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1.
Variation in FTO contributes to childhood obesity and severe adult obesity.
Nat Genet;
39(6): 724-6, 2007 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-17496892
2.
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Brain;
137(Pt 10): 2657-63, 2014 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25070513
3.
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.
PLoS Genet;
6(4): e1000916, 2010 Apr 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-20421936
4.
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population.
Hum Mol Genet;
17(12): 1798-802, 2008 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18325908
5.
Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations.
Hum Mol Genet;
17(13): 1916-21, 2008 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18375449
6.
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.
Hum Mol Genet;
17(12): 1803-13, 2008 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18325910
7.
A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2.
Diabetes;
53(3): 803-11, 2004 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-14988267
8.
Common variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 show evidence of association with adult obesity in the Greek population.
Obesity (Silver Spring);
20(2): 389-95, 2012 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21720444
9.
Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.
PLoS One;
7(6): e37423, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22701567
10.
Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.
PLoS One;
5(10): e13630, 2010 Oct 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-21049026
11.
A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity.
Obesity (Silver Spring);
17(8): 1549-53, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19300429
12.
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
Nat Genet;
41(1): 89-94, 2009 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-19060909
13.
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
Nat Genet;
41(2): 157-9, 2009 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-19151714
14.
Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population.
Obes Facts;
1(6): 305-9, 2008.
Artículo
en Inglés
| MEDLINE | ID: mdl-20054193
15.
Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.
PLoS One;
3(5): e2031, 2008 May 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-18461161
16.
Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.
Am J Hum Genet;
81(2): 338-45, 2007 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-17668382
17.
Tissue distribution and evolution of fructosamine 3-kinase and fructosamine 3-kinase-related protein.
J Biol Chem;
279(45): 46606-13, 2004 Nov 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-15331600
18.
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.
Hum Mol Genet;
11(17): 1997-2004, 2002 Aug 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-12165561
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