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 *

81 related articles for article (PubMed ID: 16198163)

  • 1. Variation in femoral length is associated with polymorphisms in RUNX2 gene.
    Ermakov S; Malkin I; Kobyliansky E; Livshits G
    Bone; 2006 Feb; 38(2):199-205. PubMed ID: 16198163
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Promoter 2 -1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck bmd in Spanish postmenopausal women.
    Bustamante M; Nogués X; Agueda L; Jurado S; Wesselius A; Cáceres E; Carreras R; Ciria M; Mellibovsky L; Balcells S; Díez-Pérez A; Grinberg D
    Calcif Tissue Int; 2007 Oct; 81(4):327-32. PubMed ID: 17878995
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of a RUNX2 promoter polymorphism with bone mineral density in postmenopausal Korean women.
    Lee HJ; Koh JM; Hwang JY; Choi KY; Lee SH; Park EK; Kim TH; Han BG; Kim GS; Kim SY; Lee JY
    Calcif Tissue Int; 2009 Jun; 84(6):439-45. PubMed ID: 19424741
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic determinants of circulating levels of tumor necrosis factor receptor II and their association with TNF-RII gene polymorphisms.
    Vistoropsky Y; Ermakov S; Toliat MR; Trofimov S; Altmüller J; Malkin I; Nürnberg P; Livshits G
    Cytokine; 2010 Jul; 51(1):28-34. PubMed ID: 20488723
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family-based association analysis of S100A8 genetic polymorphisms with aggressive periodontitis.
    Ren XY; Xu L; Meng HX; Zhao HS; Lu RF; Chen ZB; Feng XH; Shi D; Zhang L; Tian Y
    J Periodontal Res; 2009 Apr; 44(2):184-92. PubMed ID: 19210342
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association between SNP and haplotypes in PPARGC1 and adiponectin genes and bone mineral density in Chinese nuclear families.
    Zhang ZL; He JW; Qin YJ; Hu YQ; Li M; Liu YJ; Zhang H; Hu WW
    Acta Pharmacol Sin; 2007 Feb; 28(2):287-95. PubMed ID: 17241533
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of the putative genetic factors and ANKH gene polymorphisms to variation of circulating calciotropic molecules, PTH and BGP.
    Vistoropsky Y; Keter M; Malkin I; Trofimov S; Kobyliansky E; Livshits G
    Hum Mol Genet; 2007 May; 16(10):1233-40. PubMed ID: 17403715
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of C1q polymorphisms suggests association with systemic lupus erythematosus, serum C1q and CH50 levels and disease severity.
    Martens HA; Zuurman MW; de Lange AH; Nolte IM; van der Steege G; Navis GJ; Kallenberg CG; Seelen MA; Bijl M
    Ann Rheum Dis; 2009 May; 68(5):715-20. PubMed ID: 18504288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
    Dickel DE; Veenstra-VanderWeele J; Cox NJ; Wu X; Fischer DJ; Van Etten-Lee M; Himle JA; Leventhal BL; Cook EH; Hanna GL
    Arch Gen Psychiatry; 2006 Jul; 63(7):778-85. PubMed ID: 16818867
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.
    Qiu XS; Tang NL; Yeung HY; Lee KM; Hung VW; Ng BK; Ma SL; Kwok RH; Qin L; Qiu Y; Cheng JC
    Spine (Phila Pa 1976); 2007 Jul; 32(16):1748-53. PubMed ID: 17632395
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.
    Dempfle A; Wudy SA; Saar K; Hagemann S; Friedel S; Scherag A; Berthold LD; Alzen G; Gortner L; Blum WF; Hinney A; Nürnberg P; Schäfer H; Hebebrand J
    Hum Mol Genet; 2006 Sep; 15(18):2772-83. PubMed ID: 16905557
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pedigree-based quantitative genetic analysis of interindividual variation in circulating levels of IGFBP-3.
    Pantsulaia I; Trofimov S; Kobyliansky E; Livshits G
    J Bone Miner Metab; 2002; 20(3):156-63. PubMed ID: 11984698
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS; Langefeld CD; Campbell JK; Haffner SM; Norris JM; Scherzinger AL; Wagenknecht LE; Bowden DW
    Int J Obes (Lond); 2006 Sep; 30(9):1433-41. PubMed ID: 16520807
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association between polymorphisms in tumor necrosis factor (TNF) and TNF receptor genes and circulating TNF, soluble TNF receptor levels, and bone mineral density in postmenopausal Korean women.
    Kim H; Chun S; Ku SY; Suh CS; Choi YM; Kim JG
    Menopause; 2009; 16(5):1014-20. PubMed ID: 19369902
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association between PPARalpha gene polymorphisms and myocardial infarction.
    Reinhard W; Stark K; Sedlacek K; Fischer M; Baessler A; Neureuther K; Weber S; Kaess B; Wiedmann S; Mitsching S; Lieb W; Erdmann J; Meisinger C; Doering A; Tolle R; Jeron A; Riegger G; Hengstenberg C
    Clin Sci (Lond); 2008 Nov; 115(10):301-8. PubMed ID: 18336366
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association study of the genetic polymorphisms of the transcription factor 7-like 2 (TCF7L2) gene and type 2 diabetes in the Chinese population.
    Chang YC; Chang TJ; Jiang YD; Kuo SS; Lee KC; Chiu KC; Chuang LM
    Diabetes; 2007 Oct; 56(10):2631-7. PubMed ID: 17579206
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic association between Notch4 polymorphisms and Japanese schizophrenics.
    Shibata N; Ohnuma T; Higashi S; Higashi M; Usui C; Ohkubo T; Watanabe T; Kitajima A; Ueki A; Nagao M; Arai H
    Psychiatr Genet; 2006 Apr; 16(2):77-9. PubMed ID: 16538185
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RUNX2 analysis of Danish cleidocranial dysplasia families.
    Hansen L; Riis AK; Silahtaroglu A; Hove H; Lauridsen E; Eiberg H; Kreiborg S
    Clin Genet; 2011 Mar; 79(3):254-63. PubMed ID: 20560987
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation.
    Lin J; Swan GE; Shields PG; Benowitz NL; Gu J; Amos CI; de Andrade M; Spitz MR; Wu X
    Cancer Epidemiol Biomarkers Prev; 2007 Oct; 16(10):2065-71. PubMed ID: 17932354
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.