72 related articles for article (PubMed ID: 21288587)
1. A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype.
Costantini S; Prandini P; Corradi M; Pasquali A; Contreas G; Pignatti PF; Pinelli L; Trabetti E; Maffeis C
Diabetes Res Clin Pract; 2011 Apr; 92(1):e23-6. PubMed ID: 21288587
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype.
Cappelli A; Tumini S; Consoli A; Carinci S; Piersanti C; Ruggiero G; Simonella G; Soletti F; Staffolani P; Pianese L
Diabetes Res Clin Pract; 2009 Mar; 83(3):e72-4. PubMed ID: 19150152
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A novel nonsense mutation in GCK exon 9 co-segregates with diabetes phenotype.
Knebel B; Jacob S; Boxberg CV; Müller-Wieland D; Kotzka J
Exp Clin Endocrinol Diabetes; 2004 Jun; 112(6):298-301. PubMed ID: 15216446
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene.
Bennett K; James C; Mutair A; Al-Shaikh H; Sinani A; Hussain K
Pediatr Diabetes; 2011 May; 12(3 Pt 1):192-6. PubMed ID: 21518409
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.
Gloyn AL
Hum Mutat; 2003 Nov; 22(5):353-62. PubMed ID: 14517946
[TBL] [Abstract][Full Text] [Related]
11. Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations.
Pruhova S; Dusatkova P; Sumnik Z; Kolouskova S; Pedersen O; Hansen T; Cinek O; Lebl J
Pediatr Diabetes; 2010 Dec; 11(8):529-35. PubMed ID: 20337973
[TBL] [Abstract][Full Text] [Related]
12. [Mutation screening of GCK gene in Chinese early-onset diabetes population].
Zheng TS; Wu SH; Yang Z; Lu HJ; Xiang KS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):671-4. PubMed ID: 16331569
[TBL] [Abstract][Full Text] [Related]
13. Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young.
Sun F; Knebelmann B; Pueyo ME; Zouali H; Lesage S; Vaxillaire M; Passa P; Cohen D; Velho G; Antignac C
J Clin Invest; 1993 Sep; 92(3):1174-80. PubMed ID: 8376578
[TBL] [Abstract][Full Text] [Related]
14. A new de novo mutation in the GCK gene causing MODY2.
Cappelli A; Silvestri S; Tumini S; Carinci S; Cipriano P; Massi L; Staffolani P; Pianese L
Diabetes Res Clin Pract; 2011 Jul; 93(1):e41-3. PubMed ID: 21514682
[TBL] [Abstract][Full Text] [Related]
15. A novel glucokinase gene mutation and its effect on glycemic/C-peptide fluctuations in a patient with maturity-onset diabetes of the young type 2.
Loomba-Albrecht LA; Jame M; Bremer AA
Diabetes Res Clin Pract; 2010 Mar; 87(3):e23-5. PubMed ID: 20015564
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Gene symbol: GCK. Disease: diabetes, MODY.
Navas MA; Galan M; Vincent O; Roncero I; Azriel S; Boix-Pallares P; Delgado-Alvarez E; Diaz-Cadórniga F; Blázquez E
Hum Genet; 2006 Apr; 119(3):363. PubMed ID: 17230658
[No Abstract] [Full Text] [Related]
18. Minigene splicing assessment of 20 novel synonymous and intronic glucokinase gene variants identified in patients with maturity-onset diabetes of the young.
Tiulpakov A; Zubkova N; Makretskaya N; Krasnova TS; Melnikova AI; Fedyaeva AS; Vasilyev E; Petrov VM; Rubtsov PM
Hum Mutat; 2020 Jan; 41(1):129-132. PubMed ID: 31529753
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Functional characterization of two novel splicing mutations in glucokinase gene in monogenic diabetes MODY2].
Igudin EL; Spirin PV; Prasolov VS; Zubkov NA; Petriaĭkina EE; Tiul'pakov AN; Rubtsov PM
Mol Biol (Mosk); 2014; 48(2):288-94. PubMed ID: 25850297
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]