Homo sapiens solute carrier family 10 (sodium/bile acid cotransporter - Nucleotide

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The loss of hepatitis B virus receptor NTCP/SLC10A1 in human liver cancer cells is due to epigenetic silencing. [J Virol. 2024]
The loss of hepatitis B virus receptor NTCP/SLC10A1 in human liver cancer cells is due to epigenetic silencing.
Ibrahim MK, Liu C-D, Zhang L, Yu X, Kim ES, Liu Z, Jo S, Liu Y, Huang Y, Gao S-J, et al. J Virol. 2024 Oct 22; 98(10):e0118724. Epub 2024 Sep 19.
SLC10A1 rs2296651 variant (S267F mutation) predicts biochemical traits, hepatitis B virus infection susceptibility and the risk of gallstone disease. [Mol Genet Genomics. 2024]
SLC10A1 rs2296651 variant (S267F mutation) predicts biochemical traits, hepatitis B virus infection susceptibility and the risk of gallstone disease.
Ko YL, Tuan WL, Teng MS, Su WC, Wang CC, Er LK, Wu S, Hsu LA. Mol Genet Genomics. 2024 Jun 13; 299(1):62. Epub 2024 Jun 13.
Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation. [Am J Hum Genet. 2024]
Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation.
Xu ZM, Gnouamozi GE, Rüeger S, Shea PR, Buti M, Chan HL, Marcellin P, Lawless D, Naret O, Zeller M, et al. Am J Hum Genet. 2024 Jun 6; 111(6):1018-1034. Epub 2024 May 14.

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Nucleotide