The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome. - Abstract - Europe PMC
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
ABHD5 (C-9): sc-377270
ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid acyltransferase) | Gene Report | BioGPS
Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Transcription Factors ZEB1 and CREB Promote the Transcription of Bovine ABHD5 Gene | DNA and Cell Biology
ABHD5 - Wikipedia
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text
Lipase tug of war: PNPLA3 sequesters ABHD5 from ATGL | Nature Metabolism
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond - ScienceDirect
A New Patient of Chanarin Dorfman Syndrome in Egypt
Scholarly Article or Book Chapter | Clinical and genetic characterization of Chanarin-Dorfman Syndrome patients: first report of large deletions in the ABHD5 gene | ID: m900nw69t | Carolina Digital Repository
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. | Semantic Scholar
Fat breakdown: A function for CGI-58 (ABHD5) provides a new piece of the puzzle: Cell Metabolism
Loss of ABHD5 promotes the aggressiveness of prostate cancer cells | Scientific Reports
ABHD5 gene
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Human ABHD5 shRNA Plasmid | Abbexa Ltd
Frontiers | Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis
ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram
A) Sequence analysis of ABHD5 gene in the proband and her sister.... | Download Scientific Diagram
