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Journal Abstract Search

159 related items for PubMed ID: 21501964

  • 1. Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms.
    Chung PY, Beyens G, de Freitas F, Boonen S, Geusens P, Vanhoenacker F, Verbruggen L, Van Offel J, Goemaere S, Zmierczak HG, Westhovens R, Devogelaer JP, Van Hul W.
    Mol Genet Metab; 2011 Jul; 103(3):287-92. PubMed ID: 21501964
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  • 3. Paget's disease of bone: evidence for complex pathogenetic interactions.
    Chung PY, Van Hul W.
    Semin Arthritis Rheum; 2012 Apr; 41(5):619-41. PubMed ID: 21959292
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  • 4. The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes.
    Chung PY, Beyens G, Boonen S, Papapoulos S, Geusens P, Karperien M, Vanhoenacker F, Verbruggen L, Fransen E, Van Offel J, Goemaere S, Zmierczak HG, Westhovens R, Devogelaer JP, Van Hul W.
    Hum Genet; 2010 Dec; 128(6):615-26. PubMed ID: 20839008
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  • 9. Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.
    Chung PY, Beyens G, Riches PL, Van Wesenbeeck L, de Freitas F, Jennes K, Daroszewska A, Fransen E, Boonen S, Geusens P, Vanhoenacker F, Verbruggen L, Van Offel J, Goemaere S, Zmierczak HG, Westhovens R, Karperien M, Papapoulos S, Ralston SH, Devogelaer JP, Van Hul W.
    J Bone Miner Res; 2010 Dec; 25(12):2592-605. PubMed ID: 20564239
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  • 10. 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; 22(7):1062-71. PubMed ID: 17388729
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  • 12. 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; 20(2):227-31. PubMed ID: 15647816
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  • 13. Genetics of Paget's disease of bone.
    Ralston SH, Albagha OM.
    Curr Osteoporos Rep; 2014 Sep; 12(3):263-71. PubMed ID: 24988994
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  • 14. Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders.
    Lucas GJ, Daroszewska A, Ralston SH.
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P31-7. PubMed ID: 17229006
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  • 15. 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; 56(3):560-3. PubMed ID: 21917472
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  • 17. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
    Koppers M, van Blitterswijk MM, Vlam L, Rowicka PA, van Vught PW, Groen EJ, Spliet WG, Engelen-Lee J, Schelhaas HJ, de Visser M, van der Kooi AJ, van der Pol WL, Pasterkamp RJ, Veldink JH, van den Berg LH.
    Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
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  • 18. 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; 84():213-221. PubMed ID: 26772620
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  • 19. Pathogenesis of Paget's disease of bone.
    Ralston SH.
    Bone; 2008 Nov; 43(5):819-25. PubMed ID: 18672105
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  • 20. Genetics and aetiology of Pagetic disorders of bone.
    Helfrich MH, Hocking LJ.
    Arch Biochem Biophys; 2008 May 15; 473(2):172-82. PubMed ID: 18359282
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