A) Sequence analysis of ABHD5 gene in the proband and her sister.... | Download Scientific Diagram
Fat breakdown: A function for CGI-58 (ABHD5) provides a new piece of the puzzle: Cell Metabolism
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
ABHD5 - Wikipedia
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome | European Journal of Translational Myology
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
Lipase tug of war: PNPLA3 sequesters ABHD5 from ATGL | Nature Metabolism
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Schematic model of ABHD5 domain structure. The blue area marks the... | Download Scientific Diagram
ABHD5 - Wikiwand
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Endogenous and Synthetic ABHD5 Ligands Regulate ABHD5-Perilipin Interactions and Lipolysis in Fat and Muscle
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. | Semantic Scholar
Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond - ScienceDirect
Genes | Free Full-Text | Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
ABHD5 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
