Stoffel M - Search Results

1

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, Lesage S, Stoffel M, Takeda J, Passa P, et al. Froguel P, et al. Among authors: stoffel m. N Engl J Med. 1993 Mar 11;328(10):697-702. doi: 10.1056/NEJM199303113281005. N Engl J Med. 1993. PMID: 8433729 Free article.

2

Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.

Stoffel M, Froguel P, Takeda J, Zouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S, et al. Stoffel M, et al. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7698-702. doi: 10.1073/pnas.89.16.7698. Proc Natl Acad Sci U S A. 1992. PMID: 1502186 Free PMC article.

3

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.

Vionnet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, Lesage S, Velho G, Iris F, Passa P, et al. Vionnet N, et al. Among authors: stoffel m. Nature. 1992 Apr 23;356(6371):721-2. doi: 10.1038/356721a0. Nature. 1992. PMID: 1570017

4

Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.

Vaxillaire M, Vionnet N, Vigouroux C, Sun F, Espinosa R 3rd, Lebeau MM, Stoffel M, Lehto M, Beckmann JS, Detheux M, et al. Vaxillaire M, et al. Among authors: stoffel m. Diabetes. 1994 Mar;43(3):389-95. doi: 10.2337/diab.43.3.389. Diabetes. 1994. PMID: 7508874

5

Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.

Byrne MM, Sturis J, Clément K, Vionnet N, Pueyo ME, Stoffel M, Takeda J, Passa P, Cohen D, Bell GI, et al. Byrne MM, et al. Among authors: stoffel m. J Clin Invest. 1994 Mar;93(3):1120-30. doi: 10.1172/JCI117064. J Clin Invest. 1994. PMID: 8132752 Free PMC article.

6

Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships.

Gidh-Jain M, Takeda J, Xu LZ, Lange AJ, Vionnet N, Stoffel M, Froguel P, Velho G, Sun F, Cohen D, et al. Gidh-Jain M, et al. Among authors: stoffel m. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1932-6. doi: 10.1073/pnas.90.5.1932. Proc Natl Acad Sci U S A. 1993. PMID: 8446612 Free PMC article.

7

Identification of glucokinase mutations in subjects with gestational diabetes mellitus.

Stoffel M, Bell KL, Blackburn CL, Powell KL, Seo TS, Takeda J, Vionnet N, Xiang KS, Gidh-Jain M, Pilkis SJ, et al. Stoffel M, et al. Diabetes. 1993 Jun;42(6):937-40. doi: 10.2337/diab.42.6.937. Diabetes. 1993. PMID: 8495817

8

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: stoffel m. Diabetes. 1997 Jun;46(6):1062-8. doi: 10.2337/diab.46.6.1062. Diabetes. 1997. PMID: 9166680

9

Mutations of the human glucokinase gene and diabetes mellitus.

Bell GI, Froguel P, Nishi S, Pilkis SJ, Stoffel M, Takeda J, Vionnet N, Yasuda K. Bell GI, et al. Among authors: stoffel m. Trends Endocrinol Metab. 1993 Apr;4(3):86-90. doi: 10.1016/1043-2760(93)90084-r. Trends Endocrinol Metab. 1993. PMID: 18407139

10

Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13.

Nishi S, Stoffel M, Xiang K, Shows TB, Bell GI, Takeda J. Nishi S, et al. Among authors: stoffel m. Diabetologia. 1992 Aug;35(8):743-7. doi: 10.1007/BF00429094. Diabetologia. 1992. PMID: 1511800

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