124 related articles for article (PubMed ID: 17079173)
1. Prevalence and clinical phenotype of the p.Val226Met glucokinase gene mutation in French Canadians in Quebec, Canada.
Henderson M; Levy E; Delvin E; Losekoot M; Lambert M
Mol Genet Metab; 2007 Jan; 90(1):87-92. PubMed ID: 17079173
[TBL] [Abstract][Full Text] [Related]
2. Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes.
Stoffel M; Patel P; Lo YM; Hattersley AT; Lucassen AM; Page R; Bell JI; Bell GI; Turner RC; Wainscoat JS
Nat Genet; 1992 Oct; 2(2):153-6. PubMed ID: 1303265
[TBL] [Abstract][Full Text] [Related]
3. Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY). Mutations in brief no. 162. Online.
Guazzini B; Gaffi D; Mainieri D; Multari G; Cordera R; Bertolini S; Pozza G; Meschi F; Barbetti F
Hum Mutat; 1998; 12(2):136. PubMed ID: 10694920
[TBL] [Abstract][Full Text] [Related]
4. Low prevalence of MODY2 and MODY3 mutations in Brazilian individuals with clinical MODY phenotype.
Furuzawa GK; Giuffrida FM; Oliveira CS; Chacra AR; Dib SA; Reis AF
Diabetes Res Clin Pract; 2008 Sep; 81(3):e12-4. PubMed ID: 18672310
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 18399931
[TBL] [Abstract][Full Text] [Related]
6. Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young.
Mantovani V; Salardi S; Cerreta V; Bastia D; Cenci M; Ragni L; Zucchini S; Parente R; Cicognani A
Hum Mutat; 2003 Oct; 22(4):338. PubMed ID: 12955723
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 15657605
[TBL] [Abstract][Full Text] [Related]
8. Glucokinase gene mutation screening in Argentinean clinically characterized MODY patients.
Lopez AP; Foscaldi SA; Pérez MS; Krochik G; Rodríguez M; Traversa M; Puchulu FM; Hirschler V; Bergada I; Frechtel GD
Exp Clin Endocrinol Diabetes; 2009 Sep; 117(8):391-4. PubMed ID: 19358091
[TBL] [Abstract][Full Text] [Related]
9. A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians.
St-Pierre J; Vohl MC; Brisson D; Perron P; Després JP; Hudson TJ; Gaudet D
Mol Genet Metab; 2001 Mar; 72(3):209-17. PubMed ID: 11243726
[TBL] [Abstract][Full Text] [Related]
10. Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain.
Estalella I; Rica I; Perez de Nanclares G; Bilbao JR; Vazquez JA; San Pedro JI; Busturia MA; Castaño L;
Clin Endocrinol (Oxf); 2007 Oct; 67(4):538-46. PubMed ID: 17573900
[TBL] [Abstract][Full Text] [Related]
11. Clinical characteristics of mutation carriers in a large family with glucokinase diabetes (MODY2).
Shehadeh N; Bakri D; Njølstad PR; Gershoni-Baruch R
Diabet Med; 2005 Aug; 22(8):994-8. PubMed ID: 16026363
[TBL] [Abstract][Full Text] [Related]
12. Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY).
Toaima D; Näke A; Wendenburg J; Praedicow K; Rohayem J; Engel K; Galler A; Gahr M; Lee-Kirsch MA
Hum Mutat; 2005 May; 25(5):503-4. PubMed ID: 15841481
[TBL] [Abstract][Full Text] [Related]
13. [Molecular diagnosis on indication of maturity onset diabetes of the young; results from 184 patients].
Losekoot M; Broekman AJ; Breuning MH; de Koning EJ; Romijn JA; Maassen JA
Ned Tijdschr Geneeskd; 2005 Jan; 149(3):139-43. PubMed ID: 15693590
[TBL] [Abstract][Full Text] [Related]
14. The glucokinase mutation p.T206P is common among MODY patients of Jewish Ashkenazi descent.
Gozlan Y; Tenenbaum A; Shalitin S; Lebenthal Y; Oron T; Cohen O; Phillip M; Gat-Yablonski G
Pediatr Diabetes; 2012 Sep; 13(6):e14-21. PubMed ID: 21978167
[TBL] [Abstract][Full Text] [Related]
15. [From gene to disease; 'maturity-onset diabetes of the young' (MODY), monogenetic inheritable forms of diabetes mellitus].
Maassen JA; Lemkes HH; Losekoot M
Ned Tijdschr Geneeskd; 2001 Jul; 145(28):1352-3. PubMed ID: 11484433
[TBL] [Abstract][Full Text] [Related]
16. Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients.
Hwang JS; Shin CH; Yang SW; Jung SY; Huh N
Diabetes Res Clin Pract; 2006 Oct; 74(1):75-81. PubMed ID: 16632067
[TBL] [Abstract][Full Text] [Related]
17. 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; ; Bell GI; Njølstad PR
Diabetes; 2008 Apr; 57(4):1131-5. PubMed ID: 18192540
[TBL] [Abstract][Full Text] [Related]
18. Glucokinase mutations in young children with hyperglycemia.
Codner E; Deng L; Pérez-Bravo F; Román R; Lanzano P; Cassorla F; Chung WK
Diabetes Metab Res Rev; 2006; 22(5):348-55. PubMed ID: 16444761
[TBL] [Abstract][Full Text] [Related]
19. High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI.
Massa O; Meschi F; Cuesta-Munoz A; Caumo A; Cerutti F; Toni S; Cherubini V; Guazzarotti L; Sulli N; Matschinsky FM; Lorini R; Iafusco D; Barbetti F;
Diabetologia; 2001 Jul; 44(7):898-905. PubMed ID: 11508276
[TBL] [Abstract][Full Text] [Related]
20. Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish population.
Solera J; Arias P; Amiñoso C; González-Casado I; Garre P; Herranz L; Villarroel A; Cruz M; Jáñez M; Pallardo LF; Gracia R
Diabetes Res Clin Pract; 2009 Jul; 85(1):20-3. PubMed ID: 19410318
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]