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    Results: 1 to 20 of 109

    1.

    Intermediate expansions of a GAA repeat in the frataxin gene are not associated with type 2 diabetes or altered glucose-induced beta-cell function in Danish Caucasians.

    Dalgaard LT, Hansen T, Urhammer SA, Clausen JO, Eiberg H, Pedersen O.

    Diabetes. 1999 Apr;48(4):914-7.PMID: 10102712 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Altered beta-cell characteristics in impaired glucose tolerant carriers of a GAA trinucleotide repeat polymorphism in the frataxin gene.

    t Hart LM, Ruige JB, Dekker JM, Stehouwer CD, Maassen JA, Heine RJ.

    Diabetes. 1999 Apr;48(4):924-6. Erratum in: Diabetes 1999 Jul;48(7):1493. PMID: 10102715 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia.

    Bit-Avragim N, Perrot A, Schöls L, Hardt C, Kreuz FR, Zühlke C, Bubel S, Laccone F, Vogel HP, Dietz R, Osterziel KJ.

    J Mol Med. 2001;78(11):626-32.PMID: 11269509 [PubMed - indexed for MEDLINE]Related articles

    4.

    The K121Q variant of the human PC-1 gene is not associated with insulin resistance or type 2 diabetes among Danish Caucasians.

    Rasmussen SK, Urhammer SA, Pizzuti A, Echwald SM, Ekstrøm CT, Hansen L, Hansen T, Borch-Johnsen K, Frittitta L, Trischitta V, Pedersen O.

    Diabetes. 2000 Sep;49(9):1608-11.PMID: 10969849 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    The effect of two frequent amino acid variants of the hepatocyte nuclear factor-1alpha gene on estimates of the pancreatic beta-cell function in Caucasian glucose-tolerant first-degree relatives of type 2 diabetic patients.

    Urhammer SA, Møller AM, Nyholm B, Ekstrøm CT, Eiberg H, Clausen JO, Hansen T, Pedersen O, Schmitz O.

    J Clin Endocrinol Metab. 1998 Nov;83(11):3992-5.PMID: 9814481 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humans.

    Hebinck J, Hardt C, Schöls L, Vorgerd M, Briedigkeit L, Kahn CR, Ristow M.

    Diabetes. 2000 Sep;49(9):1604-7.PMID: 10969848 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene.

    Ristow M, Giannakidou E, Hebinck J, Busch K, Vorgerd M, Kotzka J, Knebel B, Mueller-Berghaus J, Epplen C, Pfeiffer A, Kahn CR, Doria A, Krone W, Mueller-Wieland D.

    Diabetes. 1998 May;47(5):851-4.PMID: 9588463 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Genetic variability of the SUR1 promoter in relation to beta-cell function and Type II diabetes mellitus.

    Hansen T, Ambye L, Grarup N, Hansen L, Echwald SM, Ferrer J, Pedersen O.

    Diabetologia. 2001 Oct;44(10):1330-4.PMID: 11692183 [PubMed - indexed for MEDLINE]Related articles

    9.

    Studies of the variability of the hepatocyte nuclear factor-1beta (HNF-1beta / TCF2) and the dimerization cofactor of HNF-1 (DcoH / PCBD) genes in relation to type 2 diabetes mellitus and beta-cell function.

    Ek J, Grarup N, Urhammer SA, Gaede PH, Drivsholm T, Borch-Johnsen K, Hansen T, Pedersen O.

    Hum Mutat. 2001 Oct;18(4):356-7.PMID: 11668623 [PubMed - indexed for MEDLINE]Related articles

    10.

    Identification of a common amino acid polymorphism in the p85alpha regulatory subunit of phosphatidylinositol 3-kinase: effects on glucose disappearance constant, glucose effectiveness, and the insulin sensitivity index.

    Hansen T, Andersen CB, Echwald SM, Urhammer SA, Clausen JO, Vestergaard H, Owens D, Hansen L, Pedersen O.

    Diabetes. 1997 Mar;46(3):494-501.PMID: 9032108 [PubMed - indexed for MEDLINE]Related articles

    11.

    Friedreich's ataxia and frataxin: molecular genetics, evolution and pathogenesis (Review).

    Palau F.

    Int J Mol Med. 2001 Jun;7(6):581-9. Review.PMID: 11351269 [PubMed - indexed for MEDLINE]Related articles

    12.

    Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxia.

    McDaniel DO, Keats B, Vedanarayanan VV, Subramony SH.

    Mov Disord. 2001 Nov;16(6):1153-8.PMID: 11748752 [PubMed - indexed for MEDLINE]Related articles

    13.

    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. Epub 2004 May 29.PMID: 15170498 [PubMed - indexed for MEDLINE]Related articles

    14.

    Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

    De Michele G, Cavalcanti F, Criscuolo C, Pianese L, Monticelli A, Filla A, Cocozza S.

    Hum Mol Genet. 1998 Nov;7(12):1901-6.PMID: 9811933 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    The FOXC2 -512C>T variant is associated with hypertriglyceridaemia and increased serum C-peptide in Danish Caucasian glucose-tolerant subjects.

    Yanagisawa K, Hingstrup Larsen L, Andersen G, Drivsholm T, Cederberg A, Westergren R, Borch-Johnsen K, Pedersen O, Enerbäck S, Hansen T.

    Diabetologia. 2003 Nov;46(11):1576-80. Epub 2003 Oct 7.PMID: 14530861 [PubMed - indexed for MEDLINE]Related articles

    16.

    Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.

    Rasmussen SK, Urhammer SA, Berglund L, Jensen JN, Hansen L, Echwald SM, Borch-Johnsen K, Horikawa Y, Mashima H, Lithell H, Cox NJ, Hansen T, Bell GI, Pedersen O.

    Diabetes. 2002 Dec;51(12):3561-7.PMID: 12453914 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Polymorphisms in the neurogenin 3 gene (NEUROG) and their relation to altered insulin secretion and diabetes in the Danish Caucasian population.

    Jensen JN, Hansen L, Ekstrøm CT, Pociot F, Nerup J, Hansen T, Pedersen O.

    Diabetologia. 2001 Jan;44(1):123-6.PMID: 11206403 [PubMed - indexed for MEDLINE]Related articles

    18.

    Intermediate expansions of a X25/frataxin gene GAA repeat and type II diabetes: assessment using parent-offspring trios.

    Lynn S, Hattersley AT, McCarthy MI, Frayling TM, Turnbull DM, Walker M.

    Diabetologia. 2000 Mar;43(3):384-5. No abstract available. PMID: 10768101 [PubMed - indexed for MEDLINE]Related articles

    19.

    Studies of variability in the PTEN gene among Danish caucasian patients with Type II diabetes mellitus.

    Hansen L, Jensen JN, Ekstrøm CT, Vestergaard H, Hansen T, Pedersen O.

    Diabetologia. 2001 Feb;44(2):237-40.PMID: 11270682 [PubMed - indexed for MEDLINE]Related articles

    20.

    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.PMID: 10491763 [PubMed - indexed for MEDLINE]Related articles

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