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Items: 20

1.

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy.

Ju JS, Weihl CC.

Hum Mol Genet. 2010 Apr 15;19(R1):R38-45. doi: 10.1093/hmg/ddq157. Epub 2010 Apr 21. Review.

2.

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.

Weihl CC, Pestronk A, Kimonis VE.

Neuromuscul Disord. 2009 May;19(5):308-15. doi: 10.1016/j.nmd.2009.01.009. Epub 2009 Apr 19. Review.

3.

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.

Guinto JB, Ritson GP, Taylor JP, Forman MS.

Acta Neuropathol. 2007 Jul;114(1):55-61. Epub 2007 Apr 25. Review.

PMID:
17457594
4.

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.

Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.

J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. Review.

PMID:
21892620
5.

[Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].

Hayashi Y.

Rinsho Shinkeigaku. 2013;53(11):947-50. Review. Japanese.

PMID:
24291843
6.

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Fanganiello RD, Kimonis VE, CĂ´rte CC, Nitrini R, Passos-Bueno MR.

Braz J Med Biol Res. 2011 Apr;44(4):374-80. Epub 2011 Mar 11. Review.

9.

Recent advances in p97/VCP/Cdc48 cellular functions.

Yamanaka K, Sasagawa Y, Ogura T.

Biochim Biophys Acta. 2012 Jan;1823(1):130-7. doi: 10.1016/j.bbamcr.2011.07.001. Epub 2011 Jul 12. Review.

10.

Structural and functional deviations in disease-associated p97 mutants.

Tang WK, Xia D.

J Struct Biol. 2012 Aug;179(2):83-92. doi: 10.1016/j.jsb.2012.04.024. Epub 2012 May 8. Review.

11.

Create and preserve: proteostasis in development and aging is governed by Cdc48/p97/VCP.

Franz A, Ackermann L, Hoppe T.

Biochim Biophys Acta. 2014 Jan;1843(1):205-15. doi: 10.1016/j.bbamcr.2013.03.031. Epub 2013 Apr 10. Review.

12.

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.

Kimonis VE, Fulchiero E, Vesa J, Watts G.

Biochim Biophys Acta. 2008 Dec;1782(12):744-8. doi: 10.1016/j.bbadis.2008.09.003. Epub 2008 Sep 18. Review.

13.

Mechanisms of disease: genetics of Paget's disease of bone and related disorders.

Daroszewska A, Ralston SH.

Nat Clin Pract Rheumatol. 2006 May;2(5):270-7. Review.

PMID:
16932700
14.

Hereditary inclusion-body myopathies.

Broccolini A, Mirabella M.

Biochim Biophys Acta. 2015 Apr;1852(4):644-50. doi: 10.1016/j.bbadis.2014.08.007. Epub 2014 Aug 19. Review.

15.

ATP-bound form of the D1 AAA domain inhibits an essential function of Cdc48p/p97.

Esaki M, Ogura T.

Biochem Cell Biol. 2010 Feb;88(1):109-17. doi: 10.1139/o09-116. Review.

PMID:
20130684
16.

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system.

Meyer H, Bug M, Bremer S.

Nat Cell Biol. 2012 Feb 2;14(2):117-23. doi: 10.1038/ncb2407. Review.

PMID:
22298039
17.

A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation.

Shinjo SK, Oba-Shinjo SM, Lerario AM, Marie SKN.

Clin Rheumatol. 2017 Nov 10. doi: 10.1007/s10067-017-3913-1. [Epub ahead of print] Review.

PMID:
29127544
18.

The AAA+ ATPase p97, a cellular multitool.

Stach L, Freemont PS.

Biochem J. 2017 Aug 17;474(17):2953-2976. doi: 10.1042/BCJ20160783. Review.

19.

Strategic role of the ubiquitin-dependent segregase p97 (VCP or Cdc48) in DNA replication.

Ramadan K, Halder S, Wiseman K, Vaz B.

Chromosoma. 2017 Feb;126(1):17-32. doi: 10.1007/s00412-016-0587-4. Epub 2016 Apr 18. Review.

PMID:
27086594
20.

VCP/p97-Mediated Unfolding as a Principle in Protein Homeostasis and Signaling.

van den Boom J, Meyer H.

Mol Cell. 2018 Jan 18;69(2):182-194. doi: 10.1016/j.molcel.2017.10.028. Epub 2017 Nov 16. Review.

PMID:
29153394

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