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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. Hocking LJ, et al. Among authors: sheppard pw. J Bone Miner Res. 2004 Jul;19(7):1122-7. doi: 10.1359/JBMR.0403015. Epub 2004 Mar 22. J Bone Miner Res. 2004. PMID: 15176995 Free article.
p62 mutations, ubiquitin recognition and Paget's disease of bone.
Layfield R, Cavey JR, Najat D, Long J, Sheppard PW, Ralston SH, Searle MS. Layfield R, et al. Among authors: sheppard pw. Biochem Soc Trans. 2006 Nov;34(Pt 5):735-7. doi: 10.1042/BST0340735. Biochem Soc Trans. 2006. PMID: 17052185
Depletion of 26S proteasomes in mouse brain neurons causes neurodegeneration and Lewy-like inclusions resembling human pale bodies.
Bedford L, Hay D, Devoy A, Paine S, Powe DG, Seth R, Gray T, Topham I, Fone K, Rezvani N, Mee M, Soane T, Layfield R, Sheppard PW, Ebendal T, Usoskin D, Lowe J, Mayer RJ. Bedford L, et al. Among authors: sheppard pw. J Neurosci. 2008 Aug 13;28(33):8189-98. doi: 10.1523/JNEUROSCI.2218-08.2008. J Neurosci. 2008. PMID: 18701681 Free PMC article.
33 results