BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 23433541)

  • 1. A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian families.
    Giuffrida FM; Calliari LE; Manna TD; Ferreira JG; Saddi-Rosa P; Kunii IS; Furuzawa GK; Dias-da-Silva MR; Reis AF
    Diabetes Res Clin Pract; 2013 May; 100(2):e42-5. PubMed ID: 23433541
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Three unreported glucokinase (GCK) missense mutations detected in the screening of thirty-two Brazilian kindreds for GCK and HNF1A-MODY.
    Weinert LS; Silveiro SP; Giuffrida FM; Cunha VT; Bulcão C; Calliari LE; Della Manna T; Kunii IS; Dotto RP; Dias-da-Silva MR; Reis AF
    Diabetes Res Clin Pract; 2014 Nov; 106(2):e44-8. PubMed ID: 25174781
    [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. Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.
    Velho G; Blanché H; Vaxillaire M; Bellanné-Chantelot C; Pardini VC; Timsit J; Passa P; Deschamps I; Robert JJ; Weber IT; Marotta D; Pilkis SJ; Lipkind GM; Bell GI; Froguel P
    Diabetologia; 1997 Feb; 40(2):217-24. PubMed ID: 9049484
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.
    López-Garrido MP; Herranz-Antolín S; Alija-Merillas MJ; Giralt P; Escribano J
    Clin Endocrinol (Oxf); 2013 Sep; 79(3):342-7. PubMed ID: 23009393
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Analysis of mutations in the glucokinase gene in people clinically characterized as MODY2 without a family history of diabetes.
    Lopez AP; de Dios A; Chiesa I; Perez MS; Frechtel GD
    Diabetes Res Clin Pract; 2016 Aug; 118():38-43. PubMed ID: 27289208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Insights into pathogenesis of five novel GCK mutations identified in Chinese MODY patients.
    Liu L; Liu Y; Ge X; Liu X; Chen C; Wang Y; Li M; Yin J; Zhang J; Chen Y; Zhang R; Jiang Y; Zhao W; Yang D; Zheng T; Lu M; Zhuang L; Jiang M
    Metabolism; 2018 Dec; 89():8-17. PubMed ID: 30257192
    [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. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Clinical follow-up of two Brazilian subjects with glucokinase-MODY (MODY2) with description of a novel mutation.
    DellaManna T; Silva MR; Chacra AR; Kunii IS; Rolim AL; Furuzawa G; Maciel RM; Reis AF
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):490-5. PubMed ID: 23295287
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional analysis of human glucokinase gene mutations causing MODY2: exploring the regulatory mechanisms of glucokinase activity.
    García-Herrero CM; Galán M; Vincent O; Flández B; Gargallo M; Delgado-Alvarez E; Blázquez E; Navas MA
    Diabetologia; 2007 Feb; 50(2):325-33. PubMed ID: 17186219
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Glucokinase mutations in pediatric patients with impaired fasting glucose.
    Aloi C; Salina A; Minuto N; Tallone R; Lugani F; Mascagni A; Mazza O; Cassanello M; Maghnie M; d'Annunzio G
    Acta Diabetol; 2017 Oct; 54(10):913-923. PubMed ID: 28726111
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.