BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 28664602)

  • 1. NEUROD1-deficient diabetes (MODY6): Identification of the first cases in Japanese and the clinical features.
    Horikawa Y; Enya M; Mabe H; Fukushima K; Takubo N; Ohashi M; Ikeda F; Hashimoto KI; Watada H; Takeda J
    Pediatr Diabetes; 2018 Mar; 19(2):236-242. PubMed ID: 28664602
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maturity onset diabetes of the young in India - a distinctive mutation pattern identified through targeted next-generation sequencing.
    Chapla A; Mruthyunjaya MD; Asha HS; Varghese D; Varshney M; Vasan SK; Venkatesan P; Nair V; Mathai S; Paul TV; Thomas N
    Clin Endocrinol (Oxf); 2015 Apr; 82(4):533-42. PubMed ID: 25041077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NEUROD1 mutation in an Italian patient with maturity onset diabetes of the young 6: a case report.
    Brodosi L; Baracco B; Mantovani V; Pironi L
    BMC Endocr Disord; 2021 Oct; 21(1):202. PubMed ID: 34654408
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A family with the Arg103Pro mutation in the NEUROD1 gene detected by next-generation sequencing - Clinical characteristics of mutation carriers.
    Szopa M; Ludwig-Galezowska AH; Radkowski P; Skupien J; Machlowska J; Klupa T; Wolkow P; Borowiec M; Mlynarski W; Malecki MT
    Eur J Med Genet; 2016 Feb; 59(2):75-9. PubMed ID: 26773576
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The first case of NEUROD1-MODY reported in Latin America.
    Abreu GM; Tarantino RM; Cabello PH; Zembrzuski VM; da Fonseca ACP; Rodacki M; Zajdenverg L; Campos Junior M
    Mol Genet Genomic Med; 2019 Dec; 7(12):e989. PubMed ID: 31578821
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY).
    Horikawa Y; Enya M
    Curr Diab Rep; 2019 Feb; 19(3):12. PubMed ID: 30793219
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus.
    Sagen JV; Baumann ME; Salvesen HB; Molven A; Søvik O; Njølstad PR
    Diabet Med; 2005 Aug; 22(8):1012-5. PubMed ID: 16026366
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification and functional analysis of mutations in the hepatocyte nuclear factor-1alpha gene in anti-islet autoantibody-negative Japanese patients with type 1 diabetes.
    Kawasaki E; Sera Y; Yamakawa K; Abe T; Ozaki M; Uotani S; Ohtsu N; Takino H; Yamasaki H; Yamaguchi Y; Matsuura N; Eguchi K
    J Clin Endocrinol Metab; 2000 Jan; 85(1):331-5. PubMed ID: 10634407
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4alpha gene in a Danish pedigree with maturity-onset diabetes of the young.
    Møller AM; Dalgaard LT; Ambye L; Hansen L; Schmitz O; Hansen T; Pedersen O
    J Clin Endocrinol Metab; 1999 Jan; 84(1):367-9. PubMed ID: 9920109
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Insulin secretion and insulin sensitivity in diabetic subgroups: studies in the prediabetic and diabetic state.
    Tripathy D; Carlsson AL; Lehto M; Isomaa B; Tuomi T; Groop L
    Diabetologia; 2000 Dec; 43(12):1476-83. PubMed ID: 11151756
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stress Induced Hyperglycemia in Early Childhood as a Clue for the Diagnosis of NEUROD1-MODY.
    Çelik NB; Lafcı NG; Savaş-Erdeve Ş; Çetinkaya S
    J Clin Res Pediatr Endocrinol; 2024 May; 16(2):218-223. PubMed ID: 36047484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.
    Lehto M; Wipemo C; Ivarsson SA; Lindgren C; Lipsanen-Nyman M; Weng J; Wibell L; Widén E; Tuomi T; Groop L
    Diabetologia; 1999 Sep; 42(9):1131-7. PubMed ID: 10447526
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1.
    Demirbilek H; Hatipoglu N; Gul U; Tatli ZU; Ellard S; Flanagan SE; De Franco E; Kurtoglu S
    Pediatr Diabetes; 2018 Aug; 19(5):898-904. PubMed ID: 29521454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretion.
    Møller AM; Ek J; Durviaux SM; Urhammer SA; Clausen JO; Eiberg H; Hansen T; Rousseau GG; Lemaigre FP; Pedersen O
    Diabetologia; 1999 Aug; 42(8):1011-6. PubMed ID: 10491763
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Large Family With Maturity-Onset Diabetes of the Young and a Novel V121I Mutation in HNF4A.
    Monney CT; Kaltenrieder V; Cousin P; Bonny C; Schorderet DF
    Hum Mutat; 2002 Sep; 20(3):230-1. PubMed ID: 12203996
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Diabetes mellitus].
    Iwasaki N
    Rinsho Byori; 2001 Feb; 49(2):161-4. PubMed ID: 11307309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the hepatocyte nuclear factor-4alpha gene in Japanese with non-insulin-dependent diabetes: a nucleotide substitution in the polypyrimidine tract of intron 1b.
    Sakurai K; Seki N; Fujii R; Yagui K; Tokuyama Y; Shimada F; Makino H; Suzuki Y; Hashimoto N; Saito Y; Egashira T; Matsui K; Kanatsuka A
    Horm Metab Res; 2000 Aug; 32(8):316-20. PubMed ID: 10983627
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.