PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23852983-8	2014	Intracellular injection of DiI into secretagogin cells revealed an average dendritic field diameter of 170 mum and an average coverage factor of 3.2.	dilC18(3) dye	27-30	secretagogin, EF-hand calcium binding protein	Homo sapiens	36-48
23685333-9	2013	DiI labeling and tissue recombination experiments show that the restriction of Tbx18 expression to the prospective ureteric mesenchyme does not reflect an active condensation process but is due to a specific loss of Tbx18 expression in the mesenchyme out of range of signals from the ureteric epithelium.	dilC18(3) dye	0-3	T-box transcription factor 18	Homo sapiens	79-84
22903314-5	2013	DiI labeling and Golli-tauGFP immunofluorescence indicate that Gli3(Xt/Pdn) cortical neurons form short and stunted axons.	dilC18(3) dye	0-3	GLI family zinc finger 3	Homo sapiens	63-67
23834820-8	2013	RESULTS: We showed that CBS was colocalized with Na(V)1.8 in colon-specific DRG neurons pre-labeled with DiI.	dilC18(3) dye	105-108	cystathionine beta synthase	Rattus norvegicus	24-27
23834820-8	2013	RESULTS: We showed that CBS was colocalized with Na(V)1.8 in colon-specific DRG neurons pre-labeled with DiI.	dilC18(3) dye	105-108	sodium voltage-gated channel alpha subunit 10	Rattus norvegicus	49-57
22898045-5	2012	Intracoronary artery transplantation was followed by the distribution of DiI-stained hCLCs into the scarred myocardial milieu.	dilC18(3) dye	73-76	ATP binding cassette subfamily B member 1	Homo sapiens	85-90
23950953-8	2013	DiI-labeled L1, internalized through the LDL receptor, became visible inside HAECs within 30 seconds.	dilC18(3) dye	0-3	low density lipoprotein receptor	Homo sapiens	41-53
23950953-9	2013	In contrast, DiI-labeled L5, internalized through LOX-1, became apparent after 5 minutes.	dilC18(3) dye	13-16	oxidized low density lipoprotein receptor 1	Homo sapiens	50-55
24088266-2	2013	The knowledge of conformational changes and its importance in binding of DII to inhA has not been explored before.	dilC18(3) dye	73-76	inhibin subunit alpha	Homo sapiens	80-84
23162434-3	2012	The application of DiI onto the ventral domain of the bulb which harbors the OR37 glomeruli resulted in the labeling of fibers within the paraventricular nucleus (PVN) and supraoptic nucleus (SO) of the hypothalamus; some of these fibers were covered with varicose-like structures.	dilC18(3) dye	19-22	olfactory receptor family 5 subfamily H member 8 (gene/pseudogene)	Homo sapiens	77-81
22898045-8	2012	Histological studies at week 12 post-transplantation demonstrated engraftment of the pre DiI-stained hCLCs into the scarred myocardium and their expression of human specific alpha-cardiac actin.	dilC18(3) dye	89-92	ATP binding cassette subfamily B member 1	Homo sapiens	101-106
22080974-5	2012	Single cell quantitative PCR was employed to measure TRPV1 expression levels in DiI-labeled colonic dorsal root ganglion (DRG) neurons.	dilC18(3) dye	80-83	transient receptor potential cation channel, subfamily V, member 1	Mus musculus	53-58
22378787-8	2012	Experiments using DiI-labeled LDL particles showed that FGF21 increased lipoprotein uptake and the effect of FGF21 was additive to that of statins.	dilC18(3) dye	18-21	fibroblast growth factor 21	Homo sapiens	56-61
22068423-9	2012	In addition, we observed that DiI-labeled hUCB-MSCs express N-cadherin in the peri-infarct area and interact with cardiomyocytes.	dilC18(3) dye	30-33	cadherin 2	Homo sapiens	60-70
22037193-7	2012	Histological analysis confirmed subepicardial scar thickness and the presence of DiI-positive cells that express connexin-43.	dilC18(3) dye	81-84	gap junction protein, alpha 1	Rattus norvegicus	113-124
22253772-8	2012	Transplantation of DiI-labeled mMSCs into WT muscle increased Pax7+ cells and facilitated formation of eMHC+DiI- fibers.	dilC18(3) dye	19-22	paired box 7	Mus musculus	62-66
21810484-10	2011	The surface expression of LDLR as well as the uptake of fluroresecent DiI-LDL was also reduced by ABCA2.	dilC18(3) dye	70-73	ATP-binding cassette, sub-family A (ABC1), member 2	Mus musculus	98-103
21501865-2	2011	The cellular uptake of p160-decorated PEO-b-PBCL micelles containing DiI fluorescent label by MDA-MB-435 cancer cells was assessed and compared to that for c(RGDfK)-decorated micelles.	dilC18(3) dye	69-72	MYB binding protein 1a	Homo sapiens	23-27
21682565-8	2011	RESULTS: DiI-labeled LOX1-targeted liposomes were prominently observed in the lesions on Day 7 after the surgery.	dilC18(3) dye	9-12	oxidized low density lipoprotein receptor 1	Rattus norvegicus	21-25
21767538-8	2011	On the other hand, in DI and DII, the tissue expression and activity of MMP-2 and -9 was very weak.	dilC18(3) dye	29-32	matrix metallopeptidase 2	Homo sapiens	72-84
21091881-12	2011	Immunofluorescence analysis demonstrated that CM-DiI-labeled BM-MSCs could stay in corporal cavernosa for at least 4 weeks and some of them expressed von Willebrand Factor, CD31, calponin, or alpha-smooth muscle actin, cells markers for endothelial cells or smooth muscle cells, respectively.	dilC18(3) dye	49-52	platelet and endothelial cell adhesion molecule 1	Rattus norvegicus	173-177
21485011-6	2011	In Ret -/- mice, DiI-labeled vagal sensory axons descended in paraesophageal trunks as far as the proximal stomach, which contains neurons, but did not enter the aganglionic bowel.	dilC18(3) dye	17-20	ret proto-oncogene	Mus musculus	3-6
21419761-15	2011	DiI labeling of the neural crest as well as quail-to-chick neural crest chimeras showed that neural crest cells migrated to and around the ectopic site of FGF8 expression.	dilC18(3) dye	0-3	fibroblast growth factor 8	Gallus gallus	155-159
21091881-12	2011	Immunofluorescence analysis demonstrated that CM-DiI-labeled BM-MSCs could stay in corporal cavernosa for at least 4 weeks and some of them expressed von Willebrand Factor, CD31, calponin, or alpha-smooth muscle actin, cells markers for endothelial cells or smooth muscle cells, respectively.	dilC18(3) dye	49-52	actin gamma 2, smooth muscle	Rattus norvegicus	192-217
19422480-7	2009	Interestingly, CM-DiI-labelled HMSCs expressed the hepatocyte-specific markers, human albumin and alpha-fetoprotein.	dilC18(3) dye	18-21	alpha fetoprotein	Homo sapiens	98-115
20304063-8	2010	The gene expression of 3beta-HSD showed a significant increase at 120min on DI and DII ((o)p<0.01) and 20alpha-HSD diminished only on DII.	dilC18(3) dye	83-86	hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1	Rattus norvegicus	23-32
21203458-7	2010	CONCLUSIONS: Large amounts of DiI and a long incubation time have proven useful in aged human brain as a marker of long axons and large cell bodies of projecting neurons such as the rubrospinal projection and for clarifying nuclear boundaries of closed nuclei (e.g., the large human pNr).	dilC18(3) dye	30-33	trace amine associated receptor 5	Homo sapiens	283-286
20220004-7	2010	DiI-labeled cell migration assay using organotypic forebrain slice cultures revealed that the number of cells migrating from the medial ganglionic eminence into the neocortex was significantly reduced in necdin-deficient embryos.	dilC18(3) dye	0-3	necdin, MAGE family member	Mus musculus	204-210
19660142-7	2009	Colon specific DRG neurons revealed by retrograde labeling DiI were all CBS-positive.	dilC18(3) dye	59-62	cystathionine beta synthase	Rattus norvegicus	72-75
19571401-4	2009	The effects of pratensein on up-regulating CLA-1 expression were demonstrated at both mRNA and protein levels, and validated by its increasing of 1,1"-dioctadecyl-3,3,3",3"-tetramethylindocarbocyanine perchlorate-labeled (DiI)-HDL uptake in HepG2 cells.	dilC18(3) dye	222-225	scavenger receptor class B member 1	Homo sapiens	43-48
19440734-7	2009	Application of the neural tracer DiI to the intestinal mucosa revealed that DiI-labelled myenteric neurons each had an oval or round cell body immunoreactive for calretinin.	dilC18(3) dye	76-79	calbindin 2	Rattus norvegicus	162-172
18079000-4	2008	96.1+/-2.6% of CFP expressing cells also were retrograde labeled with DiI indicating the bCSLO imaged fluorescent spots are RGCs.	dilC18(3) dye	70-73	complement factor properdin	Mus musculus	15-18
19111924-7	2009	We discovered that gp120 is retrogradely transported with FR along a direct pathway from the superior colliculus to the retina and anterogradely transported with DiI to several areas of the occipital cortex.	dilC18(3) dye	162-165	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	19-24
19201948-8	2009	Finally, by DiI labeling of migratory osteogenic precursor cells that contribute to the frontal and parietal bones, we show that Twist1 and EphA4 are required for the exclusion of such cells from the coronal suture.	dilC18(3) dye	12-15	Eph receptor A4	Mus musculus	140-145
19170770-4	2009	CD31(+) cells exhibit endothelial-like behavior by being able to incorporate DiI-labeled acetylated low-density lipoprotein as well as form tubular structures on matrigel.	dilC18(3) dye	77-80	platelet/endothelial cell adhesion molecule 1	Mus musculus	0-4
18644789-7	2008	Knockdown of LSR expression by small interfering RNA in mouse Hepa1-6 cells led to decreased internalization of both DiI-labeled cyclohexanedione-LDL and very low density lipoprotein in the presence of oleate.	dilC18(3) dye	117-120	lipolysis stimulated lipoprotein receptor	Mus musculus	13-16
18282574-4	2008	DiI-labeled RLPs were taken up by CHO-K1 cells stably expressing LOX-1 but not by wild-type CHO-K1 cells.	dilC18(3) dye	0-3	oxidized low density lipoprotein receptor 1	Bos taurus	65-70
18462761-8	2008	In the infracted myocardium, the number of DiI labeling cells in MSC(AdANG) group with high angiogenin expression was three-fold that in MSC(AdEGFP) group.	dilC18(3) dye	43-46	angiogenin	Rattus norvegicus	92-102
18375821-5	2008	Exposure of tumor spheroids to CM-DiI-labeled CLIP in situ confirms targeting of macrophages and not mesothelioma cells.	dilC18(3) dye	34-37	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	Mus musculus	46-50
16566941-12	2006	CM-DiI-labeled VEGF-transduced EPCs were observed in vivo and the numbers of cells increased.	dilC18(3) dye	3-6	vascular endothelial growth factor A	Homo sapiens	15-19
17289784-4	2007	Using immunofluorescence, we found that DiI-labelled neurons contained PAR(2) immunoreactivity, confirming the presence of receptors on colonic neurons.	dilC18(3) dye	40-43	coagulation factor II (thrombin) receptor-like 1	Mus musculus	71-77
17148949-4	2007	Injection of DiI into the entorhinal area of the wildtype and reeler mice at postnatal day 1 resulted in anterograde labeling of pioneer axons passing through the hippocampal fissure.	dilC18(3) dye	13-16	reelin	Mus musculus	62-68
17518674-6	2006	DiI-labeled vascular stromal fraction cells were found between adipocytes and in the connective tissue in CAL fat, and some of these cells were immunopositive for von Willebrand factor, suggesting differentiation into vascular endothelial cells.	dilC18(3) dye	0-3	filamin binding LIM protein 1	Homo sapiens	106-109
17251322-3	2007	In 13% of unidentified LS DRG neurons (not labeled with DiI) and 69% of LS colon neurons labeled with DiI, protons activated a sustained current that was significantly and reversibly attenuated by the transient receptor potential vanilloid receptor 1 (TRPV1) antagonist capsazepine.	dilC18(3) dye	102-105	transient receptor potential cation channel, subfamily V, member 1	Mus musculus	201-250
15895027-9	2006	DiI-labelled MSCs were differentiated into myofibroblast by the expression of alpha-SMA.	dilC18(3) dye	0-3	actin, aortic smooth muscle	Oryctolagus cuniculus	78-87
16376325-7	2006	IL-1beta downregulated the expression of VLDL-R in a time- and dose-dependent manner and markedly reduced the uptake of DiI-labeled beta-VLDL but not DiI-labeled low-density lipoprotein (LDL).	dilC18(3) dye	120-123	interleukin 1 beta	Rattus norvegicus	0-8
16484557-7	2006	AGE also inhibited DiI-labeled OxLDL uptake into PMA-stimulated THP-1 cells by 85.6+/-2.8% (P<0.01), but Hcy had no effects on it.	dilC18(3) dye	19-22	GLI family zinc finger 2	Homo sapiens	64-69
16376325-7	2006	IL-1beta downregulated the expression of VLDL-R in a time- and dose-dependent manner and markedly reduced the uptake of DiI-labeled beta-VLDL but not DiI-labeled low-density lipoprotein (LDL).	dilC18(3) dye	120-123	very low density lipoprotein receptor	Rattus norvegicus	41-47
16282704-7	2006	In the immunocytochemical analysis, MS7 absorbed DiI-acetylated LDL virtually, but the results of staining with anti-VE-cadherin, vWF, or CD31 antibodies were negative.	dilC18(3) dye	49-52	minisatellites detected by probe MMS7	Mus musculus	36-39
15636641-5	2005	Using ligand binding antagonists, we observed that HSPG, rather than VLDL-R or LRP, play a primary role in the uptake of DiI-labeled apoE-VLDL by mature adipocytes.	dilC18(3) dye	121-124	syndecan 2	Homo sapiens	51-55
16433624-5	2005	The circulating DiI+ HCs expressed c-Kit and half of these cells displayed blastic morphology.	dilC18(3) dye	16-19	KIT proto-oncogene receptor tyrosine kinase	Mus musculus	35-40
16115940-6	2005	For the in vivo studies, DiI-labeled HB1.F3-PEX cells were stereotactically injected into established glioma tumor in nude mice.	dilC18(3) dye	25-28	histocompatibility minor HB-1	Homo sapiens	37-40
16115940-8	2005	Histologic analysis showed that DiI-labeled HB1.F3-PEX cells migrate at the tumor boundary and cause a 90% reduction of tumor volume (P < 0.03).	dilC18(3) dye	32-35	histocompatibility minor HB-1	Homo sapiens	44-47
15977169-7	2005	Based on the correspondence of these DiI-labeled processes with immunostaining for vimentin, these cellular processes are probably derived from glial cells.	dilC18(3) dye	37-40	vimentin	Rattus norvegicus	83-91
15636641-5	2005	Using ligand binding antagonists, we observed that HSPG, rather than VLDL-R or LRP, play a primary role in the uptake of DiI-labeled apoE-VLDL by mature adipocytes.	dilC18(3) dye	121-124	apolipoprotein E	Homo sapiens	133-137
12809509-14	2003	Flow cytometry experiments show that SR-BI accounts for 75% of DiI-LDL uptake, the LDL receptor for 14%, and other pathways for 11%.	dilC18(3) dye	63-66	scavenger receptor class B member 1	Homo sapiens	37-42
15529384-7	2004	Anti-LOX-1 antibody suppressed the binding of DiI-labeled ox-LDL to chondrocytes in explant culture, suggesting that the interaction was mediated by LOX-1.	dilC18(3) dye	46-49	oxidized low density lipoprotein receptor 1	Homo sapiens	5-10
15529384-7	2004	Anti-LOX-1 antibody suppressed the binding of DiI-labeled ox-LDL to chondrocytes in explant culture, suggesting that the interaction was mediated by LOX-1.	dilC18(3) dye	46-49	oxidized low density lipoprotein receptor 1	Homo sapiens	149-154
15380451-10	2004	Upregulated expression of LOX-1 was associated with enhanced uptake of DiI-labeled Ox-LDL in smooth muscle cells.	dilC18(3) dye	71-74	oxidized low density lipoprotein receptor 1	Bos taurus	26-31
15010359-6	2004	Increased expression of LOX-1 was associated with the accumulation of DiI-labeled OxLDL (DiI-OxLDL) in ADMA- and l-NAME-pretreated HUVEC.	dilC18(3) dye	70-73	oxidized low density lipoprotein receptor 1	Homo sapiens	24-29
15200992-14	2004	Histological localization of DiI-labeled CD34-positive cells documented a direct anatomic correlation with the localization of transplanted cells on the MRI images.	dilC18(3) dye	29-32	CD34 molecule	Rattus norvegicus	41-45
15246692-6	2004	Labeling of the TG with carbocyanine dye, DiI, revealed that NGF induces local defasciculation and diversion of trigeminal axons.	dilC18(3) dye	42-45	nerve growth factor	Rattus norvegicus	61-64
15475691-9	2004	DiI labeled reative astrocytes were often apparent in close proximity to A beta plaques.	dilC18(3) dye	0-3	amyloid beta precursor protein	Homo sapiens	73-79
12424303-9	2002	[D-Pen(2), D-Pen(5)]-enkephalin (DPDPE, 1 microM) significantly decreased the frequency of GABA-mediated miniature inhibitory postsynaptic currents (IPSCs) of nine DiI-labeled LC neurons from 2.1 +/- 0.5 to 0.7 +/- 0.2 Hz without altering their amplitude and the kinetics.	dilC18(3) dye	164-167	proenkephalin	Rattus norvegicus	21-31
12435393-4	2002	DiI-labeled oxidized LDL was bound and ingested by chondrocytes via LOX-1.	dilC18(3) dye	0-3	oxidized low density lipoprotein receptor 1	Rattus norvegicus	68-73
12539569-6	2001	The results of binding experiments showed that the ability of the CHO cells transfected with the full-length cDNA of VLDL-R binding DiI-labeled beta-VLDL was higher than that of the CHO cells transfected with the mutant.	dilC18(3) dye	132-135	very low-density lipoprotein receptor	Cricetulus griseus	117-123
12089072-5	2002	Apo E was important in mediating HDL binding to the vascular wall, with a 48+/-16% increase in accumulation of DiI-labeled apo E-containing HDL (HDL3+E) compared with DiI-apo E-free HDL (HDL3-E) (P=0.003).	dilC18(3) dye	111-114	apolipoprotein E	Mus musculus	0-5
12089072-5	2002	Apo E was important in mediating HDL binding to the vascular wall, with a 48+/-16% increase in accumulation of DiI-labeled apo E-containing HDL (HDL3+E) compared with DiI-apo E-free HDL (HDL3-E) (P=0.003).	dilC18(3) dye	111-114	apolipoprotein E	Mus musculus	123-128
12089072-5	2002	Apo E was important in mediating HDL binding to the vascular wall, with a 48+/-16% increase in accumulation of DiI-labeled apo E-containing HDL (HDL3+E) compared with DiI-apo E-free HDL (HDL3-E) (P=0.003).	dilC18(3) dye	111-114	high density lipoprotein (HDL) level 3	Mus musculus	145-151
12089072-5	2002	Apo E was important in mediating HDL binding to the vascular wall, with a 48+/-16% increase in accumulation of DiI-labeled apo E-containing HDL (HDL3+E) compared with DiI-apo E-free HDL (HDL3-E) (P=0.003).	dilC18(3) dye	111-114	high density lipoprotein (HDL) level 3	Mus musculus	145-149
11839630-6	2002	Necropsy analysis of animals that received DiI-labeled VEGF-transduced EPCs confirmed that enhanced EPC incorporation demonstrated in vitro contributed to in vivo neovascularization as well.	dilC18(3) dye	43-46	vascular endothelial growth factor A	Mus musculus	55-59
11679584-9	2002	Furthermore, alpha-synuclein-positive inclusions were co-stained with DiI, a membrane-partitioning fluorescent dye, confirming the presence of lipid components in alpha-synuclein aggregates.	dilC18(3) dye	70-73	synuclein alpha	Homo sapiens	13-28
11679584-9	2002	Furthermore, alpha-synuclein-positive inclusions were co-stained with DiI, a membrane-partitioning fluorescent dye, confirming the presence of lipid components in alpha-synuclein aggregates.	dilC18(3) dye	70-73	synuclein alpha	Homo sapiens	163-178
11087627-9	2000	Focal injection of a lipophilic dye, DiI, showed that this shift was at least in part due to the posterior transformation of the original premandibular ectomesenchyme into the mandible, caused by the changed distribution of FGF8 that defines the mandibular region.	dilC18(3) dye	37-40	fibroblast growth factor 8	Gallus gallus	224-228
10085365-2	1999	Four- to eight-days in vitro slice cultures were exposed to 17beta-estradiol (EST) for an additional 4- to 8-day period, and spine density was assessed by confocal microscopy of DiI-labeled CA1 pyramidal neurons.	dilC18(3) dye	178-181	carbonic anhydrase 1	Homo sapiens	190-193
10722726-6	2000	Transient transfection of alpha-synuclein expression constructs into primary cortical neurons and counterstaining with the lipophilic fluorescent marker, DiI, demonstrates a close association between alpha-synuclein and cellular membranes.	dilC18(3) dye	154-157	synuclein alpha	Homo sapiens	26-41
10722726-6	2000	Transient transfection of alpha-synuclein expression constructs into primary cortical neurons and counterstaining with the lipophilic fluorescent marker, DiI, demonstrates a close association between alpha-synuclein and cellular membranes.	dilC18(3) dye	154-157	synuclein alpha	Homo sapiens	200-215
9919687-11	1999	It was found that HGF was able to chemotactically attract and direct the migration of DiI-labeled limb cells.	dilC18(3) dye	86-89	hepatocyte growth factor	Mus musculus	18-21
9919687-8	1999	After 36 h of culture, it was found that DiI-labeled limb cells, pretreated with HGF, migrated significantly further in the limb than labeled cells that have not been exposed to HGF.	dilC18(3) dye	41-44	hepatocyte growth factor	Mus musculus	81-84
9919687-8	1999	After 36 h of culture, it was found that DiI-labeled limb cells, pretreated with HGF, migrated significantly further in the limb than labeled cells that have not been exposed to HGF.	dilC18(3) dye	41-44	hepatocyte growth factor	Mus musculus	178-181
10936745-7	2000	GRP immunoreactivity was detected in 46 and 38% of the DiI-labelled muscle and mucosa neurones, respectively.	dilC18(3) dye	55-58	gastrin-releasing peptide	Cavia porcellus	0-3
10395792-2	1999	By coupling DiI cell labeling with ectopic implantation of FGF-4 microcarrier beads we have found that FGF-4 acts as a potent and specific chemoattractive agent for mesenchymal cells of the limb bud.	dilC18(3) dye	12-15	fibroblast growth factor 4	Gallus gallus	103-108
10199836-4	1999	Double immunofluorescence analysis of isolated monocytes revealed that the CD33(low) subset showed lower specific, ScR-mediated binding of DiI-labeled modified low-density lipoproteins (LDL) than CD33(high) cells.	dilC18(3) dye	139-142	CD33 molecule	Homo sapiens	75-79
9721907-4	1998	Cells that were immunoreactive for vasoactive intestinal polypeptide (VIP) or for substance P (SP) accounted for about 75% and 11% of DiI-labelled cells, respectively.	dilC18(3) dye	134-137	VIP peptides	Cavia porcellus	35-68
9716729-6	1998	The most striking finding was the extensive intraepithelial terminal arborizations of DiI-labelled vagal afferents in intrapulmonary airways, apparently always co-appearing with calcitonin gene-related peptide (CGRP)-immunoreactive NEBs.	dilC18(3) dye	86-89	calcitonin-related polypeptide alpha	Rattus norvegicus	211-215
9698328-5	1998	The DiI injections also reveal that the trajectories of the cdk5(-/-) thalamocortical axons are oblique and cut across the entire cortical plate, instead of being oriented tangentially in the subcortical white matter.	dilC18(3) dye	4-7	cyclin-dependent kinase 5	Mus musculus	60-64
9721907-4	1998	Cells that were immunoreactive for vasoactive intestinal polypeptide (VIP) or for substance P (SP) accounted for about 75% and 11% of DiI-labelled cells, respectively.	dilC18(3) dye	134-137	VIP peptides	Cavia porcellus	70-73
9300764-4	1997	By using the fluorescent lipophilic dye DiI in formalin-fixed human hippocampal tissue, we demonstrated that this is a continuous fiber pathway between the deep hilar region and CA2.	dilC18(3) dye	40-43	carbonic anhydrase 2	Homo sapiens	178-181
9163603-0	1997	Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein.	dilC18(3) dye	52-55	Rh blood group D antigen	Homo sapiens	127-131
9226444-8	1997	When analogous ablations are performed at the 10-12 somite stage, however, a marked increase in the numbers of DiI/Hoxa-3-positive cells from r7 are observed within the third branchial arch.	dilC18(3) dye	111-114	homeobox A3	Homo sapiens	115-121
9186055-8	1997	The results showed that FGF-2 attracted DiI-labelled proximal cells to migrate toward the implanted beads and that the migration was more extensive than that observed in the absence of FGF-2.	dilC18(3) dye	40-43	fibroblast growth factor 2	Mus musculus	24-29
9163603-0	1997	Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein.	dilC18(3) dye	52-55	Rh blood group D antigen	Homo sapiens	191-195
2062483-5	1991	In the P16 mouse, this terminal zone is more restricted, suggesting, on the basis of the anterograde DiI labeling technique, that the visual corticopontine projection matures by P16.	dilC18(3) dye	101-104	cyclin dependent kinase inhibitor 2A	Mus musculus	7-10
7789265-2	1995	DiI staining of dorsal roots indicated that limb injections of anti-NT3 reduced the spinal projection of muscle spindle afferents.	dilC18(3) dye	0-3	neurotrophin 3	Homo sapiens	68-71
7538515-4	1995	When the injection site of DiI extended into the deep layers (IV-VI) of the same cortical column, the anterograde labeling of the perforant path was accompanied by retrograde labeling of the subicular neurons and the CA1 neurons.	dilC18(3) dye	27-30	carbonic anhydrase 1	Rattus norvegicus	217-220
9254074-7	1997	CHO cells transfected with the mouse SR-BI.2 cDNA expressed significant levels of SR-BI.2 protein and acquired the ability to take up fluorescent lipid (DiI) from DiI-HDL.	dilC18(3) dye	153-156	scavenger receptor class B, member 1	Mus musculus	37-42
7560282-4	1995	Vimentin expression in the lateral radial cells decreases markedly during the second week of postnatal life: application of DiI to the ventricular surface reveals that the pial attachment of the lateral radial cells is withdrawn and that the radial processes are gradually pulled back toward the ventricular zone.	dilC18(3) dye	124-127	vimentin	Homo sapiens	0-8
8325233-14	1993	Subsequent DiI labeling revealed that in these animals the majority of MGN axons had grown past auditory cortex instead of innervating it.	dilC18(3) dye	11-14	helt bHLH transcription factor	Homo sapiens	71-74
8381454-0	1993	Rapid fluorometric assay of LDL receptor activity by DiI-labeled LDL.	dilC18(3) dye	53-56	low density lipoprotein receptor	Homo sapiens	28-40
33774421-9	2021	DII scores ranged from -4.45 to 3.15 and were positively associated with C-reactive protein (adjusted beta : 1.28, 95% confidence interval [CI]: 0.16, 2.40; P trend = 0.023) when comparing DII tertile 3 (most pro-inflammatory) to tertile 1 (most anti-inflammatory).	dilC18(3) dye	0-3	C-reactive protein	Homo sapiens	73-91
2306486-6	1990	The LDL-R activities of the cells were examined by the uptake of a fluorescence probe, DiI-labeled LDL (DiI-LDL) and analyzed by flow cytometry.	dilC18(3) dye	87-90	low density lipoprotein receptor	Homo sapiens	4-9
34354158-12	2021	Based on the current study, it could be proposed that CETP polymorphism may be associated with CVD risk factors in T2DM patients with high following insulin indices, including DII and DIL.	dilC18(3) dye	176-179	cholesteryl ester transfer protein	Homo sapiens	54-58
34922121-12	2022	CRP mediated 3.6% of the association between DII and depression in the total population in the fully adjusted model, which was statistically significant (P-trend <.001) but not clinically significant.	dilC18(3) dye	45-48	C-reactive protein	Homo sapiens	0-3
34841880-9	2022	Both fetuin-A and hs-CRP had a significant full mediator role on the association between DII and HOMA-IR (respectively; beta = 0.371 (95 % CI: -0.029-0.770), beta = 0.424 (95 % CI: -0.007-0.856)).	dilC18(3) dye	89-92	alpha 2-HS glycoprotein	Homo sapiens	5-13
34841880-9	2022	Both fetuin-A and hs-CRP had a significant full mediator role on the association between DII and HOMA-IR (respectively; beta = 0.371 (95 % CI: -0.029-0.770), beta = 0.424 (95 % CI: -0.007-0.856)).	dilC18(3) dye	89-92	C-reactive protein	Homo sapiens	21-24
34426601-7	2021	The analyses by breast cancer subtype showed that the DII was associated with breast tumors that expressed either the estrogen (ER) or progesterone (PR) hormone receptors or the Human Epidermal Growth Factor Receptor-2 (HER2), but no association was seen for the triple negative breast tumor subtype.	dilC18(3) dye	54-57	epiregulin	Homo sapiens	128-130
34426601-7	2021	The analyses by breast cancer subtype showed that the DII was associated with breast tumors that expressed either the estrogen (ER) or progesterone (PR) hormone receptors or the Human Epidermal Growth Factor Receptor-2 (HER2), but no association was seen for the triple negative breast tumor subtype.	dilC18(3) dye	54-57	erb-b2 receptor tyrosine kinase 2	Homo sapiens	178-218
34426601-7	2021	The analyses by breast cancer subtype showed that the DII was associated with breast tumors that expressed either the estrogen (ER) or progesterone (PR) hormone receptors or the Human Epidermal Growth Factor Receptor-2 (HER2), but no association was seen for the triple negative breast tumor subtype.	dilC18(3) dye	54-57	erb-b2 receptor tyrosine kinase 2	Homo sapiens	220-224
34214879-9	2021	In the case-control segment, there was a significant difference in the DII between the groups (beta = 2.51; 95% CI: 1.73; 3.27) and a higher risk of developing the disease when the DII was >=4.41 (OR = 30.25; 95% CI: 6.70; 136.47).	dilC18(3) dye	71-74	ATPase H+ transporting V0 subunit a2	Homo sapiens	95-103
34420546-9	2022	Also, a positive association between E-DII and C-reactive protein (CRP) was observed (BE-DII = 1.37, 95% CI: 0.72, 2.02), such that with each unit increase in E-E-DII, the CRP levels were increased by 1.37 units.	dilC18(3) dye	89-92	C-reactive protein	Homo sapiens	47-65
34420546-9	2022	Also, a positive association between E-DII and C-reactive protein (CRP) was observed (BE-DII = 1.37, 95% CI: 0.72, 2.02), such that with each unit increase in E-E-DII, the CRP levels were increased by 1.37 units.	dilC18(3) dye	89-92	C-reactive protein	Homo sapiens	67-70
34420546-9	2022	Also, a positive association between E-DII and C-reactive protein (CRP) was observed (BE-DII = 1.37, 95% CI: 0.72, 2.02), such that with each unit increase in E-E-DII, the CRP levels were increased by 1.37 units.	dilC18(3) dye	89-92	C-reactive protein	Homo sapiens	172-175
34532029-9	2021	Stratified analyses by obesity status showed that overweight/obese participants in the highest DII tertile had a >75% increased BrCA risk (OR of 1.77 (95% CI, 1.01-3.12)) compared with participants in the lowest tertile, after adjusting for age.	dilC18(3) dye	95-98	BRCA1 DNA repair associated	Homo sapiens	128-132
34074369-24	2021	SEM indicated that maternal serum IL-6 may be a mediator in the association between DII and birth weight.	dilC18(3) dye	84-87	interleukin 6	Homo sapiens	34-38
34249998-5	2021	Weighted multivariable regression analysis and subgroup analysis were conducted to estimate the independent relationship between DII with PTH and the HP in the population with CKD/non-CKD.	dilC18(3) dye	129-132	parathyroid hormone	Homo sapiens	138-141
35286915-16	2022	NGR-modifified could increase the distribution of PM in vivo by DiI fluorescently (p < 0.01).	dilC18(3) dye	64-67	reticulon 4 receptor	Mus musculus	0-3
35560467-10	2022	CONCLUSION: We revealed PPAR-gamma Pro12Ala polymorphism was able to intensify the effect of DIL and DII on CVD risk factors; risk-allele carriers who consumed a diet with high DIL and DII score have more likely to be obese and have higher inflammatory markers.	dilC18(3) dye	101-104	peroxisome proliferator activated receptor gamma	Homo sapiens	24-34
35624319-11	2022	In contrast, women and men >= 45 years in the 25th quartile of changes in DII were associated with a gain of 0.067 g/cm2 and 0.062 g/cm2 of total hip BMD, while those in the 75th quartile of DII was associated with a reduction of - 0.108 g/cm2 and - 0.100 g/cm2, respectively.	dilC18(3) dye	74-77	hedgehog interacting protein	Homo sapiens	146-149
35551116-13	2022	On the seventh day, some DiI-labeled BMSCs expressed cTnT and alpha-actin.	dilC18(3) dye	25-28	troponin T2, cardiac type	Rattus norvegicus	53-57
35560467-10	2022	CONCLUSION: We revealed PPAR-gamma Pro12Ala polymorphism was able to intensify the effect of DIL and DII on CVD risk factors; risk-allele carriers who consumed a diet with high DIL and DII score have more likely to be obese and have higher inflammatory markers.	dilC18(3) dye	185-188	peroxisome proliferator activated receptor gamma	Homo sapiens	24-34
2542280-3	1989	At 37 degrees C, specific binding/uptake of fluorescent (dioctadecylin-docarbocyanine, DiI) HDL was observed by cells from healthy donors as well as by those from low density lipoprotein receptor-defective patients; mitogen activated T-blasts exhibited a markedly elevated DiI-HDL uptake compared to resting T-cells.	dilC18(3) dye	87-90	low density lipoprotein receptor	Homo sapiens	163-195
35493382-3	2022	Objective: This study examined the association between DII and sex hormones and SHBG in U.S. adult women.	dilC18(3) dye	55-58	sex hormone binding globulin	Homo sapiens	80-84
35493382-9	2022	After adjusting all covariates, a per-unit DII increase in DII tertile 3 was related to an 8.05 nmol/L SHBG decrease compared to DII tertile 1 (P = 0.0366).	dilC18(3) dye	43-46	sex hormone binding globulin	Homo sapiens	103-107
35493382-9	2022	After adjusting all covariates, a per-unit DII increase in DII tertile 3 was related to an 8.05 nmol/L SHBG decrease compared to DII tertile 1 (P = 0.0366).	dilC18(3) dye	59-62	sex hormone binding globulin	Homo sapiens	103-107
35493382-14	2022	However, more well-designed studies are still needed to validate and verify the causal relationship between DII and sex hormones and SHBG.	dilC18(3) dye	108-111	sex hormone binding globulin	Homo sapiens	133-137
35619959-3	2022	However, whether DII is related to S-Klotho plasma levels is still controversial.	dilC18(3) dye	17-20	klotho	Homo sapiens	35-43
35619959-4	2022	It was the goal of this study to examine the link between DII and S-Klotho in middle-aged and elderly people.	dilC18(3) dye	58-61	klotho	Homo sapiens	68-74
35619959-8	2022	Results: There was a negative correlation between DII and S-Klotho plasma levels.	dilC18(3) dye	50-53	klotho	Homo sapiens	60-66
35619959-12	2022	Conclusion: In middle-aged and older individuals, there is a negative connection between the pro-inflammatory dietary pattern as evaluated by DII and the plasma level of S-Klotho.	dilC18(3) dye	142-145	klotho	Homo sapiens	170-178
35082755-7	2021	In male adolescents, DII was always negatively associated with TT (P-trend = 0.09), FAI (P-trend = 0.03) and E2 (P-trend = 0.01), and monotonically positively associated with SHBG (P-trend = 0.02).In female adolescents, with the increase of DII, a significant positive correlation with SHBG was observed (beta 0.017, 95%CI: 0.009,0.053) (Table 3).	dilC18(3) dye	21-24	sex hormone binding globulin	Homo sapiens	175-179
35082755-7	2021	In male adolescents, DII was always negatively associated with TT (P-trend = 0.09), FAI (P-trend = 0.03) and E2 (P-trend = 0.01), and monotonically positively associated with SHBG (P-trend = 0.02).In female adolescents, with the increase of DII, a significant positive correlation with SHBG was observed (beta 0.017, 95%CI: 0.009,0.053) (Table 3).	dilC18(3) dye	21-24	sex hormone binding globulin	Homo sapiens	286-290
35258414-4	2022	Then, stability and targeting identification of exosome-delivered bone morphogenetic protein (BMP)-2 and PLA microcapsules were measured by transmission electron microscopy (TEM), DiO/DiI staining.	dilC18(3) dye	184-187	bone morphogenetic protein 2	Oryctolagus cuniculus	66-100
7470460-4	1980	By these criteria in dimyristoyl-PC, C10 diI and C12 diI preferentially partition into the fluid phase, C14 diI and C16 diI show no preferential partition, C18 diI preferentially partitions into the gel, and C20 diI and C22 diI preferentially partition into the fluid.	dilC18(3) dye	41-44	chromosome 12 open reading frame 57	Homo sapiens	37-40
3414331-2	1988	Our experience not only shows DII with frozen semen may be used successfully in AID but that it poses interesting hypotheses, to be verified in future, of its use in association with, or as an alternative to, GIFT and IVF/ET in cases of AID failure and as a first approach to an insemination technique in AID in general.	dilC18(3) dye	30-33	activation induced cytidine deaminase	Homo sapiens	80-83
3414331-2	1988	Our experience not only shows DII with frozen semen may be used successfully in AID but that it poses interesting hypotheses, to be verified in future, of its use in association with, or as an alternative to, GIFT and IVF/ET in cases of AID failure and as a first approach to an insemination technique in AID in general.	dilC18(3) dye	30-33	activation induced cytidine deaminase	Homo sapiens	237-240
33991227-6	2021	Associations between DII and CRP were assessed using multivariate linear regression adjusting for confounders (age education, physical activity, sex and smoking).	dilC18(3) dye	21-24	C-reactive protein	Homo sapiens	29-32
33898494-3	2021	Objective: This study aimed to examine the validity of the energy-adjusted DII (E-DIITM) using high-sensitivity C-reactive protein (hs-CRP) concentration in Japanese men and women.	dilC18(3) dye	75-78	C-reactive protein	Homo sapiens	112-130
33916342-12	2021	In the 2009-2010 subset, the association of mean CAL with serum CRP was mediated by DII (52.0%, p < 0.01).	dilC18(3) dye	84-87	C-reactive protein	Homo sapiens	64-67
33345682-9	2021	Some CM-DiI-labeled cells were found to be coexpressed with CK12, Pax6, and DeltaNp63alpha in the corneal epithelium after subconjunctival injection.	dilC18(3) dye	8-11	keratin 12	Rattus norvegicus	60-64
33834376-9	2022	RESULTS: A significant decrease was found for MS (p < 0.01) and MSR (p < 0.01) across tertiles of DII.	dilC18(3) dye	98-101	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	Homo sapiens	64-67
33454278-10	2021	Lean mass index (LMI) and uric acid levels mediated the relationship between DII and S-Klotho plasma levels.	dilC18(3) dye	77-80	klotho	Homo sapiens	87-93
33529249-5	2021	Immunofluorescence was applied to identify the co-expression of TRPV1 and EP3 receptor in vagal pulmonary C-neurons (retrogradely traced by DiI).	dilC18(3) dye	140-143	transient receptor potential cation channel subfamily V member 1	Cavia porcellus	64-69
33438528-5	2021	Through molecular docking, we performed binding energy analysis of cellocidin, bruceantin, EGCG, formononetin and sesquiterpene lactones with gH DII/DIII interface, crucial for gH functions.	dilC18(3) dye	145-148	gamma-glutamyl hydrolase	Homo sapiens	142-144
33438528-5	2021	Through molecular docking, we performed binding energy analysis of cellocidin, bruceantin, EGCG, formononetin and sesquiterpene lactones with gH DII/DIII interface, crucial for gH functions.	dilC18(3) dye	145-148	gamma-glutamyl hydrolase	Homo sapiens	177-179
33345682-9	2021	Some CM-DiI-labeled cells were found to be coexpressed with CK12, Pax6, and DeltaNp63alpha in the corneal epithelium after subconjunctival injection.	dilC18(3) dye	8-11	paired box 6	Rattus norvegicus	66-70
32633666-9	2021	The maximal expression of LDLr after TGF-beta2 stimulation was consistent with the peak uptake of DiI-LDL, which was obviously highest in the RGSFs, followed by the GSFs, and then the HSFs (all p<0.05).	dilC18(3) dye	98-101	low density lipoprotein receptor	Homo sapiens	26-30
32633666-9	2021	The maximal expression of LDLr after TGF-beta2 stimulation was consistent with the peak uptake of DiI-LDL, which was obviously highest in the RGSFs, followed by the GSFs, and then the HSFs (all p<0.05).	dilC18(3) dye	98-101	transforming growth factor beta 2	Homo sapiens	37-46
31197703-10	2020	Moreover, patients and healthy subjects in second quartile of DII had significantly higher aspartate aminotransferase (AST) and alanine aminotransferase (ALT) concentrations compared with subjects in the first quartile; also healthy subjects in third quartile had significantly higher triglyceride (TG) and total cholesterol (TC) concentrations compared with subjects in second quartile (P &lt; 0.05).	dilC18(3) dye	62-65	solute carrier family 17 member 5	Homo sapiens	91-117
33088461-10	2020	The association between DII and hs-CRP was not significant (P-value >0.05).	dilC18(3) dye	24-27	C-reactive protein	Homo sapiens	35-38
32656313-5	2020	Injecting DiI dye-labeled exosomes into the same mice shows adherence of exosomes to the CD206-positive M2 macrophages on ex vivo fluorescent microscopy imaging.	dilC18(3) dye	10-13	mannose receptor, C type 1	Mus musculus	89-94
33228788-5	2020	Furthermore, after adjusting for potentials cofounders, it was revealed that the subjects with lower DII had lower monocyte chemoattractant protein-1 (MCP-1) levels in serum (beta = - 18.81, 95% CI - 35.84, - 1.79, p = 0.03).	dilC18(3) dye	101-104	C-C motif chemokine ligand 2	Homo sapiens	115-149
33228788-5	2020	Furthermore, after adjusting for potentials cofounders, it was revealed that the subjects with lower DII had lower monocyte chemoattractant protein-1 (MCP-1) levels in serum (beta = - 18.81, 95% CI - 35.84, - 1.79, p = 0.03).	dilC18(3) dye	101-104	C-C motif chemokine ligand 2	Homo sapiens	151-156
33228788-6	2020	These findings suggest an inverse and significant relationship between DII and FFM and also DII is directly related to Fat mass and the level of MCP-1.	dilC18(3) dye	92-95	FAT atypical cadherin 1	Homo sapiens	119-122
33228788-6	2020	These findings suggest an inverse and significant relationship between DII and FFM and also DII is directly related to Fat mass and the level of MCP-1.	dilC18(3) dye	92-95	C-C motif chemokine ligand 2	Homo sapiens	145-150
32326840-3	2020	ABBREVIATIONS: DiI: 1,1"-dioctadecyl-3,3,3",3"-tetramethylindocarbocyanine perchlorate; DiO: 3,3"-dioctadecyloxacarbocyanine perchlorate; NE: nuclear envelope; RanBP2: Ran-binding protein 2/Nucleoporin 358.	dilC18(3) dye	15-18	RAN binding protein 2	Homo sapiens	160-166
32326840-3	2020	ABBREVIATIONS: DiI: 1,1"-dioctadecyl-3,3,3",3"-tetramethylindocarbocyanine perchlorate; DiO: 3,3"-dioctadecyloxacarbocyanine perchlorate; NE: nuclear envelope; RanBP2: Ran-binding protein 2/Nucleoporin 358.	dilC18(3) dye	15-18	RAN binding protein 2	Homo sapiens	168-189
32326840-3	2020	ABBREVIATIONS: DiI: 1,1"-dioctadecyl-3,3,3",3"-tetramethylindocarbocyanine perchlorate; DiO: 3,3"-dioctadecyloxacarbocyanine perchlorate; NE: nuclear envelope; RanBP2: Ran-binding protein 2/Nucleoporin 358.	dilC18(3) dye	15-18	RAN binding protein 2	Homo sapiens	190-205
31197703-10	2020	Moreover, patients and healthy subjects in second quartile of DII had significantly higher aspartate aminotransferase (AST) and alanine aminotransferase (ALT) concentrations compared with subjects in the first quartile; also healthy subjects in third quartile had significantly higher triglyceride (TG) and total cholesterol (TC) concentrations compared with subjects in second quartile (P &lt; 0.05).	dilC18(3) dye	62-65	solute carrier family 17 member 5	Homo sapiens	119-122
31197703-10	2020	Moreover, patients and healthy subjects in second quartile of DII had significantly higher aspartate aminotransferase (AST) and alanine aminotransferase (ALT) concentrations compared with subjects in the first quartile; also healthy subjects in third quartile had significantly higher triglyceride (TG) and total cholesterol (TC) concentrations compared with subjects in second quartile (P &lt; 0.05).	dilC18(3) dye	62-65	glutamic--pyruvic transaminase	Homo sapiens	128-152
31574409-14	2020	Furthermore, IL-6 concentration appeared to increase across DII quartiles calculated from FFQ in men.	dilC18(3) dye	60-63	interleukin 6	Homo sapiens	13-17
31768710-6	2020	One deletion mutant protein (De-L1), whose DI-DII linker was deleted, has been established simultaneously.	dilC18(3) dye	46-49	EGF like repeats and discoidin domains 3	Homo sapiens	29-34
30229691-9	2019	Values of interleukin-6 at the 90th percentile of its distribution were 8.31 pg/ml higher among those in DII quartile 4 compared with quartile 1 ( p = 0.02).	dilC18(3) dye	105-108	interleukin 6	Homo sapiens	10-23
30557347-11	2018	Nevertheless, null mutants in unc-63 and lev-8 (essential and non-essential subunits of L-AChRs, respectively) are as sensitive to DII as the wild-type strain.	dilC18(3) dye	131-134	Acetylcholine receptor subunit alpha-type unc-63	Caenorhabditis elegans	30-36
30291843-11	2019	Moreover, the results of Golgi-cox staining and DiI staining indicated that the damage on proximal spine density caused by morphine treatment was restored by intracerebral Sfrp2 injection.	dilC18(3) dye	48-51	secreted frizzled-related protein 2	Rattus norvegicus	172-177
30557347-11	2018	Nevertheless, null mutants in unc-63 and lev-8 (essential and non-essential subunits of L-AChRs, respectively) are as sensitive to DII as the wild-type strain.	dilC18(3) dye	131-134	Uncharacterized protein	Caenorhabditis elegans	41-46
30557347-12	2018	Therefore, our results suggest that DII effects on adult nematodes rely on a previously unidentified UNC-29-containing muscle AChR, different from the classical L-AChR.	dilC18(3) dye	36-39	Acetylcholine receptor subunit beta-type unc-29	Caenorhabditis elegans	101-107
30557347-13	2018	Interestingly, DII targets appear to be different between larvae and adults, as unc-29 null mutant larvae are sensitive to the drug.	dilC18(3) dye	15-18	Acetylcholine receptor subunit beta-type unc-29	Caenorhabditis elegans	80-86
30254012-9	2018	The uptake of DiI-labeled LDL(-) was higher than that of DiI-LDL(+) in THP1-CD14 but not in THP1 cells.	dilC18(3) dye	14-17	GLI family zinc finger 2	Homo sapiens	71-75
30254012-9	2018	The uptake of DiI-labeled LDL(-) was higher than that of DiI-LDL(+) in THP1-CD14 but not in THP1 cells.	dilC18(3) dye	14-17	CD14 molecule	Homo sapiens	76-80
30271437-7	2018	After electroporation, miR-132 exosomes were labelled with DiI and added to HUVECs.	dilC18(3) dye	59-62	microRNA 132	Mus musculus	23-30
29582235-12	2018	LSEC labelled with the fluorescent tag DiI prior to implantation formed capillaries in vivo and maintained LYVE-1 and CD32b markers to 2 weeks.	dilC18(3) dye	39-42	lymphatic vessel endothelial hyaluronan receptor 1	Mus musculus	107-113
28992651-3	2018	METHODS: MSC derived from human bone marrow were labeled by DiI and administered intravascularly or endobronchially to the lungs of donor pigs after a period of 3 hours warm and 3 hours cold ischemia.	dilC18(3) dye	60-63	musculin	Homo sapiens	9-12
29257000-9	2018	CM-DiI-labeled mesenchymal stromal cells were successfully recruited to the expanded prefabricated adipose tissue, a process partly inhibited by the CXCR4 antagonist AMD3100.	dilC18(3) dye	3-6	C-X-C motif chemokine receptor 4	Rattus norvegicus	149-154
29257000-10	2018	These recruited CM-DiI-labeled mesenchymal stromal cells were found among the CXCL12 columnar cells.	dilC18(3) dye	19-22	C-X-C motif chemokine ligand 12	Rattus norvegicus	78-84
29209231-6	2017	DiI-mediated cell-fate tracing studies demonstrated that the Frzb expressing cells contribute to the formation of the dental follicle, the future periodontium.	dilC18(3) dye	0-3	frizzled related protein	Homo sapiens	61-65
29054682-7	2017	Treatment with Lipo-l-OHP, Lipo-DXR, DiI-labeled empty PEGylated liposomes or empty PEGylated liposomes caused migration of CD68+ macrophages into the dermis of hind paws.	dilC18(3) dye	37-40	CD68 molecule	Homo sapiens	124-128
27878970-9	2017	In this same sample the DII also was associated with CRP &gt;=3 mg/L (ORDIIcontinuous = 1.10; 95% CI = 1.06, 1.16).	dilC18(3) dye	24-27	C-reactive protein	Homo sapiens	53-56
27592629-7	2017	The anti-adhesion effect was assessed using DiI-labeled THP-1 and RAW264.7.	dilC18(3) dye	44-47	GLI family zinc finger 2	Homo sapiens	56-61
28166841-10	2017	The overall associations between DII and ADII and long-term CRP were not statistically significant (P trend across tertiles=0 16 for DII and 0 10 for ADII).	dilC18(3) dye	42-45	C-reactive protein	Homo sapiens	60-63
27752892-6	2016	WIN evoked inward currents via TRPA1 activation in FAST DiI-labeled TG neurons.	dilC18(3) dye	56-59	transient receptor potential cation channel, subfamily A, member 1	Rattus norvegicus	31-36
27784857-3	2016	Del-1 also inhibited DiI-labeled oxLDL uptake by scavenger receptors irrespective of the receptor type (LOX-1, SR-AI, CD36, or SR-BI) expressed in COS-7 cells, and independent of cell type (human coronary artery endothelial cells (HCAECs) or THP-1-derived macrophages).	dilC18(3) dye	21-24	EGF-like repeats and discoidin I-like domains 3	Mus musculus	0-5
27752892-7	2016	WIN enhanced mechanosensitive currents via TRPA1 activation in FAST DiI-labeled TG neurons.	dilC18(3) dye	68-71	transient receptor potential cation channel, subfamily A, member 1	Rattus norvegicus	43-48
27273864-9	2016	Blocking the function of Nogo-A with Nogo-A antibody or NEP1-40 resulted in the shift of DiI labeled axons and growth cones from the superficial half to the whole depth of the OT.	dilC18(3) dye	89-92	reticulon 4	Mus musculus	25-31
27273864-9	2016	Blocking the function of Nogo-A with Nogo-A antibody or NEP1-40 resulted in the shift of DiI labeled axons and growth cones from the superficial half to the whole depth of the OT.	dilC18(3) dye	89-92	reticulon 4	Mus musculus	37-43
27194135-12	2016	In vivo, when cell tracking was used, the number of recruited CM-DiI-labeled EPCs was significantly higher in the injured zone in mice transfused with Ad5/beta2AR-EPCs compared with non-transfected EPCs.	dilC18(3) dye	65-68	adrenergic receptor, beta 2	Mus musculus	151-167
27097549-9	2016	DiI labeling results also showed an increased formation of mature spines after inhibition of Ras/Raf/ERK1/2 signaling.	dilC18(3) dye	0-3	zinc fingers and homeoboxes 2	Mus musculus	97-100
27097549-9	2016	DiI labeling results also showed an increased formation of mature spines after inhibition of Ras/Raf/ERK1/2 signaling.	dilC18(3) dye	0-3	mitogen-activated protein kinase 3	Mus musculus	101-107
27446819-9	2015	A borderline positive association was observed between DII and the risk of insulin resistance in fully adjusted model (odds ratio = 1.66, 95 % confidence interval = 0.96-2.86, P for trend = 0.06).	dilC18(3) dye	55-58	insulin	Homo sapiens	75-82
26863067-2	2016	Autologous CM-DiI-labeled ASC-seeded (experimental group) and unseeded (control group) BAMGs were incubated in the peritoneum of male rats for 2 weeks and then harvested for bladder augmentation.	dilC18(3) dye	14-17	PYD and CARD domain containing	Rattus norvegicus	26-29
26936137-6	2016	We examined associations of DII with maternal plasma C-reactive protein and white blood cell count in the second trimester and the following perinatal outcomes: gestational diabetes, preeclampsia, length of gestation, fetal growth, mode of delivery, and duration of breastfeeding.	dilC18(3) dye	28-31	C-reactive protein	Homo sapiens	53-71
26187182-6	2015	Several potential CaMKII phosphorylation sites have been discovered, including Ser571 in the Nav1.5 DI-DII linker, but the molecular mechanism underlying CaMKII-dependent regulation of INa,L in vivo remains unknown.	dilC18(3) dye	103-106	sodium channel, voltage-gated, type V, alpha	Mus musculus	93-99
26886889-9	2016	Moreover, bimatoprost evoked inward currents via TRPA1 activation in FAST DiI-labeled TG neurons as WIN.	dilC18(3) dye	74-77	transient receptor potential cation channel, subfamily A, member 1	Rattus norvegicus	49-54
26886889-10	2016	Bimatoprost also enhanced mechanosensitivity of FAST DiI-labeled TG neurons via TRPA1 activation.	dilC18(3) dye	53-56	transient receptor potential cation channel, subfamily A, member 1	Rattus norvegicus	80-85
26621720-9	2015	In vivo, Nck knockdown suppresses enlargement of the pellet of DiI-labeled preosteoblasts/osteoblasts placed in the calvarial defects.	dilC18(3) dye	63-66	non-catalytic region of tyrosine kinase adaptor protein 1	Mus musculus	9-12
26187182-6	2015	Several potential CaMKII phosphorylation sites have been discovered, including Ser571 in the Nav1.5 DI-DII linker, but the molecular mechanism underlying CaMKII-dependent regulation of INa,L in vivo remains unknown.	dilC18(3) dye	103-106	calcium/calmodulin-dependent protein kinase II, beta	Mus musculus	18-24
26478787-1	2015	A potent class of indolinyl-thiazole based inhibitors of cellular lipid uptake mediated by scavenger receptor, class B, type I (SR-BI) was identified via a high-throughput screen of the National Institutes of Health Molecular Libraries Small Molecule Repository (NIH MLSMR) in an assay measuring the uptake of the fluorescent lipid DiI from HDL particles.	dilC18(3) dye	332-335	scavenger receptor class B member 1	Homo sapiens	91-126
25904679-8	2015	Transient receptor potential ankyrin 1 (TRPA1), TRP vanilloid 4 (TRPV4), acid-sensing ion channel (ASIC) 2 and ASIC3 channel proteins were expressed in FAST DiI-labeled TG neurons.	dilC18(3) dye	157-160	transient receptor potential cation channel, subfamily A, member 1	Rattus norvegicus	0-38
25904679-8	2015	Transient receptor potential ankyrin 1 (TRPA1), TRP vanilloid 4 (TRPV4), acid-sensing ion channel (ASIC) 2 and ASIC3 channel proteins were expressed in FAST DiI-labeled TG neurons.	dilC18(3) dye	157-160	acid sensing ion channel subunit 2	Rattus norvegicus	73-106
25904679-8	2015	Transient receptor potential ankyrin 1 (TRPA1), TRP vanilloid 4 (TRPV4), acid-sensing ion channel (ASIC) 2 and ASIC3 channel proteins were expressed in FAST DiI-labeled TG neurons.	dilC18(3) dye	157-160	acid sensing ion channel subunit 3	Rattus norvegicus	111-116
26229403-5	2015	Immunofluorescence was employed to determine the co-expression of TLR4, NF-kappaB and CBS in DiI-labeled DRG neurons.	dilC18(3) dye	93-96	toll-like receptor 4	Rattus norvegicus	66-70
26229403-5	2015	Immunofluorescence was employed to determine the co-expression of TLR4, NF-kappaB and CBS in DiI-labeled DRG neurons.	dilC18(3) dye	93-96	cystathionine beta synthase	Rattus norvegicus	86-89
25639781-8	2015	Multivariable analyses showed significant positive associations between the DII and the inflammatory markers IL-6 (&gt;1 6 pg/ml) (OR 1 19, 95 % CI 1 04, 1 36) and homocysteine (&gt;15 mumol/l) (OR 1 56, 95 % CI 1 25, 1 94).	dilC18(3) dye	76-79	interleukin 6	Homo sapiens	109-113
26478787-1	2015	A potent class of indolinyl-thiazole based inhibitors of cellular lipid uptake mediated by scavenger receptor, class B, type I (SR-BI) was identified via a high-throughput screen of the National Institutes of Health Molecular Libraries Small Molecule Repository (NIH MLSMR) in an assay measuring the uptake of the fluorescent lipid DiI from HDL particles.	dilC18(3) dye	332-335	scavenger receptor class B member 1	Homo sapiens	128-133
25190219-3	2014	We hypothesized that the DII could predict levels of high-sensitivity C-reactive protein (CRP), which is an important inflammatory marker, as well as metabolic measures that include the metabolic syndrome and its components in European adults.	dilC18(3) dye	25-28	C-reactive protein	Homo sapiens	70-88
26617436-5	2015	Here, by performing TMJ injection of a retrograde labeling tracer DiI (a fluorescent dye), I showed that maresin 1 potently inhibits capsaicin-induced TRPV1 currents and neuronal activity via Galphai-coupled G-protein coupled receptors in DiI-labeled trigeminal nociceptive neurons.	dilC18(3) dye	66-69	transient receptor potential cation channel, subfamily V, member 1	Mus musculus	151-156
25190219-3	2014	We hypothesized that the DII could predict levels of high-sensitivity C-reactive protein (CRP), which is an important inflammatory marker, as well as metabolic measures that include the metabolic syndrome and its components in European adults.	dilC18(3) dye	25-28	C-reactive protein	Homo sapiens	90-93
24621388-11	2014	Per2(-/-) reduced the retention of transplanted EPCs in the myocardium, which was associated with significantly reduced DiI expression in the myocardium of MI mice.	dilC18(3) dye	120-123	period circadian clock 2	Mus musculus	0-4
25046320-4	2014	RESULTS: Officers in DII quartiles 2 to 4 were more likely to exceed a threshold of 3.0 mg/L for C-reactive protein (odds ratio [OR] = 1.88; 95% confidence interval [95% CI] = 1.02 to 3.45; OR = 2.17; 95% CI = 1.19 to 3.95; OR = 1.57; 95% CI = 0.85 to 2.88, respectively) compared with quartile 1.	dilC18(3) dye	21-24	C-reactive protein	Homo sapiens	97-115