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Journal Abstract Search

190 related items for PubMed ID: 15365659

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  • 24. New insights into the role of sequestosome 1/p62 mutant proteins in the pathogenesis of Paget's disease of bone.
    Rea SL, Walsh JP, Layfield R, Ratajczak T, Xu J.
    Endocr Rev; 2013 Aug; 34(4):501-24. PubMed ID: 23612225
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  • 26. 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; 38(2):280-5. PubMed ID: 16199218
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  • 27. Mutant p62/SQSTM1 UBA domains linked to Paget's disease of bone differ in their abilities to function as stabilization signals.
    Heinen C, Garner TP, Long J, Böttcher C, Ralston SH, Cavey JR, Searle MS, Layfield R, Dantuma NP.
    FEBS Lett; 2010 Apr 16; 584(8):1585-90. PubMed ID: 20230821
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  • 28. The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone.
    Wright T, Rea SL, Goode A, Bennett AJ, Ratajczak T, Long JE, Searle MS, Goldring CE, Park BK, Copple IM, Layfield R.
    Bone; 2013 Feb 16; 52(2):699-706. PubMed ID: 23117207
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  • 29. Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States.
    Rhodes EC, Johnson-Pais TL, Singer FR, Ankerst DP, Bruder JM, Wisdom J, Hoon DS, Lin E, Bone HG, Simcic KJ, Leach RJ.
    Calcif Tissue Int; 2008 Apr 16; 82(4):271-7. PubMed ID: 18379713
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  • 30. Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations.
    Bolland MJ, Tong PC, Naot D, Callon KE, Wattie DJ, Gamble GD, Cundy T.
    J Bone Miner Res; 2007 Mar 16; 22(3):411-5. PubMed ID: 17181397
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  • 31. Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations.
    Eekhoff EW, Karperien M, Houtsma D, Zwinderman AH, Dragoiescu C, Kneppers AL, Papapoulos SE.
    Arthritis Rheum; 2004 May 16; 50(5):1650-4. PubMed ID: 15146436
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  • 32. 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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  • 33. Absence of somatic SQSTM1 mutations in Paget's disease of bone.
    Matthews BG, Naot D, Bava U, Callon KE, Pitto RP, McCowan SA, Wattie D, Cundy T, Cornish J, Reid IR.
    J Clin Endocrinol Metab; 2009 Feb 16; 94(2):691-4. PubMed ID: 18984666
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  • 34. Etiologic factors in Paget's disease of bone.
    Reddy SV.
    Cell Mol Life Sci; 2006 Feb 16; 63(4):391-8. PubMed ID: 16429324
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  • 35. Novel SQSTM1 mutations in patients with Paget's disease of bone in an unrelated multiethnic American population.
    Michou L, Morissette J, Gagnon ER, Marquis A, Dellabadia M, Brown JP, Siris ES.
    Bone; 2011 Mar 01; 48(3):456-60. PubMed ID: 21073987
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  • 40. Genetics of Paget's disease of bone.
    Daroszewska A, Ralston SH.
    Clin Sci (Lond); 2005 Sep 01; 109(3):257-63. PubMed ID: 16104845
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