These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 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.