236 related articles for article (PubMed ID: 26511028)
1. [A patient with familial amyotrophic lateral sclerosis associated with a new valosin-containing protein (VCP) gene mutation].
Segawa M; Hoshi A; Naruse H; Kuroda M; Bujo H; Ugawa Y
Rinsho Shinkeigaku; 2015; 55(12):914-20. PubMed ID: 26511028
[TBL] [Abstract][Full Text] [Related]
2. The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology.
Nalbandian A; Llewellyn KJ; Kitazawa M; Yin HZ; Badadani M; Khanlou N; Edwards R; Nguyen C; Mukherjee J; Mozaffar T; Watts G; Weiss J; Kimonis VE
PLoS One; 2012; 7(9):e46308. PubMed ID: 23029473
[TBL] [Abstract][Full Text] [Related]
3. The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?
Clemen CS; Winter L; Strucksberg KH; Berwanger C; Türk M; Kornblum C; Florin A; Aguilar-Pimentel JA; Amarie OV; Becker L; Garrett L; Hans W; Moreth K; Neff F; Pingen L; Rathkolb B; Rácz I; Rozman J; Treise I; Fuchs H; Gailus-Durner V; de Angelis MH; Vorgerd M; Eichinger L; Schröder R
Biochem Biophys Res Commun; 2018 Sep; 503(4):2770-2777. PubMed ID: 30100055
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 23000505
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 21892620
[TBL] [Abstract][Full Text] [Related]
6. One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia.
Abrahao A; Abath Neto O; Kok F; Zanoteli E; Santos B; Pinto WB; Barsottini OG; Oliveira AS; Pedroso JL
J Neurol Sci; 2016 Sep; 368():352-8. PubMed ID: 27538664
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 24215292
[TBL] [Abstract][Full Text] [Related]
8. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
Peyer AK; Kinter J; Hench J; Frank S; Fuhr P; Thomann S; Fischmann A; Kneifel S; Camaño P; López de Munain A; Sinnreich M; Renaud S
Neuromuscul Disord; 2013 Feb; 23(2):149-54. PubMed ID: 23140793
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic variability in three families with valosin-containing protein mutation.
Spina S; Van Laar AD; Murrell JR; Hamilton RL; Kofler JK; Epperson F; Farlow MR; Lopez OL; Quinlan J; DeKosky ST; Ghetti B
Eur J Neurol; 2013 Feb; 20(2):251-8. PubMed ID: 22900631
[TBL] [Abstract][Full Text] [Related]
10. 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; 78(1):57-64. PubMed ID: 23498975
[TBL] [Abstract][Full Text] [Related]
11. [An advanced case of myopathy and dementia with a new mutation in the valosin-containing protein gene].
Kamiyama T; Sengoku R; Sasaki M; Hayashi Y; Nishino I; Mochio S; Iguchi Y
Rinsho Shinkeigaku; 2013; 53(6):465-9. PubMed ID: 23782825
[TBL] [Abstract][Full Text] [Related]
12. 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; 2018 Apr; 37(4):1129-1136. PubMed ID: 29127544
[TBL] [Abstract][Full Text] [Related]
13. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
Wang H; Wu S
Neuromuscul Disord; 2015 Mar; 25(3):273. PubMed ID: 25497399
[No Abstract] [Full Text] [Related]
14. Motor neuron involvement in multisystem proteinopathy: implications for ALS.
Benatar M; Wuu J; Fernandez C; Weihl CC; Katzen H; Steele J; Oskarsson B; Taylor JP
Neurology; 2013 May; 80(20):1874-80. PubMed ID: 23635965
[TBL] [Abstract][Full Text] [Related]
15. Novel Variants in the
Columbres RCA; Chin Y; Pratti S; Quinn C; Gonzalez-Cuyar LF; Weiss M; Quintero-Rivera F; Kimonis V
Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980948
[TBL] [Abstract][Full Text] [Related]
16. Valosin-containing protein (VCP) is a novel IQ motif-containing GTPase activating protein 1 (IQGAP1)-interacting protein.
Itoh N; Nagai T; Watanabe T; Taki K; Nabeshima T; Kaibuchi K; Yamada K
Biochem Biophys Res Commun; 2017 Dec; 493(4):1384-1389. PubMed ID: 28970065
[TBL] [Abstract][Full Text] [Related]
17. Nucleocytoplasmic shuttling of valosin-containing protein (VCP/p97) regulated by its N domain and C-terminal region.
Song C; Wang Q; Song C; Lockett SJ; Colburn NH; Li CC; Wang JM; Rogers TJ
Biochim Biophys Acta; 2015 Jan; 1853(1):222-32. PubMed ID: 25447673
[TBL] [Abstract][Full Text] [Related]
18. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
Koppers M; van Blitterswijk MM; Vlam L; Rowicka PA; van Vught PW; Groen EJ; Spliet WG; Engelen-Lee J; Schelhaas HJ; de Visser M; van der Kooi AJ; van der Pol WL; Pasterkamp RJ; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
[TBL] [Abstract][Full Text] [Related]
19. Distal myopathy and rapidly progressive dementia associated with a novel mutation in the VCP gene: Expanding inclusion body myopathy with early-onset Paget disease and frontotemporal dementia spectrum.
Falcão de Campos C; de Carvalho M
J Clin Neurosci; 2019 Jun; 64():8-10. PubMed ID: 30955949
[TBL] [Abstract][Full Text] [Related]
20. The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.
Papadimas GK; Paraskevas GP; Zambelis T; Karagiaouris C; Bourbouli M; Bougea A; Walter MC; Schumacher NU; Krause S; Kapaki E
Acta Myol; 2017 Dec; 36(4):203-206. PubMed ID: 29770363
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]