Results 151 to 160 of about 3,060 (172)
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Neurology
Sorbitol dehydrogenase (SORD) deficiency, due to biallelic loss-of-function variants in the SORD gene, is a recently recognized cause of autosomal recessive hereditary neuropathy. Specific diagnosis is difficult on clinical grounds alone, and molecular genetic testing of SORD is complicated by the presence of a pseudogene.
Jordan Elliott Bontrager +29 more
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Sorbitol dehydrogenase (SORD) deficiency, due to biallelic loss-of-function variants in the SORD gene, is a recently recognized cause of autosomal recessive hereditary neuropathy. Specific diagnosis is difficult on clinical grounds alone, and molecular genetic testing of SORD is complicated by the presence of a pseudogene.
Jordan Elliott Bontrager +29 more
openaire +2 more sources
Isolation and identification of xylitol dehydrogenase gene from Trichoderma reesei.
Chinese journal of biotechnology, 1999A cDNA sub-library from the fungus Trichoderma reesei grown on xylan was constructed in S.cerevisiae recombinant strain H475 harboring a xylose reductase (XR) gene from Pichia stipitis. The xylitol dehydrogenase (XDH) gene was screened from sub-library on a SC selective medium in which xylose was used as a sole carbon source.
T, Wang +4 more
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Xylitol dehydrogenase from Pachysolen tannophilus
FEMS Microbiology Letters, 1984openaire +1 more source
Evidence that the geneYLR070cofSaccharomyces cerevisiaeencodes a xylitol dehydrogenase
FEBS Letters, 1999Mervi Toivari +2 more
exaly
[Histochemical studies on the demonstration of xylitol dehydrogenases].
Histochemie. Histochemistry. Histochimie, 1966D, Stiller, J, Gorski
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