Isoleucine

hydroxysteroid 17-beta dehydrogenase 10 ; Homo sapiens







7 Article(s)
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1 31654490 HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French-Canadian patients from Quebec. 2019 Dec 1
2 28875337 Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene. 2017 Dec 2
3 23834306 Transcription start sites and epigenetic analysis of the HSD17B10 proximal promoter. 2013 Jul 8 1
4 19706438 Mental retardation linked to mutations in the HSD17B10 gene interfering with neurosteroid and isoleucine metabolism. 2009 Sep 1 1
5 17618155 HSD17B10: a gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids. 2007 Sep-Oct 1
6 15860413 Multiple functions of type 10 17beta-hydroxysteroid dehydrogenase. 2005 May-Jun 1
7 11102558 Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism. 2000 Dec 1