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    Results: 1 to 20 of 244

    1.

    Interaction and association analysis of a type 1 diabetes susceptibility locus on chromosome 5q11-q13 and the 7q32 chromosomal region in Scandinavian families.

    Holm P, Rydlander B, Luthman H, Kockum I; European Consortium for IDDM Genome Studies.

    Diabetes. 2004 Jun;53(6):1584-91.PMID: 15161765 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetes.

    Barat-Houari M, Clément K, Vatin V, Dina C, Bonhomme G, Vasseur F, Guy-Grand B, Froguel P.

    Diabetes. 2002 May;51(5):1640-3.PMID: 11978668 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Association and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos.

    Bugawan TL, Mirel DB, Valdes AM, Panelo A, Pozzilli P, Erlich HA.

    Am J Hum Genet. 2003 Jun;72(6):1505-14. Epub 2003 May 13.PMID: 12748907 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Hepatocyte nuclear factor-4alpha P2 promoter haplotypes are associated with type 2 diabetes in the Japanese population.

    Hara K, Horikoshi M, Kitazato H, Ito C, Noda M, Ohashi J, Froguel P, Tokunaga K, Tobe K, Nagai R, Kadowaki T.

    Diabetes. 2006 May;55(5):1260-4.PMID: 16644680 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

    Br J Dermatol. 2005 Jan;152(1):29-36.PMID: 15656797 [PubMed - indexed for MEDLINE]Related articles

    6.

    Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population.

    Nilsson-Ardnor S, Wiklund PG, Lindgren P, Nilsson AK, Janunger T, Escher SA, Hallbeck B, Stegmayr B, Asplund K, Holmberg D.

    Stroke. 2005 Aug;36(8):1666-71. Epub 2005 Jul 14.PMID: 16020760 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32.

    Miller NH, Marosy B, Justice CM, Novak SM, Tang EY, Boyce P, Pettengil J, Doheny KF, Pugh EW, Wilson AF.

    Am J Med Genet A. 2006 May 15;140(10):1059-68.PMID: 16596674 [PubMed - indexed for MEDLINE]Related articles

    8.

    Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma.

    Malerba G, Lindgren CM, Xumerle L, Kiviluoma P, Trabetti E, Laitinen T, Galavotti R, Pescollderungg L, Boner AL, Kere J, Pignatti PF.

    Clin Exp Allergy. 2007 Jan;37(1):83-9.PMID: 17210045 [PubMed - indexed for MEDLINE]Related articles

    9.

    CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.

    Gragnoli C.

    J Cell Physiol. 2008 Nov;217(2):291-5.PMID: 18680108 [PubMed - indexed for MEDLINE]Related articles

    10.

    The TAF5L gene on chromosome 1q42 is associated with type 1 diabetes in Russian affected patients.

    Chistiakov DA, Chernisheva A, Savost'anov KV, Turakulov RI, Kuraeva TL, Dedov II, Nosikov VV.

    Autoimmunity. 2005 Jun;38(4):283-93.PMID: 16206511 [PubMed - indexed for MEDLINE]Related articles

    11.

    Fine mapping of a region on chromosome 21q21.11-q22.3 showing linkage to type 1 diabetes.

    Bergholdt R, Nerup J, Pociot F.

    J Med Genet. 2005 Jan;42(1):17-25.PMID: 15635070 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

    Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

    BMC Med Genet. 2007 Dec 6;8:74.PMID: 18053270 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.

    Kim JW, Lee YS, Cho EY, Jang YL, Park DY, Choi KS, Jeun HO, Cho SH, Jang SY, Hong KS.

    Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):281-6.PMID: 16526041 [PubMed - indexed for MEDLINE]Related articles

    15.

    Localization of a type I diabetes susceptibility locus to the variable tandem repeat region flanking the insulin gene.

    Owerbach D, Gabbay KH.

    Diabetes. 1993 Dec;42(12):1708-14.PMID: 8243816 [PubMed - indexed for MEDLINE]Related articles

    16.

    Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

    McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.

    Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12.PMID: 15108191 [PubMed - indexed for MEDLINE]Related articles

    17.

    Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity.

    Biason-Lauber A, Boehm B, Lang-Muritano M, Gauthier BR, Brun T, Wollheim CB, Schoenle EJ.

    Diabetologia. 2005 May;48(5):900-5. Epub 2005 Apr 15.PMID: 15834548 [PubMed - indexed for MEDLINE]Related articles

    18.

    Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8.

    Sale MM, FitzGerald LM, Charlesworth JC, Bowden DW, Rich SS.

    Diabetes. 2002 Dec;51 Suppl 3:S316-9.PMID: 12475769 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

    Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, Fingerlin TE, Dhanjal SK, Valle TT, Bergman RN, Tuomilehto J, Watanabe RM, Boehnke M, Collins FS.

    Diabetes. 2004 Apr;53(4):1141-9.PMID: 15047633 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

    Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP.

    Psychiatr Genet. 2002 Mar;12(1):35-41.PMID: 11901358 [PubMed - indexed for MEDLINE]Related articles

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