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401 related items for PubMed ID: 19735829

  • 1. Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.
    Liu CP, Li XG, Lou JT, Xue Y, Luo CF, Zhou XW, Chen F, Li X, Li M, Li JC.
    J Pediatr Surg; 2009 Sep; 44(9):1805-11. PubMed ID: 19735829
    [Abstract] [Full Text] [Related]

  • 2. RET 3'UTR polymorphisms and its protective role in Hirschsprung disease in southeastern Chinese.
    Pan ZW, Luo CF, Liu ZJ, Li JC.
    J Pediatr Surg; 2012 Sep; 47(9):1699-705. PubMed ID: 22974609
    [Abstract] [Full Text] [Related]

  • 3. Association study of PHOX2B as a candidate gene for Hirschsprung's disease.
    Garcia-Barceló M, Sham MH, Lui VC, Chen BL, Ott J, Tam PK.
    Gut; 2003 Apr; 52(4):563-7. PubMed ID: 12631670
    [Abstract] [Full Text] [Related]

  • 4. Ancestral RET haplotype associated with Hirschsprung's disease shows linkage disequilibrium breakpoint at -1249.
    Fernandez RM, Boru G, Peciña A, Jones K, López-Alonso M, Antiñolo G, Borrego S, Eng C.
    J Med Genet; 2005 Apr; 42(4):322-7. PubMed ID: 15805159
    [Abstract] [Full Text] [Related]

  • 5. [Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease].
    Gao H, Zhang J, Wang W, Zhang Z, Huang Y, Zhang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):697-700. PubMed ID: 19065536
    [Abstract] [Full Text] [Related]

  • 6. Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung disease.
    Fernandez RM, Ruiz-Ferrer M, Lopez-Alonso M, Antiñolo G, Borrego S.
    J Pediatr Surg; 2008 Nov; 43(11):2042-7. PubMed ID: 18970938
    [Abstract] [Full Text] [Related]

  • 7. A new haplotype of PDCD1 is associated with rheumatoid arthritis in Hong Kong Chinese.
    Kong EK, Prokunina-Olsson L, Wong WH, Lau CS, Chan TM, Alarcón-Riquelme M, Lau YL.
    Arthritis Rheum; 2005 Apr; 52(4):1058-62. PubMed ID: 15818672
    [Abstract] [Full Text] [Related]

  • 8. Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan.
    Lin YC, Lai HS, Hsu WM, Lee PI, Chen HL, Chang MH.
    J Pediatr Gastroenterol Nutr; 2008 Jan; 46(1):36-40. PubMed ID: 18162831
    [Abstract] [Full Text] [Related]

  • 9. Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.
    Fitze G, Cramer J, Serra A, Schreiber M, Roesner D, Schackert HK.
    Eur J Pediatr Surg; 2003 Jun; 13(3):152-7. PubMed ID: 12939698
    [Abstract] [Full Text] [Related]

  • 10. A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
    Griseri P, Bachetti T, Puppo F, Lantieri F, Ravazzolo R, Devoto M, Ceccherini I.
    Hum Mutat; 2005 Feb; 25(2):189-95. PubMed ID: 15643606
    [Abstract] [Full Text] [Related]

  • 11. Analysis of functional SNP in ifng/ifngr1 in Chinese Han population with tuberculosis.
    He J, Wang J, Lei D, Ding S.
    Scand J Immunol; 2010 Jun; 71(6):452-8. PubMed ID: 20500698
    [Abstract] [Full Text] [Related]

  • 12. rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
    Glas J, Seiderer J, Pasciuto G, Tillack C, Diegelmann J, Pfennig S, Konrad A, Schmechel S, Wetzke M, Török HP, Stallhofer J, Jürgens M, Griga T, Klein W, Epplen JT, Schiemann U, Mussack T, Lohse P, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Mar; 104(3):665-72. PubMed ID: 19262523
    [Abstract] [Full Text] [Related]

  • 13. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
    Fitze G, Appelt H, König IR, Görgens H, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK.
    Hum Mol Genet; 2003 Dec 15; 12(24):3207-14. PubMed ID: 14600022
    [Abstract] [Full Text] [Related]

  • 14. Genetic variants in the promoter region of the ALOX5AP gene and susceptibility of ischemic stroke.
    Ji R, Jia J, Ma X, Wu J, Zhang Y, Xu L.
    Cerebrovasc Dis; 2011 Dec 15; 32(3):261-8. PubMed ID: 21893978
    [Abstract] [Full Text] [Related]

  • 15. Correlation between genetic variations in Hox clusters and Hirschsprung's disease.
    Garcia-Barceló MM, Miao X, Lui VC, So MT, Ngan ES, Leon TY, Lau DK, Liu TT, Lao X, Guo W, Holden WT, Moore J, Tam PK.
    Ann Hum Genet; 2007 Jul 15; 71(Pt 4):526-36. PubMed ID: 17274802
    [Abstract] [Full Text] [Related]

  • 16. The ITGB2 immunomodulatory gene (CD18), enterocolitis, and Hirschsprung's disease.
    Moore SW, Sidler D, Zaahl MG.
    J Pediatr Surg; 2008 Aug 15; 43(8):1439-44. PubMed ID: 18675632
    [Abstract] [Full Text] [Related]

  • 17. A coding polymorphism of the kallikrein 1 gene is associated with essential hypertension: a tagging SNP-based association study in a Chinese Han population.
    Zhao W, Wang L, Lu X, Yang W, Huang J, Chen S, Gu D.
    J Hypertens; 2007 Sep 15; 25(9):1821-7. PubMed ID: 17762646
    [Abstract] [Full Text] [Related]

  • 18. Association of DNA repair gene XRCC1 and lung cancer susceptibility among nonsmoking Chinese women.
    Yin J, Vogel U, Ma Y, Qi R, Wang H.
    Cancer Genet Cytogenet; 2009 Jan 01; 188(1):26-31. PubMed ID: 19061777
    [Abstract] [Full Text] [Related]

  • 19. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2009 Oct 01; 44(10):1899-903. PubMed ID: 19853744
    [Abstract] [Full Text] [Related]

  • 20. Association analysis of the SOX10 polymorphism with Hirschsprung disease in the Han Chinese population.
    Pan ZW, Lou J, Luo C, Yu L, Li JC.
    J Pediatr Surg; 2011 Oct 01; 46(10):1930-4. PubMed ID: 22008330
    [Abstract] [Full Text] [Related]

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