Characterization of the human patatin-like phospholipase family - Wikidata - awgldk - TriplyDB

Characterization of the human patatin-like phospholipase family

Characterization of the human patatin-like phospholipase family

http://www.wikidata.org/entity/Q28248355

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PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions Organophosphate-sensitive lipases modulate brain lysophospholipids, ether lipids and endocannabinoids Insulin resistance in clinical and experimental alcoholic liver disease Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention Identification of an insulin-regulated lysophospholipase with homology to neuropathy target esterase Vertebrate patatin-like phospholipase domain-containing protein 4 (PNPLA4) genes and proteins: a gene with a role in retinol metabolism Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease Adiponutrin functions as a nutritionally regulated lysophosphatidic acid acyltransferase.Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes.Leptin protects host cells from Entamoeba histolytica cytotoxicity by a STAT3-dependent mechanism PNPLA3/adiponutrin functions in lipid droplet formation.The patatin-like lipase family in Gallus gallus.Genetic variance in the adiponutrin gene family and childhood obesity.Vimentin is a functional partner of hormone sensitive lipase and facilitates lipolysis.A sequence variation (I148M) in PNPLA3 associated with nonalcoholic fatty liver disease disrupts triglyceride hydrolysis.The Association between Pediatric NAFLD and Common Genetic Variants.A feed-forward loop amplifies nutritional regulation of PNPLA3 Clinical differences between alcoholic liver disease and nonalcoholic fatty liver disease.De novo assembly of Aureococcus anophagefferens transcriptomes reveals diverse responses to the low nutrient and low light conditions present during blooms.Interaction between the triglyceride lipase ATGL and the Arf1 activator GBF1.The association of PNPLA3 variants with liver enzymes in childhood obesity is driven by the interaction with abdominal fat.Genetic ablation of calcium-independent phospholipase A2gamma leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotype Global Inactivation of the Pla2g6 Gene in Mice Does Not Cause Dyslipidemia under Chow or High-fat Diet Conditions.Pnpla3/Adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome.Lipolysis - a highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores.Genetic covariance between gamma-glutamyl transpeptidase and fatty liver risk factors: role of beta2-adrenergic receptor genetic variation in twins.Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia.A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis.Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2 Genetic determinants of hepatic steatosis in man.The rs738409 (I148M) variant of the PNPLA3 gene and cirrhosis: a meta-analysis Identification of diverse lipid droplet targeting motifs in the PNPLA family of triglyceride lipases Ubiquitin activates patatin-like phospholipases from multiple bacterial species Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.PNPLA3 I148M variant in nonalcoholic fatty liver disease: demographic and ethnic characteristics and the role of the variant in nonalcoholic fatty liver fibrosis The metabolic serine hydrolases and their functions in mammalian physiology and disease.Expression and characterization of a PNPLA3 protein isoform (I148M) associated with nonalcoholic fatty liver disease.Characterization of a novel thermostable patatin-like protein from a Guaymas basin metagenomic library.PNPLA3 genetic variation in alcoholic steatosis and liver disease progression.

P2860

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P2860

Characterization of the human patatin-like phospholipase family

http://www.wikidata.org/entity/Q28248355

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2006 nî lūn-bûn

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2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Characterization of the human patatin-like phospholipase family

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Characterization of the human patatin-like phospholipase family

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Characterization of the human patatin-like phospholipase family

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type

label

Characterization of the human patatin-like phospholipase family

@ast

Characterization of the human patatin-like phospholipase family

@en

Characterization of the human patatin-like phospholipase family

@nl

prefLabel

Characterization of the human patatin-like phospholipase family

@ast

Characterization of the human patatin-like phospholipase family

@en

Characterization of the human patatin-like phospholipase family

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JLR.M600185-JLR200

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Journal of Lipid Research

P1476

Characterization of the human patatin-like phospholipase family

@en

P2093

Daniel J Crowther

http://www.w3.org/2001/XMLSchema#string

Natalie M Lambie

http://www.w3.org/2001/XMLSchema#string

Paul A Wilson

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Scott D Gardner

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Stephane A Commans

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P2860

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Identification, cloning, expression, and purification of three novel human calcium-independent phospholipase A2 family members possessing triacylglycerol lipase and acylglycerol transacylase activities

SMART, a simple modular architecture research tool: identification of signaling domains

The Pfam protein families database

I-PLA(2) activation during apoptosis promotes the exposure of membrane lysophosphatidylcholine leading to binding by natural immunoglobulin M antibodies and complement activation

The EMBL Nucleotide Sequence Database

The crystal structure, mutagenesis, and activity studies reveal that patatin is a lipid acyl hydrolase with a Ser-Asp catalytic dyad

Improved prediction of signal peptides: SignalP 3.0

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

Obese yeast: triglyceride lipolysis is functionally conserved from mammals to yeast.

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3745297

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10.1194/JLR.M600185-JLR200

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9

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16799181

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