scholarly article | Q13442814 |
P2093 | author name string | X Yu | |
J W Chu | |||
F J Sharom | |||
G DiDiodato | |||
P2860 | cites work | Phosphatidylcholine translocase: a physiological role for the mdr2 gene | Q24319732 |
Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease | Q24322810 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
ABC Transporters: From Microorganisms to Man | Q28181688 | ||
Biochemistry of multidrug resistance mediated by the multidrug transporter | Q29616476 | ||
Photoaffinity labeling of the multidrug-resistance-related P-glycoprotein with photoactive analogs of verapamil | Q33651186 | ||
Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs | Q34059522 | ||
ATP-dependent bacterial transporters and cystic fibrosis: analogy between channels and transporters | Q35323989 | ||
Interaction of multidrug-resistant Chinese hamster ovary cells with amphiphiles | Q35977177 | ||
Multidrug resistance and chemosensitization: therapeutic implications for cancer chemotherapy. | Q38014962 | ||
Characterization and functional reconstitution of the multidrug transporter | Q40456754 | ||
Allosteric regulation of [3H]vinblastine binding to P-glycoprotein of MCF-7 ADR cells by dexniguldipine | Q41334626 | ||
Tamoxifen aziridine, a novel affinity probe for P-glycoprotein in multidrug resistant cells | Q41454968 | ||
Characterization of the ATPase activity of purified Chinese hamster P-glycoprotein | Q41461421 | ||
Stoichiometric labeling of peptides by iodination on tyrosyl or histidyl residues | Q41561181 | ||
Characterization of the adenosine triphosphatase activity of Chinese hamster P-glycoprotein. | Q41572777 | ||
The effects of lipids and detergents on ATPase-active P-glycoprotein | Q41572851 | ||
Transport properties of P-glycoprotein in plasma membrane vesicles from multidrug-resistant Chinese hamster ovary cells | Q41607862 | ||
Peptide transport by the multidrug resistance pump | Q41634191 | ||
Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells. | Q41912189 | ||
Interaction of bioactive hydrophobic peptides with the human multidrug transporter | Q42068296 | ||
Interaction of prenylcysteine methyl esters with the multidrug resistance transporter | Q42068347 | ||
Characterization of the ATPase activity of P-glycoprotein from multidrug-resistant Chinese hamster ovary cells | Q42486411 | ||
Detection of P-glycoprotein in multidrug-resistant cell lines by monoclonal antibodies | Q42812351 | ||
ATPase activity of purified and reconstituted P-glycoprotein from Chinese hamster ovary cells. | Q54214354 | ||
Functional complementation of yeast ste6 by a mammalian multidrug resistance mdr gene | Q54272057 | ||
Strategies for the purification of P-glycoprotein from multidrug-resistant Chinese hamster ovary cells | Q54291890 | ||
Identification of the multidrug resistance-related membrane glycoprotein as an acceptor for calcium channel blockers. | Q54405185 | ||
ATPase activity of partially purified P-glycoprotein from multidrug-resistant Chinese hamster ovary cells | Q67520844 | ||
The intracellular content of dihydrofolate reductase: possibilities for control and implications for chemotherapy | Q70605968 | ||
Interaction of multidrug-resistant Chinese hamster ovary cells with the peptide ionophore gramicidin D | Q71611332 | ||
The effect of verapamil on the transport of peptides across the blood-brain barrier in rats: kinetic evidence for an apically polarized efflux mechanism | Q72151415 | ||
Interaction of the P-glycoprotein multidrug transporter with peptides and ionophores | Q72191051 | ||
Functional reconstitution of drug transport and ATPase activity in proteoliposomes containing partially purified P-glycoprotein | Q72656274 | ||
Covalent inhibitors of P-glycoprotein ATPase activity | Q72671369 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | hydrophobicity | Q41854968 |
P304 | page(s) | 421-428 | |
P577 | publication date | 1996-12-01 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | Synthetic hydrophobic peptides are substrates for P-glycoprotein and stimulate drug transport | |
P478 | volume | 320 ( Pt 2) |
Q38208521 | A reciprocating twin-channel model for ABC transporters. |
Q39795797 | Activators of P-glycoprotein: Structure-activity relationships and investigation of their mode of action |
Q36922557 | Approaches for enhancing oral bioavailability of peptides and proteins |
Q53405122 | Association of GSTT1 polymorphism with acute myeloid leukemia risk is dependent on smoking status. |
Q47326688 | Classification analysis of P-glycoprotein substrate specificity |
Q34563402 | Cyclodextrins in drug delivery: an updated review |
Q37058837 | Differential pharmacological regulation of drug efflux and pharmacoresistant schizophrenia |
Q37146134 | Dose-response features of neuroprotective agents: an integrative summary |
Q40703457 | Elevation of P-glycoprotein function by a catechin in green tea. |
Q39885064 | Evidence against a role of P-glycoprotein in the clearance of the Alzheimer's disease Aβ1-42 peptides |
Q40654202 | Evidence for two interacting ligand binding sites in human multidrug resistance protein 2 (ATP binding cassette C2). |
Q36895024 | Extraction of Hoechst 33342 from the cytoplasmic leaflet of the plasma membrane by P-glycoprotein. |
Q40792880 | Inhibition of P-glycoprotein transport function by grapefruit juice psoralen |
Q33784443 | Insights into the structure and substrate interactions of the P-glycoprotein multidrug transporter from spectroscopic studies |
Q41104432 | Interaction of combinations of drugs, chemosensitizers, and peptides with the P-glycoprotein multidrug transporter |
Q52571637 | Interaction of the P-glycoprotein multidrug transporter (MDR1) with high affinity peptide chemosensitizers in isolated membranes, reconstituted systems, and intact cells. |
Q41907216 | Linear and cyclic peptides as substrates and modulators of P-glycoprotein: peptide binding and effects on drug transport and accumulation |
Q43851006 | MDR1 P-glycoprotein transports endogenous opioid peptides |
Q28365282 | MDR1 causes resistance to the antitumour drug miltefosine |
Q41774328 | Modulation of drug-stimulated ATPase activity of human MDR1/P-glycoprotein by cholesterol |
Q37323494 | Molecular analysis of the multidrug transporter, P-glycoprotein |
Q34290848 | Multidrug transport by ATP binding cassette transporters: a proposed two-cylinder engine mechanism |
Q36476107 | New insights into the drug binding, transport and lipid flippase activities of the p-glycoprotein multidrug transporter. |
Q36459196 | Odyssey of a cancer nanoparticle: from injection site to site of action |
Q28372198 | Polarized transport of hydrophilic compounds across rat colonic mucosa from serosa to mucosa is temperature dependent |
Q33580765 | Polymorphisms in DNA repair genes and MDR1 and the risk for non-Hodgkin lymphoma |
Q36895030 | Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities |
Q50016751 | Proteasome inhibition and mechanism of resistance to a synthetic, library-based hexapeptide. |
Q28138732 | Retinal stimulates ATP hydrolysis by purified and reconstituted ABCR, the photoreceptor-specific ATP-binding cassette transporter responsible for Stargardt disease |
Q37709400 | Reversible dimers of the atypical antipsychotic quetiapine inhibit p-glycoprotein-mediated efflux in vitro with increased binding affinity and in situ at the blood-brain barrier. |
Q48313444 | Shedding light on drug transport: structure and function of the P-glycoprotein multidrug transporter (ABCB1). |
Q50758494 | Structure-activity relationship of P-glycoprotein substrates and modifiers. |
Q61872235 | The BH3 domain of BAD fused to the Antennapedia peptide induces apoptosis via its alpha helical structure and independent of Bcl-2 |
Q28776849 | The homodimeric ATP-binding cassette transporter LmrA mediates multidrug transport by an alternating two-site (two-cylinder engine) mechanism |
Q41818235 | The reconstituted P-glycoprotein multidrug transporter is a flippase for glucosylceramide and other simple glycosphingolipids |
Q74233348 | Two transport binding sites of P-glycoprotein are unequal yet contingent: initial rate kinetic analysis by ATP hydrolysis demonstrates intersite dependence |
Q31962046 | beta-Amyloid efflux mediated by p-glycoprotein |