Scharfmann R - Search Results

1

Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.

Bonnefond A, Vaillant E, Philippe J, Skrobek B, Lobbens S, Yengo L, Huyvaert M, Cavé H, Busiah K, Scharfmann R, Polak M, Abdul-Rasoul M, Froguel P, Vaxillaire M. Bonnefond A, et al. Among authors: scharfmann r. Diabetes Metab. 2013 May;39(3):276-80. doi: 10.1016/j.diabet.2013.02.007. Epub 2013 Apr 4. Diabetes Metab. 2013. PMID: 23562494

2

Demonstration of lactogenic receptors in rat endocrine pancreases by quantitative autoradiography.

Polak M, Scharfmann R, Ban E, Haour F, Postel-Vinay MC, Czernichow P. Polak M, et al. Among authors: scharfmann r. Diabetes. 1990 Sep;39(9):1045-9. doi: 10.2337/diab.39.9.1045. Diabetes. 1990. PMID: 2166698

3

Expression of functional nerve growth factor receptors in pancreatic beta-cell lines and fetal rat islets in primary culture.

Scharfmann R, Tazi A, Polak M, Kanaka C, Czernichow P. Scharfmann R, et al. Diabetes. 1993 Dec;42(12):1829-36. doi: 10.2337/diab.42.12.1829. Diabetes. 1993. PMID: 8243829

4

Dexamethasone regulates the expression of neuronal properties of a rat insulinoma cell line.

Atouf F, Tazi A, Polak M, Czernichow P, Scharfmann R. Atouf F, et al. Among authors: scharfmann r. J Neuroendocrinol. 1995 Dec;7(12):957-64. doi: 10.1111/j.1365-2826.1995.tb00741.x. J Neuroendocrinol. 1995. PMID: 8745274

5

Early pattern of differentiation in the human pancreas.

Polak M, Bouchareb-Banaei L, Scharfmann R, Czernichow P. Polak M, et al. Among authors: scharfmann r. Diabetes. 2000 Feb;49(2):225-32. doi: 10.2337/diabetes.49.2.225. Diabetes. 2000. PMID: 10868939

6

No evidence for linkage or for diabetes-associated mutations in the activin type 2B receptor gene (ACVR2B) in French patients with mature-onset diabetes of the young or type 2 diabetes.

Dupont S, Hani EH, Cras-Méneur C, De Matos F, Lobbens S, Lecoeur C, Vaxillaire M, Scharfmann R, Froguel P. Dupont S, et al. Among authors: scharfmann r. Diabetes. 2001 May;50(5):1219-21. doi: 10.2337/diabetes.50.5.1219. Diabetes. 2001. PMID: 11334431

7

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.

Babenko AP, Polak M, Cavé H, Busiah K, Czernichow P, Scharfmann R, Bryan J, Aguilar-Bryan L, Vaxillaire M, Froguel P. Babenko AP, et al. Among authors: scharfmann r. N Engl J Med. 2006 Aug 3;355(5):456-66. doi: 10.1056/NEJMoa055068. N Engl J Med. 2006. PMID: 16885549 Free article.

8

Transcription factor TCF7L2 genetic study in the French population: expression in human beta-cells and adipose tissue and strong association with type 2 diabetes.

Cauchi S, Meyre D, Dina C, Choquet H, Samson C, Gallina S, Balkau B, Charpentier G, Pattou F, Stetsyuk V, Scharfmann R, Staels B, Frühbeck G, Froguel P. Cauchi S, et al. Among authors: scharfmann r. Diabetes. 2006 Oct;55(10):2903-8. doi: 10.2337/db06-0474. Diabetes. 2006. PMID: 17003360

9

New ABCC8 mutations in relapsing neonatal diabetes and clinical features.

Vaxillaire M, Dechaume A, Busiah K, Cavé H, Pereira S, Scharfmann R, de Nanclares GP, Castano L, Froguel P, Polak M; SUR1-Neonatal Diabetes Study Group. Vaxillaire M, et al. Among authors: scharfmann r. Diabetes. 2007 Jun;56(6):1737-41. doi: 10.2337/db06-1540. Epub 2007 Mar 27. Diabetes. 2007. PMID: 17389331

10

Diabetes in very young children and mutations in the insulin-secreting cell potassium channel genes: therapeutic consequences.

Flechtner I, Vaxillaire M, Cavé H, Scharfmann R, Froguel P, Polak M. Flechtner I, et al. Among authors: scharfmann r. Endocr Dev. 2007;12:86-98. doi: 10.1159/000109636. Endocr Dev. 2007. PMID: 17923772

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