Work

Physiological and pharmacological functions of Mrp2, Mrp3 and Mrp4 as determined from recent studies on gene-disrupted mice

Year: 2007

Type: review

Source: Cancer and Metastasis Reviews

DOI: 10.1007/s10555-007-9039-1

Authors: Gary D. Kruh, Martin G. Belinsky, James M. Gallo, Kun Lee

Institutions: Fox Chase Cancer Center, Temple University

Language: English

Topic: Drug Transport and Resistance Mechanisms

Subfield: Oncology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Cancer Institute

Awards: Functions of MRP2 and MRP3 in Drug Disposition, Cells Designed to Deliver Anticancer Drugs by Apoptosis, G4192608636, G464542450, G5305624522, G662236807, Interactions Between Cytotoxic and Antiangiogenic Drugs, Comprehensive Cancer Center Program at Fox Chase, G921727105

OpenAlex ID: W2024317644

FWCI: 1.111

Cites: 92

Cited by: 82

Related to: 10