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Results: 1 to 20 of 132

1.

Rescue of growth defects of yeast cdc48 mutants by pathogenic IBMPFD-VCPs.

Takata T, Kimura Y, Ohnuma Y, Kawawaki J, Kakiyama Y, Tanaka K, Kakizuka A.

J Struct Biol. 2012 Aug;179(2):93-103. doi: 10.1016/j.jsb.2012.06.005. Epub 2012 Jun 19.

PMID:
22728077
[PubMed - indexed for MEDLINE]
Free Article
2.

Different dynamic movements of wild-type and pathogenic VCPs and their cofactors to damaged mitochondria in a Parkin-mediated mitochondrial quality control system.

Kimura Y, Fukushi J, Hori S, Matsuda N, Okatsu K, Kakiyama Y, Kawawaki J, Kakizuka A, Tanaka K.

Genes Cells. 2013 Dec;18(12):1131-43. doi: 10.1111/gtc.12103. Epub 2013 Nov 12.

PMID:
24215292
[PubMed - indexed for MEDLINE]
3.

A unique IBMPFD-related P97/VCP mutation with differential binding pattern and subcellular localization.

Erzurumlu Y, Kose FA, Gozen O, Gozuacik D, Toth EA, Ballar P.

Int J Biochem Cell Biol. 2013 Apr;45(4):773-82. doi: 10.1016/j.biocel.2013.01.006. Epub 2013 Jan 16.

PMID:
23333620
[PubMed - indexed for MEDLINE]
4.

Pathogenic VCP/TER94 alleles are dominant actives and contribute to neurodegeneration by altering cellular ATP level in a Drosophila IBMPFD model.

Chang YC, Hung WT, Chang YC, Chang HC, Wu CL, Chiang AS, Jackson GR, Sang TK.

PLoS Genet. 2011 Feb 3;7(2):e1001288. doi: 10.1371/journal.pgen.1001288.

PMID:
21304887
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone.

Custer SK, Neumann M, Lu H, Wright AC, Taylor JP.

Hum Mol Genet. 2010 May 1;19(9):1741-55. doi: 10.1093/hmg/ddq050. Epub 2010 Feb 10.

PMID:
20147319
[PubMed - indexed for MEDLINE]
Free Article
6.

Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Manno A, Noguchi M, Fukushi J, Motohashi Y, Kakizuka A.

Genes Cells. 2010 Aug;15(8):911-22. doi: 10.1111/j.1365-2443.2010.01428.x. Epub 2010 Jul 5.

PMID:
20604808
[PubMed - indexed for MEDLINE]
7.

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease.

Ju JS, Fuentealba RA, Miller SE, Jackson E, Piwnica-Worms D, Baloh RH, Weihl CC.

J Cell Biol. 2009 Dec 14;187(6):875-88. doi: 10.1083/jcb.200908115.

PMID:
20008565
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.

Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ, Zhang ZL.

Bone. 2013 Jan;52(1):9-16. doi: 10.1016/j.bone.2012.09.012. Epub 2012 Sep 19.

PMID:
23000505
[PubMed - indexed for MEDLINE]
9.

Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation.

Weihl CC, Dalal S, Pestronk A, Hanson PI.

Hum Mol Genet. 2006 Jan 15;15(2):189-99. Epub 2005 Dec 1.

PMID:
16321991
[PubMed - indexed for MEDLINE]
Free Article
10.

Mechanisms of Cdc48/VCP-mediated cell death: from yeast apoptosis to human disease.

Braun RJ, Zischka H.

Biochim Biophys Acta. 2008 Jul;1783(7):1418-35. doi: 10.1016/j.bbamcr.2008.01.015. Epub 2008 Feb 2. Review.

PMID:
18284922
[PubMed - indexed for MEDLINE]
Free Article
11.

VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD.

Tresse E, Salomons FA, Vesa J, Bott LC, Kimonis V, Yao TP, Dantuma NP, Taylor JP.

Autophagy. 2010 Feb;6(2):217-27. Epub 2010 Feb 22.

PMID:
20104022
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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.

PMID:
20410287
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Proteomic analysis of a drosophila IBMPFD model reveals potential pathogenic mechanisms.

Chan HT, Lee TR, Huang SH, Lee HY, Sang TK, Chan HL, Lyu PC.

Mol Biosyst. 2012 Jun;8(6):1730-41. doi: 10.1039/c2mb25037c. Epub 2012 Apr 5.

PMID:
22481368
[PubMed - indexed for MEDLINE]
14.

Neuronal-specific overexpression of a mutant valosin-containing protein associated with IBMPFD promotes aberrant ubiquitin and TDP-43 accumulation and cognitive dysfunction in transgenic mice.

Rodriguez-Ortiz CJ, Hoshino H, Cheng D, Liu-Yescevitz L, Blurton-Jones M, Wolozin B, LaFerla FM, Kitazawa M.

Am J Pathol. 2013 Aug;183(2):504-15. doi: 10.1016/j.ajpath.2013.04.014. Epub 2013 Jun 5.

PMID:
23747512
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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.

PMID:
21781992
[PubMed - indexed for MEDLINE]
Free Article
16.

Hereditary inclusion body myopathy-linked p97/VCP mutations in the NH2 domain and the D1 ring modulate p97/VCP ATPase activity and D2 ring conformation.

Halawani D, LeBlanc AC, Rouiller I, Michnick SW, Servant MJ, Latterich M.

Mol Cell Biol. 2009 Aug;29(16):4484-94. doi: 10.1128/MCB.00252-09. Epub 2009 Jun 8.

PMID:
19506019
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.

Ritson GP, Custer SK, Freibaum BD, Guinto JB, Geffel D, Moore J, Tang W, Winton MJ, Neumann M, Trojanowski JQ, Lee VM, Forman MS, Taylor JP.

J Neurosci. 2010 Jun 2;30(22):7729-39. doi: 10.1523/JNEUROSCI.5894-09.2010.

PMID:
20519548
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.

Kimonis VE, Mehta SG, Fulchiero EC, Thomasova D, Pasquali M, Boycott K, Neilan EG, Kartashov A, Forman MS, Tucker S, Kimonis K, Mumm S, Whyte MP, Smith CD, Watts GD.

Am J Med Genet A. 2008 Mar 15;146A(6):745-57. doi: 10.1002/ajmg.a.31862.

PMID:
18260132
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Pathological consequences of VCP mutations on human striated muscle.

Hübbers CU, Clemen CS, Kesper K, Böddrich A, Hofmann A, Kämäräinen O, Tolksdorf K, Stumpf M, Reichelt J, Roth U, Krause S, Watts G, Kimonis V, Wattjes MP, Reimann J, Thal DR, Biermann K, Evert BO, Lochmüller H, Wanker EE, Schoser BG, Noegel AA, Schröder R.

Brain. 2007 Feb;130(Pt 2):381-93. Epub 2006 Sep 19.

PMID:
16984901
[PubMed - indexed for MEDLINE]
Free Article
20.

Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels.

Bartolome F, Wu HC, Burchell VS, Preza E, Wray S, Mahoney CJ, Fox NC, Calvo A, Canosa A, Moglia C, Mandrioli J, Chiò A, Orrell RW, Houlden H, Hardy J, Abramov AY, Plun-Favreau H.

Neuron. 2013 Apr 10;78(1):57-64. doi: 10.1016/j.neuron.2013.02.028. Epub 2013 Mar 14.

PMID:
23498975
[PubMed - indexed for MEDLINE]
Free PMC Article

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