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Journal Abstract Search

190 related items for PubMed ID: 15365659

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  • 2. Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences.
    Hocking LJ, Lucas GJ, Daroszewska A, Cundy T, Nicholson GC, Donath J, Walsh JP, Finlayson C, Cavey JR, Ciani B, Sheppard PW, Searle MS, Layfield R, Ralston SH.
    J Bone Miner Res; 2004 Jul; 19(7):1122-7. PubMed ID: 15176995
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  • 4. 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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  • 5. 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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  • 6. 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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  • 7. 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; 18(10):1748-53. PubMed ID: 14584883
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  • 9. 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; 24(4):632-42. PubMed ID: 19049332
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  • 14. 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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  • 16. Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family.
    Falchetti A, Di Stefano M, Marini F, Del Monte F, Gozzini A, Masi L, Tanini A, Amedei A, Carossino A, Isaia G, Brandi ML.
    Arthritis Res Ther; 2005 Sep 26; 7(6):R1289-95. PubMed ID: 16277682
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  • 18. 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 26; 21(7):1136-45. PubMed ID: 16813535
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  • 19. Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American family.
    Beyens G, Wuyts W, Cleiren E, de Freitas F, Tiegs R, Van Hul W.
    Calcif Tissue Int; 2006 Nov 26; 79(5):281-8. PubMed ID: 17120186
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  • 20. Impact of p62/SQSTM1 UBA domain mutations linked to Paget's disease of bone on ubiquitin recognition.
    Garner TP, Long J, Layfield R, Searle MS.
    Biochemistry; 2011 May 31; 50(21):4665-74. PubMed ID: 21517082
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