Boutin P - Search Results

1

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: boutin p. Diabetologia. 1998 Dec;41(12):1511-5. doi: 10.1007/s001250051098. Diabetologia. 1998. PMID: 9867219

2

Genetic studies of neuropeptide Y and neuropeptide Y receptors Y1 and Y5 regions in morbid obesity.

Roche C, Boutin P, Dina C, Gyapay G, Basdevant A, Hager J, Guy-Grand B, Clément K, Froguel P. Roche C, et al. Among authors: boutin p. Diabetologia. 1997 Jun;40(6):671-5. doi: 10.1007/s001250050732. Diabetologia. 1997. PMID: 9222646

3

Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.

Chèvre JC, Hani EH, Boutin P, Vaxillaire M, Blanché H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chantelot C, Velho G, Froguel P. Chèvre JC, et al. Among authors: boutin p. Diabetologia. 1998 Sep;41(9):1017-23. doi: 10.1007/s001250051025. Diabetologia. 1998. PMID: 9754819

4

Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: how effective are the techniques of DHPLC and direct sequencing used in combination?

Boutin P, Vasseur F, Samson C, Wahl C, Froguel P. Boutin P, et al. Diabetologia. 2001 Jun;44(6):775-8. doi: 10.1007/s001250051687. Diabetologia. 2001. PMID: 11440371

5

Hypoadiponectinaemia and high risk of type 2 diabetes are associated with adiponectin-encoding (ACDC) gene promoter variants in morbid obesity: evidence for a role of ACDC in diabesity.

Vasseur F, Helbecque N, Lobbens S, Vasseur-Delannoy V, Dina C, Clément K, Boutin P, Kadowaki T, Scherer PE, Froguel P. Vasseur F, et al. Among authors: boutin p. Diabetologia. 2005 May;48(5):892-9. doi: 10.1007/s00125-005-1729-z. Epub 2005 Apr 14. Diabetologia. 2005. PMID: 15830179 Free article.

6

Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians.

Durand E, Boutin P, Meyre D, Charles MA, Clement K, Dina C, Froguel P. Durand E, et al. Among authors: boutin p. Diabetes. 2004 Sep;53(9):2483-6. doi: 10.2337/diabetes.53.9.2483. Diabetes. 2004. PMID: 15331564

7

Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population.

Durand E, Lecoeur C, Delplanque J, Benzinou M, Degraeve F, Boutin P, Marre M, Balkau B, Charpentier G, Froguel P, Meyre D. Durand E, et al. Among authors: boutin p. Obes Facts. 2008;1(6):305-9. doi: 10.1159/000178157. Epub 2008 Dec 12. Obes Facts. 2008. PMID: 20054193 Free PMC article.

8

Automated fluorescence-based screening for mutation by SSCP: use of universal M13 dye primers for labeling and detection.

Boutin P, Hani EH, Vasseur F, Roche C, Bailleul B, Hager J, Froguel P. Boutin P, et al. Biotechniques. 1997 Sep;23(3):358-62. doi: 10.2144/97233bm01. Biotechniques. 1997. PMID: 9298196 Free article. No abstract available.

9

An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young).

Boutin P, Chèvre JC, Hani EH, Gomis R, Pardini VC, Guillausseau PJ, Vaxillaire M, Velho G, Froguel P. Boutin P, et al. Diabetes. 1997 Dec;46(12):2108-9. doi: 10.2337/diab.46.12.2108. Diabetes. 1997. PMID: 9392505 No abstract available.

10

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: boutin p. J Clin Invest. 1998 Feb 1;101(3):521-6. doi: 10.1172/JCI1403. J Clin Invest. 1998. PMID: 9449683 Free PMC article.

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