The genetics of NAFLD. (Q38141714)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

22 February 2020

title

The genetics of NAFLD (English)

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22 February 2020

1

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22 February 2020

author name string

Christopher P Day

series ordinal

2

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22 February 2020

language of work or name

English

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publication date

24 September 2013

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

Nature Reviews Gastroenterology & Hepatology

22 February 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

22 February 2020

volume

10

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

22 February 2020

issue

11

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

22 February 2020

page(s)

645-655

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

AGA technical review on nonalcoholic fatty liver disease

22 February 2020

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

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HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin

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A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease

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Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

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Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease

21 January 2018

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Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

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A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians

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Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

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IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy

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21 January 2018

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The utility of radiological imaging in nonalcoholic fatty liver disease.

21 January 2018

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21 January 2018

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21 January 2018

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

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Homozygosity for the patatin-like phospholipase-3/adiponutrin I148M polymorphism influences liver fibrosis in patients with nonalcoholic fatty liver disease.

21 January 2018

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A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans

21 January 2018

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A nonsynonymous gene variant in the adiponutrin gene is associated with nonalcoholic fatty liver disease severity.

21 January 2018

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Dissociation between fatty liver and insulin resistance in humans carrying a variant of the patatin-like phospholipase 3 gene

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The association of genetic variability in patatin-like phospholipase domain-containing protein 3 (PNPLA3) with histological severity of nonalcoholic fatty liver disease

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The 148M allele of the PNPLA3 gene is associated with indices of liver damage early in life.

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A common variant in the patatin-like phospholipase 3 gene (PNPLA3) is associated with fatty liver disease in obese children and adolescents

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A common variant in the adiponutrin gene influences liver enzyme values

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A sequence variation (I148M) in PNPLA3 associated with nonalcoholic fatty liver disease disrupts triglyceride hydrolysis

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Morbid obesity exposes the association between PNPLA3 I148M (rs738409) and indices of hepatic injury in individuals of European descent

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PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease

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Expression and characterization of a PNPLA3 protein isoform (I148M) associated with nonalcoholic fatty liver disease

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Adiponutrin functions as a nutritionally regulated lysophosphatidic acid acyltransferase

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A feed-forward loop amplifies nutritional regulation of PNPLA3

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Characterization of the human patatin-like phospholipase family

21 January 2018

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The expression level of non-alcoholic fatty liver disease-related gene PNPLA3 in hepatocytes is highly influenced by hepatic lipid status

21 January 2018

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Expression, regulation, and triglyceride hydrolase activity of Adiponutrin family members.

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Patatin-like phospholipase domain-containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease

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Pnpla3/Adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome

21 January 2018

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Chronic overexpression of PNPLA3I148M in mouse liver causes hepatic steatosis

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Mouse models in non-alcoholic fatty liver disease and steatohepatitis research.

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Inhibiting triglyceride synthesis improves hepatic steatosis but exacerbates liver damage and fibrosis in obese mice with nonalcoholic steatohepatitis.

21 January 2018

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Apoptosis and necrosis in the liver: a tale of two deaths?

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Impact of pan-caspase inhibition in animal models of established steatosis and non-alcoholic steatohepatitis.

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Apoptosis in experimental NASH is associated with p53 activation and TRAIL receptor expression.

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Models of liver fibrosis: exploring the dynamic nature of inflammation and repair in a solid organ

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Characterization of European ancestry nonalcoholic fatty liver disease-associated variants in individuals of African and Hispanic descent

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Polymorphisms of microsomal triglyceride transfer protein gene and manganese superoxide dismutase gene in non-alcoholic steatohepatitis

21 January 2018

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The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population

21 January 2018

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Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD)

21 January 2018

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Association between angiotensin II type 1 receptor polymorphisms and the occurrence of nonalcoholic fatty liver disease

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Susceptibility and gene interaction study of the angiotensin II type 1 receptor (AGTR1) gene polymorphisms with non-alcoholic fatty liver disease in a multi-ethnic population

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The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver

21 January 2018

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Variant in the glucokinase regulatory protein (GCKR) gene is associated with fatty liver in obese children and adolescents

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Zf9, a Kruppel-like transcription factor up-regulated in vivo during early hepatic fibrosis

21 January 2018

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Oxidative stress, KLF6 and transforming growth factor-beta up-regulation differentiate non-alcoholic steatohepatitis progressing to fibrosis from uncomplicated steatosis in rats

21 January 2018

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Glucokinase links Krüppel-like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease

21 January 2018

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Angiotensin II activates I kappaB kinase phosphorylation of RelA at Ser 536 to promote myofibroblast survival and liver fibrosis

21 January 2018

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Pro-fibrotic polymorphisms predictive of advanced liver fibrosis in the severely obese.

21 January 2018

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Therapeutic efficacy of an angiotensin II receptor antagonist in patients with nonalcoholic steatohepatitis

21 January 2018

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Apolipoprotein B metabolism in subjects with deficiency of apolipoproteins CIII and AI. Evidence that apolipoprotein CIII inhibits catabolism of triglyceride-rich lipoproteins by lipoprotein lipase in vivo

21 January 2018

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Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease

21 January 2018

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Dissociation betweenAPOC3variants, hepatic triglyceride content and insulin resistance

21 January 2018

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Lack of effect of apolipoprotein C3 polymorphisms on indices of liver steatosis, lipid profile and insulin resistance in obese Southern Europeans

21 January 2018

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Multigenerational epigenetic adaptation of the hepatic wound-healing response

21 January 2018

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Heritability of nonalcoholic fatty liver disease

21 January 2018

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Genetic factors contribute to variation in serum alanine aminotransferase activity independent of obesity and alcohol: a study in monozygotic and dizygotic twins

21 January 2018

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Ethnic differences in the prevalence of cryptogenic cirrhosis

21 January 2018

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Ethnic differences in hepatic steatosis: an insulin resistance paradox?

21 January 2018

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Ethnicity and nonalcoholic fatty liver disease

21 January 2018

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A Germline DNA Polymorphism Enhances Alternative Splicing of theKLF6Tumor Suppressor Gene and Is Associated with Increased Prostate Cancer Risk

21 January 2018

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Unraveling the genetics of fatty liver in obese children: Additive effect of P446L GCKR and I148M PNPLA3 polymorphisms

21 January 2018

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How big a problem is non-alcoholic fatty liver disease?

21 January 2018

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A position statement on NAFLD/NASH based on the EASL 2009 special conference

31 March 2020

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Liver biopsy findings from healthy potential living liver donors: Reasons for disqualification, silent diseases and correlation with liver injury tests

31 March 2020

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One hundred consecutive hepatic biopsies in the workup of living donors for right lobe liver transplantation

31 March 2020

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Genomewide association studies--illuminating biologic pathways

31 March 2020

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Genome-wide association studies: past, present and future

31 March 2020

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Validity of real time ultrasound in the diagnosis of hepatic steatosis: a prospective study

31 March 2020

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Genetic variation in the PNPLA3 gene and hepatocellular carcinoma in USA: risk and prognosis prediction

31 March 2020

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Patatin-like phospholipase domain-containing 3 (PNPLA3) I148M (rs738409) affects hepatic VLDL secretion in humans and in vitro

31 March 2020

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From NAFLD to NASH to cirrhosis-new insights into disease mechanisms.

31 March 2020

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Association of glucokinase regulatory gene polymorphisms with risk and severity of non-alcoholic fatty liver disease: an interaction study with adiponutrin gene

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The SOD2 C47T polymorphism influences NAFLD fibrosis severity: Evidence from case-control and intra-familial allele association studies

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The APOC3 T-455C and C-482T promoter region polymorphisms are not associated with the severity of liver damage independently of PNPLA3 I148M genotype in patients with nonalcoholic fatty liver

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRGASTRO.2013.182

A gene variant of PNPLA3, but not of APOC3, is associated with histological parameters of NAFLD in an obese population.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRGASTRO.2013.182

Nonalcoholic steatohepatitis and cryptogenic cirrhosis within kindreds

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRGASTRO.2013.182

Ninety patients with nonalcoholic steatohepatitis: insulin resistance, familial tendency, and severity of disease

31 March 2020

1 reference

12 December 2020

The TDT and other family-based tests for linkage disequilibrium and association

1 reference

12 December 2020

The importance of fatty liver disease in clinical practice

1 reference

12 December 2020

PNPLA3 is regulated by glucose in human hepatocytes, and its I148M mutant slows down triglyceride hydrolysis

1 reference

12 December 2020

10.1038/NRGASTRO.2013.182

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24061205 AND SRC:MED&resulttype=core&format=json

22 February 2020

1 reference