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PDF] A New Case of Chanarin-Dorfman Syndrome with a Novel Deletion in ABHD5  Gene | Semantic Scholar
PDF] A New Case of Chanarin-Dorfman Syndrome with a Novel Deletion in ABHD5 Gene | Semantic Scholar

ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody

ABHD5 - Wikipedia
ABHD5 - Wikipedia

ABHD5 cleaves HDAC4 to benefit the heart | Nature Metabolism
ABHD5 cleaves HDAC4 to benefit the heart | Nature Metabolism

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
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/CGI-58, the Chanarin-Dorfman Syndrome Protein, Mobilises Lipid Stores  for Hepatitis C Virus Production | PLOS Pathogens
ABHD5/CGI-58, the Chanarin-Dorfman Syndrome Protein, Mobilises Lipid Stores for Hepatitis C Virus Production | PLOS Pathogens

Fat breakdown: A function for CGI-58 (ABHD5) provides a new piece of the  puzzle: Cell Metabolism
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
Loss of ABHD5 promotes the aggressiveness of prostate cancer cells | Scientific Reports

A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual  dermatological findings | Lipids in Health and Disease | Full Text
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text

A New Patient of Chanarin Dorfman Syndrome in Egypt
A New Patient of Chanarin Dorfman Syndrome in Egypt

ABHD5 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT -  Santa Cruz Biotechnology
ABHD5 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid  acyltransferase) | Gene Report | BioGPS
ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid acyltransferase) | Gene Report | BioGPS

Structural and functional insights into ABHD5, a ligand-regulated lipase  co-activator | Scientific Reports
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports

ABHD5 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT -  Santa Cruz Biotechnology
ABHD5 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody

ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody

The lipid-droplet-associated protein ABHD5 protects the heart through  proteolysis of HDAC4 | Nature Metabolism
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism

Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene -  Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online  Library
Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library

Schematic model of ABHD5 domain structure. The blue area marks the... |  Download Scientific Diagram
Schematic model of ABHD5 domain structure. The blue area marks the... | Download Scientific Diagram

Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients:  Identification of novel mutations in the ABHD5 gene. | Semantic Scholar
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. | Semantic Scholar

Lipase tug of war: PNPLA3 sequesters ABHD5 from ATGL | Nature Metabolism
Lipase tug of war: PNPLA3 sequesters ABHD5 from ATGL | Nature Metabolism

Frontiers | Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous  Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation  Analysis
Frontiers | Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis

ABHD5 suppresses mTORC1 signaling and protein synthesis. A. Gene set... |  Download Scientific Diagram
ABHD5 suppresses mTORC1 signaling and protein synthesis. A. Gene set... | Download Scientific Diagram

PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with  unusual dermatological findings
PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings

Recurrent N209* ABHD5 mutation in two unreported families with Chanarin  Dorfman Syndrome | European Journal of Translational Myology
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
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions