Pages that link to "Q28248355"
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The following pages link to Characterization of the human patatin-like phospholipase family (Q28248355):
Displaying 50 items.
- PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans (Q24301980) (← links)
- The putative peroxisomal gene Pxt1 is exclusively expressed in the testis (Q24305103) (← links)
- Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions (Q24653003) (← links)
- Organophosphate-sensitive lipases modulate brain lysophospholipids, ether lipids and endocannabinoids (Q24658124) (← links)
- Dissecting adipose tissue lipolysis: molecular regulation and implications for metabolic disease (Q26824349) (← links)
- Insulin resistance in clinical and experimental alcoholic liver disease (Q26865988) (← links)
- Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention (Q26997377) (← links)
- Identification of an insulin-regulated lysophospholipase with homology to neuropathy target esterase (Q28594789) (← links)
- Vertebrate patatin-like phospholipase domain-containing protein 4 (PNPLA4) genes and proteins: a gene with a role in retinol metabolism (Q28714402) (← links)
- Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease (Q29614897) (← links)
- Adiponutrin functions as a nutritionally regulated lysophosphatidic acid acyltransferase (Q30032295) (← links)
- Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes (Q30397602) (← links)
- Leptin protects host cells from Entamoeba histolytica cytotoxicity by a STAT3-dependent mechanism (Q30424246) (← links)
- PNPLA3/adiponutrin functions in lipid droplet formation (Q32872131) (← links)
- The patatin-like lipase family in Gallus gallus. (Q33343272) (← links)
- Genetic variance in the adiponutrin gene family and childhood obesity. (Q33434477) (← links)
- Vimentin is a functional partner of hormone sensitive lipase and facilitates lipolysis (Q33530392) (← links)
- A sequence variation (I148M) in PNPLA3 associated with nonalcoholic fatty liver disease disrupts triglyceride hydrolysis (Q33673834) (← links)
- The Association between Pediatric NAFLD and Common Genetic Variants (Q33831722) (← links)
- A feed-forward loop amplifies nutritional regulation of PNPLA3 (Q33842841) (← links)
- Clinical differences between alcoholic liver disease and nonalcoholic fatty liver disease (Q33886948) (← links)
- De novo assembly of Aureococcus anophagefferens transcriptomes reveals diverse responses to the low nutrient and low light conditions present during blooms (Q33944526) (← links)
- Interaction between the triglyceride lipase ATGL and the Arf1 activator GBF1. (Q33971142) (← links)
- The association of PNPLA3 variants with liver enzymes in childhood obesity is driven by the interaction with abdominal fat. (Q34091146) (← links)
- Genetic ablation of calcium-independent phospholipase A2gamma leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotype (Q34304761) (← links)
- Global Inactivation of the Pla2g6 Gene in Mice Does Not Cause Dyslipidemia under Chow or High-fat Diet Conditions (Q34305395) (← links)
- Pnpla3/Adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome (Q34503398) (← links)
- Lipolysis – A highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores (Q34543395) (← links)
- Genetic covariance between gamma-glutamyl transpeptidase and fatty liver risk factors: role of beta2-adrenergic receptor genetic variation in twins (Q34572645) (← links)
- Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia (Q34577092) (← links)
- A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis (Q34626025) (← links)
- Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2 (Q34634929) (← links)
- Genetic determinants of hepatic steatosis in man (Q34646183) (← links)
- The rs738409 (I148M) variant of the PNPLA3 gene and cirrhosis: a meta-analysis (Q34757399) (← links)
- Identification of diverse lipid droplet targeting motifs in the PNPLA family of triglyceride lipases (Q34761048) (← links)
- Ubiquitin activates patatin-like phospholipases from multiple bacterial species (Q34853536) (← links)
- Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes (Q34861754) (← links)
- PNPLA3 I148M variant in nonalcoholic fatty liver disease: demographic and ethnic characteristics and the role of the variant in nonalcoholic fatty liver fibrosis (Q34985968) (← links)
- The metabolic serine hydrolases and their functions in mammalian physiology and disease (Q35333042) (← links)
- Expression and characterization of a PNPLA3 protein isoform (I148M) associated with nonalcoholic fatty liver disease (Q35423296) (← links)
- Characterization of a novel thermostable patatin-like protein from a Guaymas basin metagenomic library (Q35643235) (← links)
- PNPLA3 genetic variation in alcoholic steatosis and liver disease progression (Q35737438) (← links)
- FAT SIGNALS--lipases and lipolysis in lipid metabolism and signaling (Q35859576) (← links)
- Calcium-independent phospholipases A2 and their roles in biological processes and diseases. (Q35994344) (← links)
- DAG tales: the multiple faces of diacylglycerol--stereochemistry, metabolism, and signaling (Q36074560) (← links)
- Knockdown of Pnpla6 protein results in motor neuron defects in zebrafish (Q36683054) (← links)
- Biochemistry and pathophysiology of intravascular and intracellular lipolysis (Q36708030) (← links)
- Hypermethylation reduces the expression of PNPLA7 in hepatocellular carcinoma. (Q37002835) (← links)
- Mechanism-based inhibition of iPLA2β demonstrates a highly reactive cysteine residue (C651) that interacts with the active site: mass spectrometric elucidation of the mechanisms underlying inhibition (Q37027268) (← links)
- A common variant in the adiponutrin gene influences liver enzyme values (Q37137544) (← links)