NSDHL

NSDHL

NSDHL, for NAD(P)H steroid dehydrogenase-like, encodes a sterol The dual localization of NSDHL within ER membranes and on the surface of lipid droplets.
OBJECTIVE: To analyze the dehydrogenase (NSDHL) gene in verruciform xanthoma (VX) to elucidate its potential role in the histogenesis.
Heiss et al. identified the human NSDHL gene, the homolog of the mouse gene mutant in the 'bare patches' (Bpa) and 'striated' (Str) phenotypes, at.
FIGHTING MATCH LEADS TO ILLIANA BLACKBIRDS VS. WOOSTER OILERS HOCKEY GAME WITH MULTIPLE EJECTIONS! Inferred from Sequence Orthology more info Inferred from Electronic Annotation more info Inferred from Sequence NSDHL more info Inferred from Electronic Annotation more info. These reference sequences are curated independently of the genome. Much of the NSDHL information on this page has been automatically compiled from Pubmed. HPRD Human Protein Atlas UniProt. Title: Large deletions in the NSDHL gene in two patients with CHILD syndrome. GenBankFASTASequence Viewer Graphics.

Official site: NSDHL

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NSDHL A systematic, large-scale NSDHL screen of X-chromosome coding exons in mental retardation. They include ketone bodies, fatty acids, triacylglycerols, phospholipids and sphi. Ada Hamosh, MD, MPH. The results demonstrated that Bpa and Str are allelic mutations and identified NSDHL first mammalian locus associated with an X-linked dominant, male-lethal phenotype. The following sections contain reference sequences that belong to a. Main page Contents Featured content Current events Random article Donate to Wikipedia Wikipedia store. The supernatants from three extractions were then combined and dried using a SpeedVac Savant, Fisher Scientific Inc.
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