Durand E - Search Results

1

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, Tichet J, Marre M, Weill J, Heude B, Tauber M, Lemaire K, Schuit F, Elliott P, Jørgensen T, Charpentier G, Hadjadj S, Cauchi S, Vaxillaire M, Sladek R, Visvikis-Siest S, Balkau B, Lévy-Marchal C, Pattou F, Meyre D, Blakemore AI, Jarvelin MR, Walley AJ, Hansen T, Dina C, Pedersen O, Froguel P. Bouatia-Naji N, et al. Among authors: durand e. Nat Genet. 2009 Jan;41(1):89-94. doi: 10.1038/ng.277. Epub 2008 Dec 7. Nat Genet. 2009. PMID: 19060909

2

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus.

Hani EH, Suaud L, Boutin P, Chèvre JC, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell GI, Laine B, Froguel P. Hani EH, et al. Among authors: durand e. J Clin Invest. 1998 Feb 1;101(3):521-6. doi: 10.1172/JCI1403. J Clin Invest. 1998. PMID: 9449683 Free PMC article.

3

Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians.

Hani EH, Boutin P, Durand E, Inoue H, Permutt MA, Velho G, Froguel P. Hani EH, et al. Among authors: durand e. Diabetologia. 1998 Dec;41(12):1511-5. doi: 10.1007/s001250051098. Diabetologia. 1998. PMID: 9867219

4

Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset type 2 diabetes mellitus.

Hani EH, Stoffers DA, Chèvre JC, Durand E, Stanojevic V, Dina C, Habener JF, Froguel P. Hani EH, et al. Among authors: durand e. J Clin Invest. 1999 Nov;104(9):R41-8. doi: 10.1172/JCI7469. J Clin Invest. 1999. PMID: 10545531 Free PMC article.

5

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity.

Vaisse C, Clement K, Durand E, Hercberg S, Guy-Grand B, Froguel P. Vaisse C, et al. Among authors: durand e. J Clin Invest. 2000 Jul;106(2):253-62. doi: 10.1172/JCI9238. J Clin Invest. 2000. PMID: 10903341 Free PMC article.

6

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P. Vionnet N, et al. Among authors: durand e. Am J Hum Genet. 2000 Dec;67(6):1470-80. doi: 10.1086/316887. Epub 2000 Nov 6. Am J Hum Genet. 2000. PMID: 11067779 Free PMC article.

7

Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French Caucasians.

Hani EH, Dupont S, Durand E, Dina C, Gallina S, Gantz I, Froguel P. Hani EH, et al. Among authors: durand e. J Clin Endocrinol Metab. 2001 Jun;86(6):2895-8. doi: 10.1210/jcem.86.6.7589. J Clin Endocrinol Metab. 2001. PMID: 11397906

8

No evidence for diabetes-associated mutations of PEK/EIF2AK3 gene in French patients with early-onset type II diabetes.

Vaxillaire M, Benmezroua Y, Durand E, Vasseur F, Froguel P. Vaxillaire M, et al. Among authors: durand e. Diabetologia. 2001 Jun;44(6):786. doi: 10.1007/s001250051690. Diabetologia. 2001. PMID: 11440376 No abstract available.

9

Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians.

Delplanque J, Vasseur F, Durand E, Abderrahmani A, Dina C, Waeber G, Guy-Grand B, Clement K, Weill J, Boutin P, Froguel P. Delplanque J, et al. Among authors: durand e. J Clin Endocrinol Metab. 2002 Feb;87(2):867-9. doi: 10.1210/jcem.87.2.8259. J Clin Endocrinol Metab. 2002. PMID: 11836334

10

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations.

Lubrano-Berthelier C, Durand E, Dubern B, Shapiro A, Dazin P, Weill J, Ferron C, Froguel P, Vaisse C. Lubrano-Berthelier C, et al. Among authors: durand e. Hum Mol Genet. 2003 Jan 15;12(2):145-53. doi: 10.1093/hmg/ddg016. Hum Mol Genet. 2003. PMID: 12499395

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