BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 18312624)

  • 1. Evaluating the association of common PBX1 variants with type 2 diabetes.
    Duesing K; Charpentier G; Marre M; Tichet J; Hercberg S; Balkau B; Froguel P; Gibson F
    BMC Med Genet; 2008 Feb; 9():14. PubMed ID: 18312624
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluating the association of common APOA2 variants with type 2 diabetes.
    Duesing K; Charpentier G; Marre M; Tichet J; Hercberg S; Balkau B; Froguel P; Gibson F
    BMC Med Genet; 2009 Feb; 10():13. PubMed ID: 19216768
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of PBX1 as a candidate gene for type 2 diabetes mellitus in Pima Indians.
    Thameem F; Wolford JK; Bogardus C; Prochazka M
    Biochim Biophys Acta; 2001 Mar; 1518(1-2):215-20. PubMed ID: 11267683
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of sequence variants in the pre-B cell leukemia transcription factor 1 gene: a positional and functional candidate for type 2 diabetes and impaired insulin secretion.
    Wang H; Chu W; Wang X; Zhang Z; Elbein SC
    Mol Genet Metab; 2005 Nov; 86(3):384-91. PubMed ID: 16140554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation.
    Cheung CL; Chan BY; Chan V; Ikegawa S; Kou I; Ngai H; Smith D; Luk KD; Huang QY; Mori S; Sham PC; Kung AW
    Hum Mol Genet; 2009 Feb; 18(4):679-87. PubMed ID: 19064610
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q.
    Prokopenko I; Zeggini E; Hanson RL; Mitchell BD; Rayner NW; Akan P; Baier L; Das SK; Elliott KS; Fu M; Frayling TM; Groves CJ; Gwilliam R; Scott LJ; Voight BF; Hattersley AT; Hu C; Morris AD; Ng M; Palmer CN; Tello-Ruiz M; Vaxillaire M; Wang CR; Stein L; Chan J; Jia W; Froguel P; Elbein SC; Deloukas P; Bogardus C; Shuldiner AR; McCarthy MI;
    Diabetes; 2009 Jul; 58(7):1704-9. PubMed ID: 19389826
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
    Ma W; Li Y; Wang M; Li H; Su T; Li Y; Wang S
    PLoS One; 2015; 10(6):e0130202. PubMed ID: 26075712
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of common polymorphisms in the HNF4alpha promoter on susceptibility to type 2 diabetes in the French Caucasian population.
    Vaxillaire M; Dina C; Lobbens S; Dechaume A; Vasseur-Delannoy V; Helbecque N; Charpentier G; Froguel P
    Diabetologia; 2005 Mar; 48(3):440-4. PubMed ID: 15735892
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids.
    Duesing K; Charpentier G; Marre M; Tichet J; Hercberg S; Froguel P; Gibson F
    Diabetologia; 2008 Jan; 51(1):76-81. PubMed ID: 17994215
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Strong association of common variants in the CDKN2A/CDKN2B region with type 2 diabetes in French Europids.
    Duesing K; Fatemifar G; Charpentier G; Marre M; Tichet J; Hercberg S; Balkau B; Froguel P; Gibson F
    Diabetologia; 2008 May; 51(5):821-6. PubMed ID: 18368387
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population.
    Cheyssac C; Lecoeur C; Dechaume A; Bibi A; Charpentier G; Balkau B; Marre M; Froguel P; Gibson F; Vaxillaire M
    BMC Med Genet; 2006 May; 7():44. PubMed ID: 16677372
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
    Ng MC; Miyake K; So WY; Poon EW; Lam VK; Li JK; Cox NJ; Bell GI; Chan JC
    Diabetologia; 2005 Oct; 48(10):2018-24. PubMed ID: 16132950
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case-control analysis of common variants in GIP with type 2 diabetes and related biochemical parameters in a South Indian population.
    Sugunan D; Nair AK; Kumar H; Gopalakrishnapillai A
    BMC Med Genet; 2010 Jul; 11():118. PubMed ID: 20673334
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
    Palmer ND; Hester JM; An SS; Adeyemo A; Rotimi C; Langefeld CD; Freedman BI; Ng MC; Bowden DW
    Diabetes; 2011 Feb; 60(2):662-8. PubMed ID: 20980453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.
    Vionnet N; Hani EH; Dupont S; Gallina S; Francke S; Dotte S; De Matos F; Durand E; Leprêtre F; Lecoeur C; Gallina P; Zekiri L; Dina C; Froguel P
    Am J Hum Genet; 2000 Dec; 67(6):1470-80. PubMed ID: 11067779
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association analysis of variation in/near FTO, CDKAL1, SLC30A8, HHEX, EXT2, IGF2BP2, LOC387761, and CDKN2B with type 2 diabetes and related quantitative traits in Pima Indians.
    Rong R; Hanson RL; Ortiz D; Wiedrich C; Kobes S; Knowler WC; Bogardus C; Baier LJ
    Diabetes; 2009 Feb; 58(2):478-88. PubMed ID: 19008344
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic variants of IDE-KIF11-HHEX at 10q23.33 associated with type 2 diabetes risk: a fine-mapping study in Chinese population.
    Qian Y; Lu F; Dong M; Lin Y; Li H; Chen J; Shen C; Jin G; Hu Z; Shen H
    PLoS One; 2012; 7(4):e35060. PubMed ID: 22506066
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.
    Siddiq A; Lepretre F; Hercberg S; Froguel P; Gibson F
    Diabetes; 2005 Aug; 54(8):2477-81. PubMed ID: 16046317
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Allelic expression imbalance screening of genes in chromosome 1q21-24 region to identify functional variants for Type 2 diabetes susceptibility.
    Mondal AK; Sharma NK; Elbein SC; Das SK
    Physiol Genomics; 2013 Jul; 45(13):509-20. PubMed ID: 23673729
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans.
    Cooke JN; Ng MC; Palmer ND; An SS; Hester JM; Freedman BI; Langefeld CD; Bowden DW
    Diabetes Care; 2012 Feb; 35(2):287-92. PubMed ID: 22275441
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.