Identification of an amino acid residue in multidrug resistance protein 1 critical for conferring resistance to anthracyclines (Q40816971)

24 September 2017

title

Identification of an amino acid residue in multidrug resistance protein 1 critical for conferring resistance to anthracyclines (English)

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24 September 2017

main subject

multiple drug resistance

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Zhang DW

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24 September 2017

Cole SP

series ordinal

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24 September 2017

Deeley RG

series ordinal

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24 September 2017

language of work or name

English

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publication date

23 January 2001

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Journal of Biological Chemistry

24 September 2017

published in

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24 September 2017

volume

276

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24 September 2017

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24 September 2017

page(s)

13231-13239

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Function, evolution and structure of multidrug resistance protein (MRP).

24 September 2017

cites work

1 reference

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Structural, mechanistic and clinical aspects of MRP1.

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Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

21 January 2018

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Structure of the multidrug resistance P-glycoprotein

21 January 2018

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Membrane topology of the multidrug resistance protein (MRP). A study of glycosylation-site mutants reveals an extracytosolic NH2 terminus.

21 January 2018

1 reference

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The multidrug resistance protein family.

21 January 2018

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Membrane topology distinguishes a subfamily of the ATP-binding cassette (ABC) transporters

21 January 2018

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Membrane topology and glycosylation of the human multidrug resistance-associated protein

21 January 2018

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The physiological function of drug-transporting P-glycoproteins

21 January 2018

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Cloning, transfer, and characterization of multidrug resistance protein.

21 January 2018

1 reference

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Multidrug resistance protein (MRP)-mediated transport of leukotriene C4 and chemotherapeutic agents in membrane vesicles. Demonstration of glutathione-dependent vincristine transport

21 January 2018

1 reference

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ATP-dependent 17 beta-estradiol 17-(beta-D-glucuronide) transport by multidrug resistance protein (MRP). Inhibition by cholestatic steroids

21 January 2018

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Export pumps for anionic conjugates encoded by MRP genes.

21 January 2018

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ATP-dependent transport of aflatoxin B1 and its glutathione conjugates by the product of the multidrug resistance protein (MRP) gene.

21 January 2018

1 reference

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ATP- and glutathione-dependent transport of chemotherapeutic drugs by the multidrug resistance protein MRP1.

21 January 2018

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How does P-glycoprotein recognize its substrates?

21 January 2018

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Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein

21 January 2018

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A single amino acid substitution strongly modulates the activity and substrate specificity of the mouse mdr1 and mdr3 drug efflux pumps

21 January 2018

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Epitope mapping of monoclonal antibodies specific for the 190-kDa multidrug resistance protein (MRP).

21 January 2018

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Monoclonal antibodies that inhibit the transport function of the 190-kDa multidrug resistance protein, MRP. Localization of their epitopes to the nucleotide-binding domains of the protein.

21 January 2018

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Glutathione stimulates sulfated estrogen transport by multidrug resistance protein 1.

21 January 2018

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Identification of Residues in the Drug-binding Domain of Human P-glycoprotein

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M010008200

Identification of Residues in the Drug-binding Site of Human P-glycoprotein Using a Thiol-reactive Substrate

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010008200

Drug-stimulated ATPase Activity of Human P-glycoprotein Requires Movement between Transmembrane Segments 6 and 12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010008200

Alteration of Substrate Specificity by Mutations at the His61Position in Predicted Transmembrane Domain 1 of Human MDR1/P-Glycoprotein†

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010008200

21 January 2018

Identifiers

DOI

10.1074/JBC.M010008200

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24 September 2017

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