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Journal Abstract Search

228 related items for PubMed ID: 20839008

  • 1. 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. 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; 1864(1):143-151. PubMed ID: 28993189
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  • 11. 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 Jan; 13(5):e0197543. PubMed ID: 29782529
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  • 12. Polymorphisms of CSF1 and TM7SF4 genes in a case of mild juvenile Paget's disease found using next-generation sequencing.
    Donáth J, Speer G, Kósa JP, Árvai K, Balla B, Juhász P, Lakatos P, Poór G.
    Croat Med J; 2015 Apr; 56(2):145-51. PubMed ID: 25891874
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  • 13. Effect of a rare genetic variant of TM7SF4 gene on osteoclasts of patients with Paget's disease of bone.
    Laurier E, Amiable N, Gagnon E, Brown JP, Michou L.
    BMC Med Genet; 2017 Nov 16; 18(1):133. PubMed ID: 29145829
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  • 16. Mechanisms of disease: genetics of Paget's disease of bone and related disorders.
    Daroszewska A, Ralston SH.
    Nat Clin Pract Rheumatol; 2006 May 16; 2(5):270-7. PubMed ID: 16932700
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  • 17. Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27).
    Saito-Hakoda A, Kikuchi A, Takahashi T, Yokoyama Y, Himori N, Adachi M, Ikeda R, Nomura Y, Takayama J, Kawashima J, Katsuoka F, Fujishima F, Yamaguchi T, Ito A, Hanita T, Kanno J, Aizawa T, Nakazawa T, Kawase T, Tamiya G, Yamamoto M, Fujiwara I, Kure S.
    J Bone Miner Metab; 2023 Mar 16; 41(2):193-202. PubMed ID: 36520195
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  • 18. Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease.
    Beyens G, Van Hul E, Van Driessche K, Fransen E, Devogelaer JP, Vanhoenacker F, Van Offel J, Verbruggen L, De Clerck L, Westhovens R, Van Hul W.
    Calcif Tissue Int; 2004 Aug 16; 75(2):144-52. PubMed ID: 15164150
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  • 19. 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 16; 22(7):1062-71. PubMed ID: 17388729
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  • 20. 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 16; 19(9):1506-11. PubMed ID: 15312251
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