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 *

143 related articles for article (PubMed ID: 20535137)

  • 21. No association of INS-VNTR genotype and IAA autoantibodies.
    Pérez de Nanclares G; Bilbao JR; Castano L
    Ann N Y Acad Sci; 2004 Dec; 1037():127-30. PubMed ID: 15699505
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Large-scale studies of the HphI insulin gene variable-number-of-tandem-repeats polymorphism in relation to Type 2 diabetes mellitus and insulin release.
    Hansen SK; Gjesing AP; Rasmussen SK; Glümer C; Urhammer SA; Andersen G; Rose CS; Drivsholm T; Torekov SK; Jensen DP; Ekstrøm CT; Borch-Johnsen K; Jørgensen T; McCarthy MI; Hansen T; Pedersen O
    Diabetologia; 2004 Jun; 47(6):1079-87. PubMed ID: 15170498
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A functional analysis of the role of IGF2 in IDDM2-encoded susceptibility to type 1 diabetes.
    Vafiadis P; Grabs R; Goodyer CG; Colle E; Polychronakos C
    Diabetes; 1998 May; 47(5):831-6. PubMed ID: 9588457
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Divergence between genetic determinants of IGF2 transcription levels in leukocytes and of IDDM2-encoded susceptibility to type 1 diabetes.
    Vafiadis P; Bennett ST; Todd JA; Grabs R; Polychronakos C
    J Clin Endocrinol Metab; 1998 Aug; 83(8):2933-9. PubMed ID: 9709972
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus.
    Bennett ST; Lucassen AM; Gough SC; Powell EE; Undlien DE; Pritchard LE; Merriman ME; Kawaguchi Y; Dronsfield MJ; Pociot F
    Nat Genet; 1995 Mar; 9(3):284-92. PubMed ID: 7773291
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Insulin gene VNTR, CTLA-4 +49A/G and HLA-DQB1 alleles distinguish latent autoimmune diabetes in adults from type 1 diabetes and from type 2 diabetes group.
    Haller K; Kisand K; Pisarev H; Salur L; Laisk T; Nemvalts V; Uibo R
    Tissue Antigens; 2007 Feb; 69(2):121-7. PubMed ID: 17257313
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The INS 5' variable number of tandem repeats is associated with IGF2 expression in humans.
    Paquette J; Giannoukakis N; Polychronakos C; Vafiadis P; Deal C
    J Biol Chem; 1998 Jun; 273(23):14158-64. PubMed ID: 9603916
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins.
    Scott HS; Heino M; Peterson P; Mittaz L; Lalioti MD; Betterle C; Cohen A; Seri M; Lerone M; Romeo G; Collin P; Salo M; Metcalfe R; Weetman A; Papasavvas MP; Rossier C; Nagamine K; Kudoh J; Shimizu N; Krohn KJ; Antonarakis SE
    Mol Endocrinol; 1998 Aug; 12(8):1112-9. PubMed ID: 9717837
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Insulin VNTR I/III genotype is associated with autoantibodies against glutamic acid decarboxylase in newly diagnosed type 1 diabetes.
    Rajasalu T; Haller K; Salur L; Kisand K; Tillmann V; Schlosser M; Uibo R
    Diabetes Metab Res Rev; 2007 Oct; 23(7):567-71. PubMed ID: 17461431
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A rare case of juvenile diabetes mellitus associated with APECED (autoimmune poly-endocrinopathy, candidiasis and ectodermal dystrophy) with strong X-linked familial inheritance].
    Iannello S; Campanile E; Cipolli D; Gallina M; Merola A; Puglisi S; Tabita V; Belfiore F
    Minerva Endocrinol; 1997 Jun; 22(2):51-9. PubMed ID: 9304048
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 5'-Insulin gene VNTR polymorphism is specific for type 1 diabetes: no association with celiac or Addison's disease.
    Pérez De Nanclares G; Bilbao JR; Calvo B; Vitoria JC; Vázquez F; Castaño L
    Ann N Y Acad Sci; 2003 Nov; 1005():319-23. PubMed ID: 14679083
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes: no evidence for association.
    Nithiyananthan R; Heward JM; Allahabadia A; Barnett AH; Franklyn JA; Gough SC
    J Clin Endocrinol Metab; 2000 Mar; 85(3):1320-2. PubMed ID: 10720083
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Autoimmune polyendocrinopathy--candidiasis--ectodermal dystrophy (APECED).
    Perheentupa J
    Horm Metab Res; 1996 Jul; 28(7):353-6. PubMed ID: 8858385
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
    Barratt BJ; Payne F; Lowe CE; Hermann R; Healy BC; Harold D; Concannon P; Gharani N; McCarthy MI; Olavesen MG; McCormack R; Guja C; Ionescu-Tîrgovişte C; Undlien DE; Rønningen KS; Gillespie KM; Tuomilehto-Wolf E; Tuomilehto J; Bennett ST; Clayton DG; Cordell HJ; Todd JA
    Diabetes; 2004 Jul; 53(7):1884-9. PubMed ID: 15220214
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Both polymorphic variable number of tandem repeats and autoimmune regulator modulate differential expression of insulin in human thymic epithelial cells.
    Cai CQ; Zhang T; Breslin MB; Giraud M; Lan MS
    Diabetes; 2011 Jan; 60(1):336-44. PubMed ID: 20876716
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Heterogeneity of class I INS VNTR allele association with insulin secretion in obese children.
    Le Fur S; Auffray C; Letourneur F; Cruaud C; Le Stunff C; Bougnères P
    Physiol Genomics; 2006 May; 25(3):480-4. PubMed ID: 16569775
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Screening for an AIRE-1 mutation in patients with Addison's disease, type 1 diabetes, Graves' disease and Hashimoto's thyroiditis as well as in APECED syndrome.
    Meyer G; Donner H; Herwig J; Böhles H; Usadel KH; Badenhoop K
    Clin Endocrinol (Oxf); 2001 Mar; 54(3):335-8. PubMed ID: 11298085
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.
    Cervato S; Mariniello B; Lazzarotto F; Morlin L; Zanchetta R; Radetti G; De Luca F; Valenzise M; Giordano R; Rizzo D; Giordano C; Betterle C
    Clin Endocrinol (Oxf); 2009 Mar; 70(3):421-8. PubMed ID: 18616706
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Insulin administration may trigger type 1 diabetes in Japanese type 2 diabetes patients with type 1 diabetes high-risk HLA class II and the insulin gene VNTR genotype.
    Nishida W; Nagata M; Imagawa A; Hanafusa T; Ohashi J; Takahashi K; Suehiro T; Yamada Y; Chujo D; Kawasaki E; Kawamura R; Onuma H; Osawa H; Makino H
    J Clin Endocrinol Metab; 2014 Sep; 99(9):E1793-7. PubMed ID: 24971665
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Anomalous behaviour of the 5' insulin gene polymorphism allele 814: lack of association with Type I diabetes in Basques. GEPV-N Group. Basque-Navarre Endocrinology and Paediatrics.
    Urrutia I; Calvo B; Bilbao JR; Castaño L
    Diabetologia; 1998 Sep; 41(9):1121-3. PubMed ID: 9754833
    [TBL] [Abstract][Full Text] [Related]  

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