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Journal Abstract Search

249 related items for PubMed ID: 15765181

  • 1. Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations.
    Cavey JR, Ralston SH, Hocking LJ, Sheppard PW, Ciani B, Searle MS, Layfield R.
    J Bone Miner Res; 2005 Apr; 20(4):619-24. PubMed ID: 15765181
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  • 2. Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of bone.
    Cavey JR, Ralston SH, Sheppard PW, Ciani B, Gallagher TR, Long JE, Searle MS, Layfield R.
    Calcif Tissue Int; 2006 May; 78(5):271-7. PubMed ID: 16691492
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  • 4. Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of bone.
    Layfield R, Ciani B, Ralston SH, Hocking LJ, Sheppard PW, Searle MS, Cavey JR.
    Biochem Soc Trans; 2004 Nov; 32(Pt 5):728-30. PubMed ID: 15493999
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  • 5. 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; 21(7):1136-45. PubMed ID: 16813535
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  • 8. Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations.
    Collet C, Michou L, Audran M, Chasseigneaux S, Hilliquin P, Bardin T, Lemaire I, Cornélis F, Launay JM, Orcel P, Laplanche JL.
    J Bone Miner Res; 2007 Feb; 22(2):310-7. PubMed ID: 17129171
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  • 9. p62 mutations, ubiquitin recognition and Paget's disease of bone.
    Layfield R, Cavey JR, Najat D, Long J, Sheppard PW, Ralston SH, Searle MS.
    Biochem Soc Trans; 2006 Nov; 34(Pt 5):735-7. PubMed ID: 17052185
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  • 10. Structure of the ubiquitin-associated domain of p62 (SQSTM1) and implications for mutations that cause Paget's disease of bone.
    Ciani B, Layfield R, Cavey JR, Sheppard PW, Searle MS.
    J Biol Chem; 2003 Sep 26; 278(39):37409-12. PubMed ID: 12857745
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  • 12. Genetic epidemiology of Paget's disease of bone in italy: sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone.
    Falchetti A, Di Stefano M, Marini F, Ortolani S, Ulivieri MF, Bergui S, Masi L, Cepollaro C, Benucci M, Di Munno O, Rossini M, Adami S, Del Puente A, Isaia G, Torricelli F, Brandi ML, GenePage Project.
    Calcif Tissue Int; 2009 Jan 26; 84(1):20-37. PubMed ID: 19067022
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  • 13. Three novel mutations in SQSTM1 identified in familial Paget's disease of bone.
    Johnson-Pais TL, Wisdom JH, Weldon KS, Cody JD, Hansen MF, Singer FR, Leach RJ.
    J Bone Miner Res; 2003 Oct 26; 18(10):1748-53. PubMed ID: 14584883
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  • 17. Characterization of a non-UBA domain missense mutation of sequestosome 1 (SQSTM1) in Paget's disease of bone.
    Najat D, Garner T, Hagen T, Shaw B, Sheppard PW, Falchetti A, Marini F, Brandi ML, Long JE, Cavey JR, Searle MS, Layfield R.
    J Bone Miner Res; 2009 Apr 26; 24(4):632-42. PubMed ID: 19049332
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