BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 25721872)

  • 21. 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. PubMed ID: 11719843
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.
    Froguel P; Zouali H; Vionnet N; Velho G; Vaxillaire M; Sun F; Lesage S; Stoffel M; Takeda J; Passa P
    N Engl J Med; 1993 Mar; 328(10):697-702. PubMed ID: 8433729
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of four novel mutations in the HNF-1A gene in Chinese early-onset and/or multiplex diabetes pedigrees.
    Yang Z; Wu SH; Zheng TS; Lu HJ; Xiang KS
    Chin Med J (Engl); 2006 Jul; 119(13):1072-8. PubMed ID: 16834925
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial early-onset diabetes is not a typical MODY in several Tunisian patients.
    Amara A; Chadli-Chaieb M; Ghezaiel H; Philippe J; Brahem R; Dechaume A; Saad A; Chaieb L; Froguel P; Gribaa M; Vaxillaire M
    Tunis Med; 2012 Dec; 90(12):882-7. PubMed ID: 23247789
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Identification of three new mutations of the HNF-1 alpha gene in Japanese MODY families.
    Ikema T; Shimajiri Y; Komiya I; Tawata M; Sunakawa S; Yogi H; Shimabukuro M; Takasu N
    Diabetologia; 2002 Dec; 45(12):1713-8. PubMed ID: 12488962
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Exome sequencing in children with clinically suspected maturity-onset diabetes of the young.
    Tosur M; Soler-Alfonso C; Chan KM; Khayat MM; Jhangiani SN; Meng Q; Refaey A; Muzny D; Gibbs RA; Murdock DR; Posey JE; Balasubramanyam A; Redondo MJ; Sabo A
    Pediatr Diabetes; 2021 Nov; 22(7):960-968. PubMed ID: 34387403
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of novel variants in the hepatocyte nuclear factor-1alpha gene in South Indian patients with maturity onset diabetes of young.
    Radha V; Ek J; Anuradha S; Hansen T; Pedersen O; Mohan V
    J Clin Endocrinol Metab; 2009 Jun; 94(6):1959-65. PubMed ID: 19336507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Novel INS Mutation in the C-Peptide Region Causing Hyperproinsulinemic Maturity Onset Diabetes of Youth Type 10.
    Schlegel A; Petersen WC; Holbrook AA; Iverson LK; Graham TE
    Lab Med; 2023 May; 54(3):327-332. PubMed ID: 36242597
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
    Vionnet N; Stoffel M; Takeda J; Yasuda K; Bell GI; Zouali H; Lesage S; Velho G; Iris F; Passa P
    Nature; 1992 Apr; 356(6371):721-2. PubMed ID: 1570017
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.
    Yorifuji T; Nagashima K; Kurokawa K; Kawai M; Oishi M; Akazawa Y; Hosokawa M; Yamada Y; Inagaki N; Nakahata T
    J Clin Endocrinol Metab; 2005 Jun; 90(6):3174-8. PubMed ID: 15784703
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes.
    Anuradha S; Radha V; Mohan V
    Clin Genet; 2011 Dec; 80(6):541-9. PubMed ID: 21062274
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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. PubMed ID: 10545530
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A mutation in the insulin 2 gene induces diabetes with severe pancreatic beta-cell dysfunction in the Mody mouse.
    Wang J; Takeuchi T; Tanaka S; Kubo SK; Kayo T; Lu D; Takata K; Koizumi A; Izumi T
    J Clin Invest; 1999 Jan; 103(1):27-37. PubMed ID: 9884331
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus.
    Plengvidhya N; Boonyasrisawat W; Chongjaroen N; Jungtrakoon P; Sriussadaporn S; Vannaseang S; Banchuin N; Yenchitsomanus PT
    Clin Endocrinol (Oxf); 2009 Jun; 70(6):847-53. PubMed ID: 18811724
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Biological behaviors of mutant proinsulin contribute to the phenotypic spectrum of diabetes associated with insulin gene mutations.
    Wang H; Saint-Martin C; Xu J; Ding L; Wang R; Feng W; Liu M; Shu H; Fan Z; Haataja L; Arvan P; Bellanné-Chantelot C; Cui J; Huang Y
    Mol Cell Endocrinol; 2020 Dec; 518():111025. PubMed ID: 32916194
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Nine novel mutations in maturity-onset diabetes of the young (MODY) candidate genes in 22 Spanish families.
    Barrio R; Bellanné-Chantelot C; Moreno JC; Morel V; Calle H; Alonso M; Mustieles C
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2532-9. PubMed ID: 12050210
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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. PubMed ID: 17440689
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.