Frontiers | Recent Advances on the Role of ATGL in Cancer
ABHD5 (h): 293 Lysate: sc-112234
Loss of ABHD5 promotes the aggressiveness of prostate cancer cells | Scientific Reports
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
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
ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid acyltransferase) | Gene Report | BioGPS
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. | Semantic Scholar
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
Lipase tug of war: PNPLA3 sequesters ABHD5 from ATGL | Nature Metabolism
ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Human ABHD5 shRNA Plasmid | Abbexa Ltd
Gene: ABHD5 (ENSG00000011198) - Summary - Homo_sapiens - Ensembl genome browser 109
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
Frontiers | Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome | European Journal of Translational Myology
A) Sequence analysis of ABHD5 gene in the proband and her sister.... | Download Scientific Diagram
ABHD5 - Wikipedia
Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
What is ABHD5 Gene Chanarin-Dorfman syndrome NGS Genetic DNA Test ?
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
Molecular characterization of ABHD5 gene promoter in intramuscular preadipocytes of Qinchuan cattle: Roles of Evi1 and C/EBPα - ScienceDirect
