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Journal Abstract Search

235 related items for PubMed ID: 25701875

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  • 4. Targeted Inactivation of Rin3 Increases Trabecular Bone Mass by Reducing Bone Resorption and Favouring Bone Formation.
    Vallet M, Sophocleous A, Törnqvist AE, Azfer A, Hof RV, Albagha OM, Ralston SH.
    Calcif Tissue Int; 2021 Jul; 109(1):92-102. PubMed ID: 33725152
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  • 6. Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
    Hocking LJ, Lucas GJ, Daroszewska A, Mangion J, Olavesen M, Cundy T, Nicholson GC, Ward L, Bennett ST, Wuyts W, Van Hul W, Ralston SH.
    Hum Mol Genet; 2002 Oct 15; 11(22):2735-9. PubMed ID: 12374763
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  • 7. Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene.
    Dessay M, Couture E, Maaroufi H, Fournier F, Gagnon E, Droit A, Brown JP, Michou L.
    BMC Med Genomics; 2022 Mar 03; 15(1):41. PubMed ID: 35241069
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  • 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
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  • 9. 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 30; 19(9):1506-11. PubMed ID: 15312251
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  • 10. 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 30; 1864(1):143-151. PubMed ID: 28993189
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  • 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 Jan 30; 13(5):e0197543. PubMed ID: 29782529
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  • 14. Genetic determinants of Paget's disease of bone.
    Ralston SH, Albagha OM.
    Ann N Y Acad Sci; 2011 Dec 30; 1240():53-60. PubMed ID: 22172040
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  • 17. 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 30; 75(2):144-52. PubMed ID: 15164150
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