BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 20573748)

  • 21. 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]  

  • 22. 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]  

  • 23. Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.
    Rubio-Cabezas O; Minton JA; Caswell R; Shield JP; Deiss D; Sumnik Z; Cayssials A; Herr M; Loew A; Lewis V; Ellard S; Hattersley AT
    Diabetes Care; 2009 Jan; 32(1):111-6. PubMed ID: 18931102
    [TBL] [Abstract][Full Text] [Related]  

  • 24. beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.
    Horikawa Y; Horikawa Y; Cox NJ; Iwasaki N; Ogata M; Iwamoto Y; Schwitzgebel V; German MS; Bell GI
    Diabetes; 2000 Nov; 49(11):1955-7. PubMed ID: 11078465
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
    Shaw-Smith C; Flanagan SE; Patch AM; Grulich-Henn J; Habeb AM; Hussain K; Pomahacova R; Matyka K; Abdullah M; Hattersley AT; Ellard S
    Pediatr Diabetes; 2012 Jun; 13(4):314-21. PubMed ID: 22369132
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complications.
    Tammaro P; Flanagan SE; Zadek B; Srinivasan S; Woodhead H; Hameed S; Klimes I; Hattersley AT; Ellard S; Ashcroft FM
    Diabetologia; 2008 May; 51(5):802-10. PubMed ID: 18335204
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development.
    Edghill EL; Bingham C; Slingerland AS; Minton JA; Noordam C; Ellard S; Hattersley AT
    Diabet Med; 2006 Dec; 23(12):1301-6. PubMed ID: 17116179
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.
    Senée V; Chelala C; Duchatelet S; Feng D; Blanc H; Cossec JC; Charon C; Nicolino M; Boileau P; Cavener DR; Bougnères P; Taha D; Julier C
    Nat Genet; 2006 Jun; 38(6):682-7. PubMed ID: 16715098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.
    Polak M; Dechaume A; Cavé H; Nimri R; Crosnier H; Sulmont V; de Kerdanet M; Scharfmann R; Lebenthal Y; Froguel P; Vaxillaire M;
    Diabetes; 2008 Apr; 57(4):1115-9. PubMed ID: 18171712
    [TBL] [Abstract][Full Text] [Related]  

  • 31. No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France.
    Dupont S; Vionnet N; Chèvre JC; Gallina S; Dina C; Seino Y; Yamada Y; Froguel P
    Diabetologia; 1999 Apr; 42(4):480-4. PubMed ID: 10230653
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 2 diabetes mellitus in a Polish population.
    Malecki MT; Cyganek K; Klupa T; Sieradzki J
    Acta Diabetol; 2003 Jun; 40(2):109-11. PubMed ID: 12861411
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence.
    Pinney SE; Oliver-Krasinski J; Ernst L; Hughes N; Patel P; Stoffers DA; Russo P; De León DD
    J Clin Endocrinol Metab; 2011 Jul; 96(7):1960-5. PubMed ID: 21490072
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates.
    Deeb A; Habeb A; Kaplan W; Attia S; Hadi S; Osman A; Al-Jubeh J; Flanagan S; DeFranco E; Ellard S
    Am J Med Genet A; 2016 Mar; 170(3):602-9. PubMed ID: 26463504
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.
    Gloyn AL; Pearson ER; Antcliff JF; Proks P; Bruining GJ; Slingerland AS; Howard N; Srinivasan S; Silva JM; Molnes J; Edghill EL; Frayling TM; Temple IK; Mackay D; Shield JP; Sumnik Z; van Rhijn A; Wales JK; Clark P; Gorman S; Aisenberg J; Ellard S; Njølstad PR; Ashcroft FM; Hattersley AT
    N Engl J Med; 2004 Apr; 350(18):1838-49. PubMed ID: 15115830
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.
    Habeb AM; Al-Magamsi MS; Eid IM; Ali MI; Hattersley AT; Hussain K; Ellard S
    Pediatr Diabetes; 2012 Sep; 13(6):499-505. PubMed ID: 22060631
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 gene.
    Boyraz M; Ulucan K; Taşkın N; Akçay T; Flanagan SE; Mackay DJ
    J Clin Res Pediatr Endocrinol; 2013; 5(2):125-8. PubMed ID: 23748067
    [TBL] [Abstract][Full Text] [Related]  

  • 40. DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins.
    Laborie LB; Mackay DJ; Temple IK; Molven A; Søvik O; Njølstad PR
    Eur J Pediatr; 2010 Feb; 169(2):207-13. PubMed ID: 19521719
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.