NM_000353[Secondary Source ID] - Search Results

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2002	1
2006	2
2025	0

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A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis.

Chagnon P, Michaud J, Mitchell G, Mercier J, Marion JF, Drouin E, Rasquin-Weber A, Hudson TJ, Richter A. Chagnon P, et al. Am J Hum Genet. 2002 Dec;71(6):1443-9. doi: 10.1086/344580. Epub 2002 Nov 4. Am J Hum Genet. 2002. PMID: 12417987 Free PMC article.

Differentiation of human embryonic stem cells into hepatocytes in 2D and 3D culture systems in vitro.

Baharvand H, Hashemi SM, Kazemi Ashtiani S, Farrokhi A. Baharvand H, et al. Int J Dev Biol. 2006;50(7):645-52. doi: 10.1387/ijdb.052072hb. Int J Dev Biol. 2006. PMID: 16892178 Free article.

TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.

Maydan G, Andresen BS, Madsen PP, Zeigler M, Raas-Rothschild A, Zlotogorski A, Gutman A, Korman SH. Maydan G, et al. J Inherit Metab Dis. 2006 Oct;29(5):620-6. doi: 10.1007/s10545-006-0407-8. Epub 2006 Aug 17. J Inherit Metab Dis. 2006. PMID: 16917729

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