Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population

Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population

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http://www.wikidata.org/entity/Q28215158
Q28183154
sameAs
Role of the plasma membrane transporter of organic cations OCT1 and its genetic variants in modern liver pharmacologyEstimating the contribution of genes to variation in renal drug clearance by active secretion using multiple data from clinical phase I studies.Association of genetic variation of sodium taurocholate cotransporting polypeptide with chronic hepatitis B virus infection.Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wiEthnicity-dependent polymorphism in Na+-taurocholate cotransporting polypeptide (SLC10A1) reveals a domain critical for bile acid substrate recognition.Pharmacogenetics of OATP (SLC21/SLCO), OAT and OCT (SLC22) and PEPT (SLC15) transporters in the intestine, liver and kidney.Global genetic analyses reveal strong inter-ethnic variability in the loss of activity of the organic cation transporter OCT1.Japanese single nucleotide polymorphism database for 267 possible drug-related genes.Clinical and molecular study of a pediatric patient with sodium taurocholate cotransporting polypeptide deficiency.Pharmacogenetics of drug transporters in the enterohepatic circulation.Di- and tripeptide transport in vertebrates: the contribution of teleost fish models.Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency.A dileucine motif is involved in plasma membrane expression and endocytosis of rat sodium taurocholate cotransporting polypeptide (Ntcp).Identification of DLG5 and SLC22A5 gene polymorphisms in Malaysian patients with Crohn's disease.Effect of S267F variant of NTCP on the patients with chronic hepatitis B.Genetic variations of NTCP are associated with susceptibility to HBV infection and related hepatocellular carcinoma.Association between polymorphisms in and genes and development of obesity in Chinese subjects
P2860

Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population

Item
http://www.wikidata.org/entity/Q28215158
description
2002 թուականին հրատարակուած գիտական յօդուած
@hyw
2002 թվականին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Januar 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 2002)
@en
vedecký článok (publikovaný 2002)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd in 2002)
@nl
наукова стаття, опублікована у 2002
@uk
مقالة علمية (نشرت عام 2002)
@ar
name
Catalog of 238 variations amon ...... Cs) in the Japanese population
@ast
Catalog of 238 variations amon ...... Cs) in the Japanese population
@en
Catalog of 238 variations amon ...... Cs) in the Japanese population
@nl
type
label
Catalog of 238 variations amon ...... Cs) in the Japanese population
@ast
Catalog of 238 variations amon ...... Cs) in the Japanese population
@en
Catalog of 238 variations amon ...... Cs) in the Japanese population
@nl
prefLabel
Catalog of 238 variations amon ...... Cs) in the Japanese population
@ast
Catalog of 238 variations amon ...... Cs) in the Japanese population
@en
Catalog of 238 variations amon ...... Cs) in the Japanese population
@nl
P1433
P1476
P2093
P2888
P304
P31
P3181
P356
P407
P433
P478
P577
P5875
P698
P3181
P356
P1433
P1476
Catalog of 238 variations amon ...... Cs) in the Japanese population
@en
P2093
P2888
P304
P31
P3181
P356
P407
P433
P478
P577
P5875
P698