editorial | Q871232 |
scholarly article | Q13442814 |
P2093 | author name string | Elizabeth K Speliotes | |
P2860 | cites work | Brain-derived neurotrophic factor and obesity in the WAGR syndrome | Q24644359 |
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation | Q24646434 | ||
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity | Q24650037 | ||
Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene | Q28185036 | ||
Targeted disruption of the melanocortin-4 receptor results in obesity in mice | Q28302831 | ||
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity | Q28303894 | ||
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits | Q29614593 | ||
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease | Q29614897 | ||
Obesity as a medical problem | Q29616305 | ||
A QTL genome scan of the metabolic syndrome and its component traits | Q31049216 | ||
Ninety patients with nonalcoholic steatohepatitis: insulin resistance, familial tendency, and severity of disease | Q34427653 | ||
Genetic and environmental factors in relative body weight and human adiposity | Q34461728 | ||
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes | Q34861754 | ||
Obesity – is it a genetic disorder? | Q35555011 | ||
Heritability of nonalcoholic fatty liver disease | Q36095663 | ||
Brain-derived neurotrophic factor-deficient mice develop aggressiveness and hyperphagia in conjunction with brain serotonergic abnormalities | Q36784651 | ||
Identification of SH2-B as a key regulator of leptin sensitivity, energy balance, and body weight in mice | Q47372073 | ||
Heritability and genetic loci of fatty liver in familial combined hyperlipidemia. | Q51786382 | ||
Nonalcoholic steatohepatitis and cryptogenic cirrhosis within kindreds | Q73143340 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | metabolic dysfunction–associated steatotic liver disease | Q1546498 |
P304 | page(s) | 1492-1495 | |
P577 | publication date | 2009-03-25 | |
P1433 | published in | Gastroenterology | Q4039279 |
P1476 | title | Genetics of common obesity and nonalcoholic fatty liver disease | |
P478 | volume | 136 |
Q37807577 | Advances in Hepatobiliary Pathology: Update for 2010 |
Q37251522 | Brd2 inhibits adipogenesis via the ERK1/2 signaling pathway in 3T3-L1 adipocytes |
Q51353526 | Cholesteryl ester transfer protein gene polymorphisms increase the risk of fatty liver in females independent of adiposity. |
Q34572645 | Genetic covariance between gamma-glutamyl transpeptidase and fatty liver risk factors: role of beta2-adrenergic receptor genetic variation in twins |
Q34646183 | Genetic determinants of hepatic steatosis in man. |
Q37807576 | Hepatic Neoplasia and Metabolic Diseases in Children |
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Q37873715 | Nonalcoholic fatty liver disease and diabetes mellitus: pathogenesis and treatment |
Q34390296 | Pediatric nonalcoholic fatty liver disease: A clinical and laboratory challenge |