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160 related items for PubMed ID: 27172236

  • 1. VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone.
    Usategui-Martín R, Calero-Paniagua I, García-Aparicio J, Corral-Gudino L, Del Pino Montes J, González Sarmiento R.
    Genet Test Mol Biomarkers; 2016 Jun; 20(6):335-7. PubMed ID: 27172236
    [Abstract] [Full Text] [Related]

  • 2. Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin.
    Daroszewska A, Hocking LJ, McGuigan FE, Langdahl B, Stone MD, Cundy T, Nicholson GC, Fraser WD, Ralston SH.
    J Bone Miner Res; 2004 Sep; 19(9):1506-11. PubMed ID: 15312251
    [Abstract] [Full Text] [Related]

  • 3. Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone.
    Usategui-Martín R, Gutiérrez-Cerrajero C, Jiménez-Vázquez S, Calero-Paniagua I, García-Aparicio J, Corral-Gudino L, Del Pino-Montes J, González-Sarmiento R.
    Bone; 2018 Jul; 112():19-23. PubMed ID: 29630930
    [Abstract] [Full Text] [Related]

  • 4. Pathogenesis of Paget's disease of bone.
    Ralston SH.
    Bone; 2008 Nov; 43(5):819-25. PubMed ID: 18672105
    [Abstract] [Full Text] [Related]

  • 5. Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.
    Vallet M, Soares DC, Wani S, Sophocleous A, Warner J, Salter DM, Ralston SH, Albagha OM.
    Hum Mol Genet; 2015 Jun 01; 24(11):3286-95. PubMed ID: 25701875
    [Abstract] [Full Text] [Related]

  • 6. Bone stromal cells in pagetic bone and Paget's sarcoma express RANKL and support human osteoclast formation.
    Sun SG, Lau YS, Itonaga I, Sabokbar A, Athanasou NA.
    J Pathol; 2006 May 01; 209(1):114-20. PubMed ID: 16482498
    [Abstract] [Full Text] [Related]

  • 7. Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of bone.
    Beyens G, Daroszewska A, de Freitas F, Fransen E, Vanhoenacker F, Verbruggen L, Zmierczak HG, Westhovens R, Van Offel J, Ralston SH, Devogelaer JP, Van Hul W.
    J Bone Miner Res; 2007 Jul 01; 22(7):1062-71. PubMed ID: 17388729
    [Abstract] [Full Text] [Related]

  • 8. Epigenetic analysis of Paget's disease of bone identifies differentially methylated loci that predict disease status.
    Diboun I, Wani S, Ralston SH, Albagha OM.
    Elife; 2021 Apr 30; 10():. PubMed ID: 33929316
    [Abstract] [Full Text] [Related]

  • 9. Paget's disease of bone: a disease of the osteoclast.
    Reddy SV, Kurihara N, Menaa C, Roodman GD.
    Rev Endocr Metab Disord; 2001 Apr 30; 2(2):195-201. PubMed ID: 11705325
    [Abstract] [Full Text] [Related]

  • 10. Etiology of Paget's disease and osteoclast abnormalities.
    Reddy SV.
    J Cell Biochem; 2004 Nov 01; 93(4):688-96. PubMed ID: 15389972
    [Abstract] [Full Text] [Related]

  • 11. Polymorphisms in autophagy genes are associated with paget disease of bone.
    Usategui-Martín R, García-Aparicio J, Corral-Gudino L, Calero-Paniagua I, Del Pino-Montes J, González Sarmiento R.
    PLoS One; 2015 Nov 01; 10(6):e0128984. PubMed ID: 26030385
    [Abstract] [Full Text] [Related]

  • 12. Molecular effect of an OPTN common variant associated to Paget's disease of bone.
    Silva IAL, Conceição N, Gagnon É, Brown JP, Cancela ML, Michou L.
    PLoS One; 2018 Nov 01; 13(5):e0197543. PubMed ID: 29782529
    [Abstract] [Full Text] [Related]

  • 13. VAV3 rs7528153 and VAV3-AS1 rs1185222 polymorphisms are associated with an increased risk of developing hypertension.
    Miramontes-González JP, Usategui-Martín R, Martín-Vallejo J, Ziegler M, de Isla LL, O Connor D, González-Sarmiento R.
    Eur J Intern Med; 2020 Oct 01; 80():60-65. PubMed ID: 32540412
    [Abstract] [Full Text] [Related]

  • 14. Proinflammatory cytokine gene polymorphisms and susceptibility to Paget's disease of bone: an association study.
    Gallone S, Di Stefano M, Fenoglio P, Rubino E, Criasia A, Pinessi L, Isaia G, Rainero I.
    Cytokine; 2011 Dec 01; 56(3):560-3. PubMed ID: 21917472
    [Abstract] [Full Text] [Related]

  • 15. A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype.
    Rea SL, Walsh JP, Ward L, Yip K, Ward BK, Kent GN, Steer JH, Xu J, Ratajczak T.
    J Bone Miner Res; 2006 Jul 01; 21(7):1136-45. PubMed ID: 16813535
    [Abstract] [Full Text] [Related]

  • 16. Effect of genetic variants of OPTN in the pathophysiology of Paget's disease of bone.
    Silva IAL, Conceição N, Gagnon É, Caiado H, Brown JP, Gianfrancesco F, Michou L, Cancela ML.
    Biochim Biophys Acta Mol Basis Dis; 2018 Jan 01; 1864(1):143-151. PubMed ID: 28993189
    [Abstract] [Full Text] [Related]

  • 17. Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.
    Lucas GJ, Mehta SG, Hocking LJ, Stewart TL, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Watts GD, Ralston SH, Kimonis VE.
    Bone; 2006 Feb 01; 38(2):280-5. PubMed ID: 16199218
    [Abstract] [Full Text] [Related]

  • 18. Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.
    Lucas GJ, Hocking LJ, Daroszewska A, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Meier C, Hooper MJ, Ralston SH.
    J Bone Miner Res; 2005 Feb 01; 20(2):227-31. PubMed ID: 15647816
    [Abstract] [Full Text] [Related]

  • 19. Development of a molecular test of Paget's disease of bone.
    Guay-Bélanger S, Simonyan D, Bureau A, Gagnon E, Albert C, Morissette J, Siris ES, Orcel P, Brown JP, Michou L.
    Bone; 2016 Mar 01; 84():213-221. PubMed ID: 26772620
    [Abstract] [Full Text] [Related]

  • 20. Protocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they were available?
    Langston AL, Johnston M, Robertson C, Campbell MK, Entwistle VA, Marteau TM, McCallum M, Ralston SH.
    BMC Health Serv Res; 2006 Jun 08; 6():71. PubMed ID: 16762063
    [Abstract] [Full Text] [Related]

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