716 related articles for article (PubMed ID: 25492614)
1. Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant.
Ayaki T; Ito H; Fukushima H; Inoue T; Kondo T; Ikemoto A; Asano T; Shodai A; Fujita T; Fukui S; Morino H; Nakano S; Kusaka H; Yamashita H; Ihara M; Matsumoto R; Kawamata J; Urushitani M; Kawakami H; Takahashi R
Acta Neuropathol Commun; 2014 Dec; 2():172. PubMed ID: 25492614
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosis.
Williams KL; Solski JA; Nicholson GA; Blair IP
Neurobiol Aging; 2012 Jul; 33(7):1488.e15-6. PubMed ID: 22196955
[TBL] [Abstract][Full Text] [Related]
4. Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation.
Ito H; Nakamura M; Komure O; Ayaki T; Wate R; Maruyama H; Nakamura Y; Fujita K; Kaneko S; Okamoto Y; Ihara M; Konishi T; Ogasawara K; Hirano A; Kusaka H; Kaji R; Takahashi R; Kawakami H
Acta Neuropathol; 2011 Aug; 122(2):223-9. PubMed ID: 21644038
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
Kwok CT; Wang HY; Morris AG; Smith B; Shaw C; de Belleroche J
J Neurol Sci; 2015 Feb; 349(1-2):209-13. PubMed ID: 25618255
[TBL] [Abstract][Full Text] [Related]
7. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
Tan CF; Eguchi H; Tagawa A; Onodera O; Iwasaki T; Tsujino A; Nishizawa M; Kakita A; Takahashi H
Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients.
Miller JW; Smith BN; Topp SD; Al-Chalabi A; Shaw CE; Vance C
Neurobiol Aging; 2012 Nov; 33(11):2721.e1-2. PubMed ID: 22789697
[TBL] [Abstract][Full Text] [Related]
9. Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP-43-positive inclusions of amyotrophic lateral sclerosis.
Nakamura M; Kaneko S; Wate R; Asayama S; Nakamura Y; Fujita K; Ito H; Kusaka H
Neuropathol Appl Neurobiol; 2013 Feb; 39(2):144-56. PubMed ID: 22435645
[TBL] [Abstract][Full Text] [Related]
10. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
Neumann M; Mackenzie IR; Cairns NJ; Boyer PJ; Markesbery WR; Smith CD; Taylor JP; Kretzschmar HA; Kimonis VE; Forman MS
J Neuropathol Exp Neurol; 2007 Feb; 66(2):152-7. PubMed ID: 17279000
[TBL] [Abstract][Full Text] [Related]
11. Exome sequencing reveals VCP mutations as a cause of familial ALS.
Johnson JO; Mandrioli J; Benatar M; Abramzon Y; Van Deerlin VM; Trojanowski JQ; Gibbs JR; Brunetti M; Gronka S; Wuu J; Ding J; McCluskey L; Martinez-Lage M; Falcone D; Hernandez DG; Arepalli S; Chong S; Schymick JC; Rothstein J; Landi F; Wang YD; Calvo A; Mora G; Sabatelli M; Monsurrò MR; Battistini S; Salvi F; Spataro R; Sola P; Borghero G; ; Galassi G; Scholz SW; Taylor JP; Restagno G; Chiò A; Traynor BJ
Neuron; 2010 Dec; 68(5):857-64. PubMed ID: 21145000
[TBL] [Abstract][Full Text] [Related]
12. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model.
Nakamura M; Ito H; Wate R; Nakano S; Hirano A; Kusaka H
Acta Neuropathol; 2008 Mar; 115(3):327-34. PubMed ID: 18210139
[TBL] [Abstract][Full Text] [Related]
13. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.
Kawamoto Y; Ito H; Kobayashi Y; Suzuki Y; Akiguchi I; Fujimura H; Sakoda S; Kusaka H; Hirano A; Takahashi R
Neuropathol Appl Neurobiol; 2010 Jun; 36(4):331-44. PubMed ID: 20202124
[TBL] [Abstract][Full Text] [Related]
14. VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation.
Hirano M; Nakamura Y; Saigoh K; Sakamoto H; Ueno S; Isono C; Mitsui Y; Kusunoki S
Neurobiol Aging; 2015 Mar; 36(3):1604.e1-6. PubMed ID: 25457024
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in mice.
Yin HZ; Nalbandian A; Hsu CI; Li S; Llewellyn KJ; Mozaffar T; Kimonis VE; Weiss JH
Cell Death Dis; 2012 Aug; 3(8):e374. PubMed ID: 22898872
[TBL] [Abstract][Full Text] [Related]
17. Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease.
Mori F; Tanji K; Toyoshima Y; Sasaki H; Yoshida M; Kakita A; Takahashi H; Wakabayashi K
Neuropathology; 2013 Dec; 33(6):637-44. PubMed ID: 23782134
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis.
Tiloca C; Ratti A; Pensato V; Castucci A; Sorarù G; Del Bo R; Corrado L; Cereda C; D'Ascenzo C; Comi GP; Mazzini L; Castellotti B; Ticozzi N; Gellera C; Silani V;
Neurobiol Aging; 2012 Mar; 33(3):630.e1-2. PubMed ID: 22137929
[TBL] [Abstract][Full Text] [Related]
19. An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP-43 proteinopathy.
Matsubara T; Izumi Y; Oda M; Takahashi M; Maruyama H; Miyamoto R; Watanabe C; Tachiyama Y; Morino H; Kawakami H; Saito Y; Murayama S
Neuropathology; 2021 Apr; 41(2):118-126. PubMed ID: 33415820
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]