Pages that link to "Q47649386"
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The following pages link to Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation (Q47649386):
Displaying 17 items.
- Omic studies reveal the pathogenic lipid droplet proteins in non-alcoholic fatty liver disease (Q30244335) (← links)
- Mammalian triacylglycerol metabolism: synthesis, lipolysis, and signaling (Q35235426) (← links)
- The G0/G1 switch gene 2 (G0S2): regulating metabolism and beyond (Q36972427) (← links)
- Deficiency of liver Comparative Gene Identification-58 causes steatohepatitis and fibrosis in mice (Q37002642) (← links)
- Neutral lipid storage disease: genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or CGI-58/ABHD5. (Q37463574) (← links)
- Fat in the skin: Triacylglycerol metabolism in keratinocytes and its role in the development of neutral lipid storage disease. (Q37892924) (← links)
- A Rare Cause of Fatty Liver and Elevated Aminotransferase Levels: Chanarin-Dorfman Syndrome: A Case Report (Q37945245) (← links)
- CGI-58 facilitates the mobilization of cytoplasmic triglyceride for lipoprotein secretion in hepatoma cells (Q40100342) (← links)
- Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond (Q47925533) (← links)
- Effects of abhydrolase domain containing 5 gene (ABHD5) expression and variations on chicken fat metabolism (Q51294024) (← links)
- Chanarin-Dorfman syndrome with rare renal involvement (Q51320831) (← links)
- Living Donor Liver Transplantation for Dorfman-Chanarin Syndrome With 1 Year Follow-up: Case Report (Q51827828) (← links)
- Renal involvement as a rare complication of Dorfman-Chanarin syndrome: a case report (Q51953591) (← links)
- Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome (Q58010202) (← links)
- Dorfman-Chanarin syndrome (Q63335792) (← links)
- Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene (Q64275274) (← links)
- Steatohepatitis and liver cirrhosis in Chanarin-Dorfman syndrome with a new ABDH5 mutation (Q83243469) (← links)