PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 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 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 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 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 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 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 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 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 phosphoglycolate phosphatase Mus musculus 138-142 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 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 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 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 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 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