PubMed

Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects.

del Bosque-Plata L, Lin J, Horikawa Y, Schwarz PE, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, German MS, Bell GI.

Diabetes. 2001 Mar;50(3):694-6.PMID: 11246894 [PubMed - indexed for MEDLINE]Related articlesFree article

Polymorphisms in the neurogenin 3 gene (NEUROG) and their relation to altered insulin secretion and diabetes in the Danish Caucasian population.

Jensen JN, Hansen L, Ekstrøm CT, Pociot F, Nerup J, Hansen T, Pedersen O.

Diabetologia. 2001 Jan;44(1):123-6.PMID: 11206403 [PubMed - indexed for MEDLINE]Related articles

beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.

Horikawa Y, Horikawa Y, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Schwitzgebel V, German MS, Bell GI.

Diabetes. 2000 Nov;49(11):1955-7.PMID: 11078465 [PubMed - indexed for MEDLINE]Related articlesFree article

No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France.

Dupont S, Vionnet N, Chèvre JC, Gallina S, Dina C, Seino Y, Yamada Y, Froguel P.

Diabetologia. 1999 Apr;42(4):480-4.PMID: 10230653 [PubMed - indexed for MEDLINE]Related articles

No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.

Hara M, Wang X, Paz VP, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Bell GI.

Diabetologia. 2000 Aug;43(8):1064-9.PMID: 10990086 [PubMed - indexed for MEDLINE]Related articles

Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young.

Hinokio Y, Horikawa Y, Furuta H, Cox NJ, Iwasaki N, Honda M, Ogata M, Iwamoto Y, Bell GI.

Diabetes. 2000 Feb;49(2):302-5.PMID: 10868948 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation screening of the neurogenin-3 gene in autosomal dominant diabetes.

Kim SH, Warram JH, Krolewski AS, Doria A.

J Clin Endocrinol Metab. 2001 May;86(5):2320-2.PMID: 11344245 [PubMed - indexed for MEDLINE]Related articlesFree article

Variants of neurogenin 3 gene are not associated with Type II diabetes in Japanese subjects.

Okada T, Tobe K, Hara K, Yasuda K, Kawaguchi Y, Ikegami H, Ito C, Kadowaki T.

Diabetologia. 2001 Feb;44(2):241-4.PMID: 11270683 [PubMed - indexed for MEDLINE]Related articles

MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1.

Kristinsson SY, Thorolfsdottir ET, Talseth B, Steingrimsson E, Thorsson AV, Helgason T, Hreidarsson AB, Arngrimsson R.

Diabetologia. 2001 Nov;44(11):2098-103.PMID: 11719843 [PubMed - indexed for MEDLINE]Related articles

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.

Frayling TM, Evans JC, Bulman MP, Pearson E, Allen L, Owen K, Bingham C, Hannemann M, Shepherd M, Ellard S, Hattersley AT.

Diabetes. 2001 Feb;50 Suppl 1:S94-100.PMID: 11272211 [PubMed - indexed for MEDLINE]Related articles

Mutant neurogenin-3 in congenital malabsorptive diarrhea.

Wang J, Cortina G, Wu SV, Tran R, Cho JH, Tsai MJ, Bailey TJ, Jamrich M, Ament ME, Treem WR, Hill ID, Vargas JH, Gershman G, Farmer DG, Reyen L, Martín MG.

N Engl J Med. 2006 Jul 20;355(3):270-80.PMID: 16855267 [PubMed - indexed for MEDLINE]Related articlesFree article

NEUROG3 variants and type 2 diabetes in Italians.

Milord E, Gragnoli C.

Minerva Med. 2006 Oct;97(5):373-8.PMID: 17146417 [PubMed - indexed for MEDLINE]Related articles

Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.

Domínguez-López A, Miliar-García A, Segura-Kato YX, Riba L, Esparza-López R, Ramírez-Jiménez S, Rodríguez-Torres M, Canizales-Quinteros S, Cabrera-Vásquez S, Fragoso-Ontiveros V, Aguilar-Salinas CA, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Bravo-Ríos LE, Tusié-Luna MT.

JOP. 2005 May 10;6(3):238-45.PMID: 15883474 [PubMed - indexed for MEDLINE]Related articlesFree article

Rare variants identified in the HNF- 4 alpha beta-cell-specific promoter and alternative exon 1 lack biological significance in maturity onset diabetes of the young and young onset Type II diabetes.

Mitchell SM, Vaxillaire M, Thomas H, Parrizas M, Benmezroua Y, Costa A, Hansen T, Owen KR, Tuomi T, Pirie F, Ryffel GU, Ferrer J, Froguel P, Hattersley AT, Frayling TM.

Diabetologia. 2002 Sep;45(9):1344-8. Epub 2002 Jul 19.PMID: 12242469 [PubMed - indexed for MEDLINE]Related articles

Candidate genes and late-onset type 2 diabetes mellitus. Susceptibility genes or common polymorphisms?

Hansen L.

Dan Med Bull. 2003 Nov;50(4):320-46. Review.PMID: 14694850 [PubMed - indexed for MEDLINE]Related articles

Ectopic expression of neurogenin 3 in neonatal pig pancreatic precursor cells induces (trans)differentiation to functional alpha cells.

Harb G, Heremans Y, Heimberg H, Korbutt GS.

Diabetologia. 2006 Aug;49(8):1855-63. Epub 2006 May 31.PMID: 16736130 [PubMed - indexed for MEDLINE]Related articles

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus.

Malecki MT, Jhala US, Antonellis A, Fields L, Doria A, Orban T, Saad M, Warram JH, Montminy M, Krolewski AS.

Nat Genet. 1999 Nov;23(3):323-8.PMID: 10545951 [PubMed - indexed for MEDLINE]Related articles

Insights on pathogenesis of type 2 diabetes from MODY genetics.

Weedon MN, Frayling TM.

Curr Diab Rep. 2007 Apr;7(2):131-8. Review.PMID: 17425917 [PubMed - indexed for MEDLINE]Related articles

Identification of the bHLH factor Math6 as a novel component of the embryonic pancreas transcriptional network.

Lynn FC, Sanchez L, Gomis R, German MS, Gasa R.

PLoS One. 2008 Jun 18;3(6):e2430.PMID: 18560595 [PubMed - indexed for MEDLINE]Related articlesFree article

Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity.

Utsunomiya N, Ohagi S, Sanke T, Tatsuta H, Hanabusa T, Nanjo K.

Diabetologia. 1998 Jun;41(6):701-5.PMID: 9662053 [PubMed - indexed for MEDLINE]Related articles