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Are Nucleoside Triphosphates Precursors of Mammalian Ribonucleic Acid in vivo?
- Published in:
- Nature, 1959, v. 183, n. 4668, p. 1114, doi. 10.1038/1831114c0
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- Article
A Genome-Wide Scan for Childhood Obesity-Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2.
- Published in:
- Diabetes, 2004, v. 53, n. 3, p. 803, doi. 10.2337/diabetes.53.3.803
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- Article
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1798, doi. 10.1093/hmg/ddn070
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- Article
ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity.
- Published in:
- Diabetes, 2006, v. 55, n. 2, p. 545, doi. 10.2337/diabetes.55.02.06.db05-0971
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- Article
Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.
- Published in:
- 2005
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- journal article
Craniopharyngioma and hypothalamic obesity in children.
- Published in:
- Child's Nervous System, 2009, v. 25, n. 3, p. 347, doi. 10.1007/s00381-008-0754-x
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- Article
Rfx6 directs islet formation and insulin production in mice and humans.
- Published in:
- Nature, 2010, v. 463, n. 7282, p. 775, doi. 10.1038/nature08748
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- Article
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 320, doi. 10.1038/sj.ejhg.5201754
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- Article
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 89, doi. 10.1038/ng.277
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- Article
Variation in FTO contributes to childhood obesity and severe adult obesity.
- Published in:
- Nature Genetics, 2007, v. 39, n. 6, p. 724, doi. 10.1038/ng2048
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- Article
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
- Published in:
- Nature Genetics, 2005, v. 37, n. 8, p. 863, doi. 10.1038/ng1604
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- Publication type:
- Article
Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 4, p. 1, doi. 10.1371/journal.pgen.1000916
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- Article
Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population.
- Published in:
- Obesity (19307381), 2010, v. 18, n. 8, p. 1670, doi. 10.1038/oby.2009.468
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- Article
Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity.
- Published in:
- Obesity (19307381), 2009, v. 17, n. 4, p. 745, doi. 10.1038/oby.2008.589
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- Article
INS VNTR Is Not Associated With Childhood Obesity in 1,023 Families: A Family-based Study.
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- Obesity (19307381), 2008, v. 16, n. 6, p. 1471, doi. 10.1038/oby.2008.209
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- Article
Screening of MAMLD1 Mutations in 70 Children with 46,XY DSD: Identification and Functional Analysis of Two New Mutations.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032505
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- Article
Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity.
- Published in:
- 2007
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- Publication type:
- journal article
Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?
- Published in:
- 2005
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- Publication type:
- journal article
A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children.
- Published in:
- 2002
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- Publication type:
- journal article
The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism.
- Published in:
- Endocrine (1355008X), 2023, v. 80, n. 1, p. 47, doi. 10.1007/s12020-022-03284-5
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- Article
Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths.
- Published in:
- 2016
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- journal article
Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach.
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- 2017
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- journal article
Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
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- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 3037, doi. 10.1172/JCI68035
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- Article
Monocytes of Patients with Type 1 Diabetes Harbour Enterovirus RNA.
- Published in:
- European Journal of Clinical Investigation, 2015, v. 45, n. 9, p. 918, doi. 10.1111/eci.12485
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- Article
Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population.
- Published in:
- BMC Medical Genetics, 2005, v. 6, p. 1, doi. 10.1186/1471-2350-6-11
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- Article
Description of a novel RFLP diallelic polymorphism (-127 BsgI C/G) within the 5′ region of insulin gene.
- Published in:
- Human Mutation, 1998, v. 12, n. 6, p. 435, doi. 10.1002/(SICI)1098-1004(1998)12:6<435::AID-HUMU17>3.0.CO;2-1
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- Publication type:
- Article
Randomized, double‐blind, placebo‐controlled dose‐finding study of the dipeptidyl peptidase‐4 inhibitor linagliptin in pediatric patients with type 2 diabetes.
- Published in:
- Pediatric Diabetes, 2018, v. 19, n. 4, p. 640, doi. 10.1111/pedi.12616
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- Publication type:
- Article
New insights into the pathogenesis of beckwith-wiedemann and silver-russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects.
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- Human Mutation, 2011, v. 32, n. 10, p. 1171, doi. 10.1002/humu.21558
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- Publication type:
- Article
Increased Level of Interferon-α in Blood of Patients with Insulin-Dependent Diabetes Mellitus: Relationship with Coxsackievirus B Infection.
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- Journal of Infectious Diseases, 2000, v. 181, n. 6, p. 1929, doi. 10.1086/315516
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- Article
A part of the VP4 capsid protein exhibited by coxsackievirus B4 E2 is the target of antibodies contained in plasma from patients with type 1 diabetes.
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- Journal of Medical Virology, 2008, v. 80, n. 5, p. 866, doi. 10.1002/jmv.21171
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- Article