Froguel P - Search Results

1

GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes.

Bonnefond A, Sand O, Guerin B, Durand E, De Graeve F, Huyvaert M, Rachdi L, Kerr-Conte J, Pattou F, Vaxillaire M, Polak M, Scharfmann R, Czernichow P, Froguel P. Bonnefond A, et al. Among authors: froguel p. Diabetologia. 2012 Oct;55(10):2845-2847. doi: 10.1007/s00125-012-2645-7. Epub 2012 Jul 18. Diabetologia. 2012. PMID: 22806356 No abstract available.

2

TCF7L2 rs7903146 impairs islet function and morphology in non-diabetic individuals.

Le Bacquer O, Kerr-Conte J, Gargani S, Delalleau N, Huyvaert M, Gmyr V, Froguel P, Neve B, Pattou F. Le Bacquer O, et al. Among authors: froguel p. Diabetologia. 2012 Oct;55(10):2677-2681. doi: 10.1007/s00125-012-2660-8. Epub 2012 Aug 22. Diabetologia. 2012. PMID: 22911383

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

4

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: froguel p. Diabetologia. 2001 Jun;44(6):786. doi: 10.1007/s001250051690. Diabetologia. 2001. PMID: 11440376 No abstract available.

5

Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.

Vaxillaire M, Samson C, Cavé H, Metz C, Froguel P, Polak M. Vaxillaire M, et al. Among authors: froguel p. Diabetologia. 2002 Mar;45(3):454-5. doi: 10.1007/s00125-001-0741-1. Diabetologia. 2002. PMID: 11914755 No abstract available.

6

PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian population.

Lopes C, Dina C, Durand E, Froguel P. Lopes C, et al. Among authors: froguel p. Diabetologia. 2003 Sep;46(9):1284-90. doi: 10.1007/s00125-003-1170-0. Epub 2003 Jul 11. Diabetologia. 2003. PMID: 12856128

7

Effect of common polymorphisms in the HNF4alpha promoter on susceptibility to type 2 diabetes in the French Caucasian population.

Vaxillaire M, Dina C, Lobbens S, Dechaume A, Vasseur-Delannoy V, Helbecque N, Charpentier G, Froguel P. Vaxillaire M, et al. Among authors: froguel p. Diabetologia. 2005 Mar;48(3):440-4. doi: 10.1007/s00125-004-1665-3. Epub 2005 Feb 25. Diabetologia. 2005. PMID: 15735892

8

No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects.

Cauchi S, Vaxillaire M, Choquet H, Durand E, Duval A, Polak M, Froguel P. Cauchi S, et al. Among authors: froguel p. Diabetologia. 2007 Jan;50(1):214-6. doi: 10.1007/s00125-006-0505-z. Epub 2006 Nov 9. Diabetologia. 2007. PMID: 17093940 No abstract available.

9

Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction.

Bonnefond A, Bouatia-Naji N, Simon A, Saint-Martin C, Dechaume A, de Lonlay P, Polak M, Bellanné-Chantelot C, Froguel P, Vaxillaire M. Bonnefond A, et al. Among authors: froguel p. Diabetologia. 2009 May;52(5):982-5. doi: 10.1007/s00125-009-1299-6. Epub 2009 Feb 24. Diabetologia. 2009. PMID: 19238352 No abstract available.

10

Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes.

Bonnefond A, Yengo L, Philippe J, Dechaume A, Ezzidi I, Vaillant E, Gjesing AP, Andersson EA, Czernichow S, Hercberg S, Hadjadj S, Charpentier G, Lantieri O, Balkau B, Marre M, Pedersen O, Hansen T, Froguel P, Vaxillaire M. Bonnefond A, et al. Among authors: froguel p. Diabetologia. 2013 Mar;56(3):492-6. doi: 10.1007/s00125-012-2794-8. Epub 2012 Dec 6. Diabetologia. 2013. PMID: 23224494

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