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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 - Wikipedia
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
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
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 New Patient of Chanarin Dorfman Syndrome in Egypt
ABHD5 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
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 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
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
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
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
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
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions