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2. Functional ATPase activity of p97/valosin-containing protein (VCP) is required for the quality control of endoplasmic reticulum in neuronally differentiated mammalian PC12 cells. Kobayashi T; Tanaka K; Inoue K; Kakizuka A J Biol Chem; 2002 Dec; 277(49):47358-65. PubMed ID: 12351637 [TBL] [Abstract][Full Text] [Related]
3. 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; 7(2):e1001288. PubMed ID: 21304887 [TBL] [Abstract][Full Text] [Related]
5. ATPase activity of p97/valosin-containing protein is regulated by oxidative modification of the evolutionally conserved cysteine 522 residue in Walker A motif. Noguchi M; Takata T; Kimura Y; Manno A; Murakami K; Koike M; Ohizumi H; Hori S; Kakizuka A J Biol Chem; 2005 Dec; 280(50):41332-41. PubMed ID: 16234241 [TBL] [Abstract][Full Text] [Related]
7. Pathogenic Mutations in the Valosin-containing Protein/p97(VCP) N-domain Inhibit the SUMOylation of VCP and Lead to Impaired Stress Response. Wang T; Xu W; Qin M; Yang Y; Bao P; Shen F; Zhang Z; Xu J J Biol Chem; 2016 Jul; 291(27):14373-14384. PubMed ID: 27226613 [TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 20104022 [TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 19506019 [TBL] [Abstract][Full Text] [Related]
11. Complex of Fas-associated factor 1 (FAF1) with valosin-containing protein (VCP)-Npl4-Ufd1 and polyubiquitinated proteins promotes endoplasmic reticulum-associated degradation (ERAD). Lee JJ; Park JK; Jeong J; Jeon H; Yoon JB; Kim EE; Lee KJ J Biol Chem; 2013 Mar; 288(10):6998-7011. PubMed ID: 23293021 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 23747512 [TBL] [Abstract][Full Text] [Related]
13. Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts. Vesa J; Su H; Watts GD; Krause S; Walter MC; Martin B; Smith C; Wallace DC; Kimonis VE Neuromuscul Disord; 2009 Nov; 19(11):766-72. PubMed ID: 19828315 [TBL] [Abstract][Full Text] [Related]
14. Valosin-containing protein (p97) is a regulator of endoplasmic reticulum stress and of the degradation of N-end rule and ubiquitin-fusion degradation pathway substrates in mammalian cells. Wójcik C; Rowicka M; Kudlicki A; Nowis D; McConnell E; Kujawa M; DeMartino GN Mol Biol Cell; 2006 Nov; 17(11):4606-18. PubMed ID: 16914519 [TBL] [Abstract][Full Text] [Related]
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17. 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. PubMed ID: 20604808 [TBL] [Abstract][Full Text] [Related]
18. VCP is essential for mitochondrial quality control by PINK1/Parkin and this function is impaired by VCP mutations. Kim NC; Tresse E; Kolaitis RM; Molliex A; Thomas RE; Alami NH; Wang B; Joshi A; Smith RB; Ritson GP; Winborn BJ; Moore J; Lee JY; Yao TP; Pallanck L; Kundu M; Taylor JP Neuron; 2013 Apr; 78(1):65-80. PubMed ID: 23498974 [TBL] [Abstract][Full Text] [Related]
19. Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation. Bersano A; Del Bo R; Lamperti C; Ghezzi S; Fagiolari G; Fortunato F; Ballabio E; Moggio M; Candelise L; Galimberti D; Virgilio R; Lanfranconi S; Torrente Y; Carpo M; Bresolin N; Comi GP; Corti S Neurobiol Aging; 2009 May; 30(5):752-8. PubMed ID: 17889967 [TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 19380227 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]