Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis.
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Daniel L. Koller | T. Skaar | G. Vance | D. Flockhart | K. Levy | V. Pratt | Kenneth D Levy | B. N. Beyer
[1] M. Relling,et al. FUNCTIONAL CHARACTERIZATION OF ABCC2 PROMOTER POLYMORPHISMS AND ALLELE SPECIFIC EXPRESSION , 2012, The Pharmacogenomics Journal.
[2] E. Pataraia,et al. Lack of association between ABCC2 gene variants and treatment response in epilepsy. , 2012, Pharmacogenomics.
[3] E. Poggiogalle,et al. Mutational analysis of ABCC2 gene in two siblings with neonatal‐onset Dubin Johnson syndrome , 2010, Clinical genetics.
[4] Barbara Zehnbauer,et al. Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project. , 2010, The Journal of molecular diagnostics : JMD.
[5] S. Sookoian,et al. Polymorphisms of MRP2 (ABCC2) are associated with susceptibility to nonalcoholic fatty liver disease. , 2009, The Journal of nutritional biochemistry.
[6] A. Caliebe,et al. Influence of genetic polymorphisms on intestinal expression and rifampicin-type induction of ABCC2 and on bioavailability of talinolol , 2008, Pharmacogenetics and genomics.
[7] Hassane Izzedine,et al. Association between ABCC2 gene haplotypes and tenofovir-induced proximal tubulopathy. , 2006, The Journal of infectious diseases.
[8] C. Aquilante,et al. Pharmacogenetic Characteristics of Indinavir, Zidovudine, and Lamivudine Therapy in HIV-Infected Adults: A Pilot Study , 2006, Journal of acquired immune deficiency syndromes.
[9] Michel Eichelbaum,et al. Interindividual variability of canalicular ATP‐binding‐cassette (ABC)–transporter expression in human liver , 2006, Hepatology.
[10] Ulrich Hoffmann,et al. Structure and function of the MRP2 (ABCC2) protein and its role in drug disposition , 2006, Expert opinion on drug metabolism & toxicology.
[11] M. Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[12] E. Hahn,et al. Readmissions and adverse drug reactions in internal medicine: the economic impact , 2004, Journal of internal medicine.
[13] C. J. Zheng,et al. Drug ADME‐associated protein database as a resource for facilitating pharmacogenomics research , 2004 .
[14] Y. Sugiyama,et al. Characterization of the Cellular Localization, Expression Level, and Function of SNP Variants of MRP2/ABCC2 , 2004, Pharmaceutical Research.
[15] S. Muallem,et al. Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome* , 2001, The Journal of Biological Chemistry.
[16] B. Pomeranz,et al. Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. , 1998, JAMA.
[17] K. Kohno,et al. Mutations in the Canalicular Multispecific Organic Anion Transporter (cMOAT) Gene, a Novel ABC Transporter, in Patients with Hyperbilirubinemia II/Dubin-Johnson Syndrome , 1998 .
[18] P. Zimniak. Dubin-Johnson and Rotor Syndromes: Molecular Basis and Pathogenesis , 1993, Seminars in liver disease.
[19] E. Lyon,et al. Characterization of 107 Genomic DNA Reference Materials for CYP 2 D 6 , CYP 2 C 19 , CYP 2 C 9 , VKORC 1 , and UGT 1 A 1 A GeT-RM and Association for Molecular Pathology Collaborative Project , 2010 .
[20] S. Sookoian,et al. Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancy. , 2008, Journal of hepatology.
[21] H. Kroemer,et al. Influence of polymorphisms of ABCB1 and ABCC2 on mRNA and protein expression in normal and cancerous kidney cortex , 2007, The Pharmacogenomics Journal.
[22] T. Uchiumi,et al. Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome. , 1999, American journal of human genetics.