Associated Papers
Homozygosity for a variant in SLC10A2 and infancy onset severe fat-soluble vitamin deficiency due to bile acid malabsorption.
Rungoe C et al.
Jpgn Reports, 2025
Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.
Liu Y et al.
Molecular Cancer, 2023
SLC10A2 deficiency-induced congenital chronic bile acid diarrhea and stunting.
Qie D et al.
Molecular Genetics & Genomic Medicine, 2021
The prevalence, genetic complexity and population-specific founder effects of human autosomal recessive disorders.
Xiao Q et al.
Npj Genomic Medicine, 2021
Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.
Aboul-Soud MAM et al.
Saudi Journal of Biological Sciences, 2021
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors.
Akhavanfard S et al.
Nature Communications, 2020
Targeted next generation sequencing as a tool for precision medicine.
Gulilat M et al.
Bmc Medical Genomics, 2019
Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases.
Unknown Author
Genome Biology, 2015
Importance of uncharged polar residues and proline in the proximal two-thirds (Pro107-Ser128) of the highly conserved region of mouse ileal Na+-dependent bile acid transporter, Slc10a2, in transport activity and cellular expression.
Saeki T et al.
Bmc Physiology, 2013
Genetic polymorphisms in Na+-taurocholate co-transporting polypeptide (NTCP) and ileal apical sodium-dependent bile acid transporter (ASBT) and ethnic comparisons of functional variants of NTCP among Asian populations.
Pan W et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems, 2011
Role of the intestinal bile acid transporters in bile acid and drug disposition.
Dawson PA
Handbook of Experimental Pharmacology, 2011
A variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.
Renner O et al.
Plos One, 2009
Mutational analysis of uncharged polar residues and proline in the distal one-third (Thr130-Pro142) of the highly conserved region of mouse Slc10a2.
Saeki T et al.
Bioscience, Biotechnology, and Biochemistry, 2009
Mutation screening of apical sodium-dependent bile acid transporter (SLC10A2): novel haplotype block including six newly identified variants linked to reduced expression.
Renner O et al.
Human Genetics, 2009
An association between genetic polymorphisms in the ileal sodium-dependent bile acid transporter gene and the risk of colorectal adenomas.
Wang W et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2001
Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2).
Oelkers P et al.
The Journal of Clinical Investigation, 1997
The solute carrier family 10 (SLC10): beyond bile acid transport.
Claro da Silva T et al.
Molecular Aspects of Medicine, 0