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

2

Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians.

Hani EH, Clément K, Velho G, Vionnet N, Hager J, Philippi A, Dina C, Inoue H, Permutt MA, Basdevant A, North M, Demenais F, Guy-Grand B, Froguel P. Hani EH, et al. Diabetes. 1997 Apr;46(4):688-94. doi: 10.2337/diab.46.4.688. Diabetes. 1997. PMID: 9075812

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: hani eh. Diabetologia. 1998 Sep;41(9):1017-23. doi: 10.1007/s001250051025. Diabetologia. 1998. PMID: 9754819

4

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. J Clin Endocrinol Metab. 2001 Jun;86(6):2895-8. doi: 10.1210/jcem.86.6.7589. J Clin Endocrinol Metab. 2001. PMID: 11397906

5

Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs.

Vionnet N, Hani EH, Lesage S, Philippi A, Hager J, Varret M, Stoffel M, Tanizawa Y, Chiu KC, Glaser B, Permutt MA, Passa P, Demenais F, Froguel P. Vionnet N, et al. Among authors: hani eh. Diabetes. 1997 Jun;46(6):1062-8. doi: 10.2337/diab.46.6.1062. Diabetes. 1997. PMID: 9166680

6

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. Among authors: hani eh. Biotechniques. 1997 Sep;23(3):358-62. doi: 10.2144/97233bm01. Biotechniques. 1997. PMID: 9298196 Free article. No abstract available.

7

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. Among authors: hani eh. Diabetes. 1997 Dec;46(12):2108-9. doi: 10.2337/diab.46.12.2108. Diabetes. 1997. PMID: 9392505 No abstract available.

8

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

9

Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians.

Chèvre JC, Hani EH, Stoffers DA, Habener JF, Froguel P. Chèvre JC, et al. Among authors: hani eh. Diabetes. 1998 May;47(5):843-4. doi: 10.2337/diabetes.47.5.843. Diabetes. 1998. PMID: 9588460 Clinical Trial. No abstract available.

10

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. J Clin Invest. 1999 Nov;104(9):R41-8. doi: 10.1172/JCI7469. J Clin Invest. 1999. PMID: 10545531 Free PMC article.

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