PubMed

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.

Molven A, Ringdal M, Nordbø AM, Raeder H, Støy J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, Joner G, Søvik O; Norwegian Childhood Diabetes Study Group, Bell GI, Njølstad PR.

Diabetes. 2008 Apr;57(4):1131-5. Epub 2008 Jan 11.PMID: 18192540 [PubMed - indexed for MEDLINE]Related articlesFree article

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group, Hattersley AT, Ellard S.

Diabetes. 2008 Apr;57(4):1034-42. Epub 2007 Dec 27.PMID: 18162506 [PubMed - indexed for MEDLINE]Related articlesFree article

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry.

Sagen JV, Bjørkhaug L, Molnes J, Raeder H, Grevle L, Søvik O, Molven A, Njølstad PR.

Pediatr Diabetes. 2008 Oct;9(5):442-9. Epub 2008 Apr 9.PMID: 18399931 [PubMed - indexed for MEDLINE]Related articles

Monogenic diabetes mellitus in youth. The MODY syndromes.

Winter WE, Nakamura M, House DV.

Endocrinol Metab Clin North Am. 1999 Dec;28(4):765-85. Review.PMID: 10609119 [PubMed - indexed for MEDLINE]Related articles

A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family.

Liu L, Furuta H, Minami A, Zheng T, Jia W, Nanjo K, Xiang K.

Mol Cell Biochem. 2007 Sep;303(1-2):115-20. Epub 2007 Apr 18.PMID: 17440689 [PubMed - indexed for MEDLINE]Related articles

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.

Diabetes. 2008 Apr;57(4):1115-9. Epub 2008 Jan 2.PMID: 18171712 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection.

Pearson ER, Pruhova S, Tack CJ, Johansen A, Castleden HA, Lumb PJ, Wierzbicki AS, Clark PM, Lebl J, Pedersen O, Ellard S, Hansen T, Hattersley AT.

Diabetologia. 2005 May;48(5):878-85. Epub 2005 Apr 14.PMID: 15830177 [PubMed - indexed for MEDLINE]Related articles

CTLA4 gene polymorphism contributes to the mode of onset of diabetes with antiglutamic acid decarboxylase antibody in Japanese patients: genetic analysis of diabetic patients with antiglutamic acid decarboxylase antibody.

Abe T, Yamaguchi Y, Takino H, Fujita N, Yamauchi-Degawa M, Ozaki M, Yamakawa K, Sera Y, Sakamaki H, Uotani S, Kawasaki E, Awata T, Yamasaki H, Eguchi K.

Diabet Med. 2001 Sep;18(9):726-31.PMID: 11606170 [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

Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study).

Eide SA, Raeder H, Johansson S, Midthjell K, Søvik O, Njølstad PR, Molven A.

Diabet Med. 2008 Jul;25(7):775-81.PMID: 18513305 [PubMed - indexed for MEDLINE]Related articles

Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients.

Xu JY, Dan QH, Chan V, Wat NM, Tam S, Tiu SC, Lee KF, Siu SC, Tsang MW, Fung LM, Chan KW, Lam KS.

Eur J Hum Genet. 2005 Apr;13(4):422-7.PMID: 15657605 [PubMed - indexed for MEDLINE]Related articlesFree article

Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family.

Shimada F, Makino H, Hashimoto N, Taira M, Seino S, Bell GI, Kanatsuka A, Yoshida S.

Diabetologia. 1993 May;36(5):433-7.PMID: 8314448 [PubMed - indexed for MEDLINE]Related articles

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway.

Bjørkhaug L, Sagen JV, Thorsby P, Søvik O, Molven A, Njølstad PR.

J Clin Endocrinol Metab. 2003 Feb;88(2):920-31.PMID: 12574234 [PubMed - indexed for MEDLINE]Related articlesFree article

Childhood obesity complicating the differential diagnosis of maturity-onset diabetes of the young and type 2 diabetes.

Weintrob N, Stern E, Klipper-Aurbach Y, Phillip M, Gat-Yablonski G.

Pediatr Diabetes. 2008 Feb;9(1):60-4. Epub 2007 Nov 23.PMID: 18036134 [PubMed - indexed for MEDLINE]Related articles

[Etiological dissection in common anti-islet autoantibody-negative patients with type 1 diabetes]

Zhang DM, Zhou ZG, Weng JP, Li LR, Deng H, Zhang C, Jin P, Huang G, Peng J, Xiu LL, Wang JP, Yang L.

Zhonghua Yi Xue Za Zhi. 2004 Aug 2;84(15):1247-51. Chinese. PMID: 15387959 [PubMed - indexed for MEDLINE]Related articles

Diagnosis and treatment of neonatal diabetes: a United States experience.

Støy J, Greeley SA, Paz VP, Ye H, Pastore AN, Skowron KB, Lipton RB, Cogen FR, Bell GI, Philipson LH; United States Neonatal Diabetes Working Group.

Pediatr Diabetes. 2008 Oct;9(5):450-9. Epub 2008 Jul 25.PMID: 18662362 [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

Identifying hepatic nuclear factor 1alpha mutations in children and young adults with a clinical diagnosis of type 1 diabetes.

Lambert AP, Ellard S, Allen LI, Gallen IW, Gillespie KM, Bingley PJ, Hattersley AT.

Diabetes Care. 2003 Feb;26(2):333-7.PMID: 12547858 [PubMed - indexed for MEDLINE]Related articlesFree article

Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.

Weng J, Ekelund M, Lehto M, Li H, Ekberg G, Frid A, Aberg A, Groop LC, Berntorp K.

Diabetes Care. 2002 Jan;25(1):68-71.PMID: 11772903 [PubMed - indexed for MEDLINE]Related articlesFree article

Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes.

Macfarlane WM, Frayling TM, Ellard S, Evans JC, Allen LI, Bulman MP, Ayres S, Shepherd M, Clark P, Millward A, Demaine A, Wilkin T, Docherty K, Hattersley AT.

J Clin Invest. 1999 Nov;104(9):R33-9.PMID: 10545530 [PubMed - indexed for MEDLINE]Related articlesFree article