Vaxillaire M - Search Results

1

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.

Polak M, Dechaume A, Cavé H, Nimri R, Crosnier H, Sulmont V, de Kerdanet M, Scharfmann R, Lebenthal Y, Froguel P, Vaxillaire M; French ND (Neonatal Diabetes) Study Group. Polak M, et al. Among authors: vaxillaire m. Diabetes. 2008 Apr;57(4):1115-9. doi: 10.2337/db07-1358. Epub 2008 Jan 2. Diabetes. 2008. PMID: 18171712

2

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.

Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, et al. Froguel P, et al. Among authors: vaxillaire m. Nature. 1992 Mar 12;356(6365):162-4. doi: 10.1038/356162a0. Nature. 1992. PMID: 1545870

3

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. Diabetes. 1994 Mar;43(3):389-95. doi: 10.2337/diab.43.3.389. Diabetes. 1994. PMID: 7508874

4

Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.

Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N. Lesage S, et al. Among authors: vaxillaire m. Diabetes. 1995 Oct;44(10):1243-7. doi: 10.2337/diab.44.10.1243. Diabetes. 1995. PMID: 7556965

5

Characterization of the LIM/homeodomain gene islet-1 and single nucleotide screening in NIDDM.

Riggs AC, Tanizawa Y, Aoki M, Wasson J, Ferrer J, Rabin DU, Vaxillaire M, Froguel P, Permutt MA. Riggs AC, et al. Among authors: vaxillaire m. Diabetes. 1995 Jun;44(6):689-94. doi: 10.2337/diab.44.6.689. Diabetes. 1995. PMID: 7789634

6

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q.

Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann JS, Velho G, Lathrop GM, Froguel P. Vaxillaire M, et al. Nat Genet. 1995 Apr;9(4):418-23. doi: 10.1038/ng0495-418. Nat Genet. 1995. PMID: 7795649

7

Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism [corrected].

Tanizawa Y, Riggs AC, Dagogo-Jack S, Vaxillaire M, Froguel P, Liu L, Donis-Keller H, Permutt MA. Tanizawa Y, et al. Among authors: vaxillaire m. Diabetes. 1994 Jul;43(7):935-41. doi: 10.2337/diab.43.7.935. Diabetes. 1994. PMID: 7912209

8

Arginine-induced insulin release in glucokinase-deficient subjects.

Pueyo ME, Clement K, Vaxillaire M, Passa P, Froguel P, Robert JJ, Velho G. Pueyo ME, et al. Among authors: vaxillaire m. Diabetes Care. 1994 Sep;17(9):1015-21. doi: 10.2337/diacare.17.9.1015. Diabetes Care. 1994. PMID: 7988299

9

Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.

Zouali H, Vaxillaire M, Lesage S, Sun F, Velho G, Vionnet N, Chiu K, Passa P, Permutt A, Demenais F, et al. Zouali H, et al. Among authors: vaxillaire m. Diabetes. 1993 Sep;42(9):1238-45. doi: 10.2337/diab.42.9.1238. Diabetes. 1993. PMID: 8349034

10

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: vaxillaire 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.

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