PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
17889379-6	2007	Furthermore, the observations of (i) the expression of the ABC multidrug proteins in detoxifying tissues; (ii) the induction of these transporters upon exposure to an environmental organic pollutant tributyltin (TBT); and (iii) the concentration-dependent inhibition of rhodamine efflux by TBT imply a possible role of these proteins in the export of TBT.	Rhodamines	270-279	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	59-62
17939673-0	2007	Multisignaling optical-electrochemical sensor for Hg2+ based on a rhodamine derivative with a ferrocene unit.	Rhodamines	66-75	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	50-53
17912240-7	2007	In addition, ZD6474 increases the intracellular accumulation of the P-gp substrate, rhodamine-123, and ADR, by enhancing the uptake and/or decreasing the efflux of these compounds in resistant cells.	Rhodamines	84-93	ATP binding cassette subfamily B member 1	Homo sapiens	68-72
17916018-5	2007	RESULTS: Known P-gp substrate drugs ivermectin and cyclosporin A altered rhodamine efflux by 90% and 95%, respectively.	Rhodamines	73-82	PGP	Canis lupus familiaris	15-19
17917278-9	2007	At doses of 100 and 200 microM, Cap inhibited the transport of rhodamine 123 by P-gp-mediated efflux in Caco-2 cells.	Rhodamines	63-72	ATP binding cassette subfamily B member 1	Homo sapiens	80-84
17333245-3	2007	CDCA and deoxycholic acid pre-treatment for 24-96 h (100 microM) also increased Pgp activity measured as rhodamine efflux, while cholic acid and taurocholic acid were not effective in concentrations up to 600 microM.	Rhodamines	105-114	PGP	Canis lupus familiaris	80-83
17385225-3	2007	By substituting the normal bFGF with rhodamine-labeled one (Rd-bFGF), a linear increase of the absorbance versus bilayer number was recorded.	Rhodamines	37-46	fibroblast growth factor 2	Homo sapiens	27-31
17385225-3	2007	By substituting the normal bFGF with rhodamine-labeled one (Rd-bFGF), a linear increase of the absorbance versus bilayer number was recorded.	Rhodamines	37-46	fibroblast growth factor 2	Homo sapiens	63-67
17646160-8	2007	This peptide also inhibited the resonance energy transfer between membrane-bound fluorescein-labeled fVa (donor) and rhodamine-active site-labeled S360C-APC (acceptor).	Rhodamines	117-126	APC regulator of WNT signaling pathway	Homo sapiens	153-156
17705442-13	2007	Inhibition of P-gp-mediated rhodamine efflux with AOT-alginate nanoparticles was confirmed in primary brain microvessel endothelial cells.	Rhodamines	28-37	ATP binding cassette subfamily B member 1	Homo sapiens	14-18
17652134-4	2007	Using the unmodified transcript of Escherichia coli tRNAPro as an example, which has U17 and U17a in the D loop, we show that Dus1p catalyzes conversion of one of these Us (mostly U17a) to D, and that the modified tRNA can be labeled with the fluorophores proflavin and rhodamine 110, with overall labeling yields comparable to those obtained with the native yeast tRNAPhe.	Rhodamines	270-279	tRNA dihydrouridine synthase	Saccharomyces cerevisiae S288C	126-131
17893673-6	2007	Punctate Ca(v)1.3 labeling was evident throughout the IPL and around the cell bodies in the outer nuclear (ONL), inner nuclear (INL) and on somas and axons of ganglion cells labeled with rhodamine-conjugated dextran.	Rhodamines	187-196	immunoglobulin lambda variable 2-11	Homo sapiens	9-17
17701591-3	2007	Ex vivo treatment of CLL cells with HF markedly impaired the activity of P-gp, as measured by the inhibition of the capacity of the treated cells to efflux the rhodamine 123 probe.	Rhodamines	160-169	phosphoglycolate phosphatase	Homo sapiens	73-77
17591912-5	2007	Rhodamine (Rh)-labeled bFGF-NPs were injected intravitreally and visualized by confocal microscopy to determine the localization of the nanoparticles in the retina.	Rhodamines	0-9	fibroblast growth factor 2	Homo sapiens	23-27
17591912-5	2007	Rhodamine (Rh)-labeled bFGF-NPs were injected intravitreally and visualized by confocal microscopy to determine the localization of the nanoparticles in the retina.	Rhodamines	0-2	fibroblast growth factor 2	Homo sapiens	23-27
17496218-7	2007	At the medullary sites, a specific and high-intensity binding for rhodamine-ANG-(1-7) was also shown.	Rhodamines	66-75	angiogenin	Rattus norvegicus	76-84
17635801-2	2007	In this study, the activities of two members of the superfamily of ATP-binding cassette (ABC) transport proteins, ABCB1 and ABCC (measured by rhodamine 123 efflux and Fluo-3 efflux respectively), were compared in murine bone marrow cells and thymocytes of young (3-4 weeks old), adult (2-3 months old) and old (18 months old) mice.	Rhodamines	142-151	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	114-119
17635801-2	2007	In this study, the activities of two members of the superfamily of ATP-binding cassette (ABC) transport proteins, ABCB1 and ABCC (measured by rhodamine 123 efflux and Fluo-3 efflux respectively), were compared in murine bone marrow cells and thymocytes of young (3-4 weeks old), adult (2-3 months old) and old (18 months old) mice.	Rhodamines	142-151	ATP-binding cassette, sub-family A (ABC1), member 3	Mus musculus	124-128
17530763-0	2007	Highly sensitive and selective chemosensor for Hg2+ based on the rhodamine fluorophore.	Rhodamines	65-74	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	47-50
17530811-3	2007	The (PAA-Az/PAA-Alk)-coated particles were subsequently functionalized by exploiting the free alkyne click moieties present in the film upon exposure to an azide-modified rhodamine dye.	Rhodamines	171-180	ALK receptor tyrosine kinase	Homo sapiens	16-19
17337527-6	2007	By monitoring transiently expressed green fluorescent protein fused to the actin-binding domain of mouse talin, we observed the concentration of actin bundles at the cross-pollen attachment site and actin reorganization and likely depolymerization at the self-pollen attachment site; the results correspond to those obtained by rhodamine-phalloidin staining.	Rhodamines	328-337	LOW QUALITY PROTEIN: actin	Brassica rapa	75-80
17202226-6	2007	In live cells, transiently expressed SGK1-AFP clearly colocalized with the mitochondrial marker rhodamine 123.	Rhodamines	96-105	serine/threonine-protein kinase Sgk1	Oryctolagus cuniculus	37-41
17229686-7	2007	Quantification of filamentous actin (F-actin) content by using rhodamine-conjugated phalloidin and flow cytometry showed an elevated F-actin content in NSP4-EGFP-expressing and rotavirus-infected cells in comparison with that in nonexpressing and noninfected cells.	Rhodamines	63-72	serine protease 57	Homo sapiens	152-156
17398282-5	2007	FCS measurement of the fluorophore rhodamine-labeled Abeta (Rh-Abeta) shows diffusion times: 0.1 ms, 1.1 ms and 5.9 ms.	Rhodamines	35-44	amyloid beta precursor protein	Homo sapiens	53-58
17398282-5	2007	FCS measurement of the fluorophore rhodamine-labeled Abeta (Rh-Abeta) shows diffusion times: 0.1 ms, 1.1 ms and 5.9 ms.	Rhodamines	35-44	amyloid beta precursor protein	Homo sapiens	63-68
17414424-5	2007	Histaminase counteracted free radical-mediated tissue injury, as judged by a significant decrease in the plasma and tissue levels of peroxidation and nitration products (oxidized rhodamine, malondialdehyde, nitrotyrosine), DNA damage markers (8-hydroxy-2"-deoxyguanosine, poly-adenosine diphosphate-ribosylated DNA) and consumption of tissue antioxidant enzymes (superoxide dismutase).	Rhodamines	179-188	amine oxidase, copper containing 1	Rattus norvegicus	0-11
17982279-6	2007	RESULTS: Addition of cobalamin to the cells led to an increase in MS activity, to a significant decrease in mdr-1 gene expression which is correlated to an increase in retention of the Pgp substrate Rhodamine 123.	Rhodamines	199-208	ATP binding cassette subfamily B member 1	Homo sapiens	185-188
17286965-5	2007	Furthermore, C-4 treatment significantly increases in intracellular accumulation of fluorescent P-gp substrate rhodamine 123, indicating that C-4 treatment leads to reversal of the MDR phenotype resulting from an increased accumulation of anticancer drugs by inhibiting drug efflux function of P-gp.	Rhodamines	111-120	ATP binding cassette subfamily B member 1	Homo sapiens	96-100
17266731-7	2007	The drug-sensitizing effect of overexpressed loss-of-function pdr3 mutant alleles correlated with their ability to suppress PDR5 transcription and rhodamine 6G accumulation in transformants of the wild-type and Deltapdr1 mutant strains.	Rhodamines	147-156	drug-responsive transcription factor PDR3	Saccharomyces cerevisiae S288C	62-66
16990597-2	2007	We report that the rhodamine 123 (Rho 123) dye effluxing fraction of the Lin-CD34+CD38- population contains SCID-repopulating cells (SRCs) capable of long-term repopulation in primary nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice.	Rhodamines	19-28	CD34 antigen	Mus musculus	77-81
16990597-2	2007	We report that the rhodamine 123 (Rho 123) dye effluxing fraction of the Lin-CD34+CD38- population contains SCID-repopulating cells (SRCs) capable of long-term repopulation in primary nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice.	Rhodamines	19-28	CD38 antigen	Mus musculus	82-86
17727795-0	2007	Lipid excipients Peceol and Gelucire 44/14 decrease P-glycoprotein mediated efflux of rhodamine 123 partially due to modifying P-glycoprotein protein expression within Caco-2 cells.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	52-66
17727795-0	2007	Lipid excipients Peceol and Gelucire 44/14 decrease P-glycoprotein mediated efflux of rhodamine 123 partially due to modifying P-glycoprotein protein expression within Caco-2 cells.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	127-141
17078922-5	2006	Further, the rhodamine labeled Epap-1 specifically bound to gp120 expressed on the surface of HL2/3 cells during fusion reaction thereby inhibiting viral entry.	Rhodamines	13-22	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	60-65
17078922-5	2006	Further, the rhodamine labeled Epap-1 specifically bound to gp120 expressed on the surface of HL2/3 cells during fusion reaction thereby inhibiting viral entry.	Rhodamines	13-22	intelectin 2	Homo sapiens	94-97
17054045-9	2006	P. amarus derivatives were also found to be effective in inhibiting Pgp activity as assessed by rhodamine accumulation in Lucena-1 cells, as were the classical Pgp inhibitors, cyclosporine A (160 nM), PSC-833 (2 microM) and verapamil (5 microM).	Rhodamines	96-105	phosphoglycolate phosphatase	Homo sapiens	68-71
16996216-3	2006	Expression of ABCB1 mRNA and ABCB1 activity were examined in atorvastatin-treated and control cells and PBMCs using real-time PCR and Rhodamine 123 efflux assay.	Rhodamines	134-143	ATP binding cassette subfamily B member 1	Homo sapiens	14-19
17130520-5	2006	Concurrently, SGLT1 rhodamine fluorescence intensity increased with depolarizing and decreased with hyperpolarizing voltages (DeltaF).	Rhodamines	20-29	solute carrier family 5 member 1	Homo sapiens	14-19
16910657-6	2006	Confocal images proved that some ACBP-1 localized into the nucleus (as expected) and, most significantly, it could be visualized more effectively by irradiating at the donor (fluorescein-like) part of the cassette, than the acceptor (rhodamine-like) part.	Rhodamines	234-243	carboxypeptidase N subunit 2	Homo sapiens	33-37
16782851-5	2006	Rhodamine-related fluorescence could be suppressed by preincubation with a specific inhibitor of TPP-I.	Rhodamines	0-9	tripeptidyl peptidase 1	Homo sapiens	97-102
16554405-8	2006	This work reveals the usefulness of rhodamine-based Ca2+ indicators in examining the role of intramitochondrial Ca2+ in mitochondrial (patho) physiology.	Rhodamines	36-45	carbonic anhydrase 2	Homo sapiens	52-55
16554405-8	2006	This work reveals the usefulness of rhodamine-based Ca2+ indicators in examining the role of intramitochondrial Ca2+ in mitochondrial (patho) physiology.	Rhodamines	36-45	carbonic anhydrase 2	Homo sapiens	112-115
16530756-11	2006	Rhodamine uptake after treatment with verapamil was significantly greater in D407 and MDCK-MDR1, indicating functional expression of P-gp in these two cell lines.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	86-95
16926504-1	2006	Specific interaction between green fluorescent protein (GFP)-tagged human alpha- or gamma-enolase(97-242) (alpha or gammaENO(97-242)) and the rhodamine-labeled DNA fragment containing the c-myc P2 promoter was detected by a fluorescence resonance energy transfer (FRET)-based assay, designated as a "real-time FRET assay."	Rhodamines	142-151	enolase 1	Homo sapiens	74-97
16889411-4	2006	To meet this objective, we report the synthesis and characterization of two rhodamine-conjugated probes that covalently label the active site of the PTPs in an activity-dependent manner, thus providing a direct readout of PTP activity and superior sensitivity, robustness, and quantifiability to previously reported biotinylated probes.	Rhodamines	76-85	6-pyruvoyltetrahydropterin synthase	Homo sapiens	149-153
16889411-4	2006	To meet this objective, we report the synthesis and characterization of two rhodamine-conjugated probes that covalently label the active site of the PTPs in an activity-dependent manner, thus providing a direct readout of PTP activity and superior sensitivity, robustness, and quantifiability to previously reported biotinylated probes.	Rhodamines	76-85	protein tyrosine phosphatase receptor type U	Homo sapiens	149-152
16530756-11	2006	Rhodamine uptake after treatment with verapamil was significantly greater in D407 and MDCK-MDR1, indicating functional expression of P-gp in these two cell lines.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	133-137
16601691-2	2006	The myosin V was labeled with bifunctional rhodamine on one of its calmodulin light chains.	Rhodamines	43-52	myosin VA	Gallus gallus	4-12
16129693-7	2005	Fluorescence and capacitance measurements evidenced a fast translocation of rhodamine-coupled S100A1 from the extracellular space into cardiomyocytes.	Rhodamines	76-85	S100 calcium binding protein A1	Rattus norvegicus	94-100
16614073-4	2006	We have measured the 3D orientation and stepping behavior of single bifunctional rhodamine probes attached to one of the calmodulins of the light-chain domain (LCD) of myosin V as myosin V moves along actin.	Rhodamines	81-90	myosin VA	Homo sapiens	168-176
16614073-4	2006	We have measured the 3D orientation and stepping behavior of single bifunctional rhodamine probes attached to one of the calmodulins of the light-chain domain (LCD) of myosin V as myosin V moves along actin.	Rhodamines	81-90	myosin VA	Homo sapiens	180-188
16491453-2	2006	Among the active lathyrane derivatives 1 - 3, compound 2 displayed the highest inhibition of rhodamine 123 efflux of human MDR1 gene transfected mouse lymphoma cells when compared to the untreated cells or the positive control verapamil.	Rhodamines	93-102	ATP binding cassette subfamily B member 1	Homo sapiens	123-127
16319528-6	2006	Compared KBv200/MDR1sh cells with KBv200 cells, resistance to vincristine and doxorubicin decreased from 62.4-fold to 10.5-fold and from 74.5-fold to 9.5-fold respectively, and intracellular doxorubicin accumulation enhanced from 0.30 +/- 0.08 nmoles/10(6) cells to 0.86 +/- 0.16 nmoles/10(6) cells, and the fluorescence intensity of intracellular Rhodamine 123 accumulation increased from 3.58 +/- 1.63/10(6) cells to 13.96 +/- 3.07/10(6) cells.	Rhodamines	348-357	ATP binding cassette subfamily B member 1	Homo sapiens	16-20
16380642-12	2006	Association-dissociation of the myosin head was probed with rhodamine attached at cys707 of the heavy chain of myosin.	Rhodamines	60-69	myosin heavy chain 14	Homo sapiens	32-38
16380642-12	2006	Association-dissociation of the myosin head was probed with rhodamine attached at cys707 of the heavy chain of myosin.	Rhodamines	60-69	myosin heavy chain 14	Homo sapiens	111-117
16433037-3	2006	Seven benzo[a]phenoxazines were observed to increase the amount of rhodamine 123 accumulated by resistant cells, i.e. to be new effective MDR modulators.	Rhodamines	67-76	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	138-141
16234340-4	2005	The calcium mobilization resulting from ionomycin treatment of nNOS-expressing 293T cells induced a robust increase in emission intensity, as measured using a standard rhodamine filter set.	Rhodamines	168-177	nitric oxide synthase 1	Homo sapiens	63-67
16302792-0	2005	Rhodamine-labeled 2beta-carbomethoxy-3beta-(3,4-dichlorophenyl)tropane analogues as high-affinity fluorescent probes for the dopamine transporter.	Rhodamines	0-9	solute carrier family 6 member 3	Homo sapiens	125-145
16302792-3	2005	The resulting 2-substituted (5) and N-substituted (9) rhodamine-labeled ligands provided the highest DAT binding affinities expressed in COS-7 cells (Ki= 27 and 18 nM, respectively) in the series.	Rhodamines	54-63	solute carrier family 6 member 3	Homo sapiens	101-104
16124934-7	2005	P-gp function was evaluated by the difference between rhodamine 123 transport with and without verapamil.	Rhodamines	54-63	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	0-4
16229491-5	2005	By carrying out single and sequential dual fluorescence titrations of purified P-glycoprotein with the two substrates, we observed that bound LDS-751 interacted with bound rhodamine 123.	Rhodamines	172-181	ATP binding cassette subfamily B member 1	Homo sapiens	79-93
16150484-3	2005	In the present study, the expression of PAR2 and tachykinins were investigated in rat trigeminal neurons that were identified by retrograde labeling with rhodamine dye from the nasal mucosa by using neuronal tracing in combination with immunohistochemistry.	Rhodamines	154-163	F2R like trypsin receptor 1	Rattus norvegicus	40-44
16150484-7	2005	Of the rhodamine-labeled trigeminal neurons, 52.5+/-1.8% were immunoreactive for only PAR2 expression, 7.3+/-1.9% contained tachykinins and PAR2, and 3.1+/-0.4 of the rhodamine-labeled trigeminal neurons were non-immunoreactive PAR2, but were positive for tachykinins-immunoreactivity.	Rhodamines	7-16	F2R like trypsin receptor 1	Rattus norvegicus	86-90
16150484-7	2005	Of the rhodamine-labeled trigeminal neurons, 52.5+/-1.8% were immunoreactive for only PAR2 expression, 7.3+/-1.9% contained tachykinins and PAR2, and 3.1+/-0.4 of the rhodamine-labeled trigeminal neurons were non-immunoreactive PAR2, but were positive for tachykinins-immunoreactivity.	Rhodamines	7-16	F2R like trypsin receptor 1	Rattus norvegicus	140-144
16150484-7	2005	Of the rhodamine-labeled trigeminal neurons, 52.5+/-1.8% were immunoreactive for only PAR2 expression, 7.3+/-1.9% contained tachykinins and PAR2, and 3.1+/-0.4 of the rhodamine-labeled trigeminal neurons were non-immunoreactive PAR2, but were positive for tachykinins-immunoreactivity.	Rhodamines	7-16	F2R like trypsin receptor 1	Rattus norvegicus	140-144
16103191-7	2005	Intracellular accumulation of sNS1 in Huh7 cells enhanced the fluid phase uptake of rhodamine-labeled dextran.	Rhodamines	84-93	MIR7-3 host gene	Homo sapiens	38-42
15856282-3	2005	We demonstrated by using rhodamine-phalloidin staining, the localization of actin filaments on the mitotic spindles of tobacco BY-2 cells when the cells were treated with cytochalasin D.	Rhodamines	25-34	actin	Nicotiana tabacum	76-81
15963852-5	2005	Cellular efflux of the PgP substates rhodamine and doxorubicin was abolished.	Rhodamines	37-46	ATP binding cassette subfamily B member 1	Homo sapiens	23-26
15968171-6	2005	Quantitative immunohistochemistry with rhodamine-conjugated anti-OGFr antibodies revealed twofold more OGFr expression in the central and peripheral epithelium of transfected corneas relative to naive corneas.	Rhodamines	39-48	opioid growth factor receptor	Rattus norvegicus	65-69
15968171-6	2005	Quantitative immunohistochemistry with rhodamine-conjugated anti-OGFr antibodies revealed twofold more OGFr expression in the central and peripheral epithelium of transfected corneas relative to naive corneas.	Rhodamines	39-48	opioid growth factor receptor	Rattus norvegicus	103-107
15796199-3	2005	The rhodamine 123 accumulation of the P-glycoprotein (P-gp)-expressing cells increased up to 46.4, while 2,7"-bis(2-carboxyethyl)-5(6)-carboxy-fluorescein acetoxymethyl ester (BCECF-AM) accumulation of the MRP-expressing cells increased up to 1.6, in fluorescence activity ratio (FAR).	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	38-52
16241060-0	2005	[Determination of vitamin B12 concentration by fluorescence quenching with acridine orange-rhodamine 6G energy transfer system].	Rhodamines	91-100	NADH:ubiquinone oxidoreductase subunit B3	Homo sapiens	26-29
15885661-3	2005	In IL10(-/-) enterocolitis mice, rhodamine 123 efflux was reduced by two to three-fold along the small and large intestine.	Rhodamines	33-42	interleukin 10	Mus musculus	3-7
15934943-8	2005	Tat(1-72)-mediated changes in P-gp expression were correlated with increased rhodamine 123 efflux, indicating the up-regulation of transporter functions of P-gp.	Rhodamines	77-86	tyrosine aminotransferase	Mus musculus	0-3
15934943-8	2005	Tat(1-72)-mediated changes in P-gp expression were correlated with increased rhodamine 123 efflux, indicating the up-regulation of transporter functions of P-gp.	Rhodamines	77-86	phosphoglycolate phosphatase	Mus musculus	30-34
15934943-8	2005	Tat(1-72)-mediated changes in P-gp expression were correlated with increased rhodamine 123 efflux, indicating the up-regulation of transporter functions of P-gp.	Rhodamines	77-86	phosphoglycolate phosphatase	Mus musculus	156-160
15807535-8	2005	The ABCG2 (N596Q) variant is also functional, demonstrating rhodamine 123 transport in intact cells comparable to that in cells expressing glycosylated ABCG2.	Rhodamines	60-69	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	4-9
15796199-3	2005	The rhodamine 123 accumulation of the P-glycoprotein (P-gp)-expressing cells increased up to 46.4, while 2,7"-bis(2-carboxyethyl)-5(6)-carboxy-fluorescein acetoxymethyl ester (BCECF-AM) accumulation of the MRP-expressing cells increased up to 1.6, in fluorescence activity ratio (FAR).	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	54-58
15796199-3	2005	The rhodamine 123 accumulation of the P-glycoprotein (P-gp)-expressing cells increased up to 46.4, while 2,7"-bis(2-carboxyethyl)-5(6)-carboxy-fluorescein acetoxymethyl ester (BCECF-AM) accumulation of the MRP-expressing cells increased up to 1.6, in fluorescence activity ratio (FAR).	Rhodamines	4-13	ATP binding cassette subfamily C member 1	Homo sapiens	206-209
15663893-3	2005	The amount of intracellular rhodamine (Rh123) was determined, using a fluorescence spectrophotometer, to evaluate the function of P-gp.	Rhodamines	28-37	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	130-134
15490242-9	2004	Supernatant and cells collected after circulation over normal mucin showed increased rhodamine fluorescence, indicative of oxidative burst.	Rhodamines	85-94	LOC100508689	Homo sapiens	62-67
15661399-6	2005	P-gp interaction with GC was assessed by modulation of rhodamine accumulation.	Rhodamines	55-64	phosphoglycolate phosphatase	Homo sapiens	0-4
15331656-7	2005	Furthermore, it potently blocked P-glycoprotein-mediated rhodamine 123 efflux under serum-free conditions (EC(50), approximately 8 microM), however, with reduced activity at increased serum concentrations (EC(50) at 10% serum, approximately 35 microM).	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	33-47
15486081-9	2004	FL3 cells grown on GlcNAc effluxed 5.3 times as much Cdr1p substrate rhodamine 6G, over a 10 min period, as FL3 cells grown on glucose, and this rhodamine 6G efflux was inhibited by including fluconazole in the assay.	Rhodamines	69-78	cerebellar degeneration related protein 1	Homo sapiens	53-58
15486081-9	2004	FL3 cells grown on GlcNAc effluxed 5.3 times as much Cdr1p substrate rhodamine 6G, over a 10 min period, as FL3 cells grown on glucose, and this rhodamine 6G efflux was inhibited by including fluconazole in the assay.	Rhodamines	145-154	cerebellar degeneration related protein 1	Homo sapiens	53-58
15458769-9	2004	Moreover, it was found that both celecoxib and diclofenac have the potential to inhibit the function of P-glycoprotein (P-gp) in ECC using rhodamine uptake and efflux assays.	Rhodamines	139-148	phosphoglycolate phosphatase	Mus musculus	104-118
15547738-5	2004	MDR1 functional activity was performed by a rhodamine (Rhd)-123 efflux test with or without verapamil.	Rhodamines	44-53	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
15547738-5	2004	MDR1 functional activity was performed by a rhodamine (Rhd)-123 efflux test with or without verapamil.	Rhodamines	55-58	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
15458769-9	2004	Moreover, it was found that both celecoxib and diclofenac have the potential to inhibit the function of P-glycoprotein (P-gp) in ECC using rhodamine uptake and efflux assays.	Rhodamines	139-148	phosphoglycolate phosphatase	Mus musculus	120-124
15326087-6	2004	Furthermore, AVE displaced the binding of 125I-Ang-(1-7) in Mas-transfected monkey kidney cells (COS) cells (IC50=4.75x10(-8) mol/L) and of rhodamine-Ang-(1-7) in Mas-transfected Chinese hamster ovary (CHO) cells.	Rhodamines	140-149	angiogenin, ribonuclease A family, member 6	Mus musculus	150-158
15351776-1	2004	Extracts of bitter melon, soybean, dokudami and welsh onion by 40% methanol increased the accumulation of rhodamine-123 by Caco-2 cells, suggesting that these extracts inhibited P-glycoprotein (P-gp).	Rhodamines	106-115	ATP binding cassette subfamily B member 1	Homo sapiens	178-192
15351776-1	2004	Extracts of bitter melon, soybean, dokudami and welsh onion by 40% methanol increased the accumulation of rhodamine-123 by Caco-2 cells, suggesting that these extracts inhibited P-glycoprotein (P-gp).	Rhodamines	106-115	ATP binding cassette subfamily B member 1	Homo sapiens	194-198
15138133-6	2004	The rhodamine extrusion test showed that the percentage of positive cells in MDR(+) cells was significantly lower than that in MDR1(-) cells.	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	127-131
15553233-6	2004	H17 proved to be a better P-gp inhibitor than ritonavir by resulting IC50 values and also in the cellular uptake of rhodamine.	Rhodamines	116-125	H1.7 linker histone	Homo sapiens	0-3
15158445-12	2004	While Aip2p-treated F-actin in the circular form was negligibly stained by rhodamine-labeled phalloidin (rhodamine-phalloidin) in vitro, rhodamine-phalloidin staining profiles in actin interacting protein 2 gene (AIP2)-modified cells suggested a correlation between the conformation of F-actin and the expression of Aip2p in vivo.	Rhodamines	105-114	D-lactate dehydrogenase	Saccharomyces cerevisiae S288C	6-11
15158445-12	2004	While Aip2p-treated F-actin in the circular form was negligibly stained by rhodamine-labeled phalloidin (rhodamine-phalloidin) in vitro, rhodamine-phalloidin staining profiles in actin interacting protein 2 gene (AIP2)-modified cells suggested a correlation between the conformation of F-actin and the expression of Aip2p in vivo.	Rhodamines	105-114	D-lactate dehydrogenase	Saccharomyces cerevisiae S288C	6-11
15201669-2	2004	METHODS: P-gp activity was measured by rhodamine efflux in T-cell subsets from bronchoalveolar lavage (BAL) of five healthy volunteers and 27 lung allograft recipients.	Rhodamines	39-48	ATP binding cassette subfamily B member 1	Homo sapiens	9-13
15254709-8	2004	After NS-398 treatment, Western blotting showed reduced P-gp expression and a rhodamine 123 efflux assay demonstrated a significant decrease in P-gp activity.	Rhodamines	78-87	ATP binding cassette subfamily B member 1	Homo sapiens	144-148
15020090-4	2004	Another mouse monoclonal IgG (anti-SNAP25), probed with anti-mouse IgG-rhodamine without CARD amplification, selectively visualized synaptic sites, because the maximal dilution of the other monoclonal antibody (anti-calbindin) was below the detection threshold of this anti-mouse IgG-rhodamine.	Rhodamines	71-80	synaptosome associated protein 25	Rattus norvegicus	35-41
15020090-4	2004	Another mouse monoclonal IgG (anti-SNAP25), probed with anti-mouse IgG-rhodamine without CARD amplification, selectively visualized synaptic sites, because the maximal dilution of the other monoclonal antibody (anti-calbindin) was below the detection threshold of this anti-mouse IgG-rhodamine.	Rhodamines	284-293	synaptosome associated protein 25	Rattus norvegicus	35-41
15134436-7	2004	When GALA was introduced into liposomal membranes using a cholesteryl moiety for anchoring (Chol-GALA), rhodamines were efficiently released and diffused into the cytosol.	Rhodamines	104-114	galactosidase alpha	Homo sapiens	5-9
15134436-7	2004	When GALA was introduced into liposomal membranes using a cholesteryl moiety for anchoring (Chol-GALA), rhodamines were efficiently released and diffused into the cytosol.	Rhodamines	104-114	galactosidase alpha	Homo sapiens	97-101
15138133-4	2004	P-gp functions were evaluated through the rhodamine extrusion test.	Rhodamines	42-51	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
15102327-3	2004	RESULTS: Visualization of microfilaments in onion bulb scale epidermis cells by different techniques revealed that rhodamine-phalloidin stained F-actin besides cytoplasm also in the nuclei whereas GFP-mouse talin hybrid protein did not enter the nuclei.	Rhodamines	115-124	actin	Oryctolagus cuniculus	146-151
15050634-4	2004	Eight individual rhodamine labeled peptides were identified that were specific for the kappa opioid receptor, having binding affinities ranging from 5-20 nM.	Rhodamines	17-26	opioid receptor kappa 1	Homo sapiens	87-108
15175945-9	2004	Rhodamine-phalloidin staining revealed a decreased number of actin filaments in PK-1 cells treated with troglitazone.	Rhodamines	0-9	pyruvate kinase L/R	Homo sapiens	80-84
15080706-3	2004	Adsorption of bovine serum albumin (BSA) at silica/aqueous solution interfaces resulted in changes in the polarization state of the frequency-doubled light through weak, dynamic interactions with a coadsorbed nonlinear optical probe molecule (rhodamine 6G).	Rhodamines	243-252	albumin	Homo sapiens	21-34
15022031-5	2004	As the function of Pgp might be altered in advanced age, we investigated in groups of fit and frail elderly subjects whether the efflux of the Pgp-probe rhodamine 123 from CD56(+) natural killer cells was age dependent and whether it was affected by the two SNPs.	Rhodamines	153-162	ATP binding cassette subfamily B member 1	Homo sapiens	143-146
15022031-5	2004	As the function of Pgp might be altered in advanced age, we investigated in groups of fit and frail elderly subjects whether the efflux of the Pgp-probe rhodamine 123 from CD56(+) natural killer cells was age dependent and whether it was affected by the two SNPs.	Rhodamines	153-162	neural cell adhesion molecule 1	Homo sapiens	172-176
15022031-8	2004	Using flow cytometry, rhodamine fluorescence was monitored in CD56(+) cells.	Rhodamines	22-31	neural cell adhesion molecule 1	Homo sapiens	62-66
15161039-10	2004	The rhodamine uptake was increased in L5178/MDR1 and Colo320/MDR1-LRP, but not drug-sensitive human breast cancer MCF-7 and T47D, and L5178 mouse lymphoma parent cells in the presence of alis-409 and alis-421.	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	44-48
15161039-10	2004	The rhodamine uptake was increased in L5178/MDR1 and Colo320/MDR1-LRP, but not drug-sensitive human breast cancer MCF-7 and T47D, and L5178 mouse lymphoma parent cells in the presence of alis-409 and alis-421.	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	61-65
15040543-12	2004	Basal P-gp-mediated rhodamine efflux was 61.0 +/- 4.2%.	Rhodamines	20-29	ATP binding cassette subfamily B member 1	Homo sapiens	6-10
14576174-8	2004	This was further substantiated when we observed colocalization of rhodamine-labeled TSH with TSHR-YFP within the cell and by the uptake of radiolabeled TSH.	Rhodamines	66-75	thyroid stimulating hormone receptor	Homo sapiens	93-97
15197307-2	2004	Recently, we found that the wild-type Klenow fragment of Escherichia coli DNA polymerase I is well-suited for the synthesis of DNA in a reaction set-up that contains exclusively specific rhodamine-labeled analogs of the natural pyrimidine nucleotides (dCTP and dTTP).	Rhodamines	187-196	ttp	Drosophila melanogaster	261-265
15301426-8	2004	Imidazole derivatives significantly increased the Dox accumulation and inhibited P-gp function exhibited by the increase of Rhodamine accumulation in MDR cells.	Rhodamines	124-133	ATP binding cassette subfamily B member 1	Homo sapiens	81-85
14522974-0	2003	Methanethiosulfonate derivatives of rhodamine and verapamil activate human P-glycoprotein at different sites.	Rhodamines	36-45	ATP binding cassette subfamily B member 1	Homo sapiens	75-89
14522974-8	2003	The ATPase activity of MTS-rhodamine-treated mutant F343C, however, was not stimulated further by colchicine or calcein-AM.	Rhodamines	27-36	dynein axonemal heavy chain 8	Homo sapiens	4-10
14522974-9	2003	By contrast, verapamil and Hoechst 33342 stimulated and inhibited, respectively, the ATPase activity of the MTS-rhodamine-treated mutant F343C.	Rhodamines	112-121	dynein axonemal heavy chain 8	Homo sapiens	85-91
14666249-4	2003	P-glycoprotein function was assessed by the flow cytometric rhodamine 123 assay.	Rhodamines	60-69	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
12960034-5	2003	In the present study, rhodamine-labeled (Rho-) BDNF injected into the olfactory bulb was rapidly transferred to neurons in the hlDBB.	Rhodamines	22-31	brain derived neurotrophic factor	Homo sapiens	47-51
12958156-7	2003	Interestingly, up- or down-regulation of mtCLIC protein expression changes Delta(psi)m whereas the chloride channel inhibitor NPPB reduces the Delta(psi)m in mtDNA-depleted L929 cells, measured with the fluorescent probe rhodamine 123.	Rhodamines	221-230	natriuretic peptide B	Homo sapiens	126-130
12975485-6	2003	The rhodamine 123 efflux assay showed that the efflux of rhodamine 123 in K562/DXR cells, which overexpress human P-gp, could be blocked markedly by imatinib mesilate in a dose-dependent fashion.	Rhodamines	4-13	ATP binding cassette subfamily B member 1	Homo sapiens	114-118
12975485-6	2003	The rhodamine 123 efflux assay showed that the efflux of rhodamine 123 in K562/DXR cells, which overexpress human P-gp, could be blocked markedly by imatinib mesilate in a dose-dependent fashion.	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	114-118
14563317-0	2003	The endoglin(positive) sca-1(positive) rhodamine(low) phenotype defines a near-homogeneous population of long-term repopulating hematopoietic stem cells.	Rhodamines	39-48	ataxin 1	Mus musculus	23-28
12801661-6	2003	The nano-SERS fluctuation dynamics were both photo-induced and spontaneous for rhodamine 6G, but only the photo-induced component was observable for cytochrome c.	Rhodamines	79-88	seryl-tRNA synthetase 1	Homo sapiens	9-13
12944313-0	2003	Kinetic analysis of rhodamines efflux mediated by the multidrug resistance protein (MRP1).	Rhodamines	20-30	ATP binding cassette subfamily C member 1	Homo sapiens	84-88
12944313-3	2003	However, no quantitative studies of the MRP1-mediated efflux of rhodamines have, up to now, been performed.	Rhodamines	64-74	ATP binding cassette subfamily C member 1	Homo sapiens	40-44
12944313-7	2003	MRP1-mediated transport of rhodamine was glutathione-dependent.	Rhodamines	27-36	ATP binding cassette subfamily C member 1	Homo sapiens	0-4
12944313-8	2003	The kinetics parameter, k(a) = V(M)/k(m), was very similar for the four rhodamine analogs but approximately 10-fold less than the values of the same parameter determined previously for the MRP1-mediated efflux of anthracycline.	Rhodamines	72-81	ATP binding cassette subfamily C member 1	Homo sapiens	189-193
12944313-9	2003	The findings presented here are the first to show quantitative information about the kinetics parameters for MRP1-mediated efflux of rhodamine dyes.	Rhodamines	133-142	ATP binding cassette subfamily C member 1	Homo sapiens	109-113
14567628-9	2003	A good correlation between Papp and cLogD (pH 7.4) of the compounds tested was observed, except for 3-OMG, AGN 197075, and rhodamine 123, which are substrates of carrier-mediated transport systems such as P-gp and a glucose transporter (GLUT1).	Rhodamines	123-132	ATP binding cassette subfamily B member 1	Homo sapiens	205-209
14513313-5	2003	This was established by a cosedimentation assay in cell homogenates and by colocalization of the caldesmon-related immunofluorescence with the fluorescence of filamentous actin stained with rhodamine-labelled phalloidin, demonstrated in optical sections of single cells in a confocal microscope.	Rhodamines	190-199	caldesmon 1	Gallus gallus	97-106
12805654-5	2003	PCB 104 increased the oxidative stress in endothelial cells, as determined by the increased 2",7"-dichlorofluorescein (DCF) and rhodamine 123 fluorescence.	Rhodamines	128-137	pyruvate carboxylase	Homo sapiens	0-3
12896805-1	2003	The hydrophobic estradiol-derivative RU49953 inhibits the energy-dependent interaction of yeast multidrug-transporter Pdr5p with its fluorescent drug-substrate rhodamine 6G.	Rhodamines	160-169	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	118-123
14502537-7	2003	Rhodamine 123 efflux was reduced by dexloxiglumide from 4.06 (+/-0.34) to 2.84 (+/-0.15) across Caco-2 monolayers, and from 17.3 (+/-0.9) to 8.26 (+/-1.38) across MDR1-MDCK monolayers, further indicating dexloxiglumide interaction with P-gp.	Rhodamines	0-9	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	163-167
14502537-7	2003	Rhodamine 123 efflux was reduced by dexloxiglumide from 4.06 (+/-0.34) to 2.84 (+/-0.15) across Caco-2 monolayers, and from 17.3 (+/-0.9) to 8.26 (+/-1.38) across MDR1-MDCK monolayers, further indicating dexloxiglumide interaction with P-gp.	Rhodamines	0-9	phosphoglycolate phosphatase	Mus musculus	236-240
12832070-1	2003	We have used fluorescence correlation spectroscopy to analyze the interaction of GTP-tubulin with rhodamine-labeled RB3, a neural protein of the stathmin family, and to determine the kinetic pathway of the association process.	Rhodamines	98-107	stathmin 4	Homo sapiens	116-119
12832070-1	2003	We have used fluorescence correlation spectroscopy to analyze the interaction of GTP-tubulin with rhodamine-labeled RB3, a neural protein of the stathmin family, and to determine the kinetic pathway of the association process.	Rhodamines	98-107	stathmin 1	Homo sapiens	145-153
12824231-4	2003	Rhodamine-123 (Rho-123), a P-gp substrate, was used as a P-gp probe.	Rhodamines	0-9	ATP-dependent translocase ABCB1	Oryctolagus cuniculus	57-61
12626638-0	2003	Examination of the functional activity of P-glycoprotein in the rat placental barrier using rhodamine 123.	Rhodamines	92-101	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	42-56
12824231-4	2003	Rhodamine-123 (Rho-123), a P-gp substrate, was used as a P-gp probe.	Rhodamines	0-9	ATP-dependent translocase ABCB1	Oryctolagus cuniculus	27-31
12727202-5	2003	Analysis of the mitochondria within the PC-3U cells by polarography and membrane potential-sensitive dye (Rhodamine 123) confirmed that under these experimental conditions, TGF-beta1 inhibited ATP synthesis and depolarised the mitochondria.	Rhodamines	106-115	transforming growth factor beta 1	Homo sapiens	173-182
12801910-2	2003	We have characterized the self-assembly of HsRad51 by measuring the fluorescence resonance energy transfer from the fluorescein-labeled protein to the rhodamine-labeled protein.	Rhodamines	151-160	RAD51 recombinase	Homo sapiens	43-50
12657255-1	2003	Fluorescently labeled histamine H(1) receptor antagonists were synthesized starting from N-demethylmepyramine by introduction of omega-aminoalkyl chains (2-8 methylene groups in length) followed by derivatization of the terminal NH(2) group with various fluorophores (fluorescein, naphthofluorescein, rhodamine, tetramethylrhodamine, BODIPY, dansyl, and nitrobenzoxadiazole (NBD)).	Rhodamines	301-310	histamine receptor H1	Homo sapiens	22-45
12703984-13	2003	FACS analysis showed that the concentration of rhodamine 123 was much lower in CNE2/DDP cells than in CNE2 cells (12.98 vs. 243.62).	Rhodamines	47-56	translocase of inner mitochondrial membrane 8A	Homo sapiens	84-87
12432085-3	2002	Profilin-I-EGFP was distributed throughout the cytoplasm as observed previously with rhodamine-labeled profilin, while EGFP alone accumulated in the nucleus.	Rhodamines	85-94	profilin 1	Homo sapiens	0-10
12682648-0	2003	Age-related changes of P-glycoprotein-mediated rhodamine 123 efflux in normal human bone marrow hematopoietic stem cells.	Rhodamines	47-56	ATP binding cassette subfamily B member 1	Homo sapiens	23-37
12718873-2	2003	Polarized fluorescence from bifunctional rhodamine probes attached along four alpha helices of troponin C (TnC) was measured in permeabilized skeletal muscle fibers.	Rhodamines	41-50	tenascin C	Homo sapiens	107-110
12631709-4	2003	Quantitative analysis of colocalization of EGF-rhodamine conjugate and coated pits labeled with yellow-fluorescent-protein-tagged beta2 subunit of clathrin adaptor complex AP-2 revealed that EGFR mutants lacking Grb2 binding sites do not efficiently enter coated pits.	Rhodamines	47-56	epidermal growth factor receptor	Homo sapiens	191-195
12542697-0	2003	New insights into the P-glycoprotein-mediated effluxes of rhodamines.	Rhodamines	58-68	ATP binding cassette subfamily B member 1	Homo sapiens	22-36
12542697-8	2003	The kinetic parameter, ka = VM/km, which is a measure of the efficiency of the P-gp-mediated efflux of a substrate was similar for almost all the rhodamine analogues tested.	Rhodamines	146-155	ATP binding cassette subfamily B member 1	Homo sapiens	79-83
12542697-10	2003	Our conclusion is that the compounds of these two classes of molecules, anthracyclines and rhodamines, are substrates of P-gp and that their pumping rates at limiting low substrate concentration are similar.	Rhodamines	91-101	ATP binding cassette subfamily B member 1	Homo sapiens	121-125
12542697-11	2003	The findings presented here are the first to show quantitative information about the kinetic parameters for P-gp-mediated efflux of rhodamine analogues in intact cells.	Rhodamines	132-141	ATP binding cassette subfamily B member 1	Homo sapiens	108-112
12557277-3	2003	Disruption of PDH1 in a cgcdr1::ura3 strain increased susceptibility to rhodamine 6G, cycloheximide and chloramphenicol, and also increased rhodamine 6G accumulation, all properties of pdr5 null mutants.	Rhodamines	72-81	putative 2-methylcitrate dehydratase	Saccharomyces cerevisiae S288C	14-18
12557277-3	2003	Disruption of PDH1 in a cgcdr1::ura3 strain increased susceptibility to rhodamine 6G, cycloheximide and chloramphenicol, and also increased rhodamine 6G accumulation, all properties of pdr5 null mutants.	Rhodamines	140-149	putative 2-methylcitrate dehydratase	Saccharomyces cerevisiae S288C	14-18
12557277-4	2003	Overexpression of PDH1 in S. cerevisiae complemented the pdr5 mutation by reversing susceptibility to rhodamine 6G, chloramphenicol and cycloheximide, as well as by decreasing rhodamine 6G intracellular concentration.	Rhodamines	102-111	putative 2-methylcitrate dehydratase	Saccharomyces cerevisiae S288C	18-22
12557277-4	2003	Overexpression of PDH1 in S. cerevisiae complemented the pdr5 mutation by reversing susceptibility to rhodamine 6G, chloramphenicol and cycloheximide, as well as by decreasing rhodamine 6G intracellular concentration.	Rhodamines	102-111	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	57-61
12557277-4	2003	Overexpression of PDH1 in S. cerevisiae complemented the pdr5 mutation by reversing susceptibility to rhodamine 6G, chloramphenicol and cycloheximide, as well as by decreasing rhodamine 6G intracellular concentration.	Rhodamines	176-185	putative 2-methylcitrate dehydratase	Saccharomyces cerevisiae S288C	18-22
12557277-4	2003	Overexpression of PDH1 in S. cerevisiae complemented the pdr5 mutation by reversing susceptibility to rhodamine 6G, chloramphenicol and cycloheximide, as well as by decreasing rhodamine 6G intracellular concentration.	Rhodamines	176-185	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	57-61
12557277-7	2003	Abundance of PDH1 and CgCDR1 mRNA in C. glabrata was increased by rhodamine 6G, cycloheximide and oligomycin, properties in common with PDR5.	Rhodamines	66-75	putative 2-methylcitrate dehydratase	Saccharomyces cerevisiae S288C	13-17
14585326-6	2003	Nafoxidine inhibited the Pgp pump activity as measured by rhodamine 123 efflux.	Rhodamines	58-67	phosphoglycolate phosphatase	Homo sapiens	25-28
12589678-7	2003	Selective localization of fluorescein versus rhodamine fluorescene was observed within GCs following expression of NF-M conjugated to DsRed1-E5, which shifts from fluorescein to rhodamine fluorescence within hours after expression; axonal shafts contained a more even distribution of fluorescein and rhodamine fluorescence, further indicating that GCs contained relatively higher levels of the most-recently expressed subunits.	Rhodamines	178-187	neurofilament, medium polypeptide	Mus musculus	115-119
12559037-5	2003	On the contrary, rhodamine-labeled bone matrix enters transcytotic vesicles at the central ruffled border, where the vesicle budding proteins such as clathrin, AP-2 and dynamin II are also localized.	Rhodamines	17-26	transcription factor AP-2 alpha	Homo sapiens	160-164
12559037-5	2003	On the contrary, rhodamine-labeled bone matrix enters transcytotic vesicles at the central ruffled border, where the vesicle budding proteins such as clathrin, AP-2 and dynamin II are also localized.	Rhodamines	17-26	dynamin 2	Homo sapiens	169-179
12432340-15	2002	Steady-state rhodamine accumulation was increased in the presence of compounds reported to block P-glycoprotein mediated rhodamine efflux.	Rhodamines	13-22	ATP binding cassette subfamily B member 1	Homo sapiens	97-111
12374800-7	2002	The wild-type ABCG2 and its variants, R482G and R482T, showed characteristically different drug and dye transport activities; mitoxantrone and Hoechst 33342 were transported by all transporters, whereas rhodamine 123 was only pumped by the R482G and R482T mutants.	Rhodamines	203-212	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	14-19
12223492-3	2002	One class of compounds transported by P-gp is the rhodamine dyes.	Rhodamines	50-59	phosphoglycolate phosphatase	Homo sapiens	38-42
12223492-4	2002	A P-gp deletion mutant (residues 1-379 plus 681-1025) with only the TM domains retained the ability to bind rhodamine.	Rhodamines	108-117	phosphoglycolate phosphatase	Homo sapiens	2-6
12432340-15	2002	Steady-state rhodamine accumulation was increased in the presence of compounds reported to block P-glycoprotein mediated rhodamine efflux.	Rhodamines	121-130	ATP binding cassette subfamily B member 1	Homo sapiens	97-111
12373300-11	2002	In contrast to DiOC2, rhodamine 123 was not specifically effluxed by P-gp but also by MRP1.	Rhodamines	22-31	ATP binding cassette subfamily B member 1	Homo sapiens	69-73
12373300-11	2002	In contrast to DiOC2, rhodamine 123 was not specifically effluxed by P-gp but also by MRP1.	Rhodamines	22-31	ATP binding cassette subfamily C member 1	Homo sapiens	86-90
12589934-7	2002	Functional Abcb1a/Abcb1b was detected by inhibition of rhodamine efflux by these drugs and mRNA for Abcb1a and Abcb1b were detected in these cells.	Rhodamines	55-64	ATP-binding cassette, sub-family B (MDR/TAP), member 1A	Mus musculus	11-17
12417886-5	2002	Der p 1 was labeled with rhodamine.	Rhodamines	25-34	crystallin gamma F, pseudogene	Homo sapiens	4-7
12417886-7	2002	RESULTS: Rhodamine- labeled Der p 1 was demonstrated to be taken up by MD-DCs in a dose-, time-, and temperature- dependent manner.	Rhodamines	9-18	crystallin gamma F, pseudogene	Homo sapiens	32-35
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	mannose receptor C-type 1	Homo sapiens	23-39
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	mannose receptor C-type 1	Homo sapiens	41-43
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	crystallin gamma F, pseudogene	Homo sapiens	56-59
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	mannose receptor C-type 1	Homo sapiens	115-117
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	mannose receptor C-type 1	Homo sapiens	115-117
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	crystallin gamma F, pseudogene	Homo sapiens	199-202
12417886-8	2002	The involvement of the mannose receptor (MR) in the Der p 1 uptake was demonstrated by using (1) inhibitors of the MR- mediated endocytosis (mannan and blocking anti-MR mAb), which inhibited the Der p 1 uptake from 40 % to 50 %, and (2) confocal microscopy showing the colocalization of rhodamine-labeled Der p 1 with FITC-dextran.	Rhodamines	287-296	crystallin gamma F, pseudogene	Homo sapiens	199-202
12589934-7	2002	Functional Abcb1a/Abcb1b was detected by inhibition of rhodamine efflux by these drugs and mRNA for Abcb1a and Abcb1b were detected in these cells.	Rhodamines	55-64	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	18-24
12138126-8	2002	Furthermore, using rhodamine 123 efflux assay we observed a significant increase in P-gp activity in Cox-2 overexpressing renal mesangial cells.	Rhodamines	19-28	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	84-88
12138126-8	2002	Furthermore, using rhodamine 123 efflux assay we observed a significant increase in P-gp activity in Cox-2 overexpressing renal mesangial cells.	Rhodamines	19-28	prostaglandin-endoperoxide synthase 2	Rattus norvegicus	101-106
12095981-5	2002	The fixation resulted from the interaction with the reactive anchor rhodamine and allowed the quantification of cellular DP IV activity on single cells.	Rhodamines	68-77	dipeptidyl peptidase 4	Homo sapiens	121-126
12226838-0	2002	Effect of interferons on P-glycoprotein-mediated rhodamine-123 efflux in cultured rat hepatocytes.	Rhodamines	49-58	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	25-39
12095981-6	2002	The reactivity, length, and hydrophobicity of rhodamine was characterized as the decisive factor that facilitated the determination of cellular DP IV activity.	Rhodamines	46-55	dipeptidyl peptidase 4	Homo sapiens	144-149
11985312-7	2002	Nile Red and rhodamine 6G molecules prefer the environments of the porous C18 beads.	Rhodamines	13-22	Bardet-Biedl syndrome 9	Homo sapiens	74-77
12169628-5	2002	Using rhodamine-labeled LDL, it was possible to demonstrate that during endocytosis, LDL passes through SNX17-positive compartments.	Rhodamines	6-15	sorting nexin 17	Homo sapiens	104-109
12160840-0	2002	GATA transcription in a small rhodamine 123(low)CD34(+) subpopulation of a peripheral blood-derived CD34(-)CD105(+) mesenchymal cell line.	Rhodamines	30-39	glutaminyl-tRNA amidotransferase subunit QRSL1	Homo sapiens	0-4
12160840-0	2002	GATA transcription in a small rhodamine 123(low)CD34(+) subpopulation of a peripheral blood-derived CD34(-)CD105(+) mesenchymal cell line.	Rhodamines	30-39	CD34 molecule	Homo sapiens	48-52
12160840-0	2002	GATA transcription in a small rhodamine 123(low)CD34(+) subpopulation of a peripheral blood-derived CD34(-)CD105(+) mesenchymal cell line.	Rhodamines	30-39	CD34 molecule	Homo sapiens	100-104
12195825-5	2002	After Caco-2 cells were treated with 100 IU mL-1 (6.1 ng mL-1) IL2 for 24 h, a significant diminution (21%) of P-gp transporter function was observed with rhodamine-123 substrate.	Rhodamines	155-164	interleukin 2	Homo sapiens	63-66
12195825-5	2002	After Caco-2 cells were treated with 100 IU mL-1 (6.1 ng mL-1) IL2 for 24 h, a significant diminution (21%) of P-gp transporter function was observed with rhodamine-123 substrate.	Rhodamines	155-164	ATP binding cassette subfamily B member 1	Homo sapiens	111-115
12126537-8	2002	Rhodamine-123 efflux test showed that the efflux-pump function of P-gp 12 hours after the trransfection was 19.20% in control group, 25.59% in GEM5Zf (+)- MDR1 group, and 35.02% in pT7TS-MDR1 group (all P < 0.01).	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	66-70
12126537-8	2002	Rhodamine-123 efflux test showed that the efflux-pump function of P-gp 12 hours after the trransfection was 19.20% in control group, 25.59% in GEM5Zf (+)- MDR1 group, and 35.02% in pT7TS-MDR1 group (all P < 0.01).	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	155-159
12015757-14	2002	However, rhodamine efflux from CD56-positive cells was not impaired, suggesting poor in vivo Pgp inhibition.	Rhodamines	9-18	neural cell adhesion molecule 1	Homo sapiens	31-35
12091325-3	2002	In this study, we evaluated the capacity of 4,5-dibromorhodamine methyl ester (TH9402), a photosensitizer structurally similar to rhodamine, a dye transported by Pgp, and which becomes highly cytotoxic on activation with visible light to selectively deplete alloreactive T lymphocytes.	Rhodamines	55-64	ATP binding cassette subfamily B member 1	Homo sapiens	162-165
12398423-7	2002	Rhodamine-labeled chicken vinculin added to permeabilized cells preferentially localized to focal contacts in response to cyclic strain, but not a single step increase in strain.	Rhodamines	0-9	vinculin	Gallus gallus	26-34
12063025-0	2002	Myeloid-lymphoid initiating cells (ML-IC) are highly enriched in the rhodamine-c-kit(+)CD33(-)CD38(-) fraction of umbilical cord CD34(+) cells.	Rhodamines	69-78	KIT proto-oncogene, receptor tyrosine kinase	Homo sapiens	79-84
12063025-0	2002	Myeloid-lymphoid initiating cells (ML-IC) are highly enriched in the rhodamine-c-kit(+)CD33(-)CD38(-) fraction of umbilical cord CD34(+) cells.	Rhodamines	69-78	CD33 molecule	Homo sapiens	87-91
12063025-0	2002	Myeloid-lymphoid initiating cells (ML-IC) are highly enriched in the rhodamine-c-kit(+)CD33(-)CD38(-) fraction of umbilical cord CD34(+) cells.	Rhodamines	69-78	CD34 molecule	Homo sapiens	129-133
11994059-9	2002	In contrast, P-glycoprotein function was significantly decreased in CD56+ cells of the TT compared with the CC group (rhodamine fluorescence CC vs TT: 45.6+/-7.2% vs 61.1+/-12.3%, P<0.05; 95% CI on the difference 5.6, 25.5).	Rhodamines	118-127	ATP binding cassette subfamily B member 1	Homo sapiens	13-27
11864570-4	2002	We fused kinesin to gelsolin, creating a construct that severs and caps rhodamine-phalloidin actin filaments, setting exactly one kinesin molecule on one end of each fluorescent actin filament.	Rhodamines	72-81	gelsolin	Homo sapiens	20-28
11945073-10	2002	TSA accelerated and glucocorticoid blocked export of rhodamine 123, a molecule known to be exported by PGP.	Rhodamines	53-62	ATP binding cassette subfamily B member 1	Homo sapiens	103-106
11849198-12	2002	P-glycoprotein mediated drug efflux was determined as a function of rhodamine efflux in the absence and presence of ritonavir.	Rhodamines	68-77	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
11849198-19	2002	Ritonavir (5 microm) inhibited P-glycoprotein mediated efflux in both groups producing greater intracellular accumulation of rhodamine.	Rhodamines	125-134	ATP binding cassette subfamily B member 1	Homo sapiens	31-45
11559526-5	2001	A vaccinia virus expression system confirmed that rhodamine as well as doxorubicin efflux is observed with R482T or R482G but not with the wild-type R482; all three MXR/BCRP/ABCP forms transported mitoxantrone.	Rhodamines	50-59	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	165-168
11840269-4	2002	MDR-1 (but not tNGFR) expression was associated with verapamil-sensitive rhodamine efflux and resistance to killing by etoposide.	Rhodamines	73-82	malic enzyme complex, mitochondrial	Mus musculus	0-5
11717390-0	2001	Global configuration of single titin molecules observed through chain-associated rhodamine dimers.	Rhodamines	81-90	titin	Homo sapiens	31-36
11717390-1	2001	The global configuration of individual, surface-adsorbed molecules of the giant muscle protein titin, labeled with rhodamine conjugates, was followed with confocal microscopy.	Rhodamines	115-124	titin	Homo sapiens	95-100
11801536-3	2002	Previous studies have shown that pluripotent hematopoietic stem cells overexpress the multidrug-resistant transport (MDR1) gene and efflux rhodamine, a substrate for the MDR1 transporter.	Rhodamines	139-148	ATP binding cassette subfamily B member 1	Homo sapiens	117-121
11801536-3	2002	Previous studies have shown that pluripotent hematopoietic stem cells overexpress the multidrug-resistant transport (MDR1) gene and efflux rhodamine, a substrate for the MDR1 transporter.	Rhodamines	139-148	ATP binding cassette subfamily B member 1	Homo sapiens	170-174
11990784-7	2002	Furthermore, CD56+ cells obtained from patients treated with PSC 833 demonstrate enhanced rhodamine retention in an ex vivo assay after administration of the antagonist.	Rhodamines	90-99	neural cell adhesion molecule 1	Homo sapiens	13-17
11757906-3	2001	Confocal microscopy with Hsp 25-antibody and rhodamine-labeled phalloidin clearly demonstrated the co-localization of Hsp 25 and actin filaments in the ameloblast layer, supporting our hypothesis that this molecule might serve to reinforce the ameloblast layer during enamel formation as well as the formation and maintenance of the ruffled border in ruffle-ended ameloblasts.	Rhodamines	45-54	heat shock protein family B (small) member 1	Rattus norvegicus	118-124
11585750-7	2001	Confocal fluorescence microscopy of tumor cells incubated with a rhodamine conjugate of the thermally responsive ELP showed that the cytoplasm was uniformly stained below the T(t).	Rhodamines	65-74	nuclear receptor subfamily 5 group A member 1	Homo sapiens	113-116
11587212-4	2001	P-gp and MRP activity varied strongly between the cases (rhodamine 123 efflux-blocking by PSC833: 5.4+/-7.7, and carboxyfluorescein efflux-blocking by MK-571: 4.3+/-6.7, n = 60).	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
11587212-4	2001	P-gp and MRP activity varied strongly between the cases (rhodamine 123 efflux-blocking by PSC833: 5.4+/-7.7, and carboxyfluorescein efflux-blocking by MK-571: 4.3+/-6.7, n = 60).	Rhodamines	57-66	ATP binding cassette subfamily C member 1	Homo sapiens	9-12
11745237-12	2001	Ten patients studied at the MTD for PSC 833 (4 mg/kg orally every 6 hours for 8 days) had inhibition of rhodamine efflux from CD56 positive peripheral lymphocytes as a surrogate for Pgp antagonism.	Rhodamines	104-113	neural cell adhesion molecule 1	Homo sapiens	126-130
11559526-5	2001	A vaccinia virus expression system confirmed that rhodamine as well as doxorubicin efflux is observed with R482T or R482G but not with the wild-type R482; all three MXR/BCRP/ABCP forms transported mitoxantrone.	Rhodamines	50-59	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	169-173
11559526-5	2001	A vaccinia virus expression system confirmed that rhodamine as well as doxorubicin efflux is observed with R482T or R482G but not with the wild-type R482; all three MXR/BCRP/ABCP forms transported mitoxantrone.	Rhodamines	50-59	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	174-178
11502585-5	2001	SIN-1-mediated ONOO(-) formation was confirmed by monitoring the oxidation of dihydrorhodamine 123 to rhodamine.	Rhodamines	85-94	MAPK associated protein 1	Homo sapiens	0-5
11515543-8	2001	In addition, accumulation of rhodamine 6G in the cells was detected as a result of Pdr5 inhibition by FK506.	Rhodamines	29-38	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	83-87
11518803-3	2001	After 5 min, the beta-arrestin-green fluorescent protein conjugate was visible in vesicles, where it colocalized with rhodamine-labeled TRH.	Rhodamines	118-127	thyrotropin releasing hormone	Homo sapiens	136-139
11477162-6	2001	RESULTS: A decrease of intestinal rhodamine 123 transport was observed in chronic renal failure rats, pointing to an inhibition of P-glycoprotein activity.	Rhodamines	34-43	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	131-145
11477162-9	2001	CONCLUSIONS: Intestinal secretion of rhodamine 123 is mainly mediated by P-glycoprotein.	Rhodamines	37-46	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	73-87
11237063-7	2001	With a functional rhodamine retention assay using the modulator PSC833, increased MDR1 activity was observed in the -7/7q- group as compared to the control group of patients (P = 0.05).	Rhodamines	18-27	ATP binding cassette subfamily B member 1	Homo sapiens	82-86
11445244-9	2001	EP 51389 inhibited P-gp in a dose dependent manner resulting in the intracellular accumulation of rhodamine in CH(R)C5 cells.	Rhodamines	98-107	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	19-23
11428664-7	2001	In Caco-2 cells, plasma collected from CCl4-treated rats exhibited a greater inhibitory effect on P-glycoprotein-mediated transport of rhodamine 123 than that from control rats, suggesting the accumulation of an endogenous P-glycoprotein substrate/inhibitor in the plasma of diseased rats.	Rhodamines	135-144	C-C motif chemokine ligand 4	Homo sapiens	39-43
11428664-7	2001	In Caco-2 cells, plasma collected from CCl4-treated rats exhibited a greater inhibitory effect on P-glycoprotein-mediated transport of rhodamine 123 than that from control rats, suggesting the accumulation of an endogenous P-glycoprotein substrate/inhibitor in the plasma of diseased rats.	Rhodamines	135-144	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	98-112
11428664-7	2001	In Caco-2 cells, plasma collected from CCl4-treated rats exhibited a greater inhibitory effect on P-glycoprotein-mediated transport of rhodamine 123 than that from control rats, suggesting the accumulation of an endogenous P-glycoprotein substrate/inhibitor in the plasma of diseased rats.	Rhodamines	135-144	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	223-237
11389438-3	2001	Here we demonstrate for the first time that both CapZ and Tmod are dynamic on the basis of the rapid incorporation of microinjected rhodamine-labelled actin (rho-actin) at both barbed and pointed ends and from the photobleaching of green fluorescent protein (GFP)-labelled Tmod.	Rhodamines	132-141	capping actin protein of muscle Z-line subunit alpha 2	Homo sapiens	49-53
11389438-3	2001	Here we demonstrate for the first time that both CapZ and Tmod are dynamic on the basis of the rapid incorporation of microinjected rhodamine-labelled actin (rho-actin) at both barbed and pointed ends and from the photobleaching of green fluorescent protein (GFP)-labelled Tmod.	Rhodamines	132-141	tropomodulin 1	Homo sapiens	58-62
11434506-10	2001	Subjects with CC genotype revealed a significantly lower rhodamine fluorescence (i.e. higher PGP function) compared to individuals with TT genotype (51.1 +/- 11.4% versus 67.5 +/- 9.5%, p < 0.01).	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	93-96
11434506-13	2001	In summary, subjects being homozygous for C in position 3435 of the MDR1 gene have a more pronounced efflux of rhodamine from CD56+ natural killer cells and a higher MDR1 mRNA expression in leukocytes than subjects with the TT genotype.	Rhodamines	111-120	ATP binding cassette subfamily B member 1	Homo sapiens	68-72
11434506-14	2001	Measurement of rhodamine efflux using flow-cytometry from peripheral blood cells allows assessment of genetically determined differences in P-glycoprotein function.	Rhodamines	15-24	ATP binding cassette subfamily B member 1	Homo sapiens	140-154
11406763-5	2001	While interleukin-3-containing factor combinations promoted cell proliferation they caused loss of rhodamine-123 extrusion and reduced the frequencies of cobblestone area-forming cells (CAFC).	Rhodamines	99-108	interleukin 3	Homo sapiens	6-19
11877073-7	2001	Rhodamine 123 efflux showed 16% transduced cells with P-gp function.	Rhodamines	0-9	phosphoglycolate phosphatase	Homo sapiens	54-58
11347883-2	2001	The specificity of the binding was attested by the consistent displacement of bound rhodamine-labeled EGF (Rh-EGF) following addition of 1000-fold molar excess of unlabeled EGF.	Rhodamines	84-93	epidermal growth factor	Homo sapiens	102-105
11347883-2	2001	The specificity of the binding was attested by the consistent displacement of bound rhodamine-labeled EGF (Rh-EGF) following addition of 1000-fold molar excess of unlabeled EGF.	Rhodamines	84-93	epidermal growth factor	Homo sapiens	110-113
11347883-2	2001	The specificity of the binding was attested by the consistent displacement of bound rhodamine-labeled EGF (Rh-EGF) following addition of 1000-fold molar excess of unlabeled EGF.	Rhodamines	84-93	epidermal growth factor	Homo sapiens	110-113
11327879-6	2001	A direct correlation is obtained between the efficiencies of PKC effectors to inhibit energy-dependent interaction of rhodamine 6G with yeast Pdr5p, to promote intracellular drug accumulation in various multidrug resistant cells, and to chemosensitize growth of resistant cells.	Rhodamines	118-127	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	142-147
11162533-2	2001	Using fluorescence correlation spectroscopy, we have studied binding of rhodamine-labelled human C-peptide to intact human skin fibroblasts and to detergent-solubilised extracts of fibroblasts, K-562, and IEC-6 cells.	Rhodamines	72-81	insulin	Homo sapiens	97-106
11162533-3	2001	Specificity was shown by displacement of rhodamine-labelled human C-peptide with unlabelled human C-peptide.	Rhodamines	41-50	insulin	Homo sapiens	66-75
11162533-3	2001	Specificity was shown by displacement of rhodamine-labelled human C-peptide with unlabelled human C-peptide.	Rhodamines	41-50	insulin	Homo sapiens	98-107
11212278-8	2001	Accumulation and efflux studies with the P-gp substrates, [3H]daunorubicin and rhodamine 123, demonstrated that XR9576 inhibited P-gp-mediated drug efflux.	Rhodamines	79-88	phosphoglycolate phosphatase	Mus musculus	129-133
11205902-3	2001	Flavopiridol at a concentration of 10 microM was able to prevent MRP-mediated calcein efflux, whereas Pgp-mediated transport of rhodamine 123 was unaffected at flavopiridol concentrations of up to 100 microM.	Rhodamines	128-137	phosphoglycolate phosphatase	Homo sapiens	102-105
10944537-3	2000	Here the specific interaction between Tat protein, human cyclin T1, and HIV-1 TAR RNA was analyzed by fluorescence resonance energy transfer, using fluorescein-labeled TAR RNA and a rhodamine-labeled Tat protein synthesized through solid-phase chemistry.	Rhodamines	182-191	cyclin T1	Homo sapiens	57-66
10956648-8	2000	rHDL containing only acceptor probe-labeled Q132C apoA-I showed rhodamine self-quenching.	Rhodamines	64-73	apolipoprotein A1	Homo sapiens	50-56
11104578-11	2000	Finally, it is revealed that these novel taxanes have ability to inhibit the function of the P-gp efflux pump on the basis of the Rhodamine 123 assay.	Rhodamines	130-139	ATP binding cassette subfamily B member 1	Homo sapiens	93-97
10944537-3	2000	Here the specific interaction between Tat protein, human cyclin T1, and HIV-1 TAR RNA was analyzed by fluorescence resonance energy transfer, using fluorescein-labeled TAR RNA and a rhodamine-labeled Tat protein synthesized through solid-phase chemistry.	Rhodamines	182-191	RNA binding motif protein 8A	Homo sapiens	78-81
11073100-14	2000	J774 macrophages that expressed GFP-rab5a:wt showed transiently activation and recruitment of GFP-rab5a:wt to newly formed phagosomes that contained rhodamine-labeled Escherichia coli.	Rhodamines	149-158	RAB5A, member RAS oncogene family	Mus musculus	36-41
11073100-14	2000	J774 macrophages that expressed GFP-rab5a:wt showed transiently activation and recruitment of GFP-rab5a:wt to newly formed phagosomes that contained rhodamine-labeled Escherichia coli.	Rhodamines	149-158	RAB5A, member RAS oncogene family	Mus musculus	98-103
11218898-3	2000	The positive rate and function of the mdr1 gene product P-glycoprotein (P-gp) in SKOV3/mdr1 cells after mdr1-ASON (250 micrograms/ml) treatment were determined by flow cytometry and rhodamine 123 efflux trial.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	38-42
11218898-3	2000	The positive rate and function of the mdr1 gene product P-glycoprotein (P-gp) in SKOV3/mdr1 cells after mdr1-ASON (250 micrograms/ml) treatment were determined by flow cytometry and rhodamine 123 efflux trial.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	56-70
11235562-4	2000	The functional activity of mdr1 in transfected cells was examined by rhodamine retention assay.	Rhodamines	69-78	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	27-31
11218898-3	2000	The positive rate and function of the mdr1 gene product P-glycoprotein (P-gp) in SKOV3/mdr1 cells after mdr1-ASON (250 micrograms/ml) treatment were determined by flow cytometry and rhodamine 123 efflux trial.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	72-76
11218898-6	2000	Intracellular rhodamine retension in SKOV3/mdr1 cells after mdr1-ASON treatment was increased from 32.1% to 50.7% (P < 0.01).	Rhodamines	14-23	ATP binding cassette subfamily B member 1	Homo sapiens	43-47
11218898-6	2000	Intracellular rhodamine retension in SKOV3/mdr1 cells after mdr1-ASON treatment was increased from 32.1% to 50.7% (P < 0.01).	Rhodamines	14-23	ATP binding cassette subfamily B member 1	Homo sapiens	60-64
11040353-2	2000	The in vivo function of P-glycoprotein was evaluated by measuring renal secretory and biliary clearance and brain distribution of rhodamine 123 (Rho-123), a P-glycoprotein substrate, under a steady-state plasma concentration.	Rhodamines	130-139	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	24-38
10930530-0	2000	Expression, maturation, and rhodamine-based fluorescence assay of human cathepsin K expressed in CHO cells.	Rhodamines	28-37	cathepsin K	Homo sapiens	72-83
11073069-8	2000	The subcellular localization of Hsp 25-immunoreactivity in this study appeared essentially identical to that of actin filaments as demonstrated by confocal microscopy using rhodamine-labeled phalloidin.	Rhodamines	173-182	heat shock protein family B (small) member 1	Rattus norvegicus	32-38
10882736-7	2000	This internalization was strongly inhibited by hypertonic medium (0.45 m sucrose) and paralleled localization of rhodamine-labeled transferrin, suggesting that CRLR endocytosis occurred predominantly through a clathrin-dependent pathway.	Rhodamines	113-122	calcitonin receptor like receptor	Homo sapiens	160-164
10882736-9	2000	In HEK 293 cells stably expressing CRLR-GFP and Myc-RAMPs, these rhodamine-labeled RAMPs were co-localized with CRLR-GFP in the presence and absence of the ligands.	Rhodamines	65-74	calcitonin receptor like receptor	Homo sapiens	35-39
10882736-9	2000	In HEK 293 cells stably expressing CRLR-GFP and Myc-RAMPs, these rhodamine-labeled RAMPs were co-localized with CRLR-GFP in the presence and absence of the ligands.	Rhodamines	65-74	calcitonin receptor like receptor	Homo sapiens	112-116
10930530-6	2000	The intracellular activity of cathepsin K was monitored by FACS analysis using the rhodamine substrate, which demonstrated an increased fluorescence over mock-transfected cells that was also inhibitable by (2S,3S)-trans-epoxysuccinyl-L-leucylamido-3-methylbutane ethyl ester (E64d).	Rhodamines	83-92	cathepsin K	Cricetulus griseus	30-41
11129093-7	2000	P-gp activity was determined by flow cytometry with rhodamine 123 efflux.	Rhodamines	52-61	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
11004584-1	2000	Among various dyes including congo red, thioflavin S, thioflavin T, eosin, rhodamine 6G, and phenol red, the eosin was the only dye that induced self-oligomerization of alpha-synuclein in the presence of a chemical coupling reagent of N-(ethoxycarbonyl)-2-ethoxy-1, 2-dihydroquinoline.	Rhodamines	75-84	synuclein alpha	Homo sapiens	169-184
10689111-6	2000	Two color confocal microscopy performed on fixed, permeabilized cells further showed that the EGFP green fluorescence co-localized with anti-calnexin rhodamine fluorescence in the four HLA-G isoform transfectants but only in HLA-G1 transfectant was the green EGFP fluorescence also detectable at the outer part of the cells, suggesting that the HLA-G2, -G3, and G4 were retained in the endoplasmic reticulum.	Rhodamines	150-159	major histocompatibility complex, class I, G	Homo sapiens	185-190
10903136-7	2000	To confirm a direct interaction of EGF1 with APC, rhodamine was covalently attached to the alpha-N-terminus of EGF1, and binding of the labelled EGF1 to APC was directly demonstrated using FRET.	Rhodamines	50-59	G elongation factor mitochondrial 1	Homo sapiens	35-39
10903136-7	2000	To confirm a direct interaction of EGF1 with APC, rhodamine was covalently attached to the alpha-N-terminus of EGF1, and binding of the labelled EGF1 to APC was directly demonstrated using FRET.	Rhodamines	50-59	G elongation factor mitochondrial 1	Homo sapiens	111-115
10903136-7	2000	To confirm a direct interaction of EGF1 with APC, rhodamine was covalently attached to the alpha-N-terminus of EGF1, and binding of the labelled EGF1 to APC was directly demonstrated using FRET.	Rhodamines	50-59	G elongation factor mitochondrial 1	Homo sapiens	111-115
11051045-6	2000	Using rhodamine-labeled PRL, we observed specific PRL uptake by these cells that suggested the presence of a PRL receptor.	Rhodamines	6-15	prolactin	Homo sapiens	24-27
11051045-6	2000	Using rhodamine-labeled PRL, we observed specific PRL uptake by these cells that suggested the presence of a PRL receptor.	Rhodamines	6-15	prolactin	Homo sapiens	50-53
11051045-6	2000	Using rhodamine-labeled PRL, we observed specific PRL uptake by these cells that suggested the presence of a PRL receptor.	Rhodamines	6-15	prolactin receptor	Homo sapiens	109-121
10863218-5	2000	Granular staining for alpha5beta1 with fluorescein and smooth staining for fibronectin with rhodamine were seen at the periphery of the AP muscle bundles and along the distal fibers.	Rhodamines	92-101	fibronectin 1	Homo sapiens	75-86
10841772-6	2000	The extent of high-affinity binding of prenyl-flavonoids to purified Pdr5p was correlated to their efficiency to inhibit energy-dependent quenching of rhodamine 6G fluorescence catalyzed by Pdr5p-enriched plasma membranes.	Rhodamines	151-160	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	69-74
10841772-6	2000	The extent of high-affinity binding of prenyl-flavonoids to purified Pdr5p was correlated to their efficiency to inhibit energy-dependent quenching of rhodamine 6G fluorescence catalyzed by Pdr5p-enriched plasma membranes.	Rhodamines	151-160	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	190-195
11778227-4	2000	RESULTS: Transduction of mdr1 ribozyme to A549/R cells led to decrease in mdr1 mRNA and Pgp expression; increase in rhodamine accumulation.	Rhodamines	116-125	ATP binding cassette subfamily B member 1	Homo sapiens	25-29
10726660-2	2000	The oligoribonucleotide, rC11U2C7, was labeled covalently at its 5"-terminus with fluorescein and at its 3"-terminus with rhodamine to provide a substrate for RNase L.	Rhodamines	122-131	ribonuclease L	Homo sapiens	159-166
10712705-3	2000	A T1364F mutation leads to a reduction in Pdr5p-mediated azole and rhodamine 6G resistance.	Rhodamines	67-76	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	42-47
10502397-1	1999	Cultured embryonic chicken skeletal muscle cells microinjected with rhodamine (rh)-labeled actin were stained with antibodies against nebulin and connectin (titin).	Rhodamines	68-77	actin, beta	Gallus gallus	91-96
10620493-4	2000	GFP-neurabin-II labels only a subset of F-actin within these cells, as indicated by rhodamine-phalloidin staining.	Rhodamines	84-93	protein phosphatase 1, regulatory subunit 9B	Rattus norvegicus	4-15
10631002-5	2000	A rhodamine-labeled geranylgeranylated/methylated cysteine derivative is used to measure its binding to rhoGDI.	Rhodamines	2-11	Rho GDP dissociation inhibitor alpha	Homo sapiens	104-110
10585262-3	1999	These two agents inhibited the Pgp function (rhodamine-123 excretion) as well as cell-mediated cytotoxicity, confirming that Pgp is critical for NK cell-mediated cytotoxicity.	Rhodamines	45-54	ATP binding cassette subfamily B member 1	Homo sapiens	125-128
10537179-8	1999	IF microscopy of filamentous actin using rhodamine-conjugated phalloidin revealed a significant and rapid generation of both membrane ruffling and stress fibers in response to PRL, an effect inhibited by the phosphatidylinositol 3-kinase (PI3K) inhibitor LY294002.	Rhodamines	41-50	prolactin	Homo sapiens	176-179
10560911-7	1999	The effects of MIP-1alpha were inhibited by blocking antibodies to integrin alpha4, alpha5, or beta1, and polymerization plus rearrangement of F-actin were observed in affected cells by labeling with rhodamine-conjugated phalloidine.	Rhodamines	200-209	C-C motif chemokine ligand 3	Homo sapiens	15-25
10541289-7	1999	This study found: (1) PAF C-16 and analogs inhibited Pgp-mediated efflux of rhodamine 123 by 59 to 88% in multidrug-resistant KBV-1 cells and by 85 to 97% in cultured human mesangial cells.	Rhodamines	76-85	phosphoglycolate phosphatase	Homo sapiens	53-56
10523513-6	1999	Profilin-II labeled with rhodamine on cysteine at position 58 retains its affinity for actin, PIP(2) and poly-L-proline.	Rhodamines	25-34	profilin 2	Homo sapiens	0-11
10523513-6	1999	Profilin-II labeled with rhodamine on cysteine at position 58 retains its affinity for actin, PIP(2) and poly-L-proline.	Rhodamines	25-34	prolactin induced protein	Homo sapiens	94-97
10502397-1	1999	Cultured embryonic chicken skeletal muscle cells microinjected with rhodamine (rh)-labeled actin were stained with antibodies against nebulin and connectin (titin).	Rhodamines	68-70	actin, beta	Gallus gallus	91-96
10498614-3	1999	Normal CD34(+) progenitors showed rhodamine efflux in 20% to 30% of the cells, which could be blocked by verapamil.	Rhodamines	34-43	CD34 molecule	Homo sapiens	7-11
10498614-6	1999	Triggering rhodamine dull (RhoD) CD34(+) cells to proliferate indeed resulted in a higher rhodamine retention and significantly decreased efflux modulation by verapamil (P =.04).	Rhodamines	11-20	CD34 molecule	Homo sapiens	33-37
10498614-6	1999	Triggering rhodamine dull (RhoD) CD34(+) cells to proliferate indeed resulted in a higher rhodamine retention and significantly decreased efflux modulation by verapamil (P =.04).	Rhodamines	90-99	CD34 molecule	Homo sapiens	33-37
11776553-3	1999	Pgp, a product of mdr1 gene expression, and its function were detected by flow cytometry, immunohistochemistry, and rhodamine test respectively.	Rhodamines	116-125	phosphoglycolate phosphatase	Mus musculus	0-3
11776553-3	1999	Pgp, a product of mdr1 gene expression, and its function were detected by flow cytometry, immunohistochemistry, and rhodamine test respectively.	Rhodamines	116-125	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	18-22
10496651-1	1999	PURPOSE: Previous studies demonstrated that inhibition of P glycoprotein (P-gp) by Pluronic P85 (P85) block copolymer increases apical (AP) to basolateral (BL) transport of rhodamine 123 (R123) in the polarized monolayers of bovine brain microvessel endothelial cells (BBMEC) and Caco-2 cells.	Rhodamines	173-182	phosphoglycolate phosphatase	Bos taurus	58-72
10496651-1	1999	PURPOSE: Previous studies demonstrated that inhibition of P glycoprotein (P-gp) by Pluronic P85 (P85) block copolymer increases apical (AP) to basolateral (BL) transport of rhodamine 123 (R123) in the polarized monolayers of bovine brain microvessel endothelial cells (BBMEC) and Caco-2 cells.	Rhodamines	173-182	phosphoglycolate phosphatase	Bos taurus	74-78
10496651-1	1999	PURPOSE: Previous studies demonstrated that inhibition of P glycoprotein (P-gp) by Pluronic P85 (P85) block copolymer increases apical (AP) to basolateral (BL) transport of rhodamine 123 (R123) in the polarized monolayers of bovine brain microvessel endothelial cells (BBMEC) and Caco-2 cells.	Rhodamines	173-182	phosphoinositide-3-kinase regulatory subunit 2	Homo sapiens	92-95
10496651-1	1999	PURPOSE: Previous studies demonstrated that inhibition of P glycoprotein (P-gp) by Pluronic P85 (P85) block copolymer increases apical (AP) to basolateral (BL) transport of rhodamine 123 (R123) in the polarized monolayers of bovine brain microvessel endothelial cells (BBMEC) and Caco-2 cells.	Rhodamines	173-182	phosphoinositide-3-kinase regulatory subunit 2	Homo sapiens	97-100
10438534-14	1999	Overexpression of pABC11 resulted in reduced labeling with the fluorochromes 5-chloromethylfluorescein diacetate, fluorescein diacetate, and 2",7"-bis-(2-carboxyethyl)-5 (and-6)-carboxyfluorescein acetoxymethyl ester but not with calcein or rhodamine derivatives, consistent with pABC11 being an anion transporter.	Rhodamines	241-250	ATP binding cassette subfamily C member 5	Homo sapiens	18-24
10361105-5	1999	Pgp expression and function were analyzed by flow cytometric analysis of MRK 16 binding and Rhodamine 123 retention, respectively.	Rhodamines	92-101	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
10379790-10	1999	Rhodamine efflux correlated with MDR-1 mRNA expression (r = 0.87) and with the IC50s (r = 0.60) for paclitaxel in the paired cell lines.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	33-38
9972801-9	1999	Rhodamine-labeled microspheres were identified in VIP-containing nerve cell bodies of the ferret tracheal plexus.	Rhodamines	0-9	VIP peptides	Mustela putorius furo	50-53
10336475-4	1999	A rhodamine-labeled TRH analog and fluorescein-labeled transferrin co-localized in endocytic vesicles in Fq/11 cells, indicating that endocytosis took place via the normal clathrin pathway.	Rhodamines	2-11	thyrotropin releasing hormone	Mus musculus	20-23
10212205-3	1999	Fluorescence resonance energy transfer (FRET) experiments were performed in the present study to investigate structural changes that accompany complex formation between the HMG domain B of HMG1 and a cisplatin-modified, 20-base pair double-stranded DNA probe containing fluorescein and rhodamine tethered at its two ends.	Rhodamines	286-295	high mobility group box 1 pseudogene 5	Homo sapiens	189-193
10471992-6	1999	CFM revealed that rhodamine-labeled intact caldesmon and the 20-kDa caldesmon fragment bind along nearly the entire length of the thin filaments.	Rhodamines	18-27	caldesmon	Oryctolagus cuniculus	43-52
10195430-3	1999	Functional expression of Cmdr1 in both mouse NIH 3T3 and yeast cells demonstrated that Cmdr1 represents the avian ortholog of human Mdr1, since it confers resistance to several anticancer drugs and the fluorescent dye rhodamine 6G.	Rhodamines	218-227	ATP binding cassette subfamily B member 1	Gallus gallus	25-30
10195430-3	1999	Functional expression of Cmdr1 in both mouse NIH 3T3 and yeast cells demonstrated that Cmdr1 represents the avian ortholog of human Mdr1, since it confers resistance to several anticancer drugs and the fluorescent dye rhodamine 6G.	Rhodamines	218-227	ATP binding cassette subfamily B member 1	Gallus gallus	87-92
10195430-3	1999	Functional expression of Cmdr1 in both mouse NIH 3T3 and yeast cells demonstrated that Cmdr1 represents the avian ortholog of human Mdr1, since it confers resistance to several anticancer drugs and the fluorescent dye rhodamine 6G.	Rhodamines	218-227	ATP binding cassette subfamily B member 1	Homo sapiens	132-136
10195430-8	1999	Indeed, competition experiments indicated that Cmdr1 interacts with estradiol, since rhodamine 6G efflux was efficiently blocked by estradiol in NIH 3T3 cells expressing Cmdr1.	Rhodamines	85-94	ATP binding cassette subfamily B member 1	Gallus gallus	47-52
10195430-8	1999	Indeed, competition experiments indicated that Cmdr1 interacts with estradiol, since rhodamine 6G efflux was efficiently blocked by estradiol in NIH 3T3 cells expressing Cmdr1.	Rhodamines	85-94	ATP binding cassette subfamily B member 1	Gallus gallus	170-175
9858256-6	1998	The introduction of constitutively active Rac1 resulted in an increase in rhodamine-phalloidin staining, presumably from an accumulation of actin filaments in growth cones, while dominant negative Rac1 caused a decrease in rhodamine-phalloidin staining.	Rhodamines	74-83	ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)	Gallus gallus	42-46
9920827-9	1999	P-gp function was assessed in 19 patients using rhodamine-123 efflux and its inhibition by PSC.	Rhodamines	48-57	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
9920827-10	1999	The median percentage of blasts expressing P-gp was increased (49%) for leukemic cells with PSC-inhibitable rhodamine efflux compared with 17% in cases lacking PSC-inhibitable efflux (P =.004).	Rhodamines	108-117	ATP binding cassette subfamily B member 1	Homo sapiens	43-47
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 1	Homo sapiens	62-66
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 4	Homo sapiens	71-75
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 1	Homo sapiens	133-137
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 4	Homo sapiens	221-225
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 1	Homo sapiens	261-265
9891078-5	1999	Using an approach involving exchanging homologous segments of MDR1 and MDR2 and site-directed mutagenesis, we have demonstrated that MDR1 residues Q330, V331, and L332 in transmembrane domain 6 are sufficient to allow an MDR2 backbone in the N-terminal half of P-gp to transport several MDR1 substrates, including bisantrene, colchicine, vinblastine, and rhodamine-123.	Rhodamines	355-364	ATP binding cassette subfamily B member 1	Homo sapiens	133-137
10465451-4	1999	In six cases with injections restricted to the supraoptic nucleus, rhodamine-labelled microspheres were observed in a population of tyrosine hydroxylase-positive neurons located in the A15 cells below the anterior commissure (A15 dorsal) and above the optic chiasm (A15 ventral), and the dorsal and lateral periventricular A14 cell group.	Rhodamines	67-76	tetraspanin 7	Rattus norvegicus	185-188
10465451-4	1999	In six cases with injections restricted to the supraoptic nucleus, rhodamine-labelled microspheres were observed in a population of tyrosine hydroxylase-positive neurons located in the A15 cells below the anterior commissure (A15 dorsal) and above the optic chiasm (A15 ventral), and the dorsal and lateral periventricular A14 cell group.	Rhodamines	67-76	tetraspanin 7	Rattus norvegicus	226-229
10465451-4	1999	In six cases with injections restricted to the supraoptic nucleus, rhodamine-labelled microspheres were observed in a population of tyrosine hydroxylase-positive neurons located in the A15 cells below the anterior commissure (A15 dorsal) and above the optic chiasm (A15 ventral), and the dorsal and lateral periventricular A14 cell group.	Rhodamines	67-76	tetraspanin 7	Rattus norvegicus	226-229
9864175-0	1999	Efflux of rhodamine from CD56+ cells as a surrogate marker for reversal of P-glycoprotein-mediated drug efflux by PSC 833.	Rhodamines	10-19	neural cell adhesion molecule 1	Homo sapiens	25-29
9864175-0	1999	Efflux of rhodamine from CD56+ cells as a surrogate marker for reversal of P-glycoprotein-mediated drug efflux by PSC 833.	Rhodamines	10-19	ATP binding cassette subfamily B member 1	Homo sapiens	75-89
9864175-2	1999	Efflux of rhodamine from CD56(+) cells was measured before the start of PSC 833 and at varying times thereafter.	Rhodamines	10-19	neural cell adhesion molecule 1	Homo sapiens	25-29
9864175-3	1999	Patients receiving PSC 833 had decreased rhodamine efflux from their circulating CD56(+) cells.	Rhodamines	41-50	neural cell adhesion molecule 1	Homo sapiens	81-85
9864175-9	1999	We conclude that measurement of rhodamine efflux from CD56(+) cells provides a surrogate assay with the potential for monitoring Pgp antagonism in clinical trials.	Rhodamines	32-41	neural cell adhesion molecule 1	Homo sapiens	54-58
9864175-9	1999	We conclude that measurement of rhodamine efflux from CD56(+) cells provides a surrogate assay with the potential for monitoring Pgp antagonism in clinical trials.	Rhodamines	32-41	ATP binding cassette subfamily B member 1	Homo sapiens	129-132
9858256-6	1998	The introduction of constitutively active Rac1 resulted in an increase in rhodamine-phalloidin staining, presumably from an accumulation of actin filaments in growth cones, while dominant negative Rac1 caused a decrease in rhodamine-phalloidin staining.	Rhodamines	223-232	ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)	Gallus gallus	42-46
9858256-6	1998	The introduction of constitutively active Rac1 resulted in an increase in rhodamine-phalloidin staining, presumably from an accumulation of actin filaments in growth cones, while dominant negative Rac1 caused a decrease in rhodamine-phalloidin staining.	Rhodamines	223-232	ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)	Gallus gallus	197-201
9821664-8	1998	These results imply that rhodamine 123 is secreted via P-glycoprotein in renal tubules and that the renal secretory clearance of rhodamine 123 was reduced after acute renal failure, probably because of impairment of P-glycoprotein.	Rhodamines	25-34	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	55-69
9818966-8	1998	Identification of compounds showing Pdr1p, Pdr3p-dependent, but Pdr5p-, Snq2p-, and Yor1p-independent toxicity, reflected in the case of rhodamine 6G, by efflux alterations, suggests the involvement of new drug resistance genes and is a first step toward their identification.	Rhodamines	137-146	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	64-69
9818966-8	1998	Identification of compounds showing Pdr1p, Pdr3p-dependent, but Pdr5p-, Snq2p-, and Yor1p-independent toxicity, reflected in the case of rhodamine 6G, by efflux alterations, suggests the involvement of new drug resistance genes and is a first step toward their identification.	Rhodamines	137-146	ATP-binding cassette transporter SNQ2	Saccharomyces cerevisiae S288C	72-77
9818966-8	1998	Identification of compounds showing Pdr1p, Pdr3p-dependent, but Pdr5p-, Snq2p-, and Yor1p-independent toxicity, reflected in the case of rhodamine 6G, by efflux alterations, suggests the involvement of new drug resistance genes and is a first step toward their identification.	Rhodamines	137-146	ATP-binding cassette transporter YOR1	Saccharomyces cerevisiae S288C	84-89
9888602-4	1998	Using phalloidin-rhodamine labeling of actin microfilaments, we observed that VIP and ACTH strongly affect cytoskeletal organization.	Rhodamines	17-26	vasoactive intestinal peptide	Homo sapiens	78-81
9888602-4	1998	Using phalloidin-rhodamine labeling of actin microfilaments, we observed that VIP and ACTH strongly affect cytoskeletal organization.	Rhodamines	17-26	proopiomelanocortin	Homo sapiens	86-90
9453629-4	1998	Changes in the fluorescence intensity of rhodamine-phalloidin-labeled F-actin in serial optical sections of single HGF were quantified by confocal microscopy image analysis.	Rhodamines	41-50	hepatocyte growth factor	Homo sapiens	115-118
9692365-17	1998	Rhodamine-phalloidin staining of the F-actin cytoskeleton showed disruption of the cytoskeleton with radiation exposure, increased density of F-actin filaments with KGF treatment, and resistance to disruption when cells were pretreated with KGF and exposed to radiation.	Rhodamines	0-9	fibroblast growth factor 7	Homo sapiens	165-168
9692365-17	1998	Rhodamine-phalloidin staining of the F-actin cytoskeleton showed disruption of the cytoskeleton with radiation exposure, increased density of F-actin filaments with KGF treatment, and resistance to disruption when cells were pretreated with KGF and exposed to radiation.	Rhodamines	0-9	fibroblast growth factor 7	Homo sapiens	241-244
9557616-7	1998	In mobilized PB 54% of the CD34+ cells (n=5) were rhodamine dull compared to 22% in steady-state BM (P=0.014) [n=6].	Rhodamines	50-59	CD34 molecule	Homo sapiens	27-31
9450972-4	1998	Selected mutant Pdr5 transporters were analyzed with respect to their expression levels, subcellular localization, drug resistance profiles to cycloheximide, rhodamines, antifungal azoles, steroids, and sensitivity to the inhibitor FK506.	Rhodamines	158-168	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	16-20
9417083-4	1998	Time-dependent colocalization of beta2AR-GFP with rhodamine-labeled transferrin and rhodamine-labeled dextran following agonist exposure demonstrates receptor distribution to early endosomes (sequestration) and lysosomes (down-regulation), respectively.	Rhodamines	50-59	adrenoceptor beta 2	Homo sapiens	33-40
9417083-4	1998	Time-dependent colocalization of beta2AR-GFP with rhodamine-labeled transferrin and rhodamine-labeled dextran following agonist exposure demonstrates receptor distribution to early endosomes (sequestration) and lysosomes (down-regulation), respectively.	Rhodamines	50-59	transferrin	Homo sapiens	68-79
9744774-9	1998	There was no measurable decline in the fura2 free acid fluorescence in 1 h while the fluorescence due to rhodamine 123 diminished rapidly in cells overexpressing Pgp.	Rhodamines	105-114	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	162-165
9890665-6	1998	Activity of plasma membrane Pgp was examined in parental and resistant cells due to rhodamine-accumulation assay.	Rhodamines	84-93	phosphoglycolate phosphatase	Homo sapiens	28-31
9476146-2	1998	Pgp can be detected in human cancers by immunohistochemistry, RNA probes, or by functional assays utilizing transported fluorescent dyes such as rhodamine.	Rhodamines	145-154	phosphoglycolate phosphatase	Homo sapiens	0-3
9687882-5	1998	In resistant cells, MDR is characterized by overexpression of P-gp and by the enhanced efflux, and P-gp fluorescence probe, rhodamine 123 (Rh 123).	Rhodamines	124-133	ATP binding cassette subfamily B member 1	Homo sapiens	99-103
9464818-6	1997	Using two-color flow cytometry, we observed that FITC-LPS binds to My4-saturated monocytes in association with soluble (s)CD14 present in serum as revealed by staining with rhodamine-labeled My4 mAb.	Rhodamines	173-182	CD14 molecule	Homo sapiens	122-126
9706741-4	1998	We assessed the ability of myoglobin (Mb) or hemoglobin (Hb) to oxidize dihydrorhodamine (DHR) to rhodamine (RH) in the presence of O2-/H2O2 and/or NO.	Rhodamines	79-88	myoglobin	Homo sapiens	27-36
9706741-4	1998	We assessed the ability of myoglobin (Mb) or hemoglobin (Hb) to oxidize dihydrorhodamine (DHR) to rhodamine (RH) in the presence of O2-/H2O2 and/or NO.	Rhodamines	109-111	myoglobin	Homo sapiens	27-36
9436932-3	1997	P-gp expression in the myeloma cells was determined using monoclonal antibody 4E3.16 and the rhodamine 123 functional test.	Rhodamines	93-102	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
9311609-9	1997	Rhodamine efflux data, indicated by PGP overexpression, underlined the development of this MDR mechanism in the newly established breast carcinoma lines MT-1/ADR, MT-3/ADR and MaTu/ADR.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	36-39
9397986-2	1997	We tested whether genistein, a modulator of drug resistance in tumor cells, affects biliary secretion of substrates of canalicular multispecific organic anion transporter (cmoat) (glucuronides of bilirubin and rhodamine, glutathione conjugate of bromsulphthalein) and of P-glycoprotein (Pgp) (rhodamine), respectively.	Rhodamines	210-219	ATP binding cassette subfamily C member 2	Rattus norvegicus	172-177
9397986-2	1997	We tested whether genistein, a modulator of drug resistance in tumor cells, affects biliary secretion of substrates of canalicular multispecific organic anion transporter (cmoat) (glucuronides of bilirubin and rhodamine, glutathione conjugate of bromsulphthalein) and of P-glycoprotein (Pgp) (rhodamine), respectively.	Rhodamines	293-302	ATP binding cassette subfamily C member 2	Rattus norvegicus	119-170
9397986-2	1997	We tested whether genistein, a modulator of drug resistance in tumor cells, affects biliary secretion of substrates of canalicular multispecific organic anion transporter (cmoat) (glucuronides of bilirubin and rhodamine, glutathione conjugate of bromsulphthalein) and of P-glycoprotein (Pgp) (rhodamine), respectively.	Rhodamines	293-302	ATP binding cassette subfamily C member 2	Rattus norvegicus	172-177
9310367-0	1997	Efficiency of P-glycoprotein-mediated exclusion of rhodamine dyes from multidrug-resistant cells is determined by their passive transmembrane movement rate.	Rhodamines	51-60	ATP binding cassette subfamily B member 1	Homo sapiens	14-28
9393602-4	1997	Pgp status was determined by using monoclonal antibodies JSB-1 and MRK-16 and by assessment of rhodamine efflux.	Rhodamines	95-104	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
9310367-2	1997	For this purpose, seven rhodamine dyes were examined for their P-glycoprotein-mediated exclusion from MDR cells, their localization in wild-type drug-sensitive cells, their capacity to stimulate the ATPase activity of P-glycoprotein reconstituted in proteoliposomes, and their transmembrane movement rate in artificial liposomes.	Rhodamines	24-33	ATP binding cassette subfamily B member 1	Homo sapiens	218-232
9310367-5	1997	The transmembrane movement rate proved the major factor determining the efficacy of the P-glycoprotein-mediated exclusion of rhodamine dyes from MDR cells.	Rhodamines	125-134	ATP binding cassette subfamily B member 1	Homo sapiens	88-102
9322679-5	1997	P-gp activity was defined as a ratio of mean rhodamine 123 accumulation with/without verapamil.	Rhodamines	45-54	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
9240371-3	1997	When human serum albumin (HSA) coupled to rhodamine (r) was injected, it initially filled the varicosity; within seconds, however, it began to accumulate in packets and by 15 min was punctate.	Rhodamines	13-14	albumin	Homo sapiens	26-29
9145916-5	1997	The pattern of TRH receptor immunofluorescence was the same over a wide range of receptor expression in transiently transfected COS7 cells, and all cell lines bound similar amounts of 3H- and rhodamine-labeled TRH analogs, suggesting that cell-specific differences in TRH receptor localization were not simply the result of overexpression.	Rhodamines	192-201	thyrotropin releasing hormone	Homo sapiens	210-213
9205006-4	1997	We have focused our efforts of P-gp detection on flow cytometry using a dual technique of P-gp staining with antibodies for the extracellular epitope (MRK16) and a functional analysis of P-gp using the rhodamine efflux assay and the effect of P-gp inhibitors such as SDZ PSC 833.	Rhodamines	202-211	ATP binding cassette subfamily B member 1	Homo sapiens	31-35
9145916-5	1997	The pattern of TRH receptor immunofluorescence was the same over a wide range of receptor expression in transiently transfected COS7 cells, and all cell lines bound similar amounts of 3H- and rhodamine-labeled TRH analogs, suggesting that cell-specific differences in TRH receptor localization were not simply the result of overexpression.	Rhodamines	192-201	thyrotropin releasing hormone	Homo sapiens	210-213
9108417-8	1997	Multidrug resistance investigations suggest that agressive clinical findings could be related to MDR1 gene expression as confirmed by MDR1 mRNA detection, MDR1 gene product (Pgp) expression, and a functional multidrug resistance study using rhodamine efflux by flow-cytometry.	Rhodamines	241-250	ATP binding cassette subfamily B member 1	Homo sapiens	97-101
9108099-7	1997	However, both mdr1a and mdr1b P-gps contributed to the extrusion of rhodamine from hematopoietic progenitor cells, suggesting a potential role for the endogenous mdr1-type P-gps in protection of bone marrow against cytotoxic anticancer drugs.	Rhodamines	68-77	ATP-binding cassette, sub-family B (MDR/TAP), member 1A	Mus musculus	14-19
9108099-7	1997	However, both mdr1a and mdr1b P-gps contributed to the extrusion of rhodamine from hematopoietic progenitor cells, suggesting a potential role for the endogenous mdr1-type P-gps in protection of bone marrow against cytotoxic anticancer drugs.	Rhodamines	68-77	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	24-29
9108099-7	1997	However, both mdr1a and mdr1b P-gps contributed to the extrusion of rhodamine from hematopoietic progenitor cells, suggesting a potential role for the endogenous mdr1-type P-gps in protection of bone marrow against cytotoxic anticancer drugs.	Rhodamines	68-77	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	14-18
9058588-2	1997	In this study, we developed and characterized a new antagonist analogue of cholecystokinin (D-Tyr-Gly-[(Nle28,31,D-Trp30)cholecystokinin-26-32]-phen eth yl ester) that can be tagged with a fluorescent rhodamine and radioiodinated.	Rhodamines	201-210	cholecystokinin	Homo sapiens	121-136
9050789-4	1997	Using a sheep antibody to a fragment of the third intracellular loop of the 5-HT(1A)R, we localized 5-HT(1A)R immunoreactivity (ir) to IML-projecting neurons that were retrogradely labeled with rhodamine beads injected into the IML of adult male rats.	Rhodamines	194-203	5-hydroxytryptamine receptor 1A	Rattus norvegicus	76-83
9050789-4	1997	Using a sheep antibody to a fragment of the third intracellular loop of the 5-HT(1A)R, we localized 5-HT(1A)R immunoreactivity (ir) to IML-projecting neurons that were retrogradely labeled with rhodamine beads injected into the IML of adult male rats.	Rhodamines	194-203	5-hydroxytryptamine receptor 1A	Rattus norvegicus	100-107
9150713-3	1997	The intracellular rhodamine (Rh123) contents also increased in P-gp-positive blasts and K562/ADM cells with MS-209.	Rhodamines	18-27	phosphoglycolate phosphatase	Homo sapiens	63-67
9058588-2	1997	In this study, we developed and characterized a new antagonist analogue of cholecystokinin (D-Tyr-Gly-[(Nle28,31,D-Trp30)cholecystokinin-26-32]-phen eth yl ester) that can be tagged with a fluorescent rhodamine and radioiodinated.	Rhodamines	201-210	cholecystokinin	Homo sapiens	75-90
9038218-7	1997	The mutant P-glycoprotein has a decreased affinity for PSC 833 and vinblastine and a decreased ability to transport rhodamine 123.	Rhodamines	116-125	ATP binding cassette subfamily B member 1	Homo sapiens	11-25
9588823-10	1997	Treatments of bradykinin and TNF that translocated PKC also showed cytoskeletal rearrangement of rhodamine-phalloidin stained actin, causing it to become more prevalent near cell membranes and concentrated at focal points between cells.	Rhodamines	97-106	kininogen 1	Homo sapiens	14-24
9029024-3	1997	Pgp was measured in CD34+ progenitors with a rhodamine efflux assay.	Rhodamines	45-54	phosphoglycolate phosphatase	Homo sapiens	0-3
9029024-5	1997	Pgp measured by the monoclonal antibody antibody (MoAb) MRK-16 was low in the rhodamine dull, but significantly (P < 0.04) higher than in the rhodamine bright cells.	Rhodamines	78-87	phosphoglycolate phosphatase	Homo sapiens	0-3
9029024-5	1997	Pgp measured by the monoclonal antibody antibody (MoAb) MRK-16 was low in the rhodamine dull, but significantly (P < 0.04) higher than in the rhodamine bright cells.	Rhodamines	145-154	phosphoglycolate phosphatase	Homo sapiens	0-3
9588823-10	1997	Treatments of bradykinin and TNF that translocated PKC also showed cytoskeletal rearrangement of rhodamine-phalloidin stained actin, causing it to become more prevalent near cell membranes and concentrated at focal points between cells.	Rhodamines	97-106	tumor necrosis factor	Homo sapiens	29-32
9588823-10	1997	Treatments of bradykinin and TNF that translocated PKC also showed cytoskeletal rearrangement of rhodamine-phalloidin stained actin, causing it to become more prevalent near cell membranes and concentrated at focal points between cells.	Rhodamines	97-106	protein kinase C alpha	Homo sapiens	51-54
8968602-0	1996	Fluorescence polarization of skeletal muscle fibers labeled with rhodamine isomers on the myosin heavy chain.	Rhodamines	65-74	PBV1SPCR2	Oryctolagus cuniculus	90-108
9013725-8	1997	Codistribution of merlin and F-actin filaments was found in filopodia, ruffling membranes and at the insertion points of stress fibers at cell/substrate adhesion junctions as shown by phalloidin-rhodamine staining.	Rhodamines	195-204	NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor	Homo sapiens	18-24
8977240-9	1996	The ability of Tpo and SCF to synergistically enhance the growth of Lin- Sca-1+ progenitors was predominantly observed in the more primitive rhodamine 123(lo) fraction.	Rhodamines	141-150	thrombopoietin	Mus musculus	15-18
8977240-9	1996	The ability of Tpo and SCF to synergistically enhance the growth of Lin- Sca-1+ progenitors was predominantly observed in the more primitive rhodamine 123(lo) fraction.	Rhodamines	141-150	kit ligand	Mus musculus	23-26
8977240-9	1996	The ability of Tpo and SCF to synergistically enhance the growth of Lin- Sca-1+ progenitors was predominantly observed in the more primitive rhodamine 123(lo) fraction.	Rhodamines	141-150	ataxin 1	Mus musculus	73-78
8940170-5	1996	Pdr5p extrudes rhodamines 6G and 123, from intact yeast cells in an energy-dependent manner.	Rhodamines	15-25	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	0-5
9350197-9	1997	A reliable way to measure Pgp seems to be the assessment of the active transport of fluorescent Pgp substrates, such as rhodamine 123 out of AML cells.	Rhodamines	120-129	ATP binding cassette subfamily B member 1	Homo sapiens	26-29
8939917-4	1996	Treatment with TNF and ActD resulted in the loss of 80% of rhodamine fluorescence within 6 h, a time prior to any loss of viability.	Rhodamines	59-68	tumor necrosis factor	Homo sapiens	15-18
8980395-0	1996	Acceleration of MRP-associated efflux of rhodamine 123 by genistein and related compounds.	Rhodamines	41-50	ATP binding cassette subfamily C member 1	Homo sapiens	16-19
8939917-6	1996	Potentiation of the cytotoxicity of TNF by PBzR agonists was associated with induction of the MPT, as assessed by the loss of rhodamine fluorescence.	Rhodamines	126-135	tumor necrosis factor	Homo sapiens	36-39
8781417-9	1996	In stroma-free cultures, TPO activated a quiescent CD34+Lin-Rhodamine 123lo subset of primitive hematopoietic progenitor cells into cycle, without loss of CD34 expression.	Rhodamines	60-69	CD34 molecule	Homo sapiens	51-55
8945621-6	1996	The presence of exogenous adenosine (0.5 microM) circumvented AMP-CP-induced inhibition of rhodamine efflux from EL4/ADM cells.	Rhodamines	91-100	epilepsy 4	Mus musculus	113-116
8925885-4	1996	N-terminal modification of Tat with rhodamine prevented inhibition of enzymatic activity of DP IV as well as suppression of DNA synthesis of mitogen-stimulated human T cells.	Rhodamines	36-45	tyrosine aminotransferase	Homo sapiens	27-30
8695847-4	1996	The efflux of Rh123 could be inhibited by verapamil, suggesting that rhodamine efflux from primitive hematopoietic cells is primarily due to the P-glycoprotein (P-gp) pump or another intracellular transport system affected by verapamil.	Rhodamines	69-78	ATP binding cassette subfamily B member 1	Homo sapiens	145-159
8695847-4	1996	The efflux of Rh123 could be inhibited by verapamil, suggesting that rhodamine efflux from primitive hematopoietic cells is primarily due to the P-glycoprotein (P-gp) pump or another intracellular transport system affected by verapamil.	Rhodamines	69-78	ATP binding cassette subfamily B member 1	Homo sapiens	161-165
8913436-5	1996	Mifepristone, when used at a 10 microM concentration thought to be achievable in vivo without major toxicity, was also able to markedly decrease cellular rhodamine 123 efflux occurring in CD34+ blast cells isolated from six patients suffering from myeloid acute leukemias.	Rhodamines	154-163	CD34 molecule	Homo sapiens	188-192
8913319-3	1996	However, accumulation of daunorubicin and rhodamine 123 was > 85% reduced in the P-glycoprotein-expressing subline compared to 40-50% in the MRP-expressing subline.	Rhodamines	42-51	ATP binding cassette subfamily B member 1	Homo sapiens	84-98
8650203-5	1996	Most importantly, reserpine and doxorubicin completely abolish Mdr1-mediated rhodamine resistance.	Rhodamines	77-86	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	63-67
8624264-8	1996	Staurosporine and CGP 41251 at 10 and 20 nM, respectively, decreased efflux of the P-gp probe rhodamine 123 (R123) from MCF-7/Adr cells, whereas RO 31 8220 and GF 109203X at 640 nM were inactive.	Rhodamines	94-103	ATP binding cassette subfamily B member 1	Homo sapiens	83-87
8605330-4	1996	The most purified rhodamine-bright bone marrow subset contains 80% cells that respond to calcium ionophore by increased HDC mRNA expression.	Rhodamines	18-27	histidine decarboxylase	Mus musculus	120-123
8605969-8	1996	In contrast, a high percentage of the Sca-1+Lin*- cells isolated from 14.5-day-old FL stained with the AA4.1, anti-Mac-1, and the anti-CD45RB mAbs and retained Rhodamine 123 (Rh123(bright)), whereas the Sca-1+Lin-WGA+ CRU-containing fraction of adult BM cells was found to be AA4.1-, Mac-1-, CD45RB-, and Rh123(dull).	Rhodamines	160-169	lymphocyte antigen 6 complex, locus A	Mus musculus	38-43
9350197-9	1997	A reliable way to measure Pgp seems to be the assessment of the active transport of fluorescent Pgp substrates, such as rhodamine 123 out of AML cells.	Rhodamines	120-129	ATP binding cassette subfamily B member 1	Homo sapiens	96-99
8695847-2	1996	Heterogeneous rhodamine staining is seen within the CD34+ population, and the staining patterns differ dramatically between fetal BM (FBM), adult BM (ABM) and mobilized peripheral blood (MPB).	Rhodamines	14-23	CD34 molecule	Homo sapiens	52-56
8837723-12	1996	To demonstrate that both the antibody and drug localized in the same group of prostatic epithelial cells, we used an immunoconjugate in which the PSA-IgG was labeled with rhodamine and 5"-Fu-2"-d-5"-amp with FITC.	Rhodamines	171-180	aminopeptidase puromycin sensitive	Homo sapiens	146-149
8757962-5	1996	Anti-ICAM-1 pretreatment inhibited the increase in ICAM-1 expression and the decrease in rhodamine 123 fluorescence on AH70 cells after co-culture with KC.	Rhodamines	89-98	intercellular adhesion molecule 1	Rattus norvegicus	5-11
8766007-10	1996	A third parameter influencing the interaction with the choline+ transporter is the presence of two amino groups with high pKa values or one amino group and a permanent positive charge, as is documented with the two-ring aminostyryl and rhodamine compounds, as well as three-ring aminoacridine, aminophenanthrene and cyanine compounds.	Rhodamines	236-245	solute carrier family 6 member 8	Rattus norvegicus	55-75
8925885-4	1996	N-terminal modification of Tat with rhodamine prevented inhibition of enzymatic activity of DP IV as well as suppression of DNA synthesis of mitogen-stimulated human T cells.	Rhodamines	36-45	dipeptidyl peptidase 4	Homo sapiens	92-97
8616825-7	1996	Moreover we could correlate MDR1 gene expression and modulation of rhodamine 123 efflux from the leukaemic blasts by proven P-gp MDR chemosensitizing agents such as SDZ PSC 833, dexverapamil and dexniguldipine.	Rhodamines	67-76	phosphoglycolate phosphatase	Homo sapiens	124-128
8668925-3	1996	Rhodamine 123 dye efflux measures P-glycoprotein activity and inhibition of P-glycoprotein results in dye retention.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	34-48
8668925-3	1996	Rhodamine 123 dye efflux measures P-glycoprotein activity and inhibition of P-glycoprotein results in dye retention.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	76-90
8562416-4	1996	Pgp functional activity was investigated by evaluation of verapamil influence upon rhodamine 123 efflux from the cells.	Rhodamines	83-92	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
8872748-3	1996	The active enzymes on the cell surfaces in frozen sections of human colonic carcinoma tissue were located by staining with two active site directed fluorescent inhibitors, 9-aminoacridine (9-AA) and Rhodamine labelled PAI-1 (Rh-PAI-1), followed by fluorescence microscopy.	Rhodamines	199-208	serpin family E member 1	Homo sapiens	218-223
7587721-0	1995	Flow cytometric determination of aminopeptidase activities in viable cells using fluorogenic rhodamine 110 substrates.	Rhodamines	93-102	carboxypeptidase Q	Homo sapiens	33-47
7564516-3	1995	P-gp function was measured by rhodamine 123 (Rh 123) efflux kinetics.	Rhodamines	30-39	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
7669666-1	1995	The MDR1 gene product P-glycoprotein (P-gp) extrudes several anticancer drugs including taxol and fluorescent dyes such as rhodamine (Rh123).	Rhodamines	123-132	ATP binding cassette subfamily B member 1	Homo sapiens	4-8
7669666-1	1995	The MDR1 gene product P-glycoprotein (P-gp) extrudes several anticancer drugs including taxol and fluorescent dyes such as rhodamine (Rh123).	Rhodamines	123-132	ATP binding cassette subfamily B member 1	Homo sapiens	22-36
7669666-1	1995	The MDR1 gene product P-glycoprotein (P-gp) extrudes several anticancer drugs including taxol and fluorescent dyes such as rhodamine (Rh123).	Rhodamines	123-132	ATP binding cassette subfamily B member 1	Homo sapiens	38-42
8522584-7	1995	Scanning electron microscopy and rhodamine-phalloidin staining indicates that the myosin I double mutants appear to extend a larger number of actin-filled structures, such as filopodia and crowns, than wild-type cells.	Rhodamines	33-42	myosin heavy chain 14	Homo sapiens	82-88
8522588-2	1995	To characterize the regions of CP190 responsible for its dynamic behavior, we injected rhodamine-labeled fusion proteins spanning most of CP190 into early Drosophila embryos, where their localizations were characterized using time-lapse fluorescence confocal microscopy.	Rhodamines	87-96	Centrosomal protein 190kD	Drosophila melanogaster	31-36
8586652-3	1995	These results indicate that nebulin inhibits rhodamine-phalloidin binding to actin and suggests that the unidirectional rhodamine-phalloidin binding may be due to cooperative competitive binding, i.e. phalloidin "unzips" nebulin starting from the pointed ends of the thin filaments.	Rhodamines	45-54	nebulin	Homo sapiens	28-35
7677179-9	1995	Dual labeling experiments using biotinylated fibrinogen and FITC-streptavidin as well as a monoclonal anti-GPIIIa antibody labeled with rhodamine-conjugated anti-mouse IgG demonstrated the co-localization of fibrinogen and GPIIIa.	Rhodamines	136-145	integrin subunit beta 3	Homo sapiens	107-113
7677179-9	1995	Dual labeling experiments using biotinylated fibrinogen and FITC-streptavidin as well as a monoclonal anti-GPIIIa antibody labeled with rhodamine-conjugated anti-mouse IgG demonstrated the co-localization of fibrinogen and GPIIIa.	Rhodamines	136-145	fibrinogen beta chain	Homo sapiens	208-218
7677179-9	1995	Dual labeling experiments using biotinylated fibrinogen and FITC-streptavidin as well as a monoclonal anti-GPIIIa antibody labeled with rhodamine-conjugated anti-mouse IgG demonstrated the co-localization of fibrinogen and GPIIIa.	Rhodamines	136-145	integrin subunit beta 3	Homo sapiens	223-229
7795216-10	1995	P-glycoprotein function in host marrow was confirmed by rhodamine-123 efflux.	Rhodamines	56-65	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
7477881-6	1995	In further experiments, rhodamine-conjugated latex microspheres were injected into the supraoptic nucleus to retrogradely label afferent neurons, and the brains were processed with double-immunohistochemistry for tyrosine hydroxylase and Fos-like protein.	Rhodamines	24-33	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	238-241
7552989-6	1995	Rhodamine efflux studies showed that this additional p-glycoprotein was functional and that the frequency of cells with high p-glycoprotein levels was higher in the transduced cells than in the non-transduced cells.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	53-67
7552989-6	1995	Rhodamine efflux studies showed that this additional p-glycoprotein was functional and that the frequency of cells with high p-glycoprotein levels was higher in the transduced cells than in the non-transduced cells.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	125-139
7643452-2	1995	Functional P-gp expression was examined by Rhodamine-123 efflux test, and estimated with the data by RT-PCR method.	Rhodamines	43-52	ATP binding cassette subfamily B member 1	Homo sapiens	11-15
7559918-7	1995	In contrast, CsA and PSC were more potent as inhibitors of P-gp-mediated rhodamine 123 dye efflux than the verapamil isomers.	Rhodamines	73-82	ATP binding cassette subfamily B member 1	Homo sapiens	59-63
7473775-5	1995	Fibroblasts, visualized after staining with rhodamine-labeled alpha 2-macroglobulin, were only rarely detected.	Rhodamines	44-53	alpha-2-macroglobulin	Rattus norvegicus	62-83
7507731-10	1994	Flow cytometric analysis of rhodamine 123 dye efflux indicated a functional P-gp that was efficiently blocked by verapamil or cyclosporin A (CsA).	Rhodamines	28-37	phosphoglycolate phosphatase	Homo sapiens	76-80
7787113-1	1995	Structural changes of the myosin heads were correlated with mechanical events in the cross-bridge cycle by measuring fluorescence polarization signals at high time resolution from rhodamine probes bound to myosin regulatory light chains in skeletal muscle fibers.	Rhodamines	180-189	myosin heavy chain 14	Homo sapiens	26-32
7787113-1	1995	Structural changes of the myosin heads were correlated with mechanical events in the cross-bridge cycle by measuring fluorescence polarization signals at high time resolution from rhodamine probes bound to myosin regulatory light chains in skeletal muscle fibers.	Rhodamines	180-189	myosin heavy chain 14	Homo sapiens	206-212
7895783-6	1995	IgE and IL-3 responder cells also cannot be distinguished on the basis of size, internal structure, and rhodamine (Rh) retention.	Rhodamines	115-117	interleukin 3	Mus musculus	8-12
7831321-1	1995	Endocytosis and recycling of both thyrotropin-releasing hormone (TRH) and its G-protein-coupled receptor were visualized by conventional and confocal fluorescence microscopy in pituitary cells using a rhodamine-labeled TRH analog (Rhod-TRH) and indirect immunofluorescent staining of cells stably transfected with an epitope-tagged TRH receptor (TRHR).	Rhodamines	201-210	thyrotropin releasing hormone	Homo sapiens	34-63
7831321-1	1995	Endocytosis and recycling of both thyrotropin-releasing hormone (TRH) and its G-protein-coupled receptor were visualized by conventional and confocal fluorescence microscopy in pituitary cells using a rhodamine-labeled TRH analog (Rhod-TRH) and indirect immunofluorescent staining of cells stably transfected with an epitope-tagged TRH receptor (TRHR).	Rhodamines	201-210	thyrotropin releasing hormone	Homo sapiens	65-68
7831321-1	1995	Endocytosis and recycling of both thyrotropin-releasing hormone (TRH) and its G-protein-coupled receptor were visualized by conventional and confocal fluorescence microscopy in pituitary cells using a rhodamine-labeled TRH analog (Rhod-TRH) and indirect immunofluorescent staining of cells stably transfected with an epitope-tagged TRH receptor (TRHR).	Rhodamines	201-210	thyrotropin releasing hormone	Homo sapiens	219-222
7831321-1	1995	Endocytosis and recycling of both thyrotropin-releasing hormone (TRH) and its G-protein-coupled receptor were visualized by conventional and confocal fluorescence microscopy in pituitary cells using a rhodamine-labeled TRH analog (Rhod-TRH) and indirect immunofluorescent staining of cells stably transfected with an epitope-tagged TRH receptor (TRHR).	Rhodamines	201-210	thyrotropin releasing hormone	Homo sapiens	219-222
7850770-6	1995	GC3/c1 cells after carbonyl cyanide-m-chlorophenylhydrazone rapidly lost rhodamine 123 fluorescence from mitochondria; after 1 mM sulofenur, fluorescence faded slowly.	Rhodamines	73-82	ankyrin repeat domain 36	Mus musculus	0-3
7733620-0	1995	Rhodamine 123: is it an appropriate dye to study P-glycoprotein activity in adriamycin-resistant K562 cells?	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	49-63
7733620-5	1995	Thus, in adriamycin-resistant K562 cells, the rhodamine efflux may be due to P-glycoprotein activity and also to a nonspecific targeting of dye in resistant K562 cells.	Rhodamines	46-55	ATP binding cassette subfamily B member 1	Homo sapiens	77-91
7553917-10	1995	PtK2 cells transfected with this RSV vector for 2-3 days showed disassembly of stress fibers as detected by rhodamine-phalloidin staining; in these cells the membrane actin was also greatly diminished or absent and the border of the cells was markedly retracted.	Rhodamines	108-117	protein tyrosine kinase 2	Homo sapiens	0-4
7727866-6	1994	The detection of functional GP170 can be identified by rhodamine or daunorubicin intracellular accumulation with flux cytometry or by scintigraphically imaging GP170 expression in vivo with Tc-Sestamibi.	Rhodamines	55-64	ATP binding cassette subfamily B member 1	Homo sapiens	28-33
7865127-3	1994	Rhodamine retrograde-prelabelled DA neurons were cultured on a Phastgel containing all the electrophoretically separated protein bands from CPe, and able to fish out from it their own trophic factor, a 12.5-kD protein band.	Rhodamines	0-9	carboxypeptidase E	Rattus norvegicus	140-143
7980629-4	1994	P-glycoprotein was functional in terms of rhodamine dye excretion and its susceptibility to the MDR-reversing agents.	Rhodamines	42-51	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
7513198-8	1994	P-gly function was determined for each lineage using dual-labeling for lineage and P-gly substrate (rhodamine 123).	Rhodamines	100-109	ATP binding cassette subfamily B member 1	Homo sapiens	0-5
7513198-8	1994	P-gly function was determined for each lineage using dual-labeling for lineage and P-gly substrate (rhodamine 123).	Rhodamines	100-109	ATP binding cassette subfamily B member 1	Homo sapiens	83-88
7513198-13	1994	We conclude that (1) P-gly and the MDR1 mRNA are expressed in normal leukocytes, (2) this P-gly expression is lineage specific with relatively high levels among CD56+ cells, and (3) the expression of P-gly in granulocytes is not associated with transport of the P-gly substrate, rhodamine 123, out of the cell.	Rhodamines	279-288	ATP binding cassette subfamily B member 1	Homo sapiens	21-26
7513198-13	1994	We conclude that (1) P-gly and the MDR1 mRNA are expressed in normal leukocytes, (2) this P-gly expression is lineage specific with relatively high levels among CD56+ cells, and (3) the expression of P-gly in granulocytes is not associated with transport of the P-gly substrate, rhodamine 123, out of the cell.	Rhodamines	279-288	ATP binding cassette subfamily B member 1	Homo sapiens	35-39
7513198-13	1994	We conclude that (1) P-gly and the MDR1 mRNA are expressed in normal leukocytes, (2) this P-gly expression is lineage specific with relatively high levels among CD56+ cells, and (3) the expression of P-gly in granulocytes is not associated with transport of the P-gly substrate, rhodamine 123, out of the cell.	Rhodamines	279-288	ATP binding cassette subfamily B member 1	Homo sapiens	90-95
7513198-13	1994	We conclude that (1) P-gly and the MDR1 mRNA are expressed in normal leukocytes, (2) this P-gly expression is lineage specific with relatively high levels among CD56+ cells, and (3) the expression of P-gly in granulocytes is not associated with transport of the P-gly substrate, rhodamine 123, out of the cell.	Rhodamines	279-288	ATP binding cassette subfamily B member 1	Homo sapiens	90-95
7513198-13	1994	We conclude that (1) P-gly and the MDR1 mRNA are expressed in normal leukocytes, (2) this P-gly expression is lineage specific with relatively high levels among CD56+ cells, and (3) the expression of P-gly in granulocytes is not associated with transport of the P-gly substrate, rhodamine 123, out of the cell.	Rhodamines	279-288	ATP binding cassette subfamily B member 1	Homo sapiens	90-95
7929637-5	1994	Rhodamine-labeled Fab fragments against a cytoplasmic epitope of ts-O45-G (rh-P5D4-Fabs) were microinjected into cells to visualize the intracellular viral membrane protein and to determine its mobility by FRAP with a confocal microscope.	Rhodamines	0-9	FA complementation group B	Homo sapiens	18-21
7912496-0	1994	Inhibition of rhodamine 123 secretion by cyclosporin A as a model of P-glycoprotein mediated transport in liver.	Rhodamines	14-23	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	69-83
7912496-4	1994	Both cyclosporin A and rhodamine inhibited photoaffinity labeling of immunoprecipitated P-glycoprotein with azidopine, indicating binding to hepatic P-glycoprotein.	Rhodamines	23-32	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	88-102
7912496-4	1994	Both cyclosporin A and rhodamine inhibited photoaffinity labeling of immunoprecipitated P-glycoprotein with azidopine, indicating binding to hepatic P-glycoprotein.	Rhodamines	23-32	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	149-163
7508469-3	1994	Out of six tested alkaline phosphatase activity-revealing methods, only the reaction product obtained with the Becton Dickinson CAS Red kit showed an intense red fluorescence with a rhodamine filter set and no signal with epi-polarization illumination.	Rhodamines	182-191	BCAR1 scaffold protein, Cas family member	Homo sapiens	128-131
8527682-5	1995	The system is tested on rhodamine-alpha-bungarotoxin-labeled acetylcholine receptors (AChRs) on myotubes grown in primary cultures of embryonic rat muscle, in both endogenously clustered and nonclustered regions of AChR distribution.	Rhodamines	24-33	cholinergic receptor nicotinic alpha 2 subunit	Rattus norvegicus	86-90
7540097-6	1995	To examine direct effects of PAF antagonists on toxin A in T-84 epithelial cell monolayers, rhodamine-labeled phalloidin stained F-actin demonstrated significant disruption of F-actin by toxin A that was reduced by the PAF antagonist BN 52021 or WEB 2170.	Rhodamines	92-101	PCNA clamp associated factor	Homo sapiens	219-222
7872688-7	1994	It was concluded that MRK16 and rhodamine 123 were well adapted to detect P-gp and evaluate its functional ability.	Rhodamines	32-41	ATP binding cassette subfamily B member 1	Homo sapiens	74-78
7969041-0	1994	Rhodamine efflux patterns predict P-glycoprotein substrates in the National Cancer Institute drug screen.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	34-48
7969041-4	1994	There was a significant correlation between mdr-1 expression and rhodamine efflux in the 58 cell lines (r = 0.788, p = 0.0001).	Rhodamines	65-74	ATP binding cassette subfamily B member 1	Homo sapiens	44-49
7847840-5	1994	This indicates that the rhodamine efflux is a more function-related marker for MDR than the mdr1 gene and the pgp.	Rhodamines	24-33	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	92-96
7847840-5	1994	This indicates that the rhodamine efflux is a more function-related marker for MDR than the mdr1 gene and the pgp.	Rhodamines	24-33	phosphoglycolate phosphatase	Mus musculus	110-113
8041795-4	1994	Fos-(118-211) and Jun-(225-334) polypeptides were labeled with either 5-iodoacetamidofluorescein or rhodamine X iodoacetamide on unique cysteine residues located in their DNA binding domains.	Rhodamines	100-109	Fos proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	0-3
8195695-6	1994	FACS analysis of rhodamine-phalloidin-stained MDMs showed that after incubation with IL-1 beta, but not TNF-alpha, the content of F-actin declined in MDMs, coinciding with inhibition of particle phagocytosis.	Rhodamines	17-26	interleukin 1 beta	Homo sapiens	85-94
7910786-4	1994	P-gp-mediated rhodamine 123 efflux from dye-loaded single-cell suspensions of HCT-8 cells as measured by flow cytometry was not impeded at pHo 6.8 in comparison with pHo 7.5 in standard medium, but at low pHo the inhibitory activity of R-VPL (29% vs 60% rhodamine 123 efflux inhibition) was diminished significantly, again without a reduction in the effect of PSC 833 (rhodamine 123 flux inhibition, 75%).	Rhodamines	14-23	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
7910786-4	1994	P-gp-mediated rhodamine 123 efflux from dye-loaded single-cell suspensions of HCT-8 cells as measured by flow cytometry was not impeded at pHo 6.8 in comparison with pHo 7.5 in standard medium, but at low pHo the inhibitory activity of R-VPL (29% vs 60% rhodamine 123 efflux inhibition) was diminished significantly, again without a reduction in the effect of PSC 833 (rhodamine 123 flux inhibition, 75%).	Rhodamines	254-263	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
7910786-4	1994	P-gp-mediated rhodamine 123 efflux from dye-loaded single-cell suspensions of HCT-8 cells as measured by flow cytometry was not impeded at pHo 6.8 in comparison with pHo 7.5 in standard medium, but at low pHo the inhibitory activity of R-VPL (29% vs 60% rhodamine 123 efflux inhibition) was diminished significantly, again without a reduction in the effect of PSC 833 (rhodamine 123 flux inhibition, 75%).	Rhodamines	254-263	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
8443378-4	1993	Starting from these findings, we further characterized the immature hematopoietic compartment responsible for IL-3-induced histamine synthesis using fluorescence-activated cell sorter (FACS) sorting based on rhodamine retention or wheat germ agglutinin (WGA) affinity.	Rhodamines	208-217	interleukin 3	Mus musculus	110-114
7912496-5	1994	Our results indicate that monitoring the biliary rhodamine 123 secretion in the isolated perfused liver of TR- rats offers a new system for testing modulators of P-glycoprotein like cyclosporin A.	Rhodamines	49-58	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	162-176
8105101-12	1993	MDR1 mRNA expression was significantly correlated with rhodamine 123 efflux, whereas MDR3 mRNA expression was not significantly correlated; MDR1 and MDR3 mRNA expression was not significantly associated with Rai stage, prior treatment, or disease progresssion.	Rhodamines	55-64	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
8271312-6	1993	Indeed, after incubation of oligodendrocytes with C6-NBD-ceramide and rhodamine-labeled transferrin both fluorescent labels colocalized in the Golgi system of the cell body as well as in the structures in the processes.	Rhodamines	70-79	transferrin	Rattus norvegicus	88-99
8302775-7	1993	Melanophores with either aggregated or dispersed melanosomes had low intensity rhodamine-phalloidin staining of actin filaments compared to nonpigmented cells, whereas the FITC anti-tubulin intensities were comparable in magnitude to that seen in nonpigmented cells.	Rhodamines	79-88	actin like 6A S homeolog	Xenopus laevis	112-117
7905358-0	1993	Assessment of P-glycoprotein-dependent drug transport in isolated rat hepatocytes using rhodamine 123.	Rhodamines	88-97	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	14-28
7691328-5	1993	The quiescent rhodamine 123 dull stem cell fraction was found to express the interleukin 3 (IL-3) receptor beta unit and c-kit, but not the granulocyte-macrophage colony stimulating factor (GM-CSF) receptor beta unit nor flk-2.	Rhodamines	14-23	KIT proto-oncogene, receptor tyrosine kinase	Homo sapiens	121-126
7691328-9	1993	The SCF-binding cells were found to be all rhodamine 123 bright.	Rhodamines	43-52	KIT ligand	Homo sapiens	4-7
7694687-2	1993	The results of MDR1 mRNA expression by reverse transcriptase polymerase chain reaction were confirmed by immunostaining using the anti-P-glycoprotein monoclonal antibody UIC2 and by a functional study using the rhodamine efflux test.	Rhodamines	211-220	ATP binding cassette subfamily B member 1	Homo sapiens	15-19
7693598-8	1993	When each anti-CTB IgA was mixed with 10 nM CT and applied to the apical surfaces of T84 cell monolayers, all three IgAs blocked CT-induced Cl- secretion in a dose-dependent manner and completely inhibited binding of rhodamine-labelled CT to apical cell membranes.	Rhodamines	217-226	CD79a molecule	Homo sapiens	19-22
8218101-13	1993	Direct measurement of prothrombinase complex assembly was demonstrated by using an energy transfer phenomenon between fluorescein-labeled factor Va and rhodamine-labeled factor Xa.	Rhodamines	152-161	coagulation factor X	Homo sapiens	22-36
8105110-11	1993	A verapamil-sensitive drug efflux has been demonstrated for the PC-3 and Du-145, but not for the LNCaP, cell lines, using flow cytometric measurements of the P-gp substrate rhodamine 123 efflux from preloaded cells.	Rhodamines	173-182	proprotein convertase subtilisin/kexin type 1	Homo sapiens	64-68
8105110-11	1993	A verapamil-sensitive drug efflux has been demonstrated for the PC-3 and Du-145, but not for the LNCaP, cell lines, using flow cytometric measurements of the P-gp substrate rhodamine 123 efflux from preloaded cells.	Rhodamines	173-182	ATP binding cassette subfamily B member 1	Homo sapiens	158-162
7690250-5	1993	Impaired transport of rhodamine in normal T lymphocytes treated with staurosporine demonstrates that modulation of P-glycoprotein function is not limited to cells selected for drug resistance in vitro.	Rhodamines	22-31	ATP binding cassette subfamily B member 1	Homo sapiens	115-129
8214031-3	1993	In IMCD3, 5 min of stimulation by 2.5-250 nM AVP significantly depolymerized F-actin by 13-24% in whole cell assays employing the rhodamine-phalloidin binding technique.	Rhodamines	130-139	arginine vasopressin	Rattus norvegicus	45-48
8220067-3	1993	With biotin-streptavidin-rhodamine, myosin was mainly found at the bile canaliculi level, however with confocal microscopy, the plasma membrane fluorescent staining was more apparent.	Rhodamines	25-34	myosin heavy chain 14	Homo sapiens	36-42
7683034-4	1993	Thy-1+ CD34+ cells were further characterized as CD38lo/CD45RO+/CD45RA-/CD71lo/c-kit(lo) and rhodamine 123dull.	Rhodamines	93-102	Thy-1 cell surface antigen	Homo sapiens	0-5
8384932-1	1993	The localization of topoisomerase II (topo II) in vivo was studied by recording time-lapse, three-dimensional data sets of living Drosophila melanogaster embryos injected with rhodamine-labeled topo II.	Rhodamines	176-185	Topoisomerase 2	Drosophila melanogaster	20-36
8384932-1	1993	The localization of topoisomerase II (topo II) in vivo was studied by recording time-lapse, three-dimensional data sets of living Drosophila melanogaster embryos injected with rhodamine-labeled topo II.	Rhodamines	176-185	Topoisomerase 2	Drosophila melanogaster	38-45
8384932-1	1993	The localization of topoisomerase II (topo II) in vivo was studied by recording time-lapse, three-dimensional data sets of living Drosophila melanogaster embryos injected with rhodamine-labeled topo II.	Rhodamines	176-185	Topoisomerase 2	Drosophila melanogaster	194-201
7680244-2	1993	In this study, expression of multidrug resistance P-glycoprotein on peripheral blood mononuclear cells (PBMC) of 11 patients with GLPD was examined by staining with MRK 16, a monoclonal antibody that binds to an external epitope of P-glycoprotein, and with the dye rhodamine, a known substance to be excreted from the cells through P-glycoprotein.	Rhodamines	265-274	ATP binding cassette subfamily B member 1	Homo sapiens	50-64
8432559-5	1993	Cathepsin B/L activity was measured flow cytometrically in single viable cells by the intracellular cleavage of non-fluorescent (Z-Phe-Arg)2-rhodamine 110 to the green fluorescent monoamide Z-Phe-Arg-rhodamine 110 and rhodamine 110.	Rhodamines	141-150	cathepsin B	Rattus norvegicus	0-11
8329592-2	1993	In this system, distances obtained from A-mode ultrasound will be used to compensate for decreases in fluorescence intensity due to the detector-sample separation distance r. For concentrated rhodamine, a fluorescent dye, compensation has been experimentally achieved assuming fluorescence is emitted isotropically and decreases as 1/r2.	Rhodamines	192-201	prostaglandin D2 receptor	Homo sapiens	329-333
1571946-12	1992	The effects of quenching of the fluorescent signal by the excitation beam were minimized in the following manner: a) Rhodamine anti-GFAP was substituted for more labile fluoresceine.	Rhodamines	117-126	glial fibrillary acidic protein	Homo sapiens	132-136
7682495-5	1993	CD5+ B cells were identified by double immunofluorescence staining with rhodamine-conjugated rabbit anti-human immunoglobulin and with a mouse anti-CD5 monoclonal antibody revealed by a fluorescein-conjugated goat anti-mouse immunoglobulin.	Rhodamines	72-81	CD5 molecule	Homo sapiens	0-3
1515071-0	1992	Membrane permeable fluorogenic rhodamine substrates for selective determination of cathepsin L.	Rhodamines	31-40	cathepsin L	Homo sapiens	83-94
1476678-14	1992	This colocalization confirms the association of rhodamine-tagged species with F-actin.	Rhodamines	48-57	actin, beta	Gallus gallus	80-85
1351678-8	1992	Since Thy-1 could be directly labeled with rhodamine, the effect of the size of the labeling ligand on the mobility obtained by the FRAP technique could be explored.	Rhodamines	43-52	thymus cell antigen 1, theta	Mus musculus	6-11
1599404-7	1992	The rhodamine label in bile was chloroform-soluble, but not identical to the native molecule, and was resistant to phospholipase A2 and alkaline hydrolysis.	Rhodamines	4-13	phospholipase A2 group IB	Rattus norvegicus	115-131
1639847-8	1992	Double labeling of yeast cells with affinity-purified anti-calmodulin antibody and rhodamine-conjugated phalloidin indicates that calmodulin and actin concentrate in overlapping regions during the cell cycle.	Rhodamines	83-92	calmodulin	Saccharomyces cerevisiae S288C	130-140
1377237-4	1992	One construct consisted of the nuclear import signal peptide (sp) of the SV40 large T antigen, coupled to human serum albumin (HSA) and rhodamine (r).	Rhodamines	9-10	CD24 molecule	Rattus norvegicus	127-130
1607935-3	1992	The overall staining pattern or intensity was minimally altered after stimulation, although dopamine-beta-hydroxylase (DBH) antigen, a marker for the chromaffin granule membrane, was exposed preferentially on the plasma membrane areas with lower intensity of rhodamine-phalloidin staining.	Rhodamines	259-268	dopamine beta-hydroxylase	Homo sapiens	92-117
1607935-3	1992	The overall staining pattern or intensity was minimally altered after stimulation, although dopamine-beta-hydroxylase (DBH) antigen, a marker for the chromaffin granule membrane, was exposed preferentially on the plasma membrane areas with lower intensity of rhodamine-phalloidin staining.	Rhodamines	259-268	dopamine beta-hydroxylase	Homo sapiens	119-122
1345903-1	1992	Rhodamine-labeled vinculin microinjected into chicken embryo fibroblasts and rhodamine-labeled alpha 2-macroglobulin added to the fibroblast culture medium were sequestered in endocytotic vesicles and digested.	Rhodamines	0-9	vinculin	Gallus gallus	18-26
1345903-1	1992	Rhodamine-labeled vinculin microinjected into chicken embryo fibroblasts and rhodamine-labeled alpha 2-macroglobulin added to the fibroblast culture medium were sequestered in endocytotic vesicles and digested.	Rhodamines	77-86	vinculin	Gallus gallus	18-26
1345903-1	1992	Rhodamine-labeled vinculin microinjected into chicken embryo fibroblasts and rhodamine-labeled alpha 2-macroglobulin added to the fibroblast culture medium were sequestered in endocytotic vesicles and digested.	Rhodamines	77-86	alpha-2-macroglobulin	Gallus gallus	95-116
1345903-2	1992	When a sealed microcapillary coated with fibronectin or polylysine was attached to the fibroblasts and pulled at speeds of 100-200 microns/h, stretching the plasma membrane, a variable fraction of the endosomes released the rhodamine label.	Rhodamines	224-233	fibronectin 1	Gallus gallus	41-52
1665427-6	1991	In contrast, priming with InsP6, with or without FMLP stimulation, results in a sustained assembly of F-actin as visualized with a rhodamine-phalloidin staining technique.	Rhodamines	131-140	formyl peptide receptor 1	Homo sapiens	49-53
1661732-5	1991	Coverslips coated with gelsolin, a multi-domain, calcium-dependent capping and severing protein, bound rhodamine-phalloidin-saturated filaments along their length in the presence of EGTA.	Rhodamines	103-112	Gelsolin	Drosophila melanogaster	23-31
2050110-6	1991	Fluorescence experiments with rhodamine-conjugated Tat show punctate staining on the cell surface and then localization to the cytoplasm and nucleus.	Rhodamines	30-39	tyrosine aminotransferase	Homo sapiens	51-54
1717068-7	1991	About 20% of the Lin(lineage)-c-kit+ cells were rhodamine-123low and this fraction contained more day-12 CFU-S than day-8 CFU-S. On the basis of these findings, murine hematopoietic stem cells were enriched with normal bone marrow cells.	Rhodamines	48-57	KIT proto-oncogene receptor tyrosine kinase	Mus musculus	30-35
2070071-4	1991	These procedures have allowed us to ascribe the following features to the cells mainly responsible for IL-3-induced IL-6 production: (1) they possess a low density and a relatively high forward and perpendicular light scatter (FLS/PLS); (2) they are characterized by a high rhodamine (Rh) retention; and (3) their enrichment in various subpopulations is similar to that obtained for progenitors forming colonies in the methylcellulose assay colony-forming units (CFU-C).	Rhodamines	274-283	interleukin 3	Mus musculus	103-107
2070071-4	1991	These procedures have allowed us to ascribe the following features to the cells mainly responsible for IL-3-induced IL-6 production: (1) they possess a low density and a relatively high forward and perpendicular light scatter (FLS/PLS); (2) they are characterized by a high rhodamine (Rh) retention; and (3) their enrichment in various subpopulations is similar to that obtained for progenitors forming colonies in the methylcellulose assay colony-forming units (CFU-C).	Rhodamines	274-283	interleukin 6	Mus musculus	116-120
2070071-4	1991	These procedures have allowed us to ascribe the following features to the cells mainly responsible for IL-3-induced IL-6 production: (1) they possess a low density and a relatively high forward and perpendicular light scatter (FLS/PLS); (2) they are characterized by a high rhodamine (Rh) retention; and (3) their enrichment in various subpopulations is similar to that obtained for progenitors forming colonies in the methylcellulose assay colony-forming units (CFU-C).	Rhodamines	285-287	interleukin 3	Mus musculus	103-107
2070071-4	1991	These procedures have allowed us to ascribe the following features to the cells mainly responsible for IL-3-induced IL-6 production: (1) they possess a low density and a relatively high forward and perpendicular light scatter (FLS/PLS); (2) they are characterized by a high rhodamine (Rh) retention; and (3) their enrichment in various subpopulations is similar to that obtained for progenitors forming colonies in the methylcellulose assay colony-forming units (CFU-C).	Rhodamines	285-287	interleukin 6	Mus musculus	116-120
1848561-11	1991	Visualization of microfilaments with rhodamine-conjugated phalloidin showed that PTH altered the cytoskeleton by decreasing the number of stress fibers.	Rhodamines	37-46	parathyroid hormone	Homo sapiens	81-84
1713528-2	1991	However, about one half of these GnRH neurons also project to fenestrated capillaries as evidenced by uptake and retrograde transport of both peripherally injected Fluoro-Gold and centrally injected rhodamine labeled microspheres.	Rhodamines	199-208	gonadotropin releasing hormone 1	Rattus norvegicus	33-37
1987663-7	1991	Additional studies, in which rhodamine-coupled phalloidin was used to visualize F-actin, showed that Cd2+ altered the structure of actin filaments in the cells; there was a significant reduction in the amount of junction-associated F-actin and in the number of stress fibers.	Rhodamines	29-38	CD2 molecule	Sus scrofa	101-104
34556207-3	2021	Herein, by taking advantage of frequency upconversion luminescence (FUCL) technology, we reported an FUCL probe (NRh-NDs) that can detect GST based on a rhodamine derivative structure decorated with a 2,4-dinitrobenzenesulfonyl group (NDs).	Rhodamines	153-162	glutathione S-transferase kappa 1	Homo sapiens	138-141
2144348-3	1990	The rhodamine-labeled fluorescent vasopressin analog, R-MLVP, initially bound in a diffuse manner at the cell surface of both A10 and LLC-PK1 cells and could be displaced by excess unlabeled [8-arginine]vasopressin.	Rhodamines	4-13	vasopressin	Sus scrofa	34-45
2144348-3	1990	The rhodamine-labeled fluorescent vasopressin analog, R-MLVP, initially bound in a diffuse manner at the cell surface of both A10 and LLC-PK1 cells and could be displaced by excess unlabeled [8-arginine]vasopressin.	Rhodamines	4-13	vasopressin	Sus scrofa	203-214
2134848-5	1990	Double-labeling immunohistochemical and retrograde tracing experiments evidenced that many NPY-LI neurons in the intergeniculate area contained rhodamine microspheres that had been previously injected into the ipsilateral nBOR.	Rhodamines	144-153	pro-neuropeptide Y	Columba livia	91-94
1969768-1	1990	P-glycoprotein (P-gp) is involved in the transport of a wide variety of organic compounds including a fluorescent dye, rhodamine 6G (RG), as well as anti-cancer drugs.	Rhodamines	119-128	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
1969768-1	1990	P-glycoprotein (P-gp) is involved in the transport of a wide variety of organic compounds including a fluorescent dye, rhodamine 6G (RG), as well as anti-cancer drugs.	Rhodamines	119-128	ATP binding cassette subfamily B member 1	Homo sapiens	16-20
2307704-3	1990	Fluorescein- or rhodamine-labeled antibody (12C5) specific for the head region (S1) of myosin was used as a marker to identify "embryonic" myosin.	Rhodamines	16-25	myosin, heavy chain 15	Gallus gallus	87-93
34916672-2	2022	Here we introduce HaloTag variants with either increased or decreased brightness and fluorescence lifetime compared with HaloTag7 when labeled with rhodamines.	Rhodamines	148-158	peptidoglycan recognition protein 1	Homo sapiens	121-129
34229804-6	2021	The result showed that the ratio of TIMP1/MMP-9 (in the range 0.2-1.2) and fluorescence intensity of the probe were negative linear correlation and the effects of BSA-rhodamine accumulation in tumor were individualized differences as well as correlated with the relative ratio of TIMP-1/MMP-9 in serum.	Rhodamines	167-176	tissue inhibitor of metalloproteinase 1	Mus musculus	36-41
34229804-6	2021	The result showed that the ratio of TIMP1/MMP-9 (in the range 0.2-1.2) and fluorescence intensity of the probe were negative linear correlation and the effects of BSA-rhodamine accumulation in tumor were individualized differences as well as correlated with the relative ratio of TIMP-1/MMP-9 in serum.	Rhodamines	167-176	matrix metallopeptidase 9	Mus musculus	42-47
34229804-6	2021	The result showed that the ratio of TIMP1/MMP-9 (in the range 0.2-1.2) and fluorescence intensity of the probe were negative linear correlation and the effects of BSA-rhodamine accumulation in tumor were individualized differences as well as correlated with the relative ratio of TIMP-1/MMP-9 in serum.	Rhodamines	167-176	TIMP metallopeptidase inhibitor 1	Homo sapiens	280-286
34229804-6	2021	The result showed that the ratio of TIMP1/MMP-9 (in the range 0.2-1.2) and fluorescence intensity of the probe were negative linear correlation and the effects of BSA-rhodamine accumulation in tumor were individualized differences as well as correlated with the relative ratio of TIMP-1/MMP-9 in serum.	Rhodamines	167-176	matrix metallopeptidase 9	Mus musculus	287-292
2178323-1	1990	Rat ceruloplasmin (rCp) has been labeled with the fluorophores fluorescein and rhodamine by using the isothiocyanate derivatives (FITC, RBITC).	Rhodamines	79-88	ceruloplasmin	Rattus norvegicus	4-17
2118972-4	1990	In the present work, the uptake of rhodamine 123 by Molt 16 cells stimulated by IFN-gamma or IFN-beta was measured by flow cytometry.	Rhodamines	35-44	interferon gamma	Homo sapiens	80-89
2118972-4	1990	In the present work, the uptake of rhodamine 123 by Molt 16 cells stimulated by IFN-gamma or IFN-beta was measured by flow cytometry.	Rhodamines	35-44	interferon beta 1	Homo sapiens	93-101
34816717-3	2021	Spectroscopic studies revealed trends in fluorophore efficiency based on substitution patterns at the 3"-, 6"-, and 9"-positions, providing insights to aid future designs of rhodamines/rosamines.	Rhodamines	174-184	activation induced cytidine deaminase	Homo sapiens	152-155
34643369-4	2021	RH-EDA is a hybrid of rhodamine and edaravone and exploits a  OH-specific 3-methyl-pyrazolone moiety to control its fluorescence behavior.	Rhodamines	22-31	ectodysplasin A	Homo sapiens	3-6
34351165-1	2021	This work investigates, for the first time, the application of sonochemically prepared bovine serum albumin (BSA) microspheres (BSAMS) as adsorbents of industrial organic pollutant dyes, such as rhodamine B (RhB), rhodamine 6G (Rh6G), and methylene blue (MB).	Rhodamines	214-223	albumin	Homo sapiens	94-107
34541849-8	2021	Benefiting from chemical reaction with rhodamine 6G, the AcOH gas sensor displays a short response time.	Rhodamines	39-48	gastrin	Homo sapiens	62-65
34243072-0	2021	Enhancing the tumor cell selectivity of a rhodamine-decorated iridium(III) complex by conjugating with indomethacin for COX-2 targeted photodynamic therapy.	Rhodamines	42-51	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	120-125
34339177-3	2021	HaloTag7 reaches almost diffusion-limited labeling rate constants with certain rhodamine substrates, which are more than 2 orders of magnitude higher than those of SNAP-tag for the corresponding substrates.	Rhodamines	79-88	peptidoglycan recognition protein 1	Homo sapiens	0-8
34060662-0	2021	Triangular Rhodamine Triads and Their Intrinsic Photophysics Revealed from Gas-phase Ion Fluorescence Experiments.	Rhodamines	11-20	gastrin	Homo sapiens	75-78
34231571-4	2021	Using Rhodamine 6G (R6G) as a reporter molecule, the SERS enhancement factor (EF) of the TAgNP arrays was found to be as high as 1.2 x 107 and the relative standard deviation was 6.56%.	Rhodamines	6-15	seryl-tRNA synthetase 1	Homo sapiens	53-57
34161934-6	2021	Experimental results showed that the limit of detection (LOD) of this composite SERS substrate for Rhodamine 6G (R6G) molecules was as low as 1x10-13 M, and the Raman enhancement factor was 15.68 and 2.87 times that of the AuNP and AgNP monolayer substrates respectively.	Rhodamines	99-108	seryl-tRNA synthetase 1	Homo sapiens	80-84
35234756-6	2022	The limit of detection for rhodamine 6G (R6G) molecules adsorbed on the TiO2@Ag SERS substrate is 5 x 10-14 M, and the corresponding SERS enhancement factor can reach 7.61 x 107.	Rhodamines	27-36	seryl-tRNA synthetase 1	Homo sapiens	80-84
34254096-4	2021	Upon activation by tumor-associated GGT, the probe releases highly fluorescent rhodamine that is selectively confined in tumors whereby light irradiation leads to effective tumor regression in mice.	Rhodamines	79-88	gamma-glutamyltransferase 1	Mus musculus	36-39
34149660-8	2021	Although ABC1 and ABC2 were only moderately (20% and 10%, respectively) expressed compared to the Candida albicans multidrug efflux pump CDR1, overexpression of F. keratoplasticum ABC1 caused even higher resistance levels to certain xenobiotics (e.g., rhodamine 6G and nigericin) than CDR1.	Rhodamines	252-261	protein kinase COQ8	Saccharomyces cerevisiae S288C	180-184
34069106-3	2021	Fluorescence microscopy results showed that rhodamine-encapsulated micelle was taken up by brain cancer cells, while competitive inhibition was observed in the presence of free HA and free transferrin.	Rhodamines	44-53	transferrin	Mus musculus	189-200
35234756-6	2022	The limit of detection for rhodamine 6G (R6G) molecules adsorbed on the TiO2@Ag SERS substrate is 5 x 10-14 M, and the corresponding SERS enhancement factor can reach 7.61 x 107.	Rhodamines	27-36	seryl-tRNA synthetase 1	Homo sapiens	133-137
35188523-6	2022	By multiplexing with a permeable rhodamine, we are able to differentiate extra- and intracellular SNAP- and Halo-tags, including those installed on the glucagon-like peptide-1 receptor, a prototypical class B G protein-coupled receptor.	Rhodamines	33-42	glucagon like peptide 1 receptor	Homo sapiens	152-184
2480910-8	1989	Rhodamine-losing T-lymphoma contained large amounts of the mRNA coding P-glycoprotein, the MDR efflux pump, and demonstrated increased resistance to rhodamine 123, gramicidin D, colchicine, and vincristine, the drugs belonging to the cross-resistance group for the MDR cells.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	71-85
35209208-1	2022	BACKGROUND: rhodamines are dyes widely used as fluorescent tags in cell imaging, probing of mitochondrial membrane potential, and as P-glycoprotein model substrates.	Rhodamines	12-22	ATP binding cassette subfamily B member 1	Homo sapiens	133-147
35048136-0	2022	Rhodamine-based chemosensor for Sn2+ detection and its application in nanofibrous film and bioimaging.	Rhodamines	0-9	solute carrier family 38 member 5	Homo sapiens	32-35
35048136-1	2022	A simple rhodamine-based compound CK was designed and synthesized as a fluorescent chemosensor for Sn2+ based on Sn2+-mediated cyclization.	Rhodamines	9-18	cytidine/uridine monophosphate kinase 1	Homo sapiens	34-36
35048136-1	2022	A simple rhodamine-based compound CK was designed and synthesized as a fluorescent chemosensor for Sn2+ based on Sn2+-mediated cyclization.	Rhodamines	9-18	solute carrier family 38 member 5	Homo sapiens	99-102
35048136-1	2022	A simple rhodamine-based compound CK was designed and synthesized as a fluorescent chemosensor for Sn2+ based on Sn2+-mediated cyclization.	Rhodamines	9-18	solute carrier family 38 member 5	Homo sapiens	113-116
34985062-2	2022	Two-photon excited fluorescence (TPEF) measurements and quantum chemical calculations reveal excellent two-photon properties of the employed rhodamine derivative.	Rhodamines	141-150	transmembrane protein with EGF like and two follistatin like domains 2	Homo sapiens	33-37
2630560-2	1989	Actin of reverting protoplasts was labeled with rhodamine-conjugated phalloidin and observed by conventional fluorescence microscopy and laser scanning confocal microscopy.	Rhodamines	48-57	actin	Saccharomyces cerevisiae S288C	0-5
2808706-8	1989	In contrast, the labeled SCAD band in YH2065 cells was barely detectable at 6 h and undetectable at 20 h. [35S]Methionine-labeling in the presence of rhodamine 6G demonstrated that SCAD-YH2065 was synthesized as a 44-kD precursor and imported normally into mitochondria, as were the normal SCAD and two other variant SCADs, excluding the possibility that SCAD-YH2065 is a truncated precursor that cannot be imported into mitochondria.	Rhodamines	150-159	acyl-CoA dehydrogenase short chain	Homo sapiens	25-29
2808706-8	1989	In contrast, the labeled SCAD band in YH2065 cells was barely detectable at 6 h and undetectable at 20 h. [35S]Methionine-labeling in the presence of rhodamine 6G demonstrated that SCAD-YH2065 was synthesized as a 44-kD precursor and imported normally into mitochondria, as were the normal SCAD and two other variant SCADs, excluding the possibility that SCAD-YH2065 is a truncated precursor that cannot be imported into mitochondria.	Rhodamines	150-159	acyl-CoA dehydrogenase short chain	Homo sapiens	181-185
2808706-8	1989	In contrast, the labeled SCAD band in YH2065 cells was barely detectable at 6 h and undetectable at 20 h. [35S]Methionine-labeling in the presence of rhodamine 6G demonstrated that SCAD-YH2065 was synthesized as a 44-kD precursor and imported normally into mitochondria, as were the normal SCAD and two other variant SCADs, excluding the possibility that SCAD-YH2065 is a truncated precursor that cannot be imported into mitochondria.	Rhodamines	150-159	acyl-CoA dehydrogenase short chain	Homo sapiens	181-185
2808706-8	1989	In contrast, the labeled SCAD band in YH2065 cells was barely detectable at 6 h and undetectable at 20 h. [35S]Methionine-labeling in the presence of rhodamine 6G demonstrated that SCAD-YH2065 was synthesized as a 44-kD precursor and imported normally into mitochondria, as were the normal SCAD and two other variant SCADs, excluding the possibility that SCAD-YH2065 is a truncated precursor that cannot be imported into mitochondria.	Rhodamines	150-159	acyl-CoA dehydrogenase short chain	Homo sapiens	181-185
2659755-5	1989	After these reactions, sections were stained with rhodamine-labelled rabbit antihuman IgA antiserum.	Rhodamines	50-59	CD79a molecule	Homo sapiens	86-89
2531084-4	1989	The lateral mobility of the vasopressin renal-type (V2)-receptor was measured in the basal plasma membrane of cells of the LLC-PK1 porcine epithelial line, using the technique of fluorescence microphotolysis (photobleaching) and a rhodamine-labelled analogue of vasopressin.	Rhodamines	231-240	vasopressin	Sus scrofa	28-39
2777067-1	1989	Rhodamine-conjugated phalloidin was used to analyze the actin distribution during hyphal formation in Mucor rouxii.	Rhodamines	0-9	actin	Oryctolagus cuniculus	56-61
3266692-5	1988	Nevertheless, the experiments performed on A431 cells using a fluorescent label--rhodamine--bound to EGF (EGF-R) indicate that CB, though not influencing the initial steps of endocytosis, inhibits the next step--the intracellular transport of EGF-receptor complexes from the trans-Golgi region to lysosomes.	Rhodamines	81-90	epidermal growth factor receptor	Mus musculus	101-111
2844828-2	1988	Fluorescence polarization and fluorescence photobleaching recovery experiments using rhodamine-labeled actin as a tracer showed that under conditions of low shear (shear rates of 0.05 s-1), a spatial heterogeneity of polymerized actin was observed with respect to fluorescence intensity and the diffusion coefficients with actin mobility becoming quite variable in different regions of the sample.	Rhodamines	85-94	actin, beta	Gallus gallus	103-108
3058721-3	1988	Comparison of rhodamine-labeled alpha-actinin with coinjected fluorescein-labeled myosin suggested that myosin fluorescence was localized at the A-bands of myofibrils.	Rhodamines	14-23	myosin, heavy chain 15	Gallus gallus	104-110
3266692-5	1988	Nevertheless, the experiments performed on A431 cells using a fluorescent label--rhodamine--bound to EGF (EGF-R) indicate that CB, though not influencing the initial steps of endocytosis, inhibits the next step--the intracellular transport of EGF-receptor complexes from the trans-Golgi region to lysosomes.	Rhodamines	81-90	epidermal growth factor	Mus musculus	101-104
3135511-2	1988	Retrograde transport of rhodamine-labeled fluorescent microspheres following discrete microinjection into the thoracic intermediolateral cell column was combined with immunohistochemistry to determine neuroanatomic location of thyrotropin-releasing hormone-immunoreactive neurons which project to the intermediolateral cell column in the rat.	Rhodamines	24-33	thyrotropin releasing hormone	Rattus norvegicus	227-256
3689797-1	1987	The effects of caldesmon on structural and dynamic properties of phalloidin-rhodamine-labeled F-actin in single skeletal muscle fibers were investigated by polarized microphotometry.	Rhodamines	76-85	caldesmon 1	Homo sapiens	15-24
2894318-2	1988	After 15-20 min of internalization at 37 degrees C, rhodamine-labeled EGF (EGF-Rh) accumulated into large juxtanuclear compartment consisting of closely related vesicles.	Rhodamines	52-61	epidermal growth factor	Homo sapiens	70-73
2894318-2	1988	After 15-20 min of internalization at 37 degrees C, rhodamine-labeled EGF (EGF-Rh) accumulated into large juxtanuclear compartment consisting of closely related vesicles.	Rhodamines	52-61	epidermal growth factor	Homo sapiens	75-81
3360988-2	1988	This was done by injecting rhodamine-filled latex microspheres into the nucleus tractus solitarii of rats to retrogradely label neuronal cell bodies and by processing sections from the brains of these animals to determine if the labelled neurons were immunoreactive for the catecholamine-synthesizing enzymes, dopamine-beta-hydroxylase (DBH) and phenylethanolamine-N-methyl transferase (PNMT).	Rhodamines	27-36	dopamine beta-hydroxylase	Rattus norvegicus	310-335
3360988-2	1988	This was done by injecting rhodamine-filled latex microspheres into the nucleus tractus solitarii of rats to retrogradely label neuronal cell bodies and by processing sections from the brains of these animals to determine if the labelled neurons were immunoreactive for the catecholamine-synthesizing enzymes, dopamine-beta-hydroxylase (DBH) and phenylethanolamine-N-methyl transferase (PNMT).	Rhodamines	27-36	dopamine beta-hydroxylase	Rattus norvegicus	337-340
3360988-2	1988	This was done by injecting rhodamine-filled latex microspheres into the nucleus tractus solitarii of rats to retrogradely label neuronal cell bodies and by processing sections from the brains of these animals to determine if the labelled neurons were immunoreactive for the catecholamine-synthesizing enzymes, dopamine-beta-hydroxylase (DBH) and phenylethanolamine-N-methyl transferase (PNMT).	Rhodamines	27-36	phenylethanolamine-N-methyltransferase	Rattus norvegicus	346-385
3360988-2	1988	This was done by injecting rhodamine-filled latex microspheres into the nucleus tractus solitarii of rats to retrogradely label neuronal cell bodies and by processing sections from the brains of these animals to determine if the labelled neurons were immunoreactive for the catecholamine-synthesizing enzymes, dopamine-beta-hydroxylase (DBH) and phenylethanolamine-N-methyl transferase (PNMT).	Rhodamines	27-36	phenylethanolamine-N-methyltransferase	Rattus norvegicus	387-391
3360988-4	1988	Thus, these two ventrolateral rhombencephalic cell groups accounted for nearly 80% of the total number of rhodamine-bead-labelled DBH-immunoreactive neurons in this series of experiments.	Rhodamines	106-115	dopamine beta-hydroxylase	Rattus norvegicus	130-133
3360988-5	1988	Only a small number of DBH-immunoreactive neurons of the A2/C2 cell group contained rhodamine-filled latex microspheres.	Rhodamines	84-93	dopamine beta-hydroxylase	Homo sapiens	23-26
3360988-8	1988	Only small numbers of PNMT-immunoreactive neurons of the C2 and C3 groups were found to contain rhodamine-filled latex microspheres.	Rhodamines	96-105	phenylethanolamine-N-methyltransferase	Rattus norvegicus	22-26
3782295-0	1986	Formation and alignment of Z lines in living chick myotubes microinjected with rhodamine-labeled alpha-actinin.	Rhodamines	79-88	actinin, alpha 4	Gallus gallus	97-110
3667695-1	1987	Myosin light chains labeled with rhodamine are incorporated into myosin-containing structures when microinjected into live muscle and nonmuscle cells.	Rhodamines	33-42	myosin, heavy chain 15	Gallus gallus	0-6
3667695-1	1987	Myosin light chains labeled with rhodamine are incorporated into myosin-containing structures when microinjected into live muscle and nonmuscle cells.	Rhodamines	33-42	myosin, heavy chain 15	Gallus gallus	65-71
3318045-1	1987	Dynamics of compartmentalization of epidermal growth factor (EGF) in human carcinoma A431 cells during the first hour after initiation of endocytosis was examined by methods of the organelle fractionation on a 20% Percoll gradient and of the microfluorimetric visualization of endocytosis of rhodamine-labeled EGF (EGF-R).	Rhodamines	292-301	epidermal growth factor receptor	Homo sapiens	61-64
3038101-1	1987	Rhodamines 110 and 123, and rhodamine 110 linked via peptide bonds to Arg, Cbz-Arg and Cbz-Ile-Pr-Arg interact with free base porphyrins or cytochrome C.	Rhodamines	0-10	cytochrome c, somatic	Homo sapiens	140-152
3038101-1	1987	Rhodamines 110 and 123, and rhodamine 110 linked via peptide bonds to Arg, Cbz-Arg and Cbz-Ile-Pr-Arg interact with free base porphyrins or cytochrome C.	Rhodamines	28-37	cytochrome c, somatic	Homo sapiens	140-152
3552117-4	1987	This projection originates in large part from phenylethanolamine-N-methyltransferase-immunoreactive cells (C1 adrenergic cluster) as demonstrated by immunohistochemistry combined with the retrograde transport of rhodamine-tagged microbeads.	Rhodamines	212-221	phenylethanolamine-N-methyltransferase	Rattus norvegicus	46-84
2881297-4	1987	Thy-1 was labeled with rhodamine-conjugated anti-Thy-1 monoclonal antibodies.	Rhodamines	23-32	thymus cell antigen 1, theta	Mus musculus	0-5
2881297-4	1987	Thy-1 was labeled with rhodamine-conjugated anti-Thy-1 monoclonal antibodies.	Rhodamines	23-32	thymus cell antigen 1, theta	Mus musculus	49-54
3782295-2	1986	Rhodamine-labeled alpha-actinin microinjected into living cultured chick skeletal myotubes became localized in discrete cellular structures within 1 h and remained specifically associated with structures for up to 4 d, allowing individual identified structures to be followed during development.	Rhodamines	0-9	actinin, alpha 4	Gallus gallus	18-31
3758212-2	1986	Rhodamine-labeled actin or alpha-actinin microinjected into embryonic chick cardiac fibroblasts soon became incorporated into stress fibers.	Rhodamines	0-9	actin, beta	Gallus gallus	18-23
3015981-3	1986	The EGF receptor mutants expressed on the cell surface of the COS cells were labeled with rhodamine-EGF, and the lateral diffusion coefficients of the labeled receptors were determined by the fluorescence photo-bleaching recovery method.	Rhodamines	90-99	epidermal growth factor receptor	Homo sapiens	4-16
3790516-1	1986	The fluorescence polarization from rhodamine labels specifically attached to the fast-reacting thiol of the myosin cross-bridge in glycerinated muscle fibers has been measured to determine the angular distribution of the cross-bridges in different physiological states of the fibers as a function of temperature.	Rhodamines	35-44	myosin heavy chain 14	Homo sapiens	108-114
2432803-1	1986	Rhodamine absorbed to protein was removed from rhodamine-conjugated antibody solutions by adsorption to hydrophobic macroporous beads (Bio-Beads SM-2) following gel permeation chromatography.	Rhodamines	0-9	SM2	Homo sapiens	145-149
3760196-7	1986	p alpha-ETF was detected when the cells were labeled in the presence of dinitrophenol or rhodamine 6G.	Rhodamines	89-98	electron transfer flavoprotein subunit alpha	Homo sapiens	2-11
3516661-7	1986	Indirect immunofluorescence with anti-rbc or antibrain spectrin IgG and goat antirabbit IgG conjugated with rhodamine demonstrated intense staining at the plasma membrane and throughout the cytoplasm of Y-1 cells, with little staining within the nucleus.	Rhodamines	108-117	immunoglobulin heavy variable V1-62	Mus musculus	88-91
3540192-3	1986	By staining cells with rhodamine-conjugated phalloidin, we have compared the dynamics of actin localization during the formation of buds and hyphae.	Rhodamines	23-32	actin	Saccharomyces cerevisiae S288C	89-94
3155961-8	1985	A double immunofluorescence study, involving Fab fragments of IgG L and rhodamine-conjugated antibodies to factor VIII R:Ag, demonstrated the presence of GP IIb-IIIa in megakaryocyte precursor cells.	Rhodamines	72-81	integrin subunit alpha 2b	Homo sapiens	154-160
3722280-3	1986	The distribution of F-actin filaments in the nurse cells has been studied by staining with rhodamine-conjugated phalloidin.	Rhodamines	91-100	Actin 79B	Drosophila melanogaster	20-27
3924578-1	1985	The present study describes the synthesis and biological activities of a vasopressin (VP) analog which binds covalently to receptors via a photoreactive p-azido group in position 3 and which contains a rhodamine label in position 8 for localization of hormone-receptor complexes by image-intensified fluorescence microscopy.	Rhodamines	202-211	arginine vasopressin	Homo sapiens	73-84
3924578-1	1985	The present study describes the synthesis and biological activities of a vasopressin (VP) analog which binds covalently to receptors via a photoreactive p-azido group in position 3 and which contains a rhodamine label in position 8 for localization of hormone-receptor complexes by image-intensified fluorescence microscopy.	Rhodamines	202-211	arginine vasopressin	Homo sapiens	86-88
3872076-4	1985	OKT6 antibody and S-100 protein were detected simultaneously by double labeling with FITC and rhodamine.	Rhodamines	94-103	S100 calcium binding protein A1	Homo sapiens	18-23
3496571-1	1986	Exposure of cultured human retinal pigment epithelial cells to platelet-derived growth factor, nerve growth factor or epidermal growth factor resulted in a time- and dose-dependent alteration in the distribution of actin stained by rhodamine-phalloidin.	Rhodamines	232-241	nerve growth factor	Homo sapiens	95-114
3496571-1	1986	Exposure of cultured human retinal pigment epithelial cells to platelet-derived growth factor, nerve growth factor or epidermal growth factor resulted in a time- and dose-dependent alteration in the distribution of actin stained by rhodamine-phalloidin.	Rhodamines	232-241	epidermal growth factor	Homo sapiens	118-141
2995416-1	1985	We have studied the process of transferrin endocytosis in human erythromyeloid cell line K562 using fluorescein (FL) and rhodamine (RD) labeled iron-saturated transferrin (FeTF), and a fluorescein labeled monoclonal antibody to the transferrin receptor (FL-mAB).	Rhodamines	132-134	transferrin	Homo sapiens	159-170
2995416-1	1985	We have studied the process of transferrin endocytosis in human erythromyeloid cell line K562 using fluorescein (FL) and rhodamine (RD) labeled iron-saturated transferrin (FeTF), and a fluorescein labeled monoclonal antibody to the transferrin receptor (FL-mAB).	Rhodamines	132-134	transferrin	Homo sapiens	159-170
4040842-1	1985	The pattern of localization of actin filaments was compared in whole mounts of lens epithelium of rabbit and mouse using the fluorescently-labeled actin-specific probe, rhodamine-phalloidin.	Rhodamines	169-178	actin	Oryctolagus cuniculus	147-152
2579892-2	1985	HB2 fixation was revealed using either a peroxidase- or a rhodamine-labeled anti-mouse immunoglobulin antiserum.	Rhodamines	58-67	keratin 82	Homo sapiens	0-3
7019220-1	1981	Rhodamine-conjugated antibodies specific for phenylalanine hydroxylase and serum albumin were employed as cytochemical probes to identify these two proteins in H4 hepatoma cells and in isolated rat hepatocytes.	Rhodamines	0-9	phenylalanine hydroxylase	Rattus norvegicus	45-70
6329759-5	1984	Treatment with the ionophore monensin was used to determine whether avidin is processed through the Golgi region, which was localized using rhodamine-labeled wheat germ agglutinin.	Rhodamines	140-149	avidin	Gallus gallus	68-74
6391683-2	1984	The distribution of alpha-actinin in the cells was followed for five days in culture by exposing permeabilized cells to rhodamine-labeled alpha-actinin and also by injecting the labeled alpha-actinin into living myocytes.	Rhodamines	120-129	actinin, alpha 4	Gallus gallus	138-151
6391683-2	1984	The distribution of alpha-actinin in the cells was followed for five days in culture by exposing permeabilized cells to rhodamine-labeled alpha-actinin and also by injecting the labeled alpha-actinin into living myocytes.	Rhodamines	120-129	actinin, alpha 4	Gallus gallus	138-151
6324146-3	1984	Fluorescent visualization of GnRH receptors in these cells, utilizing a bioactive rhodamine derivative of the hormone, indicated that the fluorescently labeled receptors were initially distributed uniformly on the cell surface and then formed clusters which subsequently internalized (at 37 degrees C) into endocytic vesicles.	Rhodamines	82-91	gonadotropin releasing hormone 1	Rattus norvegicus	29-33
6363632-2	1983	Fluorescent labelling of AChRs with rhodamine-conjugated alpha-bungarotoxin (R-Bgt) revealed the presence of irregularly shaped AChR clusters in wing buds at 4 1/2-5 days of incubation.	Rhodamines	36-45	cholinergic receptor nicotinic delta subunit	Gallus gallus	25-29
6341116-7	1983	Sorted rhodamine-positive cells were cultured and found to be fully functional with respect to subsequent challenge with 30 nM GnRH.	Rhodamines	7-16	gonadotropin releasing hormone 1	Rattus norvegicus	127-131
6132682-4	1982	Double label fluorescence microscopy, using fluorescein-Con-A and rhodamine immunofluorescent staining of tubulin or vimentin, indicates that during vesicle migration microtubules and 10-nm filaments are altered in their organization.	Rhodamines	66-75	vimentin	Rattus norvegicus	117-125
6406516-5	1983	Moreover, rhodamine- or fluorescein-conjugated vinculin, when added to these preparations, became specifically associated with the focal contacts regardless of whether the latter were pretreated with fragmin or not.	Rhodamines	10-19	vinculin	Gallus gallus	47-55
6305743-4	1983	This rhodamine-labeled antagonist was utilized for the microscopic visualization and localization of LHRH receptors in dispersed rat pituitary cells.	Rhodamines	5-14	gonadotropin releasing hormone 1	Rattus norvegicus	101-105
6305743-7	1983	Addition of LHRH (10(-6) M) abolished these processes, indicating specific binding sites for the rhodamine-labeled peptide to the gonadotrope cells.	Rhodamines	97-106	gonadotropin releasing hormone 1	Rattus norvegicus	12-16
6761307-3	1982	Microscopic examination of cells stained with rhodamine-labeled anti-Lyt-2 and fluorescein-labeled anti-Lyt-1 was used to measure the proportion of Lyt-1+2-, Lyt-1+2+, and Lyt-1-2+ cells in the spleen and thymus of drug-treated animals.	Rhodamines	46-55	CD8 antigen, alpha chain	Mus musculus	69-74
7028576-2	1981	A much better detection sensitivity was obtained when Paneth cells were counted by fluorescence microscopy after immunostaining for lysozyme with a rhodamine-labelled rabbit IgG conjugate.	Rhodamines	148-157	lysozyme	Homo sapiens	132-140
6170323-0	1981	Binding, surface mobility, internalization, and degradation of rhodamine-labeled alpha 2-macroglobulin.	Rhodamines	63-72	alpha-2-macroglobulin	Mus musculus	81-102
6170323-1	1981	We have used quantitative fluorescence methods to examine the fate of rhodamine-labeled alpha 2-macroglobulin (R-alpha 2 M) after binding to cell-surface receptors on NRK and Swiss 3T3 cells.	Rhodamines	70-79	alpha-2-macroglobulin	Mus musculus	88-109
7019220-1	1981	Rhodamine-conjugated antibodies specific for phenylalanine hydroxylase and serum albumin were employed as cytochemical probes to identify these two proteins in H4 hepatoma cells and in isolated rat hepatocytes.	Rhodamines	0-9	albumin	Rattus norvegicus	81-88
6111566-1	1981	After lysis in a Brij 58-polyethylene glycol medium, PtK1 cells are permeable to small molecules, such as erythrosin B, and to proteins, such as rhodamine-labeled FAB, myosin subfragment-1, and tubulin.	Rhodamines	145-154	mitogen-activated protein kinase kinase kinase 11	Homo sapiens	53-57
6788382-0	1981	The association of rhodamine - labelled alpha-actinin with actin bundles in demembranated cells.	Rhodamines	19-28	actinin alpha 1	Homo sapiens	40-53
6788382-1	1981	Rhodamine-labelled alpha-actinin was specifically bound to actin containing filament bundles of demembranated fibroblasts, and was particularly associated with their termini.	Rhodamines	0-9	actinin alpha 1	Homo sapiens	19-32
6788836-0	1981	Cytochemical localization of ornithine decarboxylase with rhodamine or biotin-labeled alpha-difluoromethylornithine.	Rhodamines	58-67	ornithine decarboxylase 1	Rattus norvegicus	29-52
6259147-2	1981	The rhodamine-derivatized peptide (Rh-GnRH) retained 40% of the receptor binding activity of [D-Lys6]GnRH, and 50% of the luteinizing hormone-releasing activity assayed in cultured pituitary cells.	Rhodamines	4-13	gonadotropin releasing hormone 1	Mus musculus	38-42
6259147-2	1981	The rhodamine-derivatized peptide (Rh-GnRH) retained 40% of the receptor binding activity of [D-Lys6]GnRH, and 50% of the luteinizing hormone-releasing activity assayed in cultured pituitary cells.	Rhodamines	4-13	gonadotropin releasing hormone 1	Mus musculus	101-105
7194696-9	1981	The photobleaching recovery curves for rhodamine-labeled bovine serum albumin reveal both an irreversibly bound state and a multiplicity of reversibly bound states.	Rhodamines	39-48	albumin	Homo sapiens	64-77
6111566-1	1981	After lysis in a Brij 58-polyethylene glycol medium, PtK1 cells are permeable to small molecules, such as erythrosin B, and to proteins, such as rhodamine-labeled FAB, myosin subfragment-1, and tubulin.	Rhodamines	145-154	FA complementation group B	Homo sapiens	163-166
6932032-4	1980	The rhodamine conjugate of nerve growth factor (R-NGF) binds initially to diffusely distributed mobile receptors (D approximately 8 X 10(-10) cm2/sec) on immature sensory and PC-12 cells.	Rhodamines	4-13	nerve growth factor	Homo sapiens	27-46
7469415-0	1980	Binding of heparin to antithrombin III: The use of dansyl and rhodamine labels.	Rhodamines	62-71	serpin family C member 1	Homo sapiens	22-38
6893813-1	1980	Living cultured fibroblasts were microinjected with rhodamine-labeled smooth muscle alpha-actinin and visualized by video-intensified fluorescence microscopy.	Rhodamines	52-61	actinin alpha 1	Homo sapiens	84-97
6932032-4	1980	The rhodamine conjugate of nerve growth factor (R-NGF) binds initially to diffusely distributed mobile receptors (D approximately 8 X 10(-10) cm2/sec) on immature sensory and PC-12 cells.	Rhodamines	4-13	nerve growth factor	Gallus gallus	50-53
6260433-2	1980	Con A, insulin and EGF receptors co-capped with each other and with cytoplasmic actin; the latter was demonstrated by anti-actin antibody (AAA) traced with fluorescein or rhodamine-labelled goat anti-human globulin.	Rhodamines	171-180	LOC521832	Bos taurus	19-22
792981-1	1976	Direct immunofluorescence technique with rhodamine-labelled rabbit anti-gastrin IgG conjugate was used for systematic mapping of the G-cell distribution in 16 resected stomachs (8 gastric ulcer patients and 8 duodenal ulcer patients with uraemia).	Rhodamines	41-50	gastrin	Homo sapiens	72-79
6153227-2	1980	Rhodamine-conjugated antibodies against fibronectin were used in this study of 22 human kidney biopsies and four histologically normal kidneys in combination with routinely employed fluorescein-conjugated antibodies against immunoglobulins, complement components, and fibrin.	Rhodamines	0-9	fibronectin 1	Homo sapiens	40-51
42903-2	1979	When rhodamine-labeled epidermal growth factor is bound to cell surface receptors on confluent monolayers of BALB/c 3T3 cells, it rapidly collects in cell surface clusters and is internalized.	Rhodamines	5-14	LOW QUALITY PROTEIN: pro-epidermal growth factor	Cricetulus griseus	23-46
42903-6	1979	The polypeptide antibiotic bacitracin inhibits clustering of rhodamine-labeled epidermal growth factor or alpha(2)-macroglobulin at 0.7 mM, and it inhibits approximately 40% of the transglutaminase activity in Chinese hamster ovary cells with a K(i) of 0.03 mM.	Rhodamines	61-70	LOW QUALITY PROTEIN: pro-epidermal growth factor	Cricetulus griseus	79-102
356052-6	1978	The binding of EGF to the surface of these cells was also visualized by immunofluorescence using rabbit antibodies to EGF and rhodamine-labeled goat anti-rabbit antibodies.	Rhodamines	126-135	epidermal growth factor	Homo sapiens	15-18
77736-4	1978	With VIM, the cellular uptake and fate of two rhodamine-labeled proteins, concanavalin A and alpha2 macroglobulin, have been followed for up to 24 hr.	Rhodamines	46-55	alpha-2-macroglobulin	Homo sapiens	93-113
7193921-7	1980	Reaction of unextracted myoblasts directly to human antiplatelet myosin conjugated to rhodamine demonstrated that the most intense reaction also occurred along the lateral edges of both human and chick myoblasts.	Rhodamines	86-95	myosin heavy chain 14	Homo sapiens	65-71
160564-1	1979	Particular thiols of the myosin subfragment 1 moieties of single glycerinated muscle fibers are covalently labeled with rhodamine.	Rhodamines	120-129	myosin heavy chain 14	Homo sapiens	25-31
152766-17	1978	Staining of isolated mouse or chicken brush borders with rhodamine-antimyosin demonstrates that myosin is localized exclusively in the terminal web.	Rhodamines	57-66	myosin, heavy chain 10, non-muscle	Gallus gallus	71-77
209452-1	1978	Highly fluorescent analogs of insulin and epidermal growth factor were prepared by the covalent attachment of these peptides to alpha-lactalbumin molecules that were highly substituted (i.e., seven to one) with rhodamine molecules.	Rhodamines	211-220	insulin	Homo sapiens	30-37
350890-2	1978	Antimyosin raised against human platelet myosin was labeled with rhodamine.	Rhodamines	65-74	myosin heavy chain 14	Homo sapiens	4-10
400891-1	1978	High titer, monospecific antibodies to human granulocyte myeloperoxidase, cathepsin G, elastase, lysozyme, and lactoferrin were conjugated with fluorescein and rhodamine and used for immunofluorescent staining of mature neutrophils obtained from 25 patients with acute and chronic leukemia.	Rhodamines	160-169	cathepsin G	Homo sapiens	74-122
72612-5	1977	Fluorescence microscopy of fixed cells using rhodamine-labeled antibodies indicated that alpha 2M is present in vesicular organelles different from primary lysosomes.	Rhodamines	45-54	alpha-2-macroglobulin	Homo sapiens	89-97
72612-6	1977	Fluorescence microscopy of living cells shows that rhodamine-labeled alpha 2M (rhodamine-alpha 2M) is taken up into similar structures.	Rhodamines	51-60	alpha-2-macroglobulin	Homo sapiens	69-77
72612-6	1977	Fluorescence microscopy of living cells shows that rhodamine-labeled alpha 2M (rhodamine-alpha 2M) is taken up into similar structures.	Rhodamines	51-60	alpha-2-macroglobulin	Homo sapiens	89-97
72612-6	1977	Fluorescence microscopy of living cells shows that rhodamine-labeled alpha 2M (rhodamine-alpha 2M) is taken up into similar structures.	Rhodamines	79-88	alpha-2-macroglobulin	Homo sapiens	69-77
72612-6	1977	Fluorescence microscopy of living cells shows that rhodamine-labeled alpha 2M (rhodamine-alpha 2M) is taken up into similar structures.	Rhodamines	79-88	alpha-2-macroglobulin	Homo sapiens	89-97
803528-4	1975	This was demonstrated best through the use of rhodamine-conjugated Fab fragments of IgM- and IgD-specific antisera which were both capped by the idiotypic antiserum.	Rhodamines	46-55	FA complementation group B	Homo sapiens	67-70
32469522-1	2020	he aim of the present paper is to study the effect of common excipients on the permeability of atenolol (as drug absorbed mainly by passive diffusion) and rhodamine (as P-Glycoprotein substrate).	Rhodamines	155-164	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	169-183
33783243-5	2021	This assay is based on the polarization of light emitted by a fluorescent rhodamine tag conjugated to a peptide corresponding to the N-terminal region of ATG16L1 (ATG16L1-N).	Rhodamines	74-83	autophagy related 16 like 1	Homo sapiens	154-161
33783243-5	2021	This assay is based on the polarization of light emitted by a fluorescent rhodamine tag conjugated to a peptide corresponding to the N-terminal region of ATG16L1 (ATG16L1-N).	Rhodamines	74-83	autophagy related 16 like 1	Homo sapiens	163-172
33722692-4	2021	Targeted anti-CD71-CPSNPs encapsulated with the fluorophore, Rhodamine WT, were preferentially internalized by breast cancer cells in co-cultures with osteoblasts.	Rhodamines	61-70	transferrin receptor	Homo sapiens	14-18
33629859-2	2021	Herein, we demonstrate that Rhodamine 6G (Rh-6G) dye conjugated DNA aptamer-attached gold nanostar (GNS)-based distance-dependent nanoparticle surface energy transfer (NSET) spectroscopy has the capability of rapid diagnosis of specific SARS-CoV-2 spike recombinant antigen or SARS-CoV-2 spike protein pseudotyped baculovirus within 10 min.	Rhodamines	28-37	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	248-253
33629859-2	2021	Herein, we demonstrate that Rhodamine 6G (Rh-6G) dye conjugated DNA aptamer-attached gold nanostar (GNS)-based distance-dependent nanoparticle surface energy transfer (NSET) spectroscopy has the capability of rapid diagnosis of specific SARS-CoV-2 spike recombinant antigen or SARS-CoV-2 spike protein pseudotyped baculovirus within 10 min.	Rhodamines	28-37	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	288-293
33383428-8	2021	On molecular docking results, triclosan and the fluorescent used as substrate (rhodamine) presented high affinity with all ABC proteins family tested, showing a greater affinity with ABCC2.	Rhodamines	79-88	ATP-binding cassette, sub-family C (CFTR/MRP), member 2	Danio rerio	183-188
32706571-3	2020	The highly ordered tip-capped nanopore arrays can induce the high sensitive and reproducible Raman signal, whose enhanced factor for rhodamine 6G (R6G) at 1358 cm-1 is 4.46x106.	Rhodamines	133-142	TOR signaling pathway regulator	Homo sapiens	19-22
33064113-1	2020	A rhodamine appended Fe(iii)-catecholate complex Fe(RhoCat)3 is reported as a smart dual-modal T1 MRI-optical imaging probe.	Rhodamines	2-11	general transcription factor IIE subunit 1	Homo sapiens	49-60
32779644-6	2020	We hypothesized that the Fe3+ ion was expected to induce the spirolactam ring-opening of the rhodamine unit due to its Lewis acid nature and preferable interactions with the N and O atoms present in NR as well as PNR.	Rhodamines	93-102	trace amine associated receptor 5	Homo sapiens	213-216
32575097-7	2020	Rhodamine 6-G was detected by SERS up to 10-12M with an analytical enhancement factor of 109for both materials using a 633 nm laser operating at 0.85 mW (5% of the nominal power).	Rhodamines	0-9	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	30-34
32373846-3	2020	Here we report on a simple gas-phase model system, synthesized with the rhodamine 575 (R575+) and rhodamine 640 (R640+) FRET pair and a covalent linker with four methylenes, R575+-(CH2)4-R640+.	Rhodamines	72-81	gastrin	Homo sapiens	27-30
32930207-4	2020	The probe RHPN consists of a rhodamine analogue and an arylhydrazide group as a response site for ONOO-.	Rhodamines	29-38	rhophilin Rho GTPase binding protein 1	Homo sapiens	10-14
32373846-3	2020	Here we report on a simple gas-phase model system, synthesized with the rhodamine 575 (R575+) and rhodamine 640 (R640+) FRET pair and a covalent linker with four methylenes, R575+-(CH2)4-R640+.	Rhodamines	98-107	gastrin	Homo sapiens	27-30
32131933-3	2020	Results The rBMECs,stimulated by glutamine,showed a high expression of P-gp(F=1.924,P=0.020)/Mdr1a(F=1.788,P=0.019) compared to the normal rBMECs.The treatment with 25.0(F=1.924,P=0.025;F=1.788,P=0.017) and 50.0 mug/mul(F=1.924,P=0.035;F=1.788,P=0.026) alpha-asarone significantly depressed the expression of P-gp/Mdr1a.The treatment with 25.0 and 50.0 mug/mul alpha-asarone significantly increased intracellular accumulation of Rhodamine 123 by 40% and 60% respectively.	Rhodamines	429-438	phosphoglycolate phosphatase	Rattus norvegicus	71-75
32478727-6	2020	Rhodamine-conjugated globular actin (G-actinRed) is diluted and loaded into a microneedle.	Rhodamines	0-9	Actin 79B	Drosophila melanogaster	30-35
32404156-6	2020	Rhodamine-labeled rhPRG4 was incubated with OA synoviocytes +- anti-CD44 or isotype control antibodies and cellular uptake of rhPRG4 was determined following a 30-min incubation and alpha-SMA expression following a 24-h incubation.	Rhodamines	0-9	CD44 antigen	Mus musculus	68-72
32404156-6	2020	Rhodamine-labeled rhPRG4 was incubated with OA synoviocytes +- anti-CD44 or isotype control antibodies and cellular uptake of rhPRG4 was determined following a 30-min incubation and alpha-SMA expression following a 24-h incubation.	Rhodamines	0-9	actin alpha 2, smooth muscle, aorta	Mus musculus	182-191
32232949-9	2020	Hence, the rotationally symmetric architecture of P-gp, which determines duality in ATP binding and rhodamine 123 interaction, also forms the basis for the existence of two independently operating outer gates.	Rhodamines	100-109	ATP binding cassette subfamily B member 1	Homo sapiens	50-54
32140458-0	2020	A Fluorescent and Colorimetric Chemosensor for Hg2+ Based on Rhodamine 6G With a Two-Step Reaction Mechanism.	Rhodamines	61-70	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	47-50
31714050-5	2019	Anti-EpCAM antibodies and galactose-rhodamine-polyacrylamide nanoparticles (Gal-Rh-PAA NPs) specifically recognizing ASGPR are modified on the surface of a graphene film that quenches the rhodamine fluorescence.	Rhodamines	36-45	asialoglycoprotein receptor 1	Homo sapiens	117-122
31419747-4	2020	In this study, using rhodamine as the acceptor and phenothiazine as the donor, we synthesized a novel mitochondrial-targeted near infrared (NIR) fluorescent probe, MIT-PZR.	Rhodamines	21-30	myelin protein zero like 1	Homo sapiens	168-171
31714050-6	2019	HCC-CTCs can be captured by anti-EpCAM antibodies and endocytose Gal-Rh-PAA NPs, recovering the rhodamine fluorescence.	Rhodamines	96-105	epithelial cell adhesion molecule	Homo sapiens	33-38
31451653-3	2019	FCP-1 links fluorescein and rhodamine dyes through a Tris[(2-pyridyl)methyl]amine bridge.	Rhodamines	28-37	FCP1	Homo sapiens	0-5
31039840-0	2019	A Novel Morpholine-Based Rhodamine Fluorescent Chemosensor for the Rapid Detection of Hg2+ Ions.	Rhodamines	25-34	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	86-89
31775672-2	2019	Fluorocoxib A, a rhodamine-conjugated analog of indomethacin, is a novel fluorescent imaging agent that selectively targets cyclooxygenase-2 (COX-2)-expressing cancers.	Rhodamines	17-26	prostaglandin-endoperoxide synthase 2	Mus musculus	124-140
31775672-2	2019	Fluorocoxib A, a rhodamine-conjugated analog of indomethacin, is a novel fluorescent imaging agent that selectively targets cyclooxygenase-2 (COX-2)-expressing cancers.	Rhodamines	17-26	prostaglandin-endoperoxide synthase 2	Mus musculus	142-147
31434345-6	2019	The enhanced cellular uptake and selective accumulation of TLS (Res) and DLS (Res) into the mitochondria were demonstrated by behavioral observation of rhodamine-labeled TLS or DLS, using confocal microscopy, and by resveratrol quantification in the intracellular organelle, using LC-MS/MS.	Rhodamines	152-161	FUS RNA binding protein	Homo sapiens	59-62
31087712-4	2019	The activity of P-glycoprotein (P-gp), as one of the membrane transporters, was determined by the rhodamine 123 (Rho 123) assay.	Rhodamines	98-107	ATP binding cassette subfamily B member 1	Homo sapiens	16-30
31087712-4	2019	The activity of P-glycoprotein (P-gp), as one of the membrane transporters, was determined by the rhodamine 123 (Rho 123) assay.	Rhodamines	98-107	ATP binding cassette subfamily B member 1	Homo sapiens	32-36
31454967-9	2019	Lyophilization of rhodamine-loaded PBCA-MB with sucrose and PVP showed that the presence of the dye does not affect the efficiency of freeze-drying, and that the dye is efficiently retained upon MB lyophilization.	Rhodamines	18-27	PBCA	Homo sapiens	35-39
31434345-6	2019	The enhanced cellular uptake and selective accumulation of TLS (Res) and DLS (Res) into the mitochondria were demonstrated by behavioral observation of rhodamine-labeled TLS or DLS, using confocal microscopy, and by resveratrol quantification in the intracellular organelle, using LC-MS/MS.	Rhodamines	152-161	FUS RNA binding protein	Homo sapiens	170-173
31166936-3	2019	Due to the enhanced visible-light absorption and efficient separation of photo-generated holes and electrons, the SnS2-SnO2 heterostructures display excellent photocatalytic performance for the degradation of rhodamine (RhB) under visible-light irradiation.	Rhodamines	209-218	sodium voltage-gated channel alpha subunit 11	Homo sapiens	114-118
31054496-1	2019	A photoinduced electron transfer (PET) and chelation-enhanced fluorescence (CHEF) regulated rhodamine-azobenzene chemosensor (L) was synthesized for chemoselective detection of Al3+, Cr3+, and Cu2+ by UV-Visible absorption study whereas Al3+ and Cr3+ by fluorimetric study in EtOH-H2O solvent.	Rhodamines	92-101	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	183-186
31054496-1	2019	A photoinduced electron transfer (PET) and chelation-enhanced fluorescence (CHEF) regulated rhodamine-azobenzene chemosensor (L) was synthesized for chemoselective detection of Al3+, Cr3+, and Cu2+ by UV-Visible absorption study whereas Al3+ and Cr3+ by fluorimetric study in EtOH-H2O solvent.	Rhodamines	92-101	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	246-249
31054496-3	2019	This is first report on rhodamine-azobenzene based Cr3+ chemosensor.	Rhodamines	24-33	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	51-54
30947123-6	2019	Ten selected non-hydrolysable derivatives were able to inhibit the P-gp-mediated rhodamine-123 efflux on K562/DOX cells, and the evaluation of their apparent permeability and ATP consumption on other cell lines suggested that the compounds can behave as unambiguous or not transported substrates.	Rhodamines	81-90	phosphoglycolate phosphatase	Homo sapiens	67-71
30958597-7	2019	Moreover, the level of active STAT3 was elevated in rhodamine 123 negative subpopulations of CSCs sorted from three melanoma cell lines.	Rhodamines	52-61	signal transducer and activator of transcription 3	Homo sapiens	30-35
31002479-3	2019	PDL is a laser that emits yellow light using Rhodamine dye as it is lasing medium.	Rhodamines	45-54	programmed cell death 1	Homo sapiens	0-3
30806015-2	2019	Herein, two derivatives of low-cost rhodamine, called sulforhodamine 101 (SR101) and sulforhodamine B (SRB), are applied as cathode interfacial layers (CILs) to effectively improve the charge-carrier transportation and collection, reduce the work function (WF) of Al counter electrode, and decrease the series resistance and charge recombination in the PSCs.	Rhodamines	36-45	chaperonin containing TCP1 subunit 4	Homo sapiens	85-101
30806015-2	2019	Herein, two derivatives of low-cost rhodamine, called sulforhodamine 101 (SR101) and sulforhodamine B (SRB), are applied as cathode interfacial layers (CILs) to effectively improve the charge-carrier transportation and collection, reduce the work function (WF) of Al counter electrode, and decrease the series resistance and charge recombination in the PSCs.	Rhodamines	36-45	chaperonin containing TCP1 subunit 4	Homo sapiens	103-106
30952726-3	2019	MATERIALS AND METHODS: In order to determine the feasibility of using an aptamer against mucin 1 (aptA) as carrier of the cytotoxic compound 1,10-phenanthroline to MCF-7 cells, as a potential radiosensitizer, was studied in experiments using circular dichroism and rhodamine labelling by fluorescent microscopy and flow cytometry.	Rhodamines	265-274	mucin 1, cell surface associated	Homo sapiens	89-96
30776197-3	2019	By introducing two additional rhodamine moieties at the termini, the resulting conjugate could also detect Hg2+ ions in a highly selective manner.	Rhodamines	30-39	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	107-110
30776197-4	2019	Upon excitation at the BODIPY core, the fluorescence emission of rhodamine at 580 nm was observed and the intensity increased substantially upon addition of Hg2+ ions due to inhibition of the PET process followed by highly efficient fluorescence resonance energy transfer (FRET) from the BODIPY core to the rhodamine moieties.	Rhodamines	65-74	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	157-160
30776197-4	2019	Upon excitation at the BODIPY core, the fluorescence emission of rhodamine at 580 nm was observed and the intensity increased substantially upon addition of Hg2+ ions due to inhibition of the PET process followed by highly efficient fluorescence resonance energy transfer (FRET) from the BODIPY core to the rhodamine moieties.	Rhodamines	307-316	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	157-160
30881339-5	2019	The cells were incubated with a pH-rhodamine-labeled human recombinant monoclonal GluN1 IgG1 autoantibody (GluN1-aAbpH-rhod) genetically engineered from clonally expanded intrathecal plasma cells from a patient with anti-NMDAR encephalitis, and the pH-rhodamine fluorescence was tracked over time.	Rhodamines	35-44	glutamate ionotropic receptor NMDA type subunit 1	Homo sapiens	107-112
30613850-8	2019	Graphical Abstract Schematic representation of Hg2+ detection by rhodamine based sensor.	Rhodamines	65-74	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	47-50
29130339-5	2019	Mechanistically, Ethyl lucidenates A could increase the intracellular accumulation of vincristine in K562/A02 cells through inhibiting the P-glycoprotein mediated drug-transport activity by rhodamine accumulation assay and cell cycle analysis.	Rhodamines	190-199	ATP binding cassette subfamily B member 1	Homo sapiens	139-153
30688455-5	2019	A total of 7 of 17 flavonoid substrates stimulated the P-gp efflux of rhodamine 123, and most substrates increased P-gp expression in KB/MDR cells.	Rhodamines	70-79	ATP binding cassette subfamily B member 1	Homo sapiens	55-59
30688455-5	2019	A total of 7 of 17 flavonoid substrates stimulated the P-gp efflux of rhodamine 123, and most substrates increased P-gp expression in KB/MDR cells.	Rhodamines	70-79	ATP binding cassette subfamily B member 1	Homo sapiens	115-119
29773368-6	2018	In addition, the multifunctional NPs increased the permeability of rhodamine 123 because the thiomer THL-fucoidan in the NPs inhibited P-glycoprotein.	Rhodamines	67-76	ATP binding cassette subfamily B member 1	Homo sapiens	135-149
30627799-0	2019	A novel tryptamine-appended rhodamine-based chemosensor for selective detection of Hg2+ present in aqueous medium and its biological applications.	Rhodamines	28-37	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	83-86
30881339-5	2019	The cells were incubated with a pH-rhodamine-labeled human recombinant monoclonal GluN1 IgG1 autoantibody (GluN1-aAbpH-rhod) genetically engineered from clonally expanded intrathecal plasma cells from a patient with anti-NMDAR encephalitis, and the pH-rhodamine fluorescence was tracked over time.	Rhodamines	35-44	glutamate ionotropic receptor NMDA type subunit 1	Homo sapiens	82-87
30538042-7	2019	Meanwhile, it was also increased the retention of P-gp substrates DOX and Rhodamine 123 (Rho-123) while did not affect the ATPase activity.	Rhodamines	74-83	ATP binding cassette subfamily B member 1	Homo sapiens	50-54
30259171-4	2018	The composite was used for SERS detection of rhodamine 6G and two antibacterial drugs (ceftriaxone and sulfadimethoxine).	Rhodamines	45-54	seryl-tRNA synthetase 1	Homo sapiens	27-31
30233326-6	2018	Our results showed that ischemia produced BBB damage and MMP-2/9 upregulation was colocalized with Rhodamine-dextran leakage.	Rhodamines	99-108	matrix metallopeptidase 2	Rattus norvegicus	57-62
30293961-0	2018	Relationship between the fluorescence intensity of rhodamine-labeled orexin A and the calcium responses in cortical neurons: An in vivo two-photon calcium imaging study.	Rhodamines	51-60	hypocretin	Mus musculus	69-77
30293961-3	2018	Here, we synthesized a rhodamine-labeled orexin A compound, enabling us to quantify the amount of orexin binding to its receptors, OX1 and OX2, which principally couple to the Gq/11 protein.	Rhodamines	23-32	hypocretin	Mus musculus	41-49
30293961-3	2018	Here, we synthesized a rhodamine-labeled orexin A compound, enabling us to quantify the amount of orexin binding to its receptors, OX1 and OX2, which principally couple to the Gq/11 protein.	Rhodamines	23-32	hypocretin	Mus musculus	41-47
30293961-3	2018	Here, we synthesized a rhodamine-labeled orexin A compound, enabling us to quantify the amount of orexin binding to its receptors, OX1 and OX2, which principally couple to the Gq/11 protein.	Rhodamines	23-32	NAD(P)H dehydrogenase, quinone 1	Mus musculus	131-134
30293961-3	2018	Here, we synthesized a rhodamine-labeled orexin A compound, enabling us to quantify the amount of orexin binding to its receptors, OX1 and OX2, which principally couple to the Gq/11 protein.	Rhodamines	23-32	CD200 antigen	Mus musculus	139-142
30293961-5	2018	Applying rhodamine-labeled orexin A (10 muM) to the cortical surface gradually and heterogeneously increased both the intensity of the rhodamine fluorescence and [Ca2+]i.	Rhodamines	9-18	hypocretin	Mus musculus	27-35
30293961-5	2018	Applying rhodamine-labeled orexin A (10 muM) to the cortical surface gradually and heterogeneously increased both the intensity of the rhodamine fluorescence and [Ca2+]i.	Rhodamines	135-144	hypocretin	Mus musculus	27-35
30293961-6	2018	Calcium responses started simultaneously with the increase in rhodamine-labeled orexin fluorescence and reached a plateau within several minutes.	Rhodamines	62-71	hypocretin	Mus musculus	80-86
29709579-2	2018	In this study we measured the inhibitory behaviour of a set of known drugs towards P-gp by using three different probe substrates (digoxin, Hoechst 33,342 and rhodamine 123).	Rhodamines	159-168	phosphoglycolate phosphatase	Homo sapiens	83-87
29698604-4	2018	Cellular uptake of PEG-CNA-RHO was detected within 30 s, and the amount internalized increased over the course of 1 h. Moreover, these copolymers were internalized within cells to a higher degree than controls consisting of either rhodamine tagged PEG or the rhodamine alone.	Rhodamines	231-240	protein phosphatase 3, catalytic subunit, alpha isoform	Mus musculus	23-26
30166110-13	2018	ATE-Hex reduced the rhodamine efflux in MES-SA/Dx5 cells, indicating that ATE-Hex could reduce the expression of P-gp.	Rhodamines	20-29	hematopoietically expressed homeobox	Homo sapiens	4-7
29458585-1	2018	We report the design and synthesis of a novel chemosensor (Rh6G-Cin) rhodamine-based indicator for selective detection of Zn2+ ion.	Rhodamines	69-78	pyridoxal phosphatase	Homo sapiens	64-67
30166110-13	2018	ATE-Hex reduced the rhodamine efflux in MES-SA/Dx5 cells, indicating that ATE-Hex could reduce the expression of P-gp.	Rhodamines	20-29	hematopoietically expressed homeobox	Homo sapiens	78-81
30166110-13	2018	ATE-Hex reduced the rhodamine efflux in MES-SA/Dx5 cells, indicating that ATE-Hex could reduce the expression of P-gp.	Rhodamines	20-29	phosphoglycolate phosphatase	Homo sapiens	113-117
29698604-4	2018	Cellular uptake of PEG-CNA-RHO was detected within 30 s, and the amount internalized increased over the course of 1 h. Moreover, these copolymers were internalized within cells to a higher degree than controls consisting of either rhodamine tagged PEG or the rhodamine alone.	Rhodamines	259-268	protein phosphatase 3, catalytic subunit, alpha isoform	Mus musculus	23-26
29748326-5	2018	After a single intravenous injection of VFI, plasma volume and mGFR can be determined on the basis of the plasma pharmacokinetics of the rhodamine derivative and fluorescein carboxymethylated dextrans, respectively.	Rhodamines	137-146	Rap guanine nucleotide exchange factor (GEF) 5	Mus musculus	63-67
30109181-5	2018	Furthermore, olmutinib could also increase the retention of doxorubicin (DOX) and rhodamine 123 (Rho 123) in ABC transporter subfamily G member 2 (ABCG2)-overexpressing cells.	Rhodamines	82-91	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	147-152
29289977-7	2018	These included a population of CCR4-CCR6- effector/memory CD4+ T cells expressing intermediate levels of the Th1-related chemokine receptor CXCR3 and abnormally high multi-drug resistance type 1 transporter (MDR1) activity as assessed by a rhodamine 123 excretion assay.	Rhodamines	240-249	C-C motif chemokine receptor 4	Homo sapiens	31-35
29763760-0	2018	Multispectroscopic and bioimaging approach for the interaction of rhodamine 6G capped gold nanoparticles with bovine serum albumin.	Rhodamines	66-75	albumin	Homo sapiens	117-130
29858657-8	2018	Carcinoembryonic antigen in sample was detected sensitively by using sensitization of rhodamine dye Rh123 as signal amplification strategy.	Rhodamines	86-95	CEA cell adhesion molecule 3	Homo sapiens	0-24
32254242-2	2018	Herein, we synthesized a novel phenyl-substituted imidazole-fused rhodamine analogue RV-1 with a long absorption wavelength at 573 nm and a large Stokes shift of about 82 nm for monitoring the changes in cellular viscosity.	Rhodamines	66-75	Friend virus susceptibility 1	Mus musculus	85-89
29808393-0	2018	A Rhodamine Derivative Based Chemosensor with High Selectivity and Quick Respond to Cr3+ in Aqueous Solution.	Rhodamines	2-11	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	84-87
29808393-1	2018	In this paper, a new kind of colorimetric chemsensor aiming at detecting Cr3+ has been synthesized, and it is based on the "Off-On" effect of a rhodamine derivative.	Rhodamines	144-153	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	73-76
29808393-4	2018	According to the fitting curve based on Benesi-Hildebrand equation and working curve of absorption strength in UV-vis spectrum, the binding pattern of Cr3+ and the rhodamine derivative follows a 1:1 stoichiometry.	Rhodamines	164-173	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	151-154
29289977-7	2018	These included a population of CCR4-CCR6- effector/memory CD4+ T cells expressing intermediate levels of the Th1-related chemokine receptor CXCR3 and abnormally high multi-drug resistance type 1 transporter (MDR1) activity as assessed by a rhodamine 123 excretion assay.	Rhodamines	240-249	C-C motif chemokine receptor 6	Homo sapiens	36-40
29725247-8	2018	Salmonella significantly decreased the efflux capabilities of P-gp, as based on the influx of Rhodamine 123 assay.	Rhodamines	94-103	ATP binding cassette subfamily B member 1	Homo sapiens	62-66
29534440-5	2018	Additionally, all of them except ATx 3 (+), caused similar results when the accumulation of the P-gp fluorescent substrate was evaluated after pre-incubating cells with the test compounds for 24 h, significantly reducing the rhodamine 123 intracellular accumulation as a result of a significant increase in P-gp activity.	Rhodamines	225-234	ataxin 3	Homo sapiens	33-38
29421572-7	2018	Two long-lasting P-gp pump modulators (9 and 10) were identified; they were able to inhibit remarkably the P-gp substrate rhodamine-123 efflux on the resistant K562/DOX cell line after 60 min.	Rhodamines	122-131	phosphoglycolate phosphatase	Homo sapiens	17-21
29421572-7	2018	Two long-lasting P-gp pump modulators (9 and 10) were identified; they were able to inhibit remarkably the P-gp substrate rhodamine-123 efflux on the resistant K562/DOX cell line after 60 min.	Rhodamines	122-131	phosphoglycolate phosphatase	Homo sapiens	107-111
29183127-1	2017	Amino pyridine-based rhodamine conjugate (APR) has been developed as a first chemosensor for selective detection and quantification of L-4-Hydroxyproline (Hyp).	Rhodamines	21-30	ribosomal protein L4	Homo sapiens	135-153
29458405-14	2018	Dacomitinib was found to significantly increase the accumulation of ABCG2 probe substrates [doxorubicin (DOX),Rhodamine 123 (Rho 123) and Hoechst 33342] by inhibiting the transporter efflux function.	Rhodamines	110-119	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	68-73
29132113-6	2018	The new approach takes advantage of Forster Resonance Energy Transfer (FRET) between, as the donor, a fluorescein-like diarsenical probe able to covalently bind a tetracysteine motif fused to the recombinant PDE5 catalytic domain and, as the acceptor, a rhodamine probe covalently bound to the pseudosubstrate cGMPS.	Rhodamines	254-263	phosphodiesterase 5A	Homo sapiens	208-212
29132113-7	2018	The FRET efficiency decreases when a competitive ligand binds the PDE5 catalytic site and displaces the cGMPS-rhodamine conjugate.	Rhodamines	110-119	phosphodiesterase 5A	Homo sapiens	66-70
29132113-8	2018	We have structurally investigated the PDE5/cGMPS-rhodamine complex by molecular modelling and have used the FRET signal to quantitatively characterize its binding equilibrium.	Rhodamines	49-58	phosphodiesterase 5A	Homo sapiens	38-42
29291440-7	2018	Oxime and particularly oxime ether formation strongly increased their inhibitory activity on the efflux of rhodamine 123 by P-glycoprotein (P-gp), while the new ecdysteroid lactam did not interfere with the efflux function.	Rhodamines	107-116	ATP binding cassette subfamily B member 1	Homo sapiens	124-138
29291440-7	2018	Oxime and particularly oxime ether formation strongly increased their inhibitory activity on the efflux of rhodamine 123 by P-glycoprotein (P-gp), while the new ecdysteroid lactam did not interfere with the efflux function.	Rhodamines	107-116	ATP binding cassette subfamily B member 1	Homo sapiens	140-144
29534440-5	2018	Additionally, all of them except ATx 3 (+), caused similar results when the accumulation of the P-gp fluorescent substrate was evaluated after pre-incubating cells with the test compounds for 24 h, significantly reducing the rhodamine 123 intracellular accumulation as a result of a significant increase in P-gp activity.	Rhodamines	225-234	ATP binding cassette subfamily B member 1	Homo sapiens	96-100
29534440-5	2018	Additionally, all of them except ATx 3 (+), caused similar results when the accumulation of the P-gp fluorescent substrate was evaluated after pre-incubating cells with the test compounds for 24 h, significantly reducing the rhodamine 123 intracellular accumulation as a result of a significant increase in P-gp activity.	Rhodamines	225-234	ATP binding cassette subfamily B member 1	Homo sapiens	307-311
29498663-6	2018	Furthermore, capsaicin and piperine increased the intracellular accumulation of the fluorescent P-glycoprotein (P-gp) substrates rhodamine and calcein and inhibited their efflux from the MDR cell lines.	Rhodamines	129-138	ATP binding cassette subfamily B member 1	Homo sapiens	96-110
29498663-6	2018	Furthermore, capsaicin and piperine increased the intracellular accumulation of the fluorescent P-glycoprotein (P-gp) substrates rhodamine and calcein and inhibited their efflux from the MDR cell lines.	Rhodamines	129-138	ATP binding cassette subfamily B member 1	Homo sapiens	112-116
29419294-4	2018	The shift of the rhodamine pi-pi* absorption maxima in going from Pt-RDM1 to Pt-RDM3 correlates well with the HOMO-LUMO energy gap measured in electrochemical experiments.	Rhodamines	17-26	RAD52 motif containing 1	Homo sapiens	69-73
29379908-7	2018	Impressively, the noted approach not only enabled the use of a new kind of enzyme substrate for ELISAs but also allowed the detection of human TNF-alpha at concentrations over 54-fold lower than that possible on commercial microwell plates primarily due to the better detectability of the rhodamine dye.	Rhodamines	289-298	tumor necrosis factor	Homo sapiens	143-152
29282978-3	2018	The effective permeability of the typical P-gp substrate rhodamine 123 (R123) in colon was significantly increased from (1.69 +- 0.22) x 10-5 cm/s in the control group to (3.39 +- 0.417) x 10-5 cm/s (p < 0.01) in the 3.5 mM IP6 group.	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	42-46
29146563-7	2018	Km and Vmax of P-gp mediated basolateral-to-apical (B-A) flux of rhodamine 123 were estimated to 332+-124muM and 111+-16pmol cm-2 min-1 (n=3, total N=6), respectively.	Rhodamines	65-74	ATP binding cassette subfamily B member 1	Homo sapiens	15-19
29128272-8	2018	LA treatment minimizes STX cytotoxicity, evaluated by trypan blue and MTT assay and both STX and STX-LA treatments were efficient to induce P-gp activity measured by rhodamine 123 dye extrusion.	Rhodamines	166-175	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Homo sapiens	89-92
29128272-8	2018	LA treatment minimizes STX cytotoxicity, evaluated by trypan blue and MTT assay and both STX and STX-LA treatments were efficient to induce P-gp activity measured by rhodamine 123 dye extrusion.	Rhodamines	166-175	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Homo sapiens	89-92
29128272-8	2018	LA treatment minimizes STX cytotoxicity, evaluated by trypan blue and MTT assay and both STX and STX-LA treatments were efficient to induce P-gp activity measured by rhodamine 123 dye extrusion.	Rhodamines	166-175	ATP binding cassette subfamily B member 1	Homo sapiens	140-144
30114704-9	2018	Mechanistically, the intracellular accumulations of doxorubicin and Rhodamine 123 were increased in ABCG2-overexpressing S1-MI-80 cells with the presence of PCI29732.	Rhodamines	68-77	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	100-105
28823086-0	2017	An Efficient Fluorescence "Turn-On" Chemosensor Comprising of Coumarin and Rhodamine Moieties for Al3+ and Hg2.	Rhodamines	75-84	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	107-110
28823086-5	2017	Graphical Abstract A potent fluorescence "turn-on" receptor (HL) based on rhodamine and coumarin moieties for the detection of Hg2+ and Al3+ is synthesized and characterized.	Rhodamines	74-83	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	127-130
29541662-4	2018	Thus, we provide solubility data on two prototypical P-gp substrates, digoxin and rhodamine 123, representing P-gp substrates with a relatively low- and high-aqueous solubility, respectively.	Rhodamines	82-91	ATP binding cassette subfamily B member 1	Homo sapiens	53-57
29541662-4	2018	Thus, we provide solubility data on two prototypical P-gp substrates, digoxin and rhodamine 123, representing P-gp substrates with a relatively low- and high-aqueous solubility, respectively.	Rhodamines	82-91	ATP binding cassette subfamily B member 1	Homo sapiens	110-114
28947254-3	2017	Here, we have internalized a rhodamine-based sensor RSL+ into living cells and monitored the mitochondrial ATP levels in cultured mouse embryonic fibroblasts.	Rhodamines	29-38	regulator of sex limited protein-Slp	Mus musculus	52-55
28624525-3	2017	Zebrafish (Danio rerio) treated with the Pxr agonist pregnenolone 16alpha-carbonitrile (PCN) showed decreased P-gp (zebrafish Abcb4) and CYP3A (zebrafish Cyp3a65) mRNA levels after 48h exposure; however, treatment with PCN also resulted in increased hepatic MDR/MXR functional activity (i.e. increased Rhodamine 123 efflux) in vivo.	Rhodamines	302-311	nuclear receptor subfamily 1, group I, member 2	Danio rerio	41-44
28825091-3	2017	P(RD-CZ) exhibits excellent selectivity for Hg2+ ions compared with Cd2+, Cu2+ Zn2+, and Fe3+ using the potentiometric technique, which depends on the increasing charge carrier transport through rhodamine-bound Hg2+ with a limit of detection (LOD) of 9.77 x 10-8 M. The P(RD-CZ) polymer film also exhibits a distinct color change from orange to purple, which is detectable even by the naked eye, in the presence of Hg2+ ions.	Rhodamines	195-204	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	44-47
28825091-3	2017	P(RD-CZ) exhibits excellent selectivity for Hg2+ ions compared with Cd2+, Cu2+ Zn2+, and Fe3+ using the potentiometric technique, which depends on the increasing charge carrier transport through rhodamine-bound Hg2+ with a limit of detection (LOD) of 9.77 x 10-8 M. The P(RD-CZ) polymer film also exhibits a distinct color change from orange to purple, which is detectable even by the naked eye, in the presence of Hg2+ ions.	Rhodamines	195-204	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	211-214
28825091-3	2017	P(RD-CZ) exhibits excellent selectivity for Hg2+ ions compared with Cd2+, Cu2+ Zn2+, and Fe3+ using the potentiometric technique, which depends on the increasing charge carrier transport through rhodamine-bound Hg2+ with a limit of detection (LOD) of 9.77 x 10-8 M. The P(RD-CZ) polymer film also exhibits a distinct color change from orange to purple, which is detectable even by the naked eye, in the presence of Hg2+ ions.	Rhodamines	195-204	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	211-214
28577240-0	2017	A Rhodamine-Based Fluorescent Chemosensor for the Detection of Pb2+, Hg2+ and Cd2.	Rhodamines	2-11	CD2 molecule	Homo sapiens	78-81
28405849-6	2017	However, accumulation of adriamycin and rhodamine 123 were increased which suggested the depression of P-gp activity.	Rhodamines	40-49	ATP binding cassette subfamily B member 1	Homo sapiens	103-107
28860472-5	2017	Surface imprinting was employed to construct a transferrin (TRA)-imprinted layer on the surface of rhodamine doped silica nanoparticles.	Rhodamines	99-108	transferrin	Homo sapiens	47-58
28860472-5	2017	Surface imprinting was employed to construct a transferrin (TRA)-imprinted layer on the surface of rhodamine doped silica nanoparticles.	Rhodamines	99-108	transferrin	Homo sapiens	60-63
28823086-1	2017	A potent fluorescence "turn-on" receptor (HL) based on rhodamine and coumarin moieties for the detection of Hg2+ and Al3+ is synthesized by condensation of rhodamine 6G hydrazide and 4-hydroxy-3-acetylcoumarin.	Rhodamines	55-64	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	108-111
28132103-5	2017	The C1236T, G2677A/T, and C3435T SNPs were determined, and the functionality of P-gp was assessed by flow cytometry (Rhodamine efflux assay).	Rhodamines	117-126	ATP binding cassette subfamily B member 1	Homo sapiens	80-84
28726724-0	2017	Theoretical Studies on Two-Photon Fluorescent Hg2+ Probes Based on the Coumarin-Rhodamine System.	Rhodamines	80-89	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	46-49
28726724-2	2017	In the present work, the optical properties of two newly-synthesized Hg2+ chemosensors based on the coumarin-rhodamine system (named Pro1 and Pro2) were systematically investigated using time-dependent density functional theory.	Rhodamines	109-118	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	69-72
28726724-2	2017	In the present work, the optical properties of two newly-synthesized Hg2+ chemosensors based on the coumarin-rhodamine system (named Pro1 and Pro2) were systematically investigated using time-dependent density functional theory.	Rhodamines	109-118	lamin A/C	Homo sapiens	133-137
28533092-9	2017	Similarly, the presence of DM did not alter the locations of other drug-binding sites since the thiol reactive forms of the substrates verapamil or rhodamine labeled the same sites in transmembrane segments 5 (I306C for verapamil) and 6 (F343C for rhodamine) whether P-gp was in native membranes or in detergent micelles.	Rhodamines	148-157	ATP binding cassette subfamily B member 1	Homo sapiens	267-271
28620179-5	2017	Quantitative analysis based on SERS detection describes an excellent reproducibility with an intensity variation less than 7% at 1649 cm-1 of Rhodamine 6G.	Rhodamines	142-151	seryl-tRNA synthetase 1	Homo sapiens	31-35
28368059-0	2017	Pd2+ fluorescent sensors based on amino and imino derivatives of rhodamine and improvement of water solubility by the formation of inclusion complexes with beta-cyclodextrin.	Rhodamines	65-74	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	0-3
28088116-6	2017	Furthermore, a Cr3+-responsive rhodamine derivative (CRD) was modified on the devised UCNPs surface to fabricate the colorimetric probe by luminescent resonance energy transfer (LRET) process.	Rhodamines	31-40	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	15-18
28235604-9	2017	The expression and function of P-gp were measured by Western blotting, quantitative real-time polymerase chain reaction (qRT-PCR) and flow cytometry using rhodamine efflux.	Rhodamines	155-164	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	31-35
28225099-5	2017	Using this approach, the muMD measures droplets at a rate of 106 droplets per sec (phi = 166 mL h-1) in 120 parallel microfluidic channels and achieves a limit of detection LOD = 1 muM Rhodamine dye, sufficient for typical droplet based assays.	Rhodamines	185-194	latexin	Homo sapiens	25-28
28303028-4	2017	Mechanistically, alectinib increased the intracellular accumulation of ABCB1/ABCG2 substrates such as doxorubicin (DOX) and Rhodamine 123 (Rho 123) by inhibiting the efflux function of the transporters in ABCB1- or ABCG2-overexpressing cells but not in their parental sensitive cells.	Rhodamines	124-133	ATP binding cassette subfamily B member 1	Homo sapiens	71-76
28303028-4	2017	Mechanistically, alectinib increased the intracellular accumulation of ABCB1/ABCG2 substrates such as doxorubicin (DOX) and Rhodamine 123 (Rho 123) by inhibiting the efflux function of the transporters in ABCB1- or ABCG2-overexpressing cells but not in their parental sensitive cells.	Rhodamines	124-133	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	77-82
28030801-9	2017	We reveal that SPP1 is overexpressed in glioma initiating cells defined by high rhodamine 123 efflux, sphere forming capacity and stemness marker expression.	Rhodamines	80-89	secreted phosphoprotein 1	Homo sapiens	15-19
27821506-3	2017	Here we identify a subset of memory CD4+ T cells capable of effluxing cellular toxins, including rhodamine (Rho), through the multidrug efflux protein MDR1 (also known as P-glycoprotein and ABCB1).	Rhodamines	97-106	CD4 molecule	Homo sapiens	36-39
28104238-4	2017	The proposed multi-stacking strategy was verified under a fluorescence microscope using Rhodamine 6G as the model analyte and a sensitivity enhancement factor (SEF) of up to 217 was achieved.	Rhodamines	88-97	transcription factor CP2	Homo sapiens	128-158
28104238-4	2017	The proposed multi-stacking strategy was verified under a fluorescence microscope using Rhodamine 6G as the model analyte and a sensitivity enhancement factor (SEF) of up to 217 was achieved.	Rhodamines	88-97	transcription factor CP2	Homo sapiens	160-163
27821506-3	2017	Here we identify a subset of memory CD4+ T cells capable of effluxing cellular toxins, including rhodamine (Rho), through the multidrug efflux protein MDR1 (also known as P-glycoprotein and ABCB1).	Rhodamines	97-106	ATP binding cassette subfamily B member 1	Homo sapiens	151-155
27821506-3	2017	Here we identify a subset of memory CD4+ T cells capable of effluxing cellular toxins, including rhodamine (Rho), through the multidrug efflux protein MDR1 (also known as P-glycoprotein and ABCB1).	Rhodamines	97-106	ATP binding cassette subfamily B member 1	Homo sapiens	190-195
28068095-4	2017	In addition, 7a induced the mitochondrial tyrosine nitration and the intracellular accumulation of rhodamine 123 by inhibiting P-gp activity in K562/A02 cells.	Rhodamines	99-108	phosphoglycolate phosphatase	Homo sapiens	127-131
28772466-1	2017	Nonlinear optical properties of a series of newly-synthesized molecular fluorescent probes for Hg2+ containing the same acceptor (rhodamine group) are analyzed by using time-dependent density functional theory in combination with analytical response theory.	Rhodamines	130-139	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	95-98
27810576-11	2017	Eight of the tested PPCPs showed effects on Abcb4 ATPase activity indicating that their effects in the dye accumulation assay may have indeed resulted from interference with Abcb4-mediated rhodamine 123 efflux.	Rhodamines	189-198	ATP-binding cassette, sub-family B (MDR/TAP), member 4	Danio rerio	44-49
27810576-11	2017	Eight of the tested PPCPs showed effects on Abcb4 ATPase activity indicating that their effects in the dye accumulation assay may have indeed resulted from interference with Abcb4-mediated rhodamine 123 efflux.	Rhodamines	189-198	ATPase H+ transporting V1 subunit C1a	Danio rerio	50-56
27810576-11	2017	Eight of the tested PPCPs showed effects on Abcb4 ATPase activity indicating that their effects in the dye accumulation assay may have indeed resulted from interference with Abcb4-mediated rhodamine 123 efflux.	Rhodamines	189-198	ATP-binding cassette, sub-family B (MDR/TAP), member 4	Danio rerio	174-179
28109303-11	2017	Huh7 and MDA-MB231 cells displayed a significantly higher Rhodamine density in the cytoplasmic phagosomes and this suggests that the mechanism of uptake of large DNA by cancer cells is likely endocytosis.	Rhodamines	58-67	MIR7-3 host gene	Homo sapiens	0-4
28114946-9	2017	Specifically, the rate of permeability of Rhodamine 123 across the BBB model (0.6 +- 0.1 x 10-3, n = 4), increased 14-fold in the presence of the P-gp inhibitor verapamil (14.7 +- 7.5 x 10-3, n = 3) and eightfold with the addition of Cyclosporine A (8.8 +- 1.8 x 10-3, n = 3).	Rhodamines	42-51	phosphoglycolate phosphatase	Homo sapiens	146-150
27026527-4	2017	In 3D ileal enteroid culture and cell culture models (MDCK, IEC-6 and IPEC-J2 cells), extrusion events were suppressed by EGF, as determined by direct counting of released cells or rhodamine-phalloidin labeling of condensed actin rings.	Rhodamines	181-190	epidermal growth factor	Sus scrofa	122-125
27864369-4	2017	Despite dramatic reduction in rhodamine 123 and calcein-AM transport, the linker-shortened mutant P-gp possesses basal ATPase activity and binds ATP only in its N-terminal nucleotide-binding domain.	Rhodamines	30-39	phosphoglycolate phosphatase	Mus musculus	98-102
27678410-8	2017	R or racemic form of tolterodine and R-tamsulosin concentration-dependently increased P-gp protein expression; the latter also enhanced P-gp efflux function in a rhodamine-based efflux assay.	Rhodamines	162-171	ATP binding cassette subfamily B member 1	Homo sapiens	136-140
27101017-4	2016	This QD/Eu-MOF is found to be an effective catalyst to complete the degradation of Rhodamine 6G dye within 50 min.	Rhodamines	83-92	lysine acetyltransferase 8	Homo sapiens	11-14
27720954-1	2016	In this present study, the secretory transport of P-gp substrates, rhodamine 123 and digoxin, was evaluated using a Caco-2/HT29-MTX co-culture characterized by an efflux mechanism and a paracellular permeability closer to the human intestinal barrier compared to the Caco-2 monolayer gold standard.	Rhodamines	67-76	phosphoglycolate phosphatase	Homo sapiens	50-54
27720954-3	2016	Labrasol  ALF and Gelucire  44/14 in saline buffer significantly decreased to 83% and 62%, the P-gp-mediated transport of rhodamine 123 across the co-culture, respectively.	Rhodamines	122-131	afamin	Homo sapiens	10-13
27720954-3	2016	Labrasol  ALF and Gelucire  44/14 in saline buffer significantly decreased to 83% and 62%, the P-gp-mediated transport of rhodamine 123 across the co-culture, respectively.	Rhodamines	122-131	phosphoglycolate phosphatase	Homo sapiens	95-99
27348457-7	2016	P-gp activities were assayed by rhodamine 123 cellular retention.	Rhodamines	32-41	phosphoglycolate phosphatase	Rattus norvegicus	0-4
27886150-6	2016	P-gp efflux activity and P-gp ATPase activity were measured using a rhodamine 123 (Rh-123) accumulation assay and a Pgp-Glo  assay; respectively.	Rhodamines	68-77	PGP	Canis lupus familiaris	0-4
29345889-11	2016	Accumulation of rhodamine encapsulated EGFR-targeted cationic liposomes was observed throughout the primary tumor bed after systemic injection.	Rhodamines	16-25	epidermal growth factor receptor	Homo sapiens	39-43
26810690-3	2016	Materials and methods In Caco-2 cell experiments, the effects of baicalin and baicalein on P-gp activity were investigated using a P-gp substrate, rhodamine 123 and non-substrate fluorescein Na, by determining their intracellular fluorescence accumulation, and their effects on P-gp expression were determined using flow cytometry.	Rhodamines	147-156	ATP binding cassette subfamily B member 1	Homo sapiens	91-95
27760768-6	2016	We then examined clathrin-mediated endocytosis after ILK inhibition using rhodamine-conjugated transferrin.	Rhodamines	74-83	transferrin	Rattus norvegicus	95-106
27545217-8	2016	The reversal of MDR by AKBA was evident in an intracellular increase in Rhodamine (Rh123), indicating that the activity of P-glycoprotein (P-gp) was blocked.	Rhodamines	72-81	ATP binding cassette subfamily B member 1	Homo sapiens	123-137
27545217-8	2016	The reversal of MDR by AKBA was evident in an intracellular increase in Rhodamine (Rh123), indicating that the activity of P-glycoprotein (P-gp) was blocked.	Rhodamines	72-81	ATP binding cassette subfamily B member 1	Homo sapiens	139-143
27857347-3	2016	The fabricated MoS<sub>2</sub>@Au NPs with higher surface area exhibit excellent Raman enhanced effect for aromatic organic molecules (rhodamine 6G and crystal violet) and achieve the best when the monolayer MoS<sub>2</sub>@AuNPs was obtained.	Rhodamines	147-156	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	15-18
27857347-3	2016	The fabricated MoS<sub>2</sub>@Au NPs with higher surface area exhibit excellent Raman enhanced effect for aromatic organic molecules (rhodamine 6G and crystal violet) and achieve the best when the monolayer MoS<sub>2</sub>@AuNPs was obtained.	Rhodamines	147-156	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	220-223
27267282-1	2016	A novel rhodamine-based dual probe Rh-2 for trivalent ferric ions (Fe(3+)) was successfully designed and synthesized, which exhibited a highly sensitive and selective recognition towards Fe(3+) with an enhanced fluorescence emission in methanol-water media (v/v=7/3, pH=7.2).	Rhodamines	8-17	Rh associated glycoprotein	Homo sapiens	35-39
27669824-8	2016	The multistacking was verified under a fluorescence microscope using Rhodamine 6G as the analyte, revealing a sensitivity enhancement factor (SEF) of 110.	Rhodamines	69-78	transcription factor CP2	Homo sapiens	110-140
27669824-8	2016	The multistacking was verified under a fluorescence microscope using Rhodamine 6G as the analyte, revealing a sensitivity enhancement factor (SEF) of 110.	Rhodamines	69-78	transcription factor CP2	Homo sapiens	142-145
27060462-0	2016	Measurement of Rhodamine 123 in Three-Dimensional Organoids: A Novel Model for P-Glycoprotein Inhibitor Screening.	Rhodamines	15-24	ATP binding cassette subfamily B member 1	Homo sapiens	79-93
27060462-3	2016	In this study, a rapid, sensitive and efficient method to measure rhodamine 123 (Rh123, P-gp substrate) in 3D organoids was developed to analyse P-gp-mediated drug transport.	Rhodamines	66-75	ATP binding cassette subfamily B member 1	Homo sapiens	88-92
27060462-3	2016	In this study, a rapid, sensitive and efficient method to measure rhodamine 123 (Rh123, P-gp substrate) in 3D organoids was developed to analyse P-gp-mediated drug transport.	Rhodamines	66-75	ATP binding cassette subfamily B member 1	Homo sapiens	145-149
27196753-3	2016	Mechanistically, osimertinib increased the intracellular accumulations of doxorubicin (DOX) and Rhodamine 123 (Rho 123) by inhibiting the efflux function of the transporters in ABCB1- or ABCG2-overexpressing cells but not in their parental sensitive cells.	Rhodamines	96-105	ATP binding cassette subfamily B member 1	Homo sapiens	177-182
27117116-1	2016	Functionalized giant unilamellar vesicles (GUVs) containing a fluorescence dye Rhodamine 6G is proposed as a marker in sandwich-type immunoassay for bovine serum albumin (BSA) and lipocalin-2 (LCN2).	Rhodamines	79-88	albumin	Homo sapiens	156-175
27117116-1	2016	Functionalized giant unilamellar vesicles (GUVs) containing a fluorescence dye Rhodamine 6G is proposed as a marker in sandwich-type immunoassay for bovine serum albumin (BSA) and lipocalin-2 (LCN2).	Rhodamines	79-88	lipocalin 2	Homo sapiens	180-191
27117116-1	2016	Functionalized giant unilamellar vesicles (GUVs) containing a fluorescence dye Rhodamine 6G is proposed as a marker in sandwich-type immunoassay for bovine serum albumin (BSA) and lipocalin-2 (LCN2).	Rhodamines	79-88	lipocalin 2	Homo sapiens	193-197
27044313-5	2016	To test this, we studied the effects of several alkylated rhodamines on the drug resistance of yeast Saccharomyces cerevisiae We found that octylrhodamine synergetically increases toxicity of Pdr5p substrate-clotrimazole, while the others were less effective.	Rhodamines	58-68	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	192-197
27044313-6	2016	Next, we compared the contributions of three major pleiotropic ABC-transporters (Pdr5p, Yor1p, Snq2p) on the accumulation of the alkylated rhodamines.	Rhodamines	139-149	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	81-86
27044313-6	2016	Next, we compared the contributions of three major pleiotropic ABC-transporters (Pdr5p, Yor1p, Snq2p) on the accumulation of the alkylated rhodamines.	Rhodamines	139-149	ATP-binding cassette transporter YOR1	Saccharomyces cerevisiae S288C	88-93
27044313-6	2016	Next, we compared the contributions of three major pleiotropic ABC-transporters (Pdr5p, Yor1p, Snq2p) on the accumulation of the alkylated rhodamines.	Rhodamines	139-149	ATP-binding cassette transporter SNQ2	Saccharomyces cerevisiae S288C	95-100
27044313-8	2016	Interestingly, among the tested alkylated rhodamines, inactivation of Pdr5p had the strongest effect on the accumulation of octylrhodamine inside the cells, which is consistent with the fact that clotrimazole is a substrate of Pdr5p.	Rhodamines	42-52	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	70-75
27001764-0	2016	Geographical Distribution of MDR1 Expression in Leishmania Isolates, from Greece and Cyprus, Measured by the Rhodamine-123 Efflux Potential of the Isolates, Using Flow Cytometry.	Rhodamines	109-118	ATP binding cassette subfamily B member 1	Homo sapiens	29-33
27077878-4	2016	14/16 of these P-gp inhibitors were found to increase rhodamine 123 accumulation in P-gp-overexpressing MCF7R cells, thus allowing the determination of their P-gp inhibitory potential, i.e., their half maximal inhibitor concentration (IC50) value towards P-gp-mediated transport of the dye.	Rhodamines	54-63	ATP binding cassette subfamily B member 1	Homo sapiens	15-19
27077878-4	2016	14/16 of these P-gp inhibitors were found to increase rhodamine 123 accumulation in P-gp-overexpressing MCF7R cells, thus allowing the determination of their P-gp inhibitory potential, i.e., their half maximal inhibitor concentration (IC50) value towards P-gp-mediated transport of the dye.	Rhodamines	54-63	ATP binding cassette subfamily B member 1	Homo sapiens	84-88
27077878-4	2016	14/16 of these P-gp inhibitors were found to increase rhodamine 123 accumulation in P-gp-overexpressing MCF7R cells, thus allowing the determination of their P-gp inhibitory potential, i.e., their half maximal inhibitor concentration (IC50) value towards P-gp-mediated transport of the dye.	Rhodamines	54-63	ATP binding cassette subfamily B member 1	Homo sapiens	84-88
27077878-4	2016	14/16 of these P-gp inhibitors were found to increase rhodamine 123 accumulation in P-gp-overexpressing MCF7R cells, thus allowing the determination of their P-gp inhibitory potential, i.e., their half maximal inhibitor concentration (IC50) value towards P-gp-mediated transport of the dye.	Rhodamines	54-63	ATP binding cassette subfamily B member 1	Homo sapiens	84-88
26288998-6	2016	The enhancement ratios of Papp calculated from the ratio between Papp of rhodamine 123 in the presence of P-gp inhibitors and Papp of rhodamine 123 alone were 2.36, 2.09, and 1.84-fold in the presence of PAA-Cys-2MNA, PAA-Cys, and PAA, respectively.	Rhodamines	73-82	ATP binding cassette subfamily B member 1	Homo sapiens	106-110
27140215-3	2016	The bone-abrading method was used to detect the effects of intracerebroventricular application of 40 mug/kg bw TNF-alpha on cerebral venular leakage of fluorescein isothiocyanate (FITC)- albulmin and the rolling and adhesion of leukocytes on venules with fluorescence tracer rhodamine 6G.	Rhodamines	275-284	tumor necrosis factor	Mus musculus	111-120
26258802-6	2016	The enhancement ratios of Papp calculated from the ratio between Papp of rhodamine 123 in the presence of P-gp inhibitors and Papp of rhodamine 123 alone were 2.36, 2.09, and 1.84-fold in the presence of PAA-Cys-2MNA, PAA-Cys, and PAA, respectively.	Rhodamines	73-82	ATP binding cassette subfamily B member 1	Homo sapiens	106-110
26968974-0	2016	Effects of Polyoxyethylene Alkyl Ethers on the Intestinal Transport and Absorption of Rhodamine 123: A P-glycoprotein Substrate by In Vitro and In Vivo Studies.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	103-117
26555574-0	2016	Environmentally Robust Rhodamine Reporters for Probe-based Cellular Detection of the Cancer-linked Oxidoreductase hNQO1.	Rhodamines	23-32	NAD(P)H quinone dehydrogenase 1	Homo sapiens	114-119
26687436-3	2015	In contrast to common logic, we used SERS intensity gradients of Rhodamine 6G to quantitatively calculate the concentration of chloride ions at specific positions on a microfluidic chip.	Rhodamines	65-74	seryl-tRNA synthetase 1	Homo sapiens	37-41
27212149-1	2016	OBJECTIVE: The aim of this work was to verify the usefulness and efficacy of treating superficial vascular lesions of the face using rhodamine intense pulsed light (r-IPL).	Rhodamines	133-142	pleckstrin homology like domain family A member 2	Homo sapiens	167-170
26486517-7	2015	Pgp function was assessed by a rhodamine efflux assay and (99m)Tc-sestamibi scintigraphy.	Rhodamines	31-40	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
26506420-4	2015	Furthermore, cetuximab markedly increased intracellular accumulation of doxorubicin (DOX) and rhodamine 123 (Rho 123) in ABCB1-overexpressing MDR cancer cells in a concentration-dependent manner.	Rhodamines	94-103	ATP binding cassette subfamily B member 1	Homo sapiens	121-126
26402516-1	2015	A rhodamine-based molecule, Rh-OH, is synthesized.	Rhodamines	2-11	ras homolog family member H	Homo sapiens	28-33
26153782-8	2015	In five EBV-T-LPDs patients, P-gp function was detected by Rhodamine-123 efflux assay in these cells.	Rhodamines	59-68	ATP binding cassette subfamily B member 1	Homo sapiens	29-33
26462065-1	2015	Using apoferritin (AFt) as a carrier, a novel ratiometric luminescence probe based on luminescence resonance energy transfer (LRET) between a Tb(3+) complex (PTTA-Tb(3+)) and a rhodamine derivative (Rh-NO), PTTA-Tb(3+)@AFt-Rh-NO, has been designed and prepared for the specific recognition and time-gated luminescence detection of nitric oxide (NO) in living samples.	Rhodamines	177-186	ferritin heavy chain 1	Homo sapiens	6-17
26462065-1	2015	Using apoferritin (AFt) as a carrier, a novel ratiometric luminescence probe based on luminescence resonance energy transfer (LRET) between a Tb(3+) complex (PTTA-Tb(3+)) and a rhodamine derivative (Rh-NO), PTTA-Tb(3+)@AFt-Rh-NO, has been designed and prepared for the specific recognition and time-gated luminescence detection of nitric oxide (NO) in living samples.	Rhodamines	177-186	ferritin heavy chain 1	Homo sapiens	19-22
26265061-7	2015	P-gp inhibitory potential of Pl-g-CH was proved by flow cytometry and fluorescence microscopy where the much enhanced fluorescence intensity of Rhodamine 123 (Rho-123, P-gp substrate) was observed in the presence of Pl-g-CH.	Rhodamines	144-153	phosphoglycolate phosphatase	Homo sapiens	0-4
26265061-7	2015	P-gp inhibitory potential of Pl-g-CH was proved by flow cytometry and fluorescence microscopy where the much enhanced fluorescence intensity of Rhodamine 123 (Rho-123, P-gp substrate) was observed in the presence of Pl-g-CH.	Rhodamines	144-153	phosphoglycolate phosphatase	Homo sapiens	168-172
26291333-6	2015	FD18 (1 muM) can increase accumulation of doxorubicin by 2.7-fold, daunorubicin (2.1-fold), and rhodamine 123 (5.2-fold) in LCC6MDR.	Rhodamines	96-105	latexin	Homo sapiens	8-11
25841120-3	2015	Using CA125 as the antigen and Rhodamine-6G (R6G)-conjugated immunogolds, a SERS immunosensor was self-assembled by antigen-antibody interaction.	Rhodamines	31-40	mucin 16, cell surface associated	Homo sapiens	6-11
26174773-4	2015	Cys residues were introduced at 12 positions in hSERT to enable covalent attachment of a rhodamine-based fluorophore.	Rhodamines	89-98	solute carrier family 6 member 4	Homo sapiens	48-53
26757548-5	2015	When pretreatment with MRP2 siRNA-3 or P-gp siRNA-2, the efflux of methotrexate or rhodamine decreased significantly and the intra-cellular concentration increased.	Rhodamines	83-92	ATP binding cassette subfamily C member 2	Homo sapiens	23-35
26757548-5	2015	When pretreatment with MRP2 siRNA-3 or P-gp siRNA-2, the efflux of methotrexate or rhodamine decreased significantly and the intra-cellular concentration increased.	Rhodamines	83-92	phosphoglycolate phosphatase	Homo sapiens	39-43
26295572-3	2015	The results showed that the rhodamine 123 (Rh123) accumulation, an indicator of P-gp activity, in Caco-2, KBv and RBMECs was increased by (-)CLA (1 or 5 mumol/L) at 8.2%-28.5%, but reduced by (+)CLA at 11.7%-25.9%, showing stereoselectivity in their regulation of P-gp activity.	Rhodamines	28-37	ATP binding cassette subfamily B member 1	Homo sapiens	80-84
26295572-3	2015	The results showed that the rhodamine 123 (Rh123) accumulation, an indicator of P-gp activity, in Caco-2, KBv and RBMECs was increased by (-)CLA (1 or 5 mumol/L) at 8.2%-28.5%, but reduced by (+)CLA at 11.7%-25.9%, showing stereoselectivity in their regulation of P-gp activity.	Rhodamines	28-37	ATP binding cassette subfamily B member 1	Homo sapiens	264-268
25995342-3	2015	EXPERIMENTAL DESIGN: ABCB1 efflux activity was determined using a rhodamine efflux assay.	Rhodamines	66-75	ATP binding cassette subfamily B member 1	Homo sapiens	21-26
26350141-5	2015	Microarray and real-time PCR analysis showed that ABCB1 mRNA is upregulated in these cells, and P-glycoprotein (P-gp) expression as well as function were confirmed by immunoblot and rhodamine exclusion assays.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	50-55
26350141-5	2015	Microarray and real-time PCR analysis showed that ABCB1 mRNA is upregulated in these cells, and P-glycoprotein (P-gp) expression as well as function were confirmed by immunoblot and rhodamine exclusion assays.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	96-110
26350141-5	2015	Microarray and real-time PCR analysis showed that ABCB1 mRNA is upregulated in these cells, and P-glycoprotein (P-gp) expression as well as function were confirmed by immunoblot and rhodamine exclusion assays.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	112-116
26018271-1	2015	OBJECTIVE: To investigate the role of capsaicin in regulating permeation of P-gp substrate rhodamine 123 (R123) across the jejunum, ileum and colon membranes of rats.	Rhodamines	91-100	phosphoglycolate phosphatase	Rattus norvegicus	76-80
26219569-7	2015	Interestingly, all resistant cells showed the induction of P-gp at the protein and RNA levels, which was associated with an increased efflux of the P-gp substrate rhodamine 123 (Rho123).	Rhodamines	163-172	ATP binding cassette subfamily B member 1	Homo sapiens	59-63
26219569-7	2015	Interestingly, all resistant cells showed the induction of P-gp at the protein and RNA levels, which was associated with an increased efflux of the P-gp substrate rhodamine 123 (Rho123).	Rhodamines	163-172	ATP binding cassette subfamily B member 1	Homo sapiens	148-152
25981393-4	2015	We also prepare dye-based SERS nanoprobes by sandwiching a typical Raman reporter such as Rhodamine B (RhB), Crystal Violet (CV) and Rhodamine 6G (R6G) between the nanostars and the nGO coating.	Rhodamines	90-99	seryl-tRNA synthetase 1	Homo sapiens	26-30
25725134-6	2015	The P-gp efflux efficiency was assessed by rhodamine 123 transport.	Rhodamines	43-52	phosphoglycolate phosphatase	Homo sapiens	4-8
25857708-3	2015	Rhodamine derivatives are validated fluorescent probes for measurement of mitochondrial membrane potential and also Pgp function.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	116-119
25857708-4	2015	The aim of this study was to investigate whether 2"[(18)F]-fluoroethylrhodamine B ((18)FRB) a halogenated rhodamine derivative previously synthesized for PET assessment of myocardial perfusion preserved its Pgp substrate character.	Rhodamines	70-79	ATP binding cassette subfamily B member 1	Homo sapiens	207-210
25857708-8	2015	Dissipation of the mitochondrial proton gradient by a proton ionophore CCCP decreased the accumulation of rhodamine 123 (R123) and (18)FRB into Pgp(-) cells.	Rhodamines	106-115	ATP binding cassette subfamily B member 1	Homo sapiens	144-147
25586740-3	2015	In the present study, miR-10a silencing in human DDP-resistant lung cancer A549/DDP cells was demonstrated to improve DDP sensitivity, apoptosis, intracellular rhodamine-123 content as well as the expression and activity of caspase-3/8.	Rhodamines	160-169	microRNA 10a	Homo sapiens	22-29
25765837-7	2015	The lignans can increase the retention of the P-gp substrate rhodamine 123 in CEM/ADR 5000 cells, indicating that lignans can inhibit the activity of P-gp.	Rhodamines	61-70	phosphoglycolate phosphatase	Homo sapiens	46-50
26197581-1	2015	In the present paper, the authors studied fluorescence resonance energy transfer (FRET) phenomenon between silver triangular nanoplates and bovine serum albumin (BSA)/Rhodamine 6G fluorescence complex, and established a fluorescence method for the detection of cobalt ions.	Rhodamines	167-176	albumin	Homo sapiens	147-160
26197581-2	2015	We found that when increasing the silver triangular nanoplates added to certain concentrations of fluorescent bovine serum albumin (BSA)/Rhodamine 6G complex, the fluorescence of Rhodamine 6G would be quenched up to 80% due to the FRET between the quencher and donor.	Rhodamines	137-146	albumin	Homo sapiens	117-130
25829763-7	2015	Further, the ability of ES to inhibit multi drug resistant (MDR) transporters (ABC-B1 and ABC-G2) was determined by Rhodamine (Rho) and Mitoxantrone (MXR) efflux assays.	Rhodamines	116-125	ATP binding cassette subfamily B member 1	Homo sapiens	79-85
25829763-7	2015	Further, the ability of ES to inhibit multi drug resistant (MDR) transporters (ABC-B1 and ABC-G2) was determined by Rhodamine (Rho) and Mitoxantrone (MXR) efflux assays.	Rhodamines	116-125	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	90-96
25829763-7	2015	Further, the ability of ES to inhibit multi drug resistant (MDR) transporters (ABC-B1 and ABC-G2) was determined by Rhodamine (Rho) and Mitoxantrone (MXR) efflux assays.	Rhodamines	116-119	ATP binding cassette subfamily B member 1	Homo sapiens	79-85
25829763-7	2015	Further, the ability of ES to inhibit multi drug resistant (MDR) transporters (ABC-B1 and ABC-G2) was determined by Rhodamine (Rho) and Mitoxantrone (MXR) efflux assays.	Rhodamines	116-119	ATP binding cassette subfamily G member 2 (Junior blood group)	Homo sapiens	90-96
25666715-1	2015	Two new rhodamine derivatives (L1 and L2) were synthesized, characterized and their ion recognition property has been investigated.	Rhodamines	8-17	L1 cell adhesion molecule	Homo sapiens	31-40
25730814-0	2015	Rhodamine-123: a p-glycoprotein marker complex with sodium lauryl sulfate.	Rhodamines	0-9	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	17-31
25765837-7	2015	The lignans can increase the retention of the P-gp substrate rhodamine 123 in CEM/ADR 5000 cells, indicating that lignans can inhibit the activity of P-gp.	Rhodamines	61-70	phosphoglycolate phosphatase	Homo sapiens	150-154
25686090-6	2015	In addition, multicopies of SNQ2 or PDR5 conferred resistance to rhodamine 6G (R6G), which was widely used as a substrate for transport assay.	Rhodamines	65-74	ATP-binding cassette transporter SNQ2	Saccharomyces cerevisiae S288C	28-32
25676275-4	2015	The expression of P-gp was detected by cell immunofluorescense analysis and the activity of P-gp was evaluated by Rhodamine 123 efflux experiment.	Rhodamines	114-123	ATP binding cassette subfamily B member 1	Homo sapiens	92-96
25445037-8	2015	Most DHPs, particularly compounds bearing 3-nitrophenyl (A2B2 and A3B2) and 4-nitrophenyl (A3B1 and A4B1) moieties at C4 significantly inhibited rhodamine 123 efflux at 5-25 microM, showing that the mechanism of MDR reversal by these agents is P-gp transporter modulation.	Rhodamines	145-154	ATP binding cassette subfamily B member 1	Homo sapiens	244-248
25470220-4	2015	Compound 7 h also enhanced the effects of other MDR-related cytotoxic agents (paclitaxel, vinblastine, and daunorubicin), increased the accumulation of DOX and blocked P-gp-mediated rhodamine 123 efflux function in K562/A02 MDR cells.	Rhodamines	182-191	ATP binding cassette subfamily B member 1	Homo sapiens	168-172
25510469-7	2015	When a CaF2/ZnS DBR was grown, without heating the substrate during deposition, on top of a thin film containing the fluorescent dye Rhodamine 6G, the fluorescence intensity showed no degradation compared to an uncoated film, in contrast to a MgF2/ZnS DBR coating grown with substrate heating which showed a 92% reduction in signal.	Rhodamines	133-142	CCR4-NOT transcription complex subunit 8	Homo sapiens	7-11
25686090-6	2015	In addition, multicopies of SNQ2 or PDR5 conferred resistance to rhodamine 6G (R6G), which was widely used as a substrate for transport assay.	Rhodamines	65-74	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	36-40
26046259-8	2015	Methyl-G increased the intracellular concentration of a known Pgp substrate, Rhodamine 123 in SF-295 cells.	Rhodamines	77-86	ATP binding cassette subfamily B member 1	Homo sapiens	62-65
25403403-3	2014	On the other hand, the fluorescence distribution plot showed predominant location of CD133(+) cancer cells among cells stained with neither DyeCycle Violet DNA-binding dye, nor rhodamine 123 mitochondrial dye.	Rhodamines	177-186	prominin 1	Homo sapiens	85-90
25433164-11	2015	Functionality of P-gp assessed with Rhodamine permeability did not change with passage number in Caco-2 cells with any of the protocols but increased in both protocols in MDCK and MDCK-MDR1 cells.	Rhodamines	36-45	phosphoglycolate phosphatase	Homo sapiens	17-21
25545265-1	2014	The reagent Rh-C, incorporating a rhodamine moiety and a coumarin backbone and prepared via click chemistry, was developed as the first single molecule for detecting Cu2+, Fe3+ and Cr3+.	Rhodamines	34-43	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	181-184
26088979-5	2014	The 3D-NPG nanostructures were found to effectively enhance the SERS sensitivity of rhodamine 6G (R6G) molecules with a concentration up to 10(-8) M.	Rhodamines	84-93	seryl-tRNA synthetase 1	Homo sapiens	64-68
25372840-9	2014	The intracellular level of ATP decreased 44%, 46% in the presence of 12.5.25 microM 3-Bromopyruvate, whereas the accumulation of rhodamine 123 and epirubicin (two typical P-glycoprotein substrates) in cells was significantly increased.	Rhodamines	129-138	ATP binding cassette subfamily B member 1	Homo sapiens	171-185
25189757-8	2014	The CNF surface bound AgNPs were easily fabricated into freestanding CNF/AgNPs films that showed excellent surface enhanced Raman scattering of Rhodamine 6G with analytical enhancement factor of 5 x 10(3) in contrast to none from the CNF/AgNSs film.	Rhodamines	144-153	NPHS1 adhesion molecule, nephrin	Homo sapiens	4-7
24734954-5	2014	MDR-1 function was assessed by Rhodamine efflux in presence or absence of verapamil.	Rhodamines	31-40	ATP binding cassette subfamily B member 1	Homo sapiens	0-5
25189757-8	2014	The CNF surface bound AgNPs were easily fabricated into freestanding CNF/AgNPs films that showed excellent surface enhanced Raman scattering of Rhodamine 6G with analytical enhancement factor of 5 x 10(3) in contrast to none from the CNF/AgNSs film.	Rhodamines	144-153	NPHS1 adhesion molecule, nephrin	Homo sapiens	69-72
25189757-8	2014	The CNF surface bound AgNPs were easily fabricated into freestanding CNF/AgNPs films that showed excellent surface enhanced Raman scattering of Rhodamine 6G with analytical enhancement factor of 5 x 10(3) in contrast to none from the CNF/AgNSs film.	Rhodamines	144-153	NPHS1 adhesion molecule, nephrin	Homo sapiens	69-72
25478314-0	2014	Rhodamine-Appended Bipyridine: XOR and OR Logic Operations Integrated in an Example of Controlled Metal Migration.	Rhodamines	0-9	xanthine dehydrogenase	Homo sapiens	31-34
25050613-0	2014	Synthesis and characterization of macromolecular rhodamine tethers and their interactions with P-glycoprotein.	Rhodamines	49-58	ATP binding cassette subfamily B member 1	Homo sapiens	95-109
24814693-6	2014	DAPK3 siRNA or a pharmacological inhibitor of DAPK3 inhibited PDGF-BB-induced lamellipodia formation as determined by rhodamine-phalloidin staining.	Rhodamines	118-127	death-associated protein kinase 3	Rattus norvegicus	0-5
24814693-6	2014	DAPK3 siRNA or a pharmacological inhibitor of DAPK3 inhibited PDGF-BB-induced lamellipodia formation as determined by rhodamine-phalloidin staining.	Rhodamines	118-127	death-associated protein kinase 3	Rattus norvegicus	46-51
25108566-5	2014	RESULTS: Both fAd and gAd increased RhoA activity, phosphorylation of the Rho/ROCK signaling target cofilin and actin polymerization to form filamentous actin as determined by rhodamine-phallodin immunofluorescence and quantitative analysis of filamentous to globular actin ratio.	Rhodamines	176-185	presenilin 1	Homo sapiens	14-17
25108566-5	2014	RESULTS: Both fAd and gAd increased RhoA activity, phosphorylation of the Rho/ROCK signaling target cofilin and actin polymerization to form filamentous actin as determined by rhodamine-phallodin immunofluorescence and quantitative analysis of filamentous to globular actin ratio.	Rhodamines	176-185	glutamate decarboxylase 1	Homo sapiens	22-25
25166911-3	2014	The entrapped cargo of rhodamine 6G was shown to be selectively released from PoPs upon exposure to divalent cations including the alpha-synuclein-specific pathophysiological ligand of Ca(2+).	Rhodamines	23-32	synuclein alpha	Homo sapiens	131-146
24967548-6	2014	In addition, p53 protein inexpression, mediated by rhodamine nanoparticles, demonstrates the ability of the proposed system to target mitochondria; due to the different genetic code in mitochondria, p53 protein cannot be expressed.	Rhodamines	51-60	tumor protein p53	Homo sapiens	13-16
25050613-1	2014	Rhodamine dyes are well-known P-glycoprotein (P-gp) substrates that have played an important role in the detection of inhibitors and other substrates of P-gp, as well as in the understanding of P-gp function.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	30-44
25050613-1	2014	Rhodamine dyes are well-known P-glycoprotein (P-gp) substrates that have played an important role in the detection of inhibitors and other substrates of P-gp, as well as in the understanding of P-gp function.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	46-50
25050613-1	2014	Rhodamine dyes are well-known P-glycoprotein (P-gp) substrates that have played an important role in the detection of inhibitors and other substrates of P-gp, as well as in the understanding of P-gp function.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	153-157
25050613-1	2014	Rhodamine dyes are well-known P-glycoprotein (P-gp) substrates that have played an important role in the detection of inhibitors and other substrates of P-gp, as well as in the understanding of P-gp function.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	153-157
25050613-2	2014	Macromolecular conjugates of rhodamines could prove useful as tethers for further probing of P-gp structure and function.	Rhodamines	29-39	ATP binding cassette subfamily B member 1	Homo sapiens	93-97
25121365-6	2014	P-gp activity was measured by flow cytometry using rhodamine efflux.	Rhodamines	51-60	phosphoglycolate phosphatase	Homo sapiens	0-4
24704556-6	2014	Furthermore, it could also increase the retention of ABCB1 substrates doxorubicin and rhodamine 123 in HepG2/ADM and MCF-7/ADR cells.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	53-58
24704556-6	2014	Furthermore, it could also increase the retention of ABCB1 substrates doxorubicin and rhodamine 123 in HepG2/ADM and MCF-7/ADR cells.	Rhodamines	86-95	adrenomedullin	Homo sapiens	109-112
26420981-6	2014	rhodamine-labelled PBCA NP variations into rats and monitored the survival and morphology of retrogradely labelled neurons by in vivo confocal neuroimaging (ICON) for five weeks.	Rhodamines	0-9	PBCA	Homo sapiens	19-23
24512977-7	2014	Based on these profiles, gelatin and PLGA NPs were used to encapsulate plasmid DNA encoding yellow fluorescent protein (YFP) or rhodamine-conjugated erythropoietin (EPO) for inhalational delivery to rats.	Rhodamines	128-137	erythropoietin	Rattus norvegicus	149-163
24512977-7	2014	Based on these profiles, gelatin and PLGA NPs were used to encapsulate plasmid DNA encoding yellow fluorescent protein (YFP) or rhodamine-conjugated erythropoietin (EPO) for inhalational delivery to rats.	Rhodamines	128-137	erythropoietin	Rattus norvegicus	165-168
24738437-6	2014	The as-synthesized ANAs array exhibited a remarkable SERS activity and Raman signal reproducibility to rhodamine 6G, a concentration down to 10(-13) M can be identified.	Rhodamines	103-112	seryl-tRNA synthetase 1	Homo sapiens	53-57
24948896-2	2014	LFP has been widely used as an electrode material of a lithium ion battery, but we observed that commercial LFP (LFP-C) could act as a good Fenton-like catalyst to decompose rhodamine 6G.	Rhodamines	174-183	lamin A/C	Homo sapiens	0-3
24733388-5	2014	The completely "regenerated" Pdr5 protein was severely impaired in its function of ATP hydrolysis and of rhodamine 6G transport.	Rhodamines	105-114	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	29-33
24948896-2	2014	LFP has been widely used as an electrode material of a lithium ion battery, but we observed that commercial LFP (LFP-C) could act as a good Fenton-like catalyst to decompose rhodamine 6G.	Rhodamines	174-183	lamin A/C	Homo sapiens	108-111
24948896-2	2014	LFP has been widely used as an electrode material of a lithium ion battery, but we observed that commercial LFP (LFP-C) could act as a good Fenton-like catalyst to decompose rhodamine 6G.	Rhodamines	174-183	lamin A/C	Homo sapiens	113-118
24944746-1	2014	Novel rhodamine-labeled ligands, based on (S)-citalopram, were synthesized and evaluated for uptake inhibition at the human serotonin, dopamine, and norepinephrine transporters (hSERT, hDAT, and hNET, respectively) and for binding at SERT, in transiently transfected COS7 cells.	Rhodamines	6-15	solute carrier family 6 member 4	Homo sapiens	179-183
24805805-4	2014	The performance of S-SERS is evaluated by the detection of Rhodamine 6G, urea, and its mixture with acetaminophen, in a physiologically relevant concentration range, along with the corresponding SERS spectroscopic maps.	Rhodamines	59-68	seryl-tRNA synthetase 1	Homo sapiens	21-25
24558643-1	2014	The effect of substituents on FRET in two newly designed rhodamine-based Hg(2+) ion selective chemosensors (L1 and L2) has been explored by a systematic experimental and theoretical study.	Rhodamines	57-66	L1 cell adhesion molecule	Homo sapiens	108-117
24735764-13	2014	CONCLUSIONS: This study showed reduced function of P-glycoprotein in ischemia-reperfusion injury as reflected by decreased biliary excretion of Rhodamine 123, as well as reduced protein expression of the transporter.	Rhodamines	144-153	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	51-65
24602286-12	2014	In addition, intracellular accumulation of Rhodamine 123 significantly increased in MCF-7/ADR cells transfected with ETS1 siRNA, indicating that silencing of ETS1 may reduce drug efflux.	Rhodamines	43-52	ETS proto-oncogene 1, transcription factor	Homo sapiens	117-121
24602286-12	2014	In addition, intracellular accumulation of Rhodamine 123 significantly increased in MCF-7/ADR cells transfected with ETS1 siRNA, indicating that silencing of ETS1 may reduce drug efflux.	Rhodamines	43-52	ETS proto-oncogene 1, transcription factor	Homo sapiens	158-162
24493631-6	2014	In situ intestinal perfusion experiments also showed that CK, Ppd, and Ppt increased the absorption rate constant and permeability coefficient of rhodamine 123.	Rhodamines	146-155	tachykinin precursor 1	Homo sapiens	71-74
22913740-0	2014	The mitochondrial fluorescent dye rhodamine 123 is a high-affinity substrate for organic cation transporters (OCTs) 1 and 2.	Rhodamines	34-43	solute carrier family 22 member 1	Homo sapiens	81-123
22913740-4	2014	This increase of rhodamine 123 influxes was found to be a saturable carrier-mediated process, with low K(m) values (K(m) = 0.54 mum and K(m) = 0.61 mum for transport of the dye in hOCT1- and hOCT2-positive HEK293 cells, respectively).	Rhodamines	17-26	solute carrier family 22 member 1	Homo sapiens	180-185
22913740-4	2014	This increase of rhodamine 123 influxes was found to be a saturable carrier-mediated process, with low K(m) values (K(m) = 0.54 mum and K(m) = 0.61 mum for transport of the dye in hOCT1- and hOCT2-positive HEK293 cells, respectively).	Rhodamines	17-26	solute carrier family 22 member 2	Homo sapiens	191-196
23728918-0	2014	Rhodamine-marked bombesin: a novel means for prostate cancer fluorescence imaging.	Rhodamines	0-9	gastrin releasing peptide	Homo sapiens	17-25
23728918-4	2014	These novel rhodamine fluorescent conjugates were used to study the targeting and uptake of bombesin on a cellular level.	Rhodamines	12-21	gastrin releasing peptide	Homo sapiens	92-100
24621983-5	2014	The impact of the 1199G>A SNP on ABCB1 activity towards rhodamine (Rh123), doxorubicin, vinblastine, tacrolimus and cyclosporine A was assessed by accumulation, cytotoxicity and/or kinetic experiments.	Rhodamines	59-68	ATP binding cassette subfamily B member 1	Homo sapiens	36-41
24504599-1	2014	In this work, we investigated Greek Leishmania isolates (n = 70) for their individual MDR1-gene-related p-gp (belonging to the ABC-B subfamily of permeases) expression levels by means of flow cytometric analysis of Rhodamine 123 extrusion kinetics.	Rhodamines	215-224	ATP binding cassette subfamily B member 1	Homo sapiens	86-90
32261280-0	2014	Self-focusing Au@SiO2 nanorods with rhodamine 6G as highly sensitive SERS substrate for carcinoembryonic antigen detection.	Rhodamines	36-45	CEA cell adhesion molecule 3	Homo sapiens	88-112
24471913-2	2014	The rhodamine-labeled C-peptide entered renal tubular cells and localized in nuclei, both in the presence and absence of insulin; preincubations with the unlabeled compound inhibited internalization.	Rhodamines	4-13	insulin	Oryctolagus cuniculus	121-128
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 1	Homo sapiens	42-47
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 2	Homo sapiens	53-58
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 1	Homo sapiens	131-136
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 2	Homo sapiens	141-146
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 1	Homo sapiens	131-136
22913740-6	2014	In addition, the dye was found to inhibit hOCT1- and hOCT2-mediated uptake of tetraethylammonium (TEA), a model substrate for both hOCT1 and hOCT2; rhodamine 123 appeared nevertheless to be a more potent inhibitor of hOCT1-mediated TEA transport (IC50 = 0.37 mum) than of that mediated by hOCT2 (IC50 = 61.5 mum).	Rhodamines	148-157	solute carrier family 22 member 2	Homo sapiens	141-146
22913740-7	2014	Taken together, these data demonstrate that rhodamine 123 is a high-affinity substrate for both hOCT1 and hOCT2.	Rhodamines	44-53	solute carrier family 22 member 1	Homo sapiens	96-101
22913740-7	2014	Taken together, these data demonstrate that rhodamine 123 is a high-affinity substrate for both hOCT1 and hOCT2.	Rhodamines	44-53	solute carrier family 22 member 2	Homo sapiens	106-111
24117322-5	2013	The results demonstrate that a maximum enhancement factor can reach ~10(5) with a detectable concentration as low as 10(-10) M for rhodamine 6G (R6G) molecules, indicating that the as-obtained unique nanostructure will be a promising candidate for SERS applications.	Rhodamines	131-140	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	248-252
24130053-6	2013	Here, using a ubiquitin-rhodamine-based high-throughput screening, we identified small-molecule inhibitors of USP1 and investigated their therapeutic potential for leukemia.	Rhodamines	24-33	ubiquitin specific peptidase 1	Homo sapiens	110-114
24107183-2	2013	Here we describe a nanosensor for caspase-1 ratiometric measurements, consisting of a rhodamine-labeled, caspase-1 cleavable peptide linked to quantum dots (QDs).	Rhodamines	86-95	caspase 1	Homo sapiens	34-43
24107183-2	2013	Here we describe a nanosensor for caspase-1 ratiometric measurements, consisting of a rhodamine-labeled, caspase-1 cleavable peptide linked to quantum dots (QDs).	Rhodamines	86-95	caspase 1	Homo sapiens	105-114
24237849-5	2013	ABPP was performed by reacting urines (n = 18) with a rhodamine-tagged fluorophosphonate probe and visualizing on SDS-PAGE.	Rhodamines	54-63	amyloid beta precursor protein	Homo sapiens	0-4
24036383-0	2013	Rhodamine-loaded intercellular adhesion molecule-1-targeted microbubbles for dual-modality imaging under controlled shear stresses.	Rhodamines	0-9	intercellular adhesion molecule 1	Homo sapiens	17-50
23872169-3	2013	METHODS: The signal transduction pathway of PI3-K/AKT and the downstream signaling proteins had been studied in an early stage of colon carcinogenesis (DMH induced) by gene and protein expression, apoptotic studies by colonocyte apoptotic bleb assay, intracellular calcium level by fluorescence spectrometry, mitochondrial membrane potential by Rhodamine 123 flow cytometry and Reactive oxygen species measurement.	Rhodamines	345-354	AKT serine/threonine kinase 1	Rattus norvegicus	50-53
24036383-3	2013	METHODS AND RESULTS: Using 2-photon laser scanning microscopy and contrast-enhanced ultrasound, intercellular adhesion molecule-1-targeted and rhodamine-loaded microbubbles were shown to be specifically bound to tumor necrosis factor-alpha-stimulated human umbilical vein endothelial cells and murine carotid arteries (44 wild-type mice) at shear stresses ranging from 1.25 to 120 dyn/cm(2).	Rhodamines	143-152	tumor necrosis factor	Homo sapiens	212-239
24041929-4	2013	rhodamine 123 acts as a good substrate for P-glycoprotein, and agents that block P-glycoprotein have been found to increase the retention of rhodamine in cells.	Rhodamines	0-9	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	43-57
24041929-4	2013	rhodamine 123 acts as a good substrate for P-glycoprotein, and agents that block P-glycoprotein have been found to increase the retention of rhodamine in cells.	Rhodamines	141-150	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	81-95
23271055-5	2013	Tau synergized with Hsc70, but not Hsp72, to promote microtubule assembly at nearly twice the rate of either Hsp70 homologue in reconstituted, ATP-regenerating Xenopus extracts supplemented with rhodamine-labeled tubulin and human recombinant Hsp72 and Hsc70.	Rhodamines	195-204	microtubule associated protein tau	Homo sapiens	0-3
23897240-4	2013	In everted intestinal sacs, AP inhibited serosal-mucosal transport of rhodamine 123 (R123), a prototypical P-gp substrate.	Rhodamines	70-79	ATP binding cassette subfamily B member 1	Homo sapiens	107-111
23897419-1	2013	Venlafaxine, and to a lesser extent desvenlafaxine, has previously been shown to induce the expression of the drug efflux transporters P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) in whole cells and alter the cellular permeability of a known drug efflux probe (rhodamine 123).	Rhodamines	282-291	phosphoglycolate phosphatase	Mus musculus	135-149
23897419-1	2013	Venlafaxine, and to a lesser extent desvenlafaxine, has previously been shown to induce the expression of the drug efflux transporters P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) in whole cells and alter the cellular permeability of a known drug efflux probe (rhodamine 123).	Rhodamines	282-291	phosphoglycolate phosphatase	Mus musculus	151-155
23897419-1	2013	Venlafaxine, and to a lesser extent desvenlafaxine, has previously been shown to induce the expression of the drug efflux transporters P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) in whole cells and alter the cellular permeability of a known drug efflux probe (rhodamine 123).	Rhodamines	282-291	ATP binding cassette subfamily G member 2 (Junior blood group)	Mus musculus	161-193
23897419-1	2013	Venlafaxine, and to a lesser extent desvenlafaxine, has previously been shown to induce the expression of the drug efflux transporters P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) in whole cells and alter the cellular permeability of a known drug efflux probe (rhodamine 123).	Rhodamines	282-291	ATP binding cassette subfamily G member 2 (Junior blood group)	Mus musculus	195-199
23608541-3	2013	The quenching intensity of the fluorescence images for rhodamine-labeled ssDNA fitted well with the changes in SPR.	Rhodamines	55-64	sepiapterin reductase	Homo sapiens	111-114
23380148-1	2013	A novel FRET fluorescent sensor for Hg2+ imaging in living cells is rationally designed based on a coumarin-rhodamine platform.	Rhodamines	108-117	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	36-39
23380148-3	2013	After addition of increasing concentrations of Hg2+, it result in the decrease of coumarin emission at 467 nm and a new emission profile of rhodamine at 590 nm gradually increased.	Rhodamines	140-149	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	47-50
23524533-4	2013	P-gp expression was determined by western blot and activity determined by rhodamine efflux assay.	Rhodamines	74-83	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
23618585-9	2013	After 30 minutes of efflux, rhodamine 123 fluorescence intensity was significantly lower in BIU-87/ADM cells (5.55 vs 51.45, p = 0.004) and co-cultured BIU-87 cells than in BIU-87 cells (14.22 vs 51.45, p <0.001), indicating that P-glycoprotein was functional.	Rhodamines	28-37	ATP binding cassette subfamily B member 1	Homo sapiens	233-247
23594094-5	2013	Confocal microscopy confirmed the Tf receptor-mediated endocytosis of rhodamine-labeled Tf-modified micelles after staining the micelle-treated cells with the endosomal marker Tf-Alexa488.	Rhodamines	70-79	transferrin	Homo sapiens	34-36
23594094-5	2013	Confocal microscopy confirmed the Tf receptor-mediated endocytosis of rhodamine-labeled Tf-modified micelles after staining the micelle-treated cells with the endosomal marker Tf-Alexa488.	Rhodamines	70-79	transferrin	Homo sapiens	88-90
23743668-5	2013	METHODS: Rhodamine (Rh123) efflux was used to study ABCB1 activity, with or without the addition of the ABCB1 inhibitor verapamil.	Rhodamines	9-18	ATP binding cassette subfamily B member 1	Homo sapiens	52-57
23705772-1	2013	A series of deep red fluorescent dyes (CR1 to CR3) was developed via introduction of a coumarin moiety into the rhodamine molecular skeleton.	Rhodamines	112-121	complement C3b/C4b receptor 1 (Knops blood group)	Homo sapiens	39-42
23705772-1	2013	A series of deep red fluorescent dyes (CR1 to CR3) was developed via introduction of a coumarin moiety into the rhodamine molecular skeleton.	Rhodamines	112-121	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	46-49
23799018-6	2013	In turn, apelin 14 was conjugated to rhodamine-encapsulating liposomes and administered to tumor-bearing mice.	Rhodamines	37-46	apelin	Mus musculus	9-15
23468132-8	2013	In addition, ABCB1 and ABCB4 mediated the efflux of rhodamine 123 and rhodamine 6G from nonraft membranes, which was not affected by taurocholate.	Rhodamines	52-61	ATP binding cassette subfamily B member 1	Homo sapiens	13-18
23468132-8	2013	In addition, ABCB1 and ABCB4 mediated the efflux of rhodamine 123 and rhodamine 6G from nonraft membranes, which was not affected by taurocholate.	Rhodamines	52-61	ATP binding cassette subfamily B member 4	Homo sapiens	23-28
23457297-6	2013	The direct interaction of BmCrzR with BmCrz was confirmed by a rhodamine-labeled BmCrz peptide.	Rhodamines	63-72	neuropeptide receptor A21	Bombyx mori	26-32
23457297-6	2013	The direct interaction of BmCrzR with BmCrz was confirmed by a rhodamine-labeled BmCrz peptide.	Rhodamines	63-72	pro-corazonin	Bombyx mori	26-31
23457297-6	2013	The direct interaction of BmCrzR with BmCrz was confirmed by a rhodamine-labeled BmCrz peptide.	Rhodamines	63-72	pro-corazonin	Bombyx mori	38-43
23423264-0	2013	A rhodamine derivative as a "lock" and SCN- as a "key": visible light excitable SCN- sensing in living cells.	Rhodamines	2-11	sorcin	Homo sapiens	80-83
23423264-1	2013	A visible light excitable rhodamine based probe operates as a SCN(-) selective fluorescent "turn-on" sensor for living cell imaging with a detection limit of 0.01 muM, which is much lower than the normal SCN(-) level in the human body.	Rhodamines	26-35	sorcin	Homo sapiens	62-65
23423264-1	2013	A visible light excitable rhodamine based probe operates as a SCN(-) selective fluorescent "turn-on" sensor for living cell imaging with a detection limit of 0.01 muM, which is much lower than the normal SCN(-) level in the human body.	Rhodamines	26-35	latexin	Homo sapiens	163-166
23423264-1	2013	A visible light excitable rhodamine based probe operates as a SCN(-) selective fluorescent "turn-on" sensor for living cell imaging with a detection limit of 0.01 muM, which is much lower than the normal SCN(-) level in the human body.	Rhodamines	26-35	sorcin	Homo sapiens	204-207
23423264-2	2013	A "lock" and "key" model has been proposed to explain the fluorescence enhancement of the rhodamine probe in the presence of SCN(-).	Rhodamines	90-99	sorcin	Homo sapiens	125-128
23528086-2	2013	We used high-speed polarized total internal reflection fluorescence (polTIRF) microscopy to study the structural dynamics of single myosin V molecules that had been labeled with bifunctional rhodamine linked to one of the calmodulins along the lever arm.	Rhodamines	191-200	myosin VA	Homo sapiens	132-140
23507591-4	2013	For example, gGlu-HMRG, a novel spirocyclized rhodamine-based fluorescence probe for gamma-glutamyltranspeptidase(GGT), which is well-known to be upregulated in various cancer cells, was successfully developed.	Rhodamines	46-55	gamma-glutamyltransferase light chain 5 pseudogene	Homo sapiens	85-118
23356389-4	2013	For Pdr5, five compounds could be identified that inhibited rhodamine 6G transport more efficiently than zosuquidar.	Rhodamines	60-69	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	4-8
23356389-6	2013	Furthermore, the determination of IC(50) values for rhodamine 6G transport of Pdr5 with representative compounds reveals values between 0.3 and 0.9 muM.	Rhodamines	52-61	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	78-82
23393332-2	2013	A fluorescent probe for detecting HER2/neu-expressing cells was generated by conjugation of the humanized anti-HER2/neu antibody trastuzumab with rhodamine.	Rhodamines	146-155	erb-b2 receptor tyrosine kinase 2	Mus musculus	34-38
23393332-2	2013	A fluorescent probe for detecting HER2/neu-expressing cells was generated by conjugation of the humanized anti-HER2/neu antibody trastuzumab with rhodamine.	Rhodamines	146-155	erb-b2 receptor tyrosine kinase 2	Mus musculus	39-42
23393332-2	2013	A fluorescent probe for detecting HER2/neu-expressing cells was generated by conjugation of the humanized anti-HER2/neu antibody trastuzumab with rhodamine.	Rhodamines	146-155	erb-b2 receptor tyrosine kinase 2	Mus musculus	111-115
23393332-2	2013	A fluorescent probe for detecting HER2/neu-expressing cells was generated by conjugation of the humanized anti-HER2/neu antibody trastuzumab with rhodamine.	Rhodamines	146-155	erb-b2 receptor tyrosine kinase 2	Mus musculus	116-119
23393332-4	2013	All tumor-bearing mice were given a single intravenous injection of either rhodamine-conjugated anti-HER2/neu probe, or conjugated control IgG antibody, when LN metastasis developed.	Rhodamines	75-84	erb-b2 receptor tyrosine kinase 2	Mus musculus	101-105
23393332-4	2013	All tumor-bearing mice were given a single intravenous injection of either rhodamine-conjugated anti-HER2/neu probe, or conjugated control IgG antibody, when LN metastasis developed.	Rhodamines	75-84	erb-b2 receptor tyrosine kinase 2	Mus musculus	106-109
23393332-5	2013	Each animal was imaged with both green and red fluorescence to assess in vivo binding of the rhodamine-conjugated anti-HER2/neu probe to the tumors and LN metastases.	Rhodamines	93-102	erb-b2 receptor tyrosine kinase 2	Mus musculus	119-123
23393332-5	2013	Each animal was imaged with both green and red fluorescence to assess in vivo binding of the rhodamine-conjugated anti-HER2/neu probe to the tumors and LN metastases.	Rhodamines	93-102	erb-b2 receptor tyrosine kinase 2	Mus musculus	124-127
23393332-8	2013	The primary tumors and LN metastases from the animals which were treated with rhodamine-conjugated anti-HER2/neu probe exhibited a visible red fluorescence signal.	Rhodamines	78-87	erb-b2 receptor tyrosine kinase 2	Mus musculus	104-108
23393332-8	2013	The primary tumors and LN metastases from the animals which were treated with rhodamine-conjugated anti-HER2/neu probe exhibited a visible red fluorescence signal.	Rhodamines	78-87	erb-b2 receptor tyrosine kinase 2	Mus musculus	109-112
23393332-10	2013	Sensitivity of 78% (14 out of 18) and specificity of 100% (20 out of 20) could be achieved with the rhodamine-conjugated anti-HER2/neu probe for the detection of LN metastasis.	Rhodamines	100-109	erb-b2 receptor tyrosine kinase 2	Mus musculus	126-130
23393332-10	2013	Sensitivity of 78% (14 out of 18) and specificity of 100% (20 out of 20) could be achieved with the rhodamine-conjugated anti-HER2/neu probe for the detection of LN metastasis.	Rhodamines	100-109	erb-b2 receptor tyrosine kinase 2	Mus musculus	131-134
23172365-8	2013	Finally, the water soluble azide-reactive phosphine probe, rho-TEO-phosphine (21) (rho: rhodamine), has been designed and applied to attach a chromophore to azido-(K1)RNase A via Staudinger ligation at physiological pH indicating that the introduced azido group is accessible and could be addressed by other established azide-reactive bioorthogonal reaction schemes.	Rhodamines	88-97	ribonuclease A family member 1, pancreatic	Homo sapiens	167-174
23166305-9	2013	The downregulation of miR-145 in Caco-2 cells, an epithelial cell line derived from human colon, increased P-gp expression and efflux activity of rhodamine 123, but not MDR1 mRNA level.	Rhodamines	146-155	microRNA 145	Homo sapiens	22-29
23216707-6	2013	Pgp activity was evaluated in PBMC using the Rhodamine 123 efflux assay.	Rhodamines	45-54	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
23302031-1	2013	We have synthesized a new indole functionalized rhodamine derivative L(1) which specifically binds to Cu(2+) in the presence of large excess of other competing ions with visually observable changes in their electronic and fluorescence spectral behavior.	Rhodamines	48-57	immunoglobulin kappa variable 1-16	Homo sapiens	69-73
23035695-5	2012	Concomitantly, P-gp protein expression increased 2.5-fold and was accompanied by a 20-35% reduction in cellular accumulation of the P-gp substrates, rhodamine 6G (R6G), and HiLyte Fluor 488-labeled human amyloid beta 1-42 (hAbeta(42)).	Rhodamines	149-158	phosphoglycolate phosphatase	Homo sapiens	15-19
24025574-0	2013	A fluorescent chemosensor for Hg2+ based on a rhodamine derivative in an aqueous solution.	Rhodamines	46-55	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	30-33
23168018-0	2013	A rhodamine-labeled citalopram analogue as a high-affinity fluorescent probe for the serotonin transporter.	Rhodamines	2-11	solute carrier family 6 member 4	Homo sapiens	85-106
23168018-3	2013	The resulting rhodamine-labeled ligand 8 inhibited [(3)H]5-HT uptake in COS-7 cells (K(i)=225 nM) with similar potency to the tropane-based JHC 1-064 (1), but with higher specificity towards the SERT relative to the transporters for dopamine and norepinephrine.	Rhodamines	14-23	solute carrier family 6 member 4	Homo sapiens	195-199
23646714-4	2013	In addition, scFV-SCLs (effective diameter: 185.7 nm; polydispersity index: 0.236) can significantly boost rhodamine 123 cellular accumulation in the cytoplasm.	Rhodamines	107-116	immunglobulin heavy chain variable region	Homo sapiens	13-17
23234641-4	2013	Here we validate the new dye-probe beta-amyloid (1-40) HiLyte Fluor  TR-labeled (Ab-HiLyte) (Anaspec) P-gp mediated transport in the ex vivo rat everted gut sac assay by using MC18 or MC266, a fully characterized P-gp inhibitor and substrate, respectively, and compare it with the commonly used dye rhodamine.	Rhodamines	299-308	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	102-106
23234641-4	2013	Here we validate the new dye-probe beta-amyloid (1-40) HiLyte Fluor  TR-labeled (Ab-HiLyte) (Anaspec) P-gp mediated transport in the ex vivo rat everted gut sac assay by using MC18 or MC266, a fully characterized P-gp inhibitor and substrate, respectively, and compare it with the commonly used dye rhodamine.	Rhodamines	299-308	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	213-217
23150440-2	2013	Here, we describe a detailed protocol to identify small molecules capable of targeting p53-MDM2/MDMX interactions using a fluorescence polarization assay with Rhodamine-labeled p53 peptides.	Rhodamines	159-168	tumor protein p53	Homo sapiens	87-90
23150440-2	2013	Here, we describe a detailed protocol to identify small molecules capable of targeting p53-MDM2/MDMX interactions using a fluorescence polarization assay with Rhodamine-labeled p53 peptides.	Rhodamines	159-168	MDM2 proto-oncogene	Homo sapiens	91-95
23150440-2	2013	Here, we describe a detailed protocol to identify small molecules capable of targeting p53-MDM2/MDMX interactions using a fluorescence polarization assay with Rhodamine-labeled p53 peptides.	Rhodamines	159-168	MDM4 regulator of p53	Homo sapiens	96-100
23150440-2	2013	Here, we describe a detailed protocol to identify small molecules capable of targeting p53-MDM2/MDMX interactions using a fluorescence polarization assay with Rhodamine-labeled p53 peptides.	Rhodamines	159-168	tumor protein p53	Homo sapiens	177-180
23144078-10	2013	Using rhodamine-labeled NP and U251 glioma cell-derived xenografts, we demonstrated that the NP-TRAIL were found in the tumor site and induced a significant increase in glioma cell apoptosis, a decrease in tumor volume, and increased animal survival.	Rhodamines	6-15	TNF superfamily member 10	Homo sapiens	96-101
22695925-1	2012	A novel rhodamine derivative (Rh-C), synthesized by the reaction of rhodamine ethylenediamine and cinnamoyl chloride, was evaluated as a chemoselective Hg(2+) ion sensor.	Rhodamines	8-17	HCL2	Homo sapiens	30-34
22965487-2	2012	METHODS AND RESULTS: Rhodamine absorption displayed saturation kinetics with a K(m)  of 1.1 muM and a pH-optimum of 8.5 and was stimulated by flavone four-fold in its V(max) .	Rhodamines	21-30	latexin	Homo sapiens	92-95
22981987-8	2012	Half-maximum effect concentrations (IC(50)) for inhibition of Pgp-mediated rhodamine 123 efflux from CCRFvcr1000 cells were 375+-60nM for MC113 versus 8.5+-2.5nM for tariquidar.	Rhodamines	75-84	phosphoglycolate phosphatase	Mus musculus	62-65
22932925-0	2012	FRET-based ratiometric detection of Hg2+ and biothiols using naphthalimide-rhodamine dyads.	Rhodamines	75-84	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	36-39
22705940-6	2012	The sliding velocity of rhodamine-phalloidin-bound actin filaments on HMM was measured using an in vitro motility assay.	Rhodamines	24-33	actin	Oryctolagus cuniculus	51-56
22900779-6	2012	The IC(50) values of (-)-THP and (+)-THP on rhodamine 123 (P-gp substrate) efflux were 48.6 and 20.0 microM, respectively, which showed obvious stereoselective difference.	Rhodamines	44-53	ATP binding cassette subfamily B member 1	Homo sapiens	59-63
23183822-10	2012	Of note, miR-211- and pM-treated CSC demonstrated increased drug retention capacity, as observed by MDR1/P-gp mediated-Rhodamine 123 drug efflux activity assay.	Rhodamines	119-128	microRNA 211	Homo sapiens	9-16
23183822-10	2012	Of note, miR-211- and pM-treated CSC demonstrated increased drug retention capacity, as observed by MDR1/P-gp mediated-Rhodamine 123 drug efflux activity assay.	Rhodamines	119-128	ATP binding cassette subfamily B member 1	Homo sapiens	100-104
23183822-10	2012	Of note, miR-211- and pM-treated CSC demonstrated increased drug retention capacity, as observed by MDR1/P-gp mediated-Rhodamine 123 drug efflux activity assay.	Rhodamines	119-128	phosphoglycolate phosphatase	Homo sapiens	105-109
22858611-1	2012	Rhodamine S could emit strong and stable room temperature phosphorescence (RTP) on polyamide membrane (PAM) in the presence of heavy atom perturber Pb(2+).	Rhodamines	0-11	MORN repeat containing 4	Homo sapiens	75-78
22858611-1	2012	Rhodamine S could emit strong and stable room temperature phosphorescence (RTP) on polyamide membrane (PAM) in the presence of heavy atom perturber Pb(2+).	Rhodamines	0-11	peptidylglycine alpha-amidating monooxygenase	Homo sapiens	103-106
23202936-9	2012	FACS analysis demonstrated a correlation of cell labeling between FITC-CaIX-P1 and rhodamine-labeled anti-CAIX-mAb in both HCT116 and HT29 cells.	Rhodamines	83-92	carbonic anhydrase 9	Homo sapiens	106-110
22451472-3	2012	Multidrug resistance protein 1 blockade by the specific inhibitor reduced the percentage of rhodamine 123(low) cells in LDCs from aged mice (54.8% +- 2.6% to 13.2% +- 2.5%, p < .01).	Rhodamines	92-101	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	0-30
22875192-1	2012	A new coumarin-rhodamine conjugate constitutes a unique example of the interrupted PET coupled TBET response for developing an imaging reagent for determining the intracellular distribution of Hg(2+) in MCF7 cells exposed to [Hg(2+)] as low as 2 ppb.	Rhodamines	15-24	T-box transcription factor 21	Homo sapiens	95-99
22525746-6	2012	RESULTS: In rhodamine 123 efflux assay drugs inhibitory potency to P-gp could be ranked quetiapine>N-desmethylclozapine>clozapine>olanzapine.	Rhodamines	12-21	phosphoglycolate phosphatase	Mus musculus	67-71
22583690-2	2012	METHODS: To confirm that TNF-alpha induces epithelial barrier hyperpermeability by disrupting tight junction, Caco-2 cells were exposed to TNF-alpha, and changes in epithelial permeability (via TER assay), F-actin dynamics (via Rhodamine-phalloidin staining) and tight junction protein expression (via western blot) were monitored.	Rhodamines	228-237	tumor necrosis factor	Homo sapiens	25-34
22931670-3	2012	The results showed that after pretreated with S1P, the level of superoxide anion released by fMLP-activated neutrophils significantly increased; the Rhodamine 123 mean fluorescence intensity in S1P primed fMLP-activated neutrophils group was significantly higher than that in fMLP treatment group; PI3K and Akt proteins involved in the signal pathway of neutrophil respiratory burst.	Rhodamines	149-158	formyl peptide receptor 1	Homo sapiens	93-97
22931670-3	2012	The results showed that after pretreated with S1P, the level of superoxide anion released by fMLP-activated neutrophils significantly increased; the Rhodamine 123 mean fluorescence intensity in S1P primed fMLP-activated neutrophils group was significantly higher than that in fMLP treatment group; PI3K and Akt proteins involved in the signal pathway of neutrophil respiratory burst.	Rhodamines	149-158	formyl peptide receptor 1	Homo sapiens	205-209
22931670-3	2012	The results showed that after pretreated with S1P, the level of superoxide anion released by fMLP-activated neutrophils significantly increased; the Rhodamine 123 mean fluorescence intensity in S1P primed fMLP-activated neutrophils group was significantly higher than that in fMLP treatment group; PI3K and Akt proteins involved in the signal pathway of neutrophil respiratory burst.	Rhodamines	149-158	formyl peptide receptor 1	Homo sapiens	205-209
22931670-3	2012	The results showed that after pretreated with S1P, the level of superoxide anion released by fMLP-activated neutrophils significantly increased; the Rhodamine 123 mean fluorescence intensity in S1P primed fMLP-activated neutrophils group was significantly higher than that in fMLP treatment group; PI3K and Akt proteins involved in the signal pathway of neutrophil respiratory burst.	Rhodamines	149-158	AKT serine/threonine kinase 1	Homo sapiens	307-310
22506763-6	2012	This assay, which monitors the kinetics of the fluorescence polarization signal increase upon PRMT1 labeling by a rhodamine-containing cysteine-reactive probe, successfully identified two novel inhibitors selective for PRMT1 over other SAM-dependent methyltransferases.	Rhodamines	114-123	protein arginine methyltransferase 1	Homo sapiens	94-99
22506763-6	2012	This assay, which monitors the kinetics of the fluorescence polarization signal increase upon PRMT1 labeling by a rhodamine-containing cysteine-reactive probe, successfully identified two novel inhibitors selective for PRMT1 over other SAM-dependent methyltransferases.	Rhodamines	114-123	protein arginine methyltransferase 1	Homo sapiens	219-224
22386863-6	2012	The P-glycoprotein (P-gp) function assay in MES-Dx5 cells showed the potential of gelucire-based NPs in inhibiting rhodamine 123 efflux.	Rhodamines	115-124	phosphoglycolate phosphatase	Mus musculus	4-18
21882172-0	2012	Spectroscopic investigations to reveal the nature of interactions between the haem protein myoglobin and the dye rhodamine 6G.	Rhodamines	113-122	myoglobin	Homo sapiens	91-100
22386863-6	2012	The P-glycoprotein (P-gp) function assay in MES-Dx5 cells showed the potential of gelucire-based NPs in inhibiting rhodamine 123 efflux.	Rhodamines	115-124	phosphoglycolate phosphatase	Mus musculus	20-24
22550304-0	2012	Fluorescent labeling of calmodulin with bifunctional rhodamine.	Rhodamines	53-62	calmodulin 2	Gallus gallus	24-34
22550304-3	2012	This protocol describes how to label chicken calmodulin (CaM) with bifunctional rhodamine (BR) at two engineered cysteine (Cys) residues (P66C and A73C) so that it cross-links the two Cys sites.	Rhodamines	80-89	calmodulin 2	Gallus gallus	45-55
22550304-3	2012	This protocol describes how to label chicken calmodulin (CaM) with bifunctional rhodamine (BR) at two engineered cysteine (Cys) residues (P66C and A73C) so that it cross-links the two Cys sites.	Rhodamines	80-89	calmodulin 2	Gallus gallus	57-60
22354094-3	2012	The nano-patterned SERS substrate, with excellent control and reproducibility of plasmon-polaritons generation, shows very efficient enhanced Raman signal in the presence of intrinsically fluorescent molecules such as cresyl violet, rhodamine, and green fluorescent protein.	Rhodamines	233-242	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	19-23
22212563-5	2012	Apatinib treatment markedly increased the intracellular accumulation of doxorubicin and rhodamine 123 in K562/ADR cells and the accumulation of rhodamine 123 in the primary leukemia blasts with ABCB1 overexpression.	Rhodamines	144-153	ATP binding cassette subfamily B member 1	Homo sapiens	194-199
22226881-6	2012	It also significantly increased intracellular accumulation (21-fold) of rhodamine 123 in HEK293 MDR1 cells.	Rhodamines	72-81	ATP binding cassette subfamily B member 1	Homo sapiens	96-100
22420656-4	2012	METHODS: P-gp drug efflux activity was measured by an in-situ closed loop method with Rhodamine 123, a P-gp substrate.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	9-13
22420656-4	2012	METHODS: P-gp drug efflux activity was measured by an in-situ closed loop method with Rhodamine 123, a P-gp substrate.	Rhodamines	86-95	ATP binding cassette subfamily B member 1	Homo sapiens	103-107
22420656-7	2012	KEY FINDINGS: ETP and morphine significantly decreased the intestinal Rhodamine 123 efflux activity of P-gp.	Rhodamines	70-79	ATP binding cassette subfamily B member 1	Homo sapiens	103-107
21797847-3	2012	EXPERIMENTAL APPROACH: Intravital microscopy was used to determine whether ETR/B(2)R drives the accumulation of rhodamine-labelled leucocytes in the hamster cheek pouch (HCP).	Rhodamines	112-121	bradykinin receptor B2	Homo sapiens	79-84
22201267-2	2012	By use of a photostable rhodamine attached specifically to Halo-tagged proteins in mitochondrial membranes, we were able to track and localize single protein complexes such as Tom20 and ATP synthase in suborganellar structures in live cells.	Rhodamines	24-33	translocase of outer mitochondrial membrane 20	Homo sapiens	176-181
22300338-0	2012	New fluorogenic sensors for Hg2+ ions: through-bond energy transfer from pentaquinone to rhodamine.	Rhodamines	89-98	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	28-31
22234375-5	2012	The architecture of the SERS-active substrate was varied using three adsorption strategies for incorporating a laser dye (rhodamine): alongside the nanoparticles into the polymer matrix, during the polymer cure and within nanoholes lithographed on the polymer.	Rhodamines	122-131	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	24-28
22234375-6	2012	As a proof-of-concept, we obtained the SERS spectra of rhodamine for the three types of substrates.	Rhodamines	55-64	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	39-43
22234375-8	2012	In the case of arrays of nanoholes, rhodamine molecules could be adsorbed directly on the gold surface, then yielding a well-resolved SERS spectrum for a small amount of analyte owing to the short-range interactions and the large longitudinal field component inside the nanoholes.	Rhodamines	36-45	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	134-138
25786599-6	2012	In addition, we demonstrate that rhodamine-loaded MB can also be used for in vivo and ex vivo experimental setups, e.g., for analyzing MB binding to inflamed carotids using two-photon laser scanning microscopy, and for validating the binding of VEGFR2-targeted MB to tumor endothelium.	Rhodamines	33-42	kinase insert domain receptor	Homo sapiens	245-251
22176300-5	2012	Significantly, the new CS1-6 NIR dyes are superior to the traditional rhodamine dyes with both absorption and emission in the NIR region while retaining the rhodamine-like fluorescence ON-OFF switching mechanism.	Rhodamines	70-79	chorionic somatomammotropin hormone 1	Homo sapiens	23-28
22291144-2	2012	To better understand how myoV navigates along actin, we used polarized total internal reflection fluorescence microscopy to examine angular changes of bifunctional rhodamine probes on the lever arms of single myoV molecules in vitro.	Rhodamines	164-173	myosin VA	Homo sapiens	209-213
22148475-5	2012	Incubation of MCF-7/Vin cells with 1 caused an increase in uptake and notably lowered the efflux rate of rhodamine 123.	Rhodamines	105-114	long intergenic non-protein coding RNA 1191	Homo sapiens	20-23
22176300-5	2012	Significantly, the new CS1-6 NIR dyes are superior to the traditional rhodamine dyes with both absorption and emission in the NIR region while retaining the rhodamine-like fluorescence ON-OFF switching mechanism.	Rhodamines	157-166	chorionic somatomammotropin hormone 1	Homo sapiens	23-28
22403486-14	2012	Further, biodistribution studies of rhodamine-loaded nanoparticles demonstrated that modification with the SynB peptide could not only improve the ability of PEG-GS nanoparticles to evade capture in the reticuloendothelial system but also enhance their efficiency in crossing the blood-brain barrier.	Rhodamines	36-45	syncytin b	Mus musculus	107-111
22470447-3	2012	Rhodamine 123, a member of the rhodamine family of flurone dyes, has been used to examine membrane transport by the ABCB1 gene product, MDR1.	Rhodamines	31-40	ATP binding cassette subfamily B member 1	Homo sapiens	116-121
22416063-10	2012	Rhodamine efflux from CD56+ PBMCs was a statistically significant 51%-100% lower (p < .0001) with CBT-1 .	Rhodamines	0-9	succinate dehydrogenase complex subunit D	Homo sapiens	101-106
22470447-3	2012	Rhodamine 123, a member of the rhodamine family of flurone dyes, has been used to examine membrane transport by the ABCB1 gene product, MDR1.	Rhodamines	31-40	ATP binding cassette subfamily B member 1	Homo sapiens	136-140
22018584-0	2012	Reversible "off-on" fluorescent chemosensor for Hg2+ based on rhodamine derivative.	Rhodamines	62-71	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	48-51
21920352-1	2011	P-Glycoprotein (Pgp) inhibition by three sets of four isomers of N,N-bis(cyclohexanol)amine aryl esters was assessed on rhodamine 123 (R123) efflux in human MDR1-gene transfected mouse T-lymphoma L5178 cells and on Sf9 ATPase activity.	Rhodamines	120-129	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
21920352-1	2011	P-Glycoprotein (Pgp) inhibition by three sets of four isomers of N,N-bis(cyclohexanol)amine aryl esters was assessed on rhodamine 123 (R123) efflux in human MDR1-gene transfected mouse T-lymphoma L5178 cells and on Sf9 ATPase activity.	Rhodamines	120-129	ATP binding cassette subfamily B member 1	Homo sapiens	16-19
22027958-0	2011	Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor.	Rhodamines	20-29	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	137-140
21685928-4	2011	P-GP function was investigated via measuring tissue-to-plasma concentration ratios and body fluid excretion percentages of rhodamine 123.	Rhodamines	123-132	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	0-4
20676745-6	2011	The results demonstrated that increased intracellular accumulation of rhodamine 123 and increased fluorescence of calcein were observed after YC-1 treatment.	Rhodamines	70-79	RNA binding motif single stranded interacting protein 1	Homo sapiens	142-146
21851848-8	2011	Accumulation studies demonstrated 31-38% decrease in rhodamine 123 intracellular levels when LS-180 cells were treated with the investigated compounds as a result of P-gp induction.	Rhodamines	53-62	ATP binding cassette subfamily B member 1	Homo sapiens	166-170
21731939-0	2011	A new rhodamine based colorimetric "off-on" fluorescence sensor selective for Pd2+ along with the first bound X-ray crystal structure.	Rhodamines	6-15	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	78-81
21763326-7	2011	KEY FINDINGS: MDR1 blockade by the specific inhibitor verapamil reduced the percentage of rhodamine 123(low) cells in LDCs (from 31.8+-6.3% to 11.8+-2.8%, p<0.02).	Rhodamines	90-99	ATP binding cassette subfamily B member 1	Homo sapiens	14-18
20196146-5	2011	Rhodamine assay also revealed that hydrocinchonine, cinchonine, and quinidine effectively enhanced the accumulation of a P-gp substrate, rhodamine in TAX-treated MES-SA/DX5 cells compared with TAX-treated control.	Rhodamines	0-9	phosphoglycolate phosphatase	Homo sapiens	121-125
20196146-5	2011	Rhodamine assay also revealed that hydrocinchonine, cinchonine, and quinidine effectively enhanced the accumulation of a P-gp substrate, rhodamine in TAX-treated MES-SA/DX5 cells compared with TAX-treated control.	Rhodamines	137-146	phosphoglycolate phosphatase	Homo sapiens	121-125
21502729-3	2011	The presence of ORF2-EGFP fusion protein was demonstrated by dual signals of green fluorescence and anti-PCV2 antibodies conjugated with rhodamine in an immunofluorescence assay (IFA).	Rhodamines	137-146	capsid protein	Porcine circovirus 2	16-20
21711510-10	2011	Moreover, the markedly increased Abcb1a/Abcb1b expression was correlated to an efficient Rhodamine 123 efflux, which was completely inhibited by verapamil, a well-known Abcb1a/Abcb1b inhibitor.	Rhodamines	89-98	ATP-binding cassette, sub-family B (MDR/TAP), member 1A	Mus musculus	33-39
21786801-6	2011	All the coumarin-, cresyl violet- and rhodamine-based fluorogenic probes turned out to be good substrates for most GSTs, especially for GSTA(1-1), in terms of strong fluorescence increases (71-1200-fold), high k(cat)/K(m) values (10(4)-10(7) M(-1) s(-1)) and significant rate enhancements (10(6)-10(9)-fold).	Rhodamines	38-47	hematopoietic prostaglandin D synthase	Homo sapiens	115-119
21786801-6	2011	All the coumarin-, cresyl violet- and rhodamine-based fluorogenic probes turned out to be good substrates for most GSTs, especially for GSTA(1-1), in terms of strong fluorescence increases (71-1200-fold), high k(cat)/K(m) values (10(4)-10(7) M(-1) s(-1)) and significant rate enhancements (10(6)-10(9)-fold).	Rhodamines	38-47	glutathione S-transferase alpha 1	Homo sapiens	136-144
21372002-7	2011	The MPO-NAA-induced production of reactive oxygen species was assessed using oxidation of dihydrorhodamine (DHR) to rhodamine.	Rhodamines	97-106	myeloperoxidase	Homo sapiens	4-7
21711510-10	2011	Moreover, the markedly increased Abcb1a/Abcb1b expression was correlated to an efficient Rhodamine 123 efflux, which was completely inhibited by verapamil, a well-known Abcb1a/Abcb1b inhibitor.	Rhodamines	89-98	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	40-46
21711510-10	2011	Moreover, the markedly increased Abcb1a/Abcb1b expression was correlated to an efficient Rhodamine 123 efflux, which was completely inhibited by verapamil, a well-known Abcb1a/Abcb1b inhibitor.	Rhodamines	89-98	ATP-binding cassette, sub-family B (MDR/TAP), member 1A	Mus musculus	169-175
21711510-10	2011	Moreover, the markedly increased Abcb1a/Abcb1b expression was correlated to an efficient Rhodamine 123 efflux, which was completely inhibited by verapamil, a well-known Abcb1a/Abcb1b inhibitor.	Rhodamines	89-98	ATP-binding cassette, sub-family B (MDR/TAP), member 1B	Mus musculus	176-182
21421215-5	2011	The sensitivity and reproducibility of the substrate were confirmed using a common SERS probe molecule, rhodamine 6G.	Rhodamines	104-113	seryl-tRNA synthetase 1	Homo sapiens	83-87
21262289-6	2011	Rhodamine labeled EGa1-micelles showed substantially higher binding as well as uptake by EGFR over-expressing cancer cells (A431 and UM-SCC-14C) than untargeted rhodamine labeled micelles.	Rhodamines	0-9	epidermal growth factor receptor	Mus musculus	89-93
21289467-6	2011	The elevation of the oocyte Pgp level was associated with increased activity of rhodamine 6G efflux from the oocyte, and its efflux was suppressed by verapamil, an inhibitor of Pgp.	Rhodamines	80-89	ATP binding cassette subfamily B member 1	Homo sapiens	28-31
21729546-7	2011	The acidification resulted in the increased rhodamine 123 accumulation in HL-60, MSC and CD34(+) cells without P-gp activity.	Rhodamines	44-53	CD34 molecule	Homo sapiens	89-93
21452853-9	2011	Consistent with these results, FSBA blocked efflux of rhodamine 123 from P-gp-expressing cells.	Rhodamines	54-63	ATP binding cassette subfamily B member 1	Homo sapiens	73-77
21684029-6	2011	Rhodamine labeled EGa1-micelles showed substantially higher binding as well as uptake by EGFR over-expressing cancer cells (A431 and UM-SCC-14C) than untargeted rhodamine labeled micelles.	Rhodamines	0-9	epidermal growth factor receptor	Mus musculus	89-93
21385940-5	2011	Qualitative analysis using rhodamine-conjugated phalloidin immunofluorescence indicated that leptin stimulated actin cytoskeletal reorganization and enhanced stress fiber formation.	Rhodamines	27-36	leptin	Rattus norvegicus	93-99
21780390-1	2011	Luminescent nanorods of potassium acid phthalate (KAP) doped with rhodamine 6G (Rh 6G) dye molecules were grown by template assisted crystallization.	Rhodamines	66-75	napsin A aspartic peptidase	Homo sapiens	50-53
20857089-4	2011	Cytotoxicity of doxorubicin (0-100 muM) and paraquat (0-1,000 muM) was evaluated for a maximum period of 96 h. In doxorubicin-exposed cells, P-gp expression and transport activity were evaluated by flow cytometry, using a fluorescein isothiocyanate-conjugated antibody and the P-gp fluorescent subtract rhodamine 123, respectively.	Rhodamines	303-312	ATP binding cassette subfamily B member 1	Homo sapiens	141-145
21286625-0	2011	A highly specific rhodamine-based colorimetric probe for hypochlorites: a new sensing strategy and real application in tap water.	Rhodamines	18-27	nuclear RNA export factor 1	Homo sapiens	119-122
21097518-11	2011	Microscopic studies revealed that the vascular constrained, rhodamine-labeled alpha(v)beta(3)-GNBs homed specifically to immature neovasculature (PECAM(+), Tie-2(-)) along the immediate tumor periphery, but not to nearby mature microvasculature (PECAM(+), Tie-2(+)).	Rhodamines	60-69	platelet/endothelial cell adhesion molecule 1	Mus musculus	146-151
21097518-11	2011	Microscopic studies revealed that the vascular constrained, rhodamine-labeled alpha(v)beta(3)-GNBs homed specifically to immature neovasculature (PECAM(+), Tie-2(-)) along the immediate tumor periphery, but not to nearby mature microvasculature (PECAM(+), Tie-2(+)).	Rhodamines	60-69	TEK receptor tyrosine kinase	Mus musculus	156-161
21097518-11	2011	Microscopic studies revealed that the vascular constrained, rhodamine-labeled alpha(v)beta(3)-GNBs homed specifically to immature neovasculature (PECAM(+), Tie-2(-)) along the immediate tumor periphery, but not to nearby mature microvasculature (PECAM(+), Tie-2(+)).	Rhodamines	60-69	platelet/endothelial cell adhesion molecule 1	Mus musculus	246-251
21097518-11	2011	Microscopic studies revealed that the vascular constrained, rhodamine-labeled alpha(v)beta(3)-GNBs homed specifically to immature neovasculature (PECAM(+), Tie-2(-)) along the immediate tumor periphery, but not to nearby mature microvasculature (PECAM(+), Tie-2(+)).	Rhodamines	60-69	TEK receptor tyrosine kinase	Mus musculus	256-261
20955791-8	2011	Changes in expression were confined mostly to MDR1 and CYP3A4: in LS180 cells, treatment for 3 days increased MDR1 and CYP3A4 but not MRP2 mRNA, and elevated P-gp and CYP3A4 protein expression that led to decreased cellular accumulation of [(3)H]digoxin and rhodamine 123, and enhanced testosterone 6beta-hydroxylase activity towards T2007, respectively.	Rhodamines	258-267	ATP binding cassette subfamily B member 1	Homo sapiens	46-50
21081657-8	2011	Tariquidar inhibited Pgp-mediated rhodamine efflux from CD56(+) cells and reduced (99m)Tc-sestamibi clearance from the liver.	Rhodamines	34-43	ATP binding cassette subfamily B member 1	Homo sapiens	21-24
21145107-7	2011	Drug transport in BCEC-1 was investigated by FACS analysis using the fluorescent P-gp substrate Rhodamine 123.	Rhodamines	96-105	phosphoglycolate phosphatase	Bos taurus	81-85
21145107-8	2011	Inhibition of Rhodamine 123 efflux by the P-gp inhibitors Verapamil and PSC833 confirmed functional expression of P-gp in BCEC-1.	Rhodamines	14-23	phosphoglycolate phosphatase	Bos taurus	42-46
21145107-8	2011	Inhibition of Rhodamine 123 efflux by the P-gp inhibitors Verapamil and PSC833 confirmed functional expression of P-gp in BCEC-1.	Rhodamines	14-23	phosphoglycolate phosphatase	Bos taurus	114-118
20955791-3	2011	P-gp and CYP3A4 activities were assayed by [(3)H]digoxin and rhodamine 123 cellular retention and testosterone 6beta-hydroxylation, respectively.	Rhodamines	61-70	phosphoglycolate phosphatase	Homo sapiens	0-4
20955791-8	2011	Changes in expression were confined mostly to MDR1 and CYP3A4: in LS180 cells, treatment for 3 days increased MDR1 and CYP3A4 but not MRP2 mRNA, and elevated P-gp and CYP3A4 protein expression that led to decreased cellular accumulation of [(3)H]digoxin and rhodamine 123, and enhanced testosterone 6beta-hydroxylase activity towards T2007, respectively.	Rhodamines	258-267	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	55-61
21057677-2	2010	The emission behavior of ABPX series is directly opposite to the concentration quenching of conventional rhodamine dyes.	Rhodamines	105-114	filamin A	Homo sapiens	25-29
20955791-3	2011	P-gp and CYP3A4 activities were assayed by [(3)H]digoxin and rhodamine 123 cellular retention and testosterone 6beta-hydroxylation, respectively.	Rhodamines	61-70	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	9-15
20955690-6	2011	MDR1 activity was increased by 50% in APAP treated rats, as evaluated by serosal to mucosal secretion of rhodamine 123 in everted intestinal sacs.	Rhodamines	105-114	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	0-4
21147877-6	2011	We quantitatively assessed the filamentous to globular actin ratio and show that increased stress fiber formation, visualized by rhodamine-phalloidin immunofluorescence, in response to adiponectin, is achieved via stimulating Ras homolog gene family A (RhoA) activity, determined using G-LISA RhoA activation assay kit.	Rhodamines	129-138	adiponectin, C1Q and collagen domain containing	Rattus norvegicus	185-196
21147877-6	2011	We quantitatively assessed the filamentous to globular actin ratio and show that increased stress fiber formation, visualized by rhodamine-phalloidin immunofluorescence, in response to adiponectin, is achieved via stimulating Ras homolog gene family A (RhoA) activity, determined using G-LISA RhoA activation assay kit.	Rhodamines	129-138	ras homolog family member A	Rattus norvegicus	253-257
21147877-6	2011	We quantitatively assessed the filamentous to globular actin ratio and show that increased stress fiber formation, visualized by rhodamine-phalloidin immunofluorescence, in response to adiponectin, is achieved via stimulating Ras homolog gene family A (RhoA) activity, determined using G-LISA RhoA activation assay kit.	Rhodamines	129-138	ras homolog family member A	Rattus norvegicus	293-297
22358098-7	2011	Moreover, DIOXOL (at 10 muM) significantly inhibited P-gp transport function by more than twofold comparing to control, untreated cells that was demonstrated using rhodamine 123-based functional test.	Rhodamines	164-173	phosphoglycolate phosphatase	Homo sapiens	53-57
19788373-1	2010	Primitive marrow lineage-negative rhodamine low and Hoechst low (LRH) stem cells isolated on the basis of quiescence respond to the cytokines thrombopoietin, FLT3L, and steel factor by synchronously progressing through cell cycle.	Rhodamines	34-43	thrombopoietin	Mus musculus	142-156
20844484-3	2010	In patients with hypothyroidism, normalization of thyroid function was associated with a 1.8-fold increase in mRNA expression and a 26% increase in rhodamine efflux from CD56(+) cells.	Rhodamines	148-157	neural cell adhesion molecule 1	Homo sapiens	170-174
20846144-5	2010	The energy-dependent efflux of rhodamine 6G was increased by VMR1 deletion.	Rhodamines	31-40	putative ATP-binding cassette multidrug transporter VMR1	Saccharomyces cerevisiae S288C	61-65
20608983-3	2010	Here, we report that loss of the type 2A-related serine/threonine protein phosphatase Sit4p renders yeast cells sensitive to cycloheximide, azoles, daunorubicin and rhodamine 6G.	Rhodamines	165-174	type 2A-related serine/threonine-protein phosphatase SIT4	Saccharomyces cerevisiae S288C	86-91
20499920-4	2010	These gold nanoparticle structures were shown to yield a large SERS enhancement for Rhodamine 6G.	Rhodamines	84-93	seryl-tRNA synthetase 1	Homo sapiens	63-67
20132313-6	2010	These compounds almost completely inhibited the efflux of the Pdr5p fluorescent substrate Rhodamine 6G and at 25 muM chemosensitized the Pdr5p-overexpressing strain AD124567 to fluconazole (0.4 mg mL(-1)).	Rhodamines	90-99	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	62-67
20132313-6	2010	These compounds almost completely inhibited the efflux of the Pdr5p fluorescent substrate Rhodamine 6G and at 25 muM chemosensitized the Pdr5p-overexpressing strain AD124567 to fluconazole (0.4 mg mL(-1)).	Rhodamines	90-99	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	137-142
20417333-1	2010	We introduce a new rhodamine-based fluorescent chemosensor, FD8 which exhibits a distinct two-photon excited fluorescence (TPEF) on/off characteristic upon binding Cr(3+) ions.	Rhodamines	19-28	transmembrane protein with EGF like and two follistatin like domains 2	Homo sapiens	123-127
20188976-1	2010	A new Rhodamine-based chemosensor RBSN designed for the selective detection of Hg(2+) in aqueous media is synthesized and structural characterized.	Rhodamines	6-15	rabenosyn, RAB effector	Homo sapiens	34-38
20230790-4	2010	In vitro, the P-gp antagonist PSC833, a non-calcineurin-inhibitory cyclosporine A analogue, specifically inhibited cellular efflux of the P-gp substrate rhodamine-123 in wild-type CD3(+) T cells and MHC class II(+) APCs but not their P-gp knockout counterparts that lacked rhodamine-123 efflux capacity.	Rhodamines	153-162	phosphoglycolate phosphatase	Mus musculus	14-18
20230790-4	2010	In vitro, the P-gp antagonist PSC833, a non-calcineurin-inhibitory cyclosporine A analogue, specifically inhibited cellular efflux of the P-gp substrate rhodamine-123 in wild-type CD3(+) T cells and MHC class II(+) APCs but not their P-gp knockout counterparts that lacked rhodamine-123 efflux capacity.	Rhodamines	153-162	phosphoglycolate phosphatase	Mus musculus	138-142
20230790-4	2010	In vitro, the P-gp antagonist PSC833, a non-calcineurin-inhibitory cyclosporine A analogue, specifically inhibited cellular efflux of the P-gp substrate rhodamine-123 in wild-type CD3(+) T cells and MHC class II(+) APCs but not their P-gp knockout counterparts that lacked rhodamine-123 efflux capacity.	Rhodamines	153-162	CD3 antigen, epsilon polypeptide	Mus musculus	180-183
20230790-4	2010	In vitro, the P-gp antagonist PSC833, a non-calcineurin-inhibitory cyclosporine A analogue, specifically inhibited cellular efflux of the P-gp substrate rhodamine-123 in wild-type CD3(+) T cells and MHC class II(+) APCs but not their P-gp knockout counterparts that lacked rhodamine-123 efflux capacity.	Rhodamines	153-162	phosphoglycolate phosphatase	Mus musculus	138-142
20623626-8	2010	MCF-7-Chk cells effluxed twice as much rhodamine-123 compared to MCF-7 cells.	Rhodamines	39-48	choline kinase alpha	Homo sapiens	6-9
19898868-6	2010	Doxorubicin also induced up-regulation of P-gp functional activities, as intracellular retention of rhodamine was decreased; however, 2.0 microg/ml tetrandrine significantly inhibited the overexpression of doxorubicin-induced mdr1 mRNA/P-gp.	Rhodamines	100-109	phosphoglycolate phosphatase	Homo sapiens	42-46
20146400-5	2010	The introduction of the D853Y mutation into gain-of-function Pdr3p suppressed the transcription of the PDR3 and PDR5 genes and reduced both the rhodamine 6G efflux rate and the drug resistance level in corresponding double mutants.	Rhodamines	144-153	drug-responsive transcription factor PDR3	Saccharomyces cerevisiae S288C	61-66
20146400-5	2010	The introduction of the D853Y mutation into gain-of-function Pdr3p suppressed the transcription of the PDR3 and PDR5 genes and reduced both the rhodamine 6G efflux rate and the drug resistance level in corresponding double mutants.	Rhodamines	144-153	drug-responsive transcription factor PDR3	Saccharomyces cerevisiae S288C	103-107
20146400-5	2010	The introduction of the D853Y mutation into gain-of-function Pdr3p suppressed the transcription of the PDR3 and PDR5 genes and reduced both the rhodamine 6G efflux rate and the drug resistance level in corresponding double mutants.	Rhodamines	144-153	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	112-116
19788373-1	2010	Primitive marrow lineage-negative rhodamine low and Hoechst low (LRH) stem cells isolated on the basis of quiescence respond to the cytokines thrombopoietin, FLT3L, and steel factor by synchronously progressing through cell cycle.	Rhodamines	34-43	FMS-like tyrosine kinase 3 ligand	Mus musculus	158-163
19954837-5	2010	To further understand the bi-functionality, we labeled the SPT7pTL and PGA-alpha-MSH with YOYO-1 and Rhodamine, respectively, to follow its intracellular pathway by confocal microscopy.	Rhodamines	101-110	proopiomelanocortin	Homo sapiens	75-84
20298597-6	2010	GIVaPLA2 enzyme activity was analyzed using [14C-PAPC] as specific substrate F-actin polymerization and cell structure were examined after rhodamine-phalloidin staining.	Rhodamines	139-148	coiled-coil domain containing 88A	Homo sapiens	0-8
20121943-9	2010	Thus, P-glycoprotein appears to pump rhodamines from the cytoplasmic leaflet either to the outer leaflet or to the outer medium.	Rhodamines	37-47	ATP binding cassette subfamily B member 1	Homo sapiens	6-20
19761200-2	2009	In response to binding cationic lipophilic compounds, including ethidium and rhodamine 6G, QacR dissociates from the qacA operator alleviating repression.	Rhodamines	77-86	QacA	Staphylococcus aureus	117-121
19933268-0	2010	Impact of disease-causing SUR1 mutations on the KATP channel subunit interface probed with a rhodamine protection assay.	Rhodamines	93-102	ATP binding cassette subfamily C member 8	Homo sapiens	26-30
19933268-2	2010	The conformation of the interface between these two subunits can be monitored using a rhodamine 123 (Rho) protection assay because Rho blocks Kir6.2 with an efficiency that depends on the relative position of transmembrane domain (TMD) 0 of the associated SUR (Hosy, E., Derand, R., Revilloud, J., and Vivaudou, M. (2007) J. Physiol.	Rhodamines	86-95	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	142-148
19933268-2	2010	The conformation of the interface between these two subunits can be monitored using a rhodamine 123 (Rho) protection assay because Rho blocks Kir6.2 with an efficiency that depends on the relative position of transmembrane domain (TMD) 0 of the associated SUR (Hosy, E., Derand, R., Revilloud, J., and Vivaudou, M. (2007) J. Physiol.	Rhodamines	86-95	ATP binding cassette subfamily C member 8	Homo sapiens	256-259
19783150-3	2010	In addition to being lipophilic cations, like (99m)Tc-MIBI, rhodamine dyes are known to accumulate in the myocardium and are substrates for Pgp, the protein implicated in MDR1 multidrug resistance.	Rhodamines	60-69	phosphoglycolate phosphatase	Homo sapiens	140-143
19783150-3	2010	In addition to being lipophilic cations, like (99m)Tc-MIBI, rhodamine dyes are known to accumulate in the myocardium and are substrates for Pgp, the protein implicated in MDR1 multidrug resistance.	Rhodamines	60-69	ATP binding cassette subfamily B member 1	Homo sapiens	171-175
19684997-2	2009	Exposure to a known mammalian inhibitor (verapamil, 10 1M) and inducer (rhodamine 123, 3 1M) on the transport protein P-glycoprotein (Pgp) was investigated in the liver of the western mosquitofish and bluegill sunfish.	Rhodamines	72-81	ATP binding cassette subfamily B member 1	Homo sapiens	118-132
19684997-2	2009	Exposure to a known mammalian inhibitor (verapamil, 10 1M) and inducer (rhodamine 123, 3 1M) on the transport protein P-glycoprotein (Pgp) was investigated in the liver of the western mosquitofish and bluegill sunfish.	Rhodamines	72-81	ATP binding cassette subfamily B member 1	Homo sapiens	134-137
19761200-2	2009	In response to binding cationic lipophilic compounds, including ethidium and rhodamine 6G, QacR dissociates from the qacA operator alleviating repression.	Rhodamines	77-86	QacR	Staphylococcus aureus	91-95
19481575-1	2009	We evaluated the benefits of a novel formulation of vasoactive intestinal peptide (VIP) based on the incorporation of VIP-loaded rhodamine-conjugated liposomes (VIP-Rh-Lip) within hyaluronic acid (HA) gel (Gel-VIP-Rh-Lip) for the treatment of endotoxin-induced uveitis (EIU) in comparison with VIP-Rh-Lip alone.	Rhodamines	129-138	vasoactive intestinal peptide	Rattus norvegicus	83-86
19481575-1	2009	We evaluated the benefits of a novel formulation of vasoactive intestinal peptide (VIP) based on the incorporation of VIP-loaded rhodamine-conjugated liposomes (VIP-Rh-Lip) within hyaluronic acid (HA) gel (Gel-VIP-Rh-Lip) for the treatment of endotoxin-induced uveitis (EIU) in comparison with VIP-Rh-Lip alone.	Rhodamines	129-138	vasoactive intestinal peptide	Rattus norvegicus	118-121
19481575-1	2009	We evaluated the benefits of a novel formulation of vasoactive intestinal peptide (VIP) based on the incorporation of VIP-loaded rhodamine-conjugated liposomes (VIP-Rh-Lip) within hyaluronic acid (HA) gel (Gel-VIP-Rh-Lip) for the treatment of endotoxin-induced uveitis (EIU) in comparison with VIP-Rh-Lip alone.	Rhodamines	129-138	vasoactive intestinal peptide	Rattus norvegicus	118-121
19481575-1	2009	We evaluated the benefits of a novel formulation of vasoactive intestinal peptide (VIP) based on the incorporation of VIP-loaded rhodamine-conjugated liposomes (VIP-Rh-Lip) within hyaluronic acid (HA) gel (Gel-VIP-Rh-Lip) for the treatment of endotoxin-induced uveitis (EIU) in comparison with VIP-Rh-Lip alone.	Rhodamines	129-138	vasoactive intestinal peptide	Rattus norvegicus	118-121
19481575-1	2009	We evaluated the benefits of a novel formulation of vasoactive intestinal peptide (VIP) based on the incorporation of VIP-loaded rhodamine-conjugated liposomes (VIP-Rh-Lip) within hyaluronic acid (HA) gel (Gel-VIP-Rh-Lip) for the treatment of endotoxin-induced uveitis (EIU) in comparison with VIP-Rh-Lip alone.	Rhodamines	129-138	vasoactive intestinal peptide	Rattus norvegicus	118-121
19814863-6	2009	Verapamil, a competitive inhibitor of P-gp, significantly inhibited ileal clearance of rhodamine 123 to the lumen at 24 h after reperfusion, suggesting that P-gp was working at this time.	Rhodamines	87-96	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	38-42
19814863-6	2009	Verapamil, a competitive inhibitor of P-gp, significantly inhibited ileal clearance of rhodamine 123 to the lumen at 24 h after reperfusion, suggesting that P-gp was working at this time.	Rhodamines	87-96	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	157-161
19760117-5	2010	Laser scanning microscopy of fungal cells exposed to rhodamine-labeled Pr-1 revealed that the protein accumulated and was localized on the cell surface.	Rhodamines	53-62	transmembrane protein 37	Homo sapiens	71-75
19834649-7	2010	These experiments demonstrated that: i) both constructs expressed in the generated transfected cell line are functional; ii) the estimated pEYFP-actin: endogenous beta-actin ratio is within the limits required for the functional integrity of the actin filaments; and iii) pEYFP-actin and rhodamine-phalloidine-stained F-actin structures colocalize and display comparable reorganization patterns in pharmacologically challenged cells.	Rhodamines	288-297	POTE ankyrin domain family member F	Homo sapiens	163-173
20460821-2	2010	KP018 from Ellipeiopsis cherrevensis and AT80 from Ancistrocladus tectorius increased both rhodamine 123, a typical P-gp substrate, and [(3)H]paclitaxel uptake in PR-HepG2 cells.	Rhodamines	91-100	ATP binding cassette subfamily B member 1	Homo sapiens	116-120
19726755-5	2010	Membrane vesicles from stably transfected CHO cells expressing recombinant SMDR2 show significant increases in rhodamine transport and ATP hydrolysis compared with those from control cells or cells transfected with empty vector.	Rhodamines	111-120	smdr2	Schistosoma mansoni	75-80
19907082-4	2009	In the first section, rhodamine-derived Hg2+ ion sensors have been reviewed according to the essential mechanisms that work together with the spirolactam ring opening reaction.	Rhodamines	22-31	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	40-43
19761200-6	2009	Furthermore, although mutation of the majority of residues contacting rhodamine 6G exerted moderate effects on QacR-rhodamine 6G binding, mutation of Leu(54) and Gln(96), and cumulative mutations involving these with Tyr(93) and Tyr(123), imparted a dramatic decrease in QacR-rhodamine 6G binding affinity.	Rhodamines	70-79	QacR	Staphylococcus aureus	111-115
19761200-6	2009	Furthermore, although mutation of the majority of residues contacting rhodamine 6G exerted moderate effects on QacR-rhodamine 6G binding, mutation of Leu(54) and Gln(96), and cumulative mutations involving these with Tyr(93) and Tyr(123), imparted a dramatic decrease in QacR-rhodamine 6G binding affinity.	Rhodamines	70-79	QacR	Staphylococcus aureus	271-275
19761200-6	2009	Furthermore, although mutation of the majority of residues contacting rhodamine 6G exerted moderate effects on QacR-rhodamine 6G binding, mutation of Leu(54) and Gln(96), and cumulative mutations involving these with Tyr(93) and Tyr(123), imparted a dramatic decrease in QacR-rhodamine 6G binding affinity.	Rhodamines	116-125	QacR	Staphylococcus aureus	111-115
19761200-6	2009	Furthermore, although mutation of the majority of residues contacting rhodamine 6G exerted moderate effects on QacR-rhodamine 6G binding, mutation of Leu(54) and Gln(96), and cumulative mutations involving these with Tyr(93) and Tyr(123), imparted a dramatic decrease in QacR-rhodamine 6G binding affinity.	Rhodamines	116-125	QacR	Staphylococcus aureus	111-115
19761200-8	2009	Additionally, despite maintaining a high affinity for ethidium, QacR mutants involving Leu(54), Tyr(93), Gln(96), and Tyr(123), which denote the interface between the rhodamine 6G and ethidium subpockets, were unable to be induced from operator DNA in the presence of ethidium in S. aureus.	Rhodamines	167-176	QacR	Staphylococcus aureus	64-68
19947169-6	2009	The effects of guggulsterone on P-glycoprotein activity were evaluated by measuring rhodamine 123 (Rh123)-associated mean fluorescence intensity and P-glycoprotein expression on the basis of the flow cytometric technology, respectively.	Rhodamines	84-93	ATP binding cassette subfamily B member 1	Homo sapiens	32-46
19576864-6	2009	Additional evidence was obtained from time-resolved in situ fluorescence spectroscopic monitoring of the Pgp efflux dynamics in transfected Caco-2 cells which yielded significantly reduced transporter efficiencies for the Pgp substrate Rhodamine 123.	Rhodamines	236-245	ATP binding cassette subfamily B member 1	Homo sapiens	105-108
19576864-6	2009	Additional evidence was obtained from time-resolved in situ fluorescence spectroscopic monitoring of the Pgp efflux dynamics in transfected Caco-2 cells which yielded significantly reduced transporter efficiencies for the Pgp substrate Rhodamine 123.	Rhodamines	236-245	ATP binding cassette subfamily B member 1	Homo sapiens	222-225
19538007-7	2009	Surface charge of liposomes did not affect the rhodamine retention, whereas the incorporation of cholesterol and polyethyleneglycol-attached lipids was effective in further increasing the rhodamine retention in MCF-7/Pgp cells.	Rhodamines	188-197	ATP binding cassette subfamily B member 1	Homo sapiens	217-220
19596835-8	2009	We also find that a rhodamine dye conjugated to a 5beta-reduced 3alpha-hydroxy steroid is a particularly potent and effective photopotentiator, with minimal baseline receptor activity up to 10 muM.	Rhodamines	20-29	latexin	Homo sapiens	193-196
19297331-10	2009	As expected, surface binding of rhodamine-labeled EGF increased with green fluorescent protein-EGFR expression level.	Rhodamines	32-41	epidermal growth factor receptor	Homo sapiens	95-99
19616959-1	2009	Two kinds of rhodamine modified beta-cyclodextrins (R-1 and R-2), which are coupled up ethylene diamine (EDA) and tetraethylene pentamine (TEPA) between Rh B and beta-cyclodextrin, respectively, have been synthesized.	Rhodamines	13-22	CD1b molecule	Homo sapiens	32-63
19465096-4	2009	P-glycoprotein (P-gp) does not affect melatonin absorption but transported rhodamine 123, a well-known P-gp substrate.	Rhodamines	75-84	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	0-14
19465096-4	2009	P-glycoprotein (P-gp) does not affect melatonin absorption but transported rhodamine 123, a well-known P-gp substrate.	Rhodamines	75-84	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	16-20
19465096-4	2009	P-glycoprotein (P-gp) does not affect melatonin absorption but transported rhodamine 123, a well-known P-gp substrate.	Rhodamines	75-84	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	103-107
19480464-5	2009	Rhodamine derivatives were conjugated to avidin and trastuzumab, which target D-galactose receptor and HER2/neu antigen, respectively.	Rhodamines	0-9	erb-b2 receptor tyrosine kinase 2	Mus musculus	103-111
19538007-0	2009	Liposome composition is important for retention of liposomal rhodamine in P-glycoprotein-overexpressing cancer cells.	Rhodamines	61-70	ATP binding cassette subfamily B member 1	Homo sapiens	74-88
19538007-5	2009	Pgp-expression decreased the rhodamine retention in MCF-7 cells, suggesting that Pgp is functional.	Rhodamines	29-38	ATP binding cassette subfamily B member 1	Homo sapiens	0-3
19538007-5	2009	Pgp-expression decreased the rhodamine retention in MCF-7 cells, suggesting that Pgp is functional.	Rhodamines	29-38	ATP binding cassette subfamily B member 1	Homo sapiens	81-84
19538007-6	2009	Liposome loading increased rhodamine retention in MCF-7/Pgp cells, but not in MCF-7/WT cells.	Rhodamines	27-36	ATP binding cassette subfamily B member 1	Homo sapiens	56-59
19564743-3	2009	P-gp function was measured using the verapamil-sensitive Rhodamine efflux.	Rhodamines	57-66	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
19549365-7	2009	The function of P-gp in K562/A02 cells weakened along with decrease of intracellular acidification, the intracellular acidification significantly increased the accumulation of Rhodamine 123 (Rh 123) and suppressed the efflux of Rh 123 mediated by P-gp.	Rhodamines	176-185	phosphoglycolate phosphatase	Homo sapiens	16-20
19402665-0	2009	Rhodamine inhibitors of P-glycoprotein: an amide/thioamide "switch" for ATPase activity.	Rhodamines	0-9	ATP binding cassette subfamily B member 1	Homo sapiens	24-38
19402665-0	2009	Rhodamine inhibitors of P-glycoprotein: an amide/thioamide "switch" for ATPase activity.	Rhodamines	0-9	dynein axonemal heavy chain 8	Homo sapiens	72-78
19474307-5	2009	The rhodamine-, OR Green-, or Cy3-labeled ligands had high binding affinity for DAT and enabled specific labeling of DAT in live neurons and visualization by confocal imaging.	Rhodamines	4-13	solute carrier family 6 member 3	Homo sapiens	80-83
19474307-5	2009	The rhodamine-, OR Green-, or Cy3-labeled ligands had high binding affinity for DAT and enabled specific labeling of DAT in live neurons and visualization by confocal imaging.	Rhodamines	4-13	solute carrier family 6 member 3	Homo sapiens	117-120
19232637-11	2009	A Raman probe, Rhodamine 6G (Rh 6G), has been found to be suited for the surface modification of the gold particles and it has also been demonstrated that the larger particles show better SERS signal than the corresponding smaller ones.	Rhodamines	15-24	seryl-tRNA synthetase 1	Homo sapiens	188-192
19429419-3	2009	The change in the mRNA expression of MDR1 was accompanied by a change in the CsA-dependent intracellular accumulation of rhodamine 123.	Rhodamines	121-130	ATP binding cassette subfamily B member 1	Homo sapiens	37-41
19188399-9	2009	They also correlated with the 50% inhibitory concentration for inhibition of Pdr5p-mediated transport of rhodamine 6G in isolated plasma membranes.	Rhodamines	105-114	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	77-82
19174508-7	2009	Compared with WT, stimulation-induced increases in rhodamine-123 fluorescence were approximately 5 times larger in motor terminals from presymptomatic mice expressing mutations of human superoxide dismutase I (SOD1) that cause familial amyotrophic lateral sclerosis (SOD1-G85R, which lacks dismutase activity; SOD1-G93A, which retains dismutase activity).	Rhodamines	51-60	superoxide dismutase 1	Homo sapiens	210-214
19041851-4	2009	Moreover, expression of P-gp and BCRP was lower in hCMEC/D3 than in human brain microvessels but remain functional as shown by rhodamine 123 efflux assay.	Rhodamines	127-136	phosphoglycolate phosphatase	Homo sapiens	24-28
19041851-4	2009	Moreover, expression of P-gp and BCRP was lower in hCMEC/D3 than in human brain microvessels but remain functional as shown by rhodamine 123 efflux assay.	Rhodamines	127-136	BCR pseudogene 1	Homo sapiens	33-37
19194580-3	2009	These properties are mechanistically ascribed to the transfer from rhodamine spirolactam to the thiazoline-derived open-ring rhodamine via Hg2+ induced desulfurization.	Rhodamines	67-76	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	139-142
19174508-7	2009	Compared with WT, stimulation-induced increases in rhodamine-123 fluorescence were approximately 5 times larger in motor terminals from presymptomatic mice expressing mutations of human superoxide dismutase I (SOD1) that cause familial amyotrophic lateral sclerosis (SOD1-G85R, which lacks dismutase activity; SOD1-G93A, which retains dismutase activity).	Rhodamines	51-60	superoxide dismutase 1	Homo sapiens	267-271
19174508-7	2009	Compared with WT, stimulation-induced increases in rhodamine-123 fluorescence were approximately 5 times larger in motor terminals from presymptomatic mice expressing mutations of human superoxide dismutase I (SOD1) that cause familial amyotrophic lateral sclerosis (SOD1-G85R, which lacks dismutase activity; SOD1-G93A, which retains dismutase activity).	Rhodamines	51-60	superoxide dismutase 1	Homo sapiens	267-271
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	74-84	ATP binding cassette subfamily C member 1	Homo sapiens	8-12
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	74-84	ATP binding cassette subfamily C member 1	Homo sapiens	88-92
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	74-84	ATP binding cassette subfamily C member 1	Homo sapiens	88-92
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	156-166	ATP binding cassette subfamily C member 1	Homo sapiens	8-12
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	156-166	ATP binding cassette subfamily C member 1	Homo sapiens	88-92
19120455-8	2009	Because MRP1 was expressed in all the cell lines tested and the efflux of rhodamines in MRP1 over-expressing cells was abolished by NBD-Cl, it appears that rhodamines are excluded from these cells by MRP1.	Rhodamines	156-166	ATP binding cassette subfamily C member 1	Homo sapiens	88-92
19120455-11	2009	The innate resistance provided by MRP1 to cells prevents rhodamine dyes, and possibly drugs such as doxorubicin, from achieving equilibration of their concentration in the cytoplasm with their concentration in the external medium.	Rhodamines	57-66	ATP binding cassette subfamily C member 1	Homo sapiens	34-38
19232006-2	2009	injection of vasoactive intestinal peptide (VIP) loaded in rhodamine-conjugated liposomes (VIP-Rh-Lip) on experimental autoimmune uveoretinitis (EAU).	Rhodamines	59-68	vasoactive intestinal peptide	Rattus norvegicus	44-47
19179882-10	2009	Hepatocyte extrusion of rhodamine dye, a measure of MDR1 function, declined only in the TPN with lipid group.	Rhodamines	24-33	malic enzyme complex, mitochondrial	Mus musculus	52-56
18592293-9	2008	SGLT1 G507C rhodamine fluorescence intensity increased with depolarizing and decreased with hyperpolarizing voltages.	Rhodamines	12-21	solute carrier family 5 member 1	Homo sapiens	0-5
19124148-5	2009	The inhibition of efflux activity was measured via the increased rhodamine uptake by mouse lymphoma cells transfected in human MDR1 gene and in human brain capillary endothelial cells.	Rhodamines	65-74	ATP binding cassette subfamily B member 1	Homo sapiens	127-131
18845169-7	2008	KB3-1 significantly enhanced the accumulation and retention of a P-gp substrate, rhodamine-123 in the P-gp-expressing MES-SA/DX5 uterine sarcoma cells but not in the P-gp-negative MES-SA cells at non-toxic concentrations of 1 microM and 3 microM.	Rhodamines	81-90	ATP binding cassette subfamily B member 1	Homo sapiens	65-69
18845169-7	2008	KB3-1 significantly enhanced the accumulation and retention of a P-gp substrate, rhodamine-123 in the P-gp-expressing MES-SA/DX5 uterine sarcoma cells but not in the P-gp-negative MES-SA cells at non-toxic concentrations of 1 microM and 3 microM.	Rhodamines	81-90	ATP binding cassette subfamily B member 1	Homo sapiens	102-106
18845169-7	2008	KB3-1 significantly enhanced the accumulation and retention of a P-gp substrate, rhodamine-123 in the P-gp-expressing MES-SA/DX5 uterine sarcoma cells but not in the P-gp-negative MES-SA cells at non-toxic concentrations of 1 microM and 3 microM.	Rhodamines	81-90	ATP binding cassette subfamily B member 1	Homo sapiens	102-106
19031139-10	2008	There was positive correlation between the percentage of Rhodamine 123 low staining cells and positive msi-1 cells in each group (r=0.867, P<0.01).	Rhodamines	57-66	musashi RNA-binding protein 1	Mus musculus	103-108
18799096-5	2008	P-gp-mediated transport activity of cells was detected by rhodamine 123 efflux assay.	Rhodamines	58-67	ATP binding cassette subfamily B member 1	Homo sapiens	0-4
17941015-8	2008	The in vitro Rhodamine 123 efflux experiment using MDR KB(v200) cells revealed that when cells were pretreated with folate-attached and FG020326-loaded micelles, the P-glycoprotein (P-gp) drug efflux function was significantly inhibited.	Rhodamines	13-22	ATP binding cassette subfamily B member 1	Homo sapiens	166-180
18403942-1	2008	OBJECTIVES: The present study was aimed at evaluation of in vivo biliary and renal excretion of rhodamine 123 (Rho123), a P-glycoprotein (P-gp) substrate, in rats during either acute or chronic cholestasis induced by bile duct obstruction (BDO).	Rhodamines	96-105	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	122-136
18403942-1	2008	OBJECTIVES: The present study was aimed at evaluation of in vivo biliary and renal excretion of rhodamine 123 (Rho123), a P-glycoprotein (P-gp) substrate, in rats during either acute or chronic cholestasis induced by bile duct obstruction (BDO).	Rhodamines	96-105	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	138-142
19881253-5	2009	The uptake of [(3)H]paclitaxel and rhodamine 123 increased by verapamil, a P-gp inhibitor.	Rhodamines	35-44	ATP binding cassette subfamily B member 1	Homo sapiens	75-79
20053600-2	2009	P-glycoprotein activity in lymphocytes was measured by the Rhodamine 123 efflux assay using flow cytometry, in the presence and absence of verapamil, a P-glycoprotein inhibitor.	Rhodamines	59-68	ATP binding cassette subfamily B member 1	Homo sapiens	0-14
18945821-4	2009	The designed agents were potent inhibitors of rhodamine 123 efflux in cultured cancer cell lines that display high levels of P-gp expression at the cell surface and in transfected cells expressing P-gp.	Rhodamines	46-55	ATP binding cassette subfamily B member 1	Homo sapiens	125-129
18945821-4	2009	The designed agents were potent inhibitors of rhodamine 123 efflux in cultured cancer cell lines that display high levels of P-gp expression at the cell surface and in transfected cells expressing P-gp.	Rhodamines	46-55	ATP binding cassette subfamily B member 1	Homo sapiens	197-201
19309222-10	2009	Rhodamine retention alone and in the presence of cyclosporine was the lowest in imatinib-resistant K-562R-0.1 cell line, what suggest high PGP activity in this cell line.	Rhodamines	0-9	phosphoglycolate phosphatase	Homo sapiens	139-142
18559252-3	2008	Because tight dimerization will result in complete energy transfer from donor to acceptor, we have used the same experimental system of fluorescein- and rhodamine-labeled G380R mutants of FGFR3 for the experimental assessment of the proximity FRET corrections using fluorescence lifetime measurements.	Rhodamines	153-162	fibroblast growth factor receptor 3	Homo sapiens	188-193
18637679-1	2008	A new chemosensor RF1 that combines a ferrocene unit and a rhodamine block via the linkage of a carbohydrazone binding unit was designed and prepared for the highly selective detection of Hg (2+) in natural water.	Rhodamines	59-68	mitochondrial translation release factor 1	Homo sapiens	18-21
18637679-5	2008	Hg (2+)-binding also arouses the absorption of the rhodamine moiety in RF1 significantly with the chromogenic detection limit for Hg (2+) at 50 ppb.	Rhodamines	51-60	mitochondrial translation release factor 1	Homo sapiens	71-74
18633498-1	2008	On the basis of fluorescent resonance energy transfer from 1,8-naphthalimide to rhodamine, a fluorophore dyad (FD8) containing rhodamine and a naphthalimide moiety was synthesized as a Cr3+-selective fluorescent probe for monitoring Cr3+ in living cells with ratiometric fluorescent methods.	Rhodamines	80-89	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	185-188
18633498-1	2008	On the basis of fluorescent resonance energy transfer from 1,8-naphthalimide to rhodamine, a fluorophore dyad (FD8) containing rhodamine and a naphthalimide moiety was synthesized as a Cr3+-selective fluorescent probe for monitoring Cr3+ in living cells with ratiometric fluorescent methods.	Rhodamines	127-136	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	185-188
18612518-1	2008	Isotopically substituted rhodamine dyes provide ideal probes for the study of single-molecule surface enhanced Raman scattering (SM-SERS) events through multiple-analyte techniques.	Rhodamines	25-34	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	132-136
18489122-3	2008	Here we show that rhodamine-phalloidin binds both Arp2/3 complex and the VCA domain of Arp2/3 complex activator, hWASp, with dissociation equilibrium constants of about 100 nM.	Rhodamines	18-27	actin related protein 2	Homo sapiens	50-54
18489122-3	2008	Here we show that rhodamine-phalloidin binds both Arp2/3 complex and the VCA domain of Arp2/3 complex activator, hWASp, with dissociation equilibrium constants of about 100 nM.	Rhodamines	18-27	actin related protein 2	Homo sapiens	87-91
18489122-3	2008	Here we show that rhodamine-phalloidin binds both Arp2/3 complex and the VCA domain of Arp2/3 complex activator, hWASp, with dissociation equilibrium constants of about 100 nM.	Rhodamines	18-27	WASP actin nucleation promoting factor	Homo sapiens	113-118
18205807-5	2008	In the rpd3 Delta and rom2 Delta mutants, the level of PDR5 mRNA and the rate of rhodamine 6G efflux were reduced.	Rhodamines	81-90	histone deacetylase RPD3	Saccharomyces cerevisiae S288C	7-11
18205807-5	2008	In the rpd3 Delta and rom2 Delta mutants, the level of PDR5 mRNA and the rate of rhodamine 6G efflux were reduced.	Rhodamines	81-90	Rho family guanine nucleotide exchange factor ROM2	Saccharomyces cerevisiae S288C	22-26
18646325-5	2008	Flow cytometry was also used to determine the efflux activity associated with P-gp; with this process, refluxed fluorescent P-gp substrate, rhodamine 123 (Rho123), was determined by the subsequently identified P-gp-positive PBMC subset.	Rhodamines	140-149	ATP binding cassette subfamily B member 1	Homo sapiens	78-82
18646325-5	2008	Flow cytometry was also used to determine the efflux activity associated with P-gp; with this process, refluxed fluorescent P-gp substrate, rhodamine 123 (Rho123), was determined by the subsequently identified P-gp-positive PBMC subset.	Rhodamines	140-149	ATP binding cassette subfamily B member 1	Homo sapiens	124-128
18646325-5	2008	Flow cytometry was also used to determine the efflux activity associated with P-gp; with this process, refluxed fluorescent P-gp substrate, rhodamine 123 (Rho123), was determined by the subsequently identified P-gp-positive PBMC subset.	Rhodamines	140-149	ATP binding cassette subfamily B member 1	Homo sapiens	124-128
18046703-6	2007	Ultraviolet (UV) illumination of the aorta allowed the identification of regions with high macrophage content, while MSR-targeted rhodamine micelles could be detected with fluorescence microscopy and were found to be associated with macrophages.	Rhodamines	130-139	macrophage scavenger receptor 1	Mus musculus	117-120
18356296-0	2008	A mutation of the H-loop selectively affects rhodamine transport by the yeast multidrug ABC transporter Pdr5.	Rhodamines	45-54	ATP-binding cassette multidrug transporter PDR5	Saccharomyces cerevisiae S288C	104-108
18234154-5	2008	CBT-1 completely inhibited rhodamine 123 transport from Pgp-overexpressing cells at a concentration of 1muM.	Rhodamines	27-36	succinate dehydrogenase complex subunit D	Homo sapiens	0-5
18234154-5	2008	CBT-1 completely inhibited rhodamine 123 transport from Pgp-overexpressing cells at a concentration of 1muM.	Rhodamines	27-36	ATP binding cassette subfamily B member 1	Homo sapiens	56-59
18234154-10	2008	Serum levels of CBT-1 in samples obtained from eight patients receiving CBT-1 increased intracellular rhodamine 123 levels in CD56+ cells 2.1- to 5.7-fold in an ex vivo assay.	Rhodamines	102-111	succinate dehydrogenase complex subunit D	Homo sapiens	16-21
18234154-10	2008	Serum levels of CBT-1 in samples obtained from eight patients receiving CBT-1 increased intracellular rhodamine 123 levels in CD56+ cells 2.1- to 5.7-fold in an ex vivo assay.	Rhodamines	102-111	succinate dehydrogenase complex subunit D	Homo sapiens	72-77
17647225-10	2008	Based on the rhodamine accumulation study, the increased cytotoxicity is possibly due to the P-gp inhibition by CPGS.	Rhodamines	13-22	ATP binding cassette subfamily B member 1	Homo sapiens	93-97
18221354-10	2008	Intraperitoneal administration of monoclonal antibodies to CD11b (rat IgG2b) to C3H/HeN mice inhibited UVB-induced oxidative stress generated by both epidermal and dermal cells as is evident by relative fluorescence intensity of oxidized rhodamine.	Rhodamines	238-247	integrin alpha M	Mus musculus	59-64
18221354-10	2008	Intraperitoneal administration of monoclonal antibodies to CD11b (rat IgG2b) to C3H/HeN mice inhibited UVB-induced oxidative stress generated by both epidermal and dermal cells as is evident by relative fluorescence intensity of oxidized rhodamine.	Rhodamines	238-247	immunoglobulin heavy constant gamma 2B	Mus musculus	70-75
18302483-4	2008	After 12 days, MDR1 expression was determined by the rhodamine efflux assay.	Rhodamines	53-62	ATP binding cassette subfamily B member 1	Homo sapiens	15-19
18059369-5	2008	Rhodamine-labeled DNA nanoparticles colocalize with nucleolin on the cell surface, as well as in the cytoplasm and nucleus, but not with transferrin or markers of early endosome or lysosome following cellular uptake.	Rhodamines	0-9	nucleolin	Homo sapiens	52-61
17942408-4	2007	Rhodamine-phalloidin staining revealed increase stress fiber formation in vascular smooth muscle cells of profilin 1 compared with 88R/L and control.	Rhodamines	0-9	profilin 1	Mus musculus	106-116
18451986-0	2007	Ocular and systemic bio-distribution of rhodamine-conjugated liposomes loaded with VIP injected into the vitreous of Lewis rats.	Rhodamines	40-49	vasoactive intestinal peptide	Rattus norvegicus	83-86
18451986-2	2007	The purpose of the present study was to define the biodistribution of rhodamine-conjugated liposomes loaded with vasoactive intestinal peptide (VIP), an immunosuppressive neuropeptide, following their intravitreal (IVT) injection in normal rats.	Rhodamines	70-79	vasoactive intestinal peptide	Rattus norvegicus	144-147
17873103-4	2008	Fluorescent-labeled microspheres composed of poly lactic-coglycolic acid (PLGA) were loaded with rhodamine-labeled PF-4/CTF and formulated to release their contents over time.	Rhodamines	97-106	platelet factor 4	Homo sapiens	115-119
17964793-2	2008	Herein, we describe the development of a novel screen for PAD4 inhibitors that is based on a PAD4-targeted Activity-Based Protein Profiling reagent, denoted Rhodamine-conjugated F-Amidine (RFA).	Rhodamines	157-166	peptidyl arginine deiminase 4	Homo sapiens	58-62
17964793-2	2008	Herein, we describe the development of a novel screen for PAD4 inhibitors that is based on a PAD4-targeted Activity-Based Protein Profiling reagent, denoted Rhodamine-conjugated F-Amidine (RFA).	Rhodamines	157-166	peptidyl arginine deiminase 4	Homo sapiens	93-97
17950691-6	2008	273 (1998) 12612-12622], we show that Yor1p also confers resistance to rhodamine 6G and to doxorubicin.	Rhodamines	71-80	ATP-binding cassette transporter YOR1	Saccharomyces cerevisiae S288C	38-43
18989812-9	2008	The PLA(2) and Mel activities were measured indirectly by changes in turbidity at 400(n m), rhodamine leak-out, and hemolysis.	Rhodamines	92-101	phospholipase A2 group IB	Homo sapiens	4-10
18369935-6	2008	Fusion of labeled v-SNARE liposomes with unlabeled t-SNARE liposomes increases the distance between NBD and rhodamine, increasing the NBD fluorescence.	Rhodamines	108-117	vesicle transport through interaction with t-SNAREs 1B	Homo sapiens	18-25
18234965-9	2008	Silencing the expression of the DNA binding subunit of NF-kappaB, p50, by small interfering RNA vector resulted in a decrease of MDR1 function by rhodamine 123 efflux assay in T167 cells exposed to 2 Gy.	Rhodamines	146-155	nuclear factor kappa B subunit 1	Homo sapiens	66-69
18234965-9	2008	Silencing the expression of the DNA binding subunit of NF-kappaB, p50, by small interfering RNA vector resulted in a decrease of MDR1 function by rhodamine 123 efflux assay in T167 cells exposed to 2 Gy.	Rhodamines	146-155	ATP binding cassette subfamily B member 1	Homo sapiens	129-133