718 related articles for article (PubMed ID: 25492614)
21. A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse.
Nalbandian A; Llewellyn KJ; Badadani M; Yin HZ; Nguyen C; Katheria V; Watts G; Mukherjee J; Vesa J; Caiozzo V; Mozaffar T; Weiss JH; Kimonis VE
Muscle Nerve; 2013 Feb; 47(2):260-70. PubMed ID: 23169451
[TBL] [Abstract][Full Text] [Related]
22. Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.
Zou ZY; Liu MS; Li XG; Cui LY
Neurobiol Aging; 2013 May; 34(5):1519.e3-4. PubMed ID: 23102936
[TBL] [Abstract][Full Text] [Related]
23. [Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].
Arai T; Hasegawa M; Nishihara M; Nonaka T; Kametani F; Yoshida M; Hashizume Y; Beach TG; Morita M; Nakano I; Oda T; Tsuchiya K; Akiyama H
Rinsho Shinkeigaku; 2008 Nov; 48(11):990-3. PubMed ID: 19198141
[TBL] [Abstract][Full Text] [Related]
24. Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis.
Abramzon Y; Johnson JO; Scholz SW; Taylor JP; Brunetti M; Calvo A; Mandrioli J; Benatar M; Mora G; Restagno G; Chiò A; Traynor BJ
Neurobiol Aging; 2012 Sep; 33(9):2231.e1-2231.e6. PubMed ID: 22572540
[TBL] [Abstract][Full Text] [Related]
25. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
Turner BJ; Bäumer D; Parkinson NJ; Scaber J; Ansorge O; Talbot K
BMC Neurosci; 2008 Oct; 9():104. PubMed ID: 18957104
[TBL] [Abstract][Full Text] [Related]
26. An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions.
Matsuoka T; Fujii N; Kondo A; Iwaki A; Hokonohara T; Honda H; Sasaki K; Suzuki SO; Iwaki T
Neuropathology; 2011 Feb; 31(1):71-6. PubMed ID: 20573033
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
[TBL] [Abstract][Full Text] [Related]
29. Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders.
Hortobágyi T; Troakes C; Nishimura AL; Vance C; van Swieten JC; Seelaar H; King A; Al-Sarraj S; Rogelj B; Shaw CE
Acta Neuropathol; 2011 Apr; 121(4):519-27. PubMed ID: 21360076
[TBL] [Abstract][Full Text] [Related]
30. Increased expression of valosin-containing protein in the skin of patients with amyotrophic lateral sclerosis.
Ishikawa H; Yasui K; Oketa Y; Suzuki M; Ono S
J Clin Neurosci; 2012 Apr; 19(4):522-6. PubMed ID: 22321369
[TBL] [Abstract][Full Text] [Related]
31. Nuclear TAR DNA binding protein 43 expression in spinal cord neurons correlates with the clinical course in amyotrophic lateral sclerosis.
Sumi H; Kato S; Mochimaru Y; Fujimura H; Etoh M; Sakoda S
J Neuropathol Exp Neurol; 2009 Jan; 68(1):37-47. PubMed ID: 19104447
[TBL] [Abstract][Full Text] [Related]
32. VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death.
Gitcho MA; Strider J; Carter D; Taylor-Reinwald L; Forman MS; Goate AM; Cairns NJ
J Biol Chem; 2009 May; 284(18):12384-98. PubMed ID: 19237541
[TBL] [Abstract][Full Text] [Related]
33. Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions.
Nishihira Y; Tan CF; Onodera O; Toyoshima Y; Yamada M; Morita T; Nishizawa M; Kakita A; Takahashi H
Acta Neuropathol; 2008 Aug; 116(2):169-82. PubMed ID: 18481073
[TBL] [Abstract][Full Text] [Related]
34. Decreased cystatin C immunoreactivity in spinal motor neurons and astrocytes in amyotrophic lateral sclerosis.
Mori F; Tanji K; Miki Y; Wakabayashi K
J Neuropathol Exp Neurol; 2009 Nov; 68(11):1200-6. PubMed ID: 19816197
[TBL] [Abstract][Full Text] [Related]
35. Primary lateral sclerosis: upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration--immunohistochemical and biochemical analyses of TDP-43.
Kosaka T; Fu YJ; Shiga A; Ishidaira H; Tan CF; Tani T; Koike R; Onodera O; Nishizawa M; Kakita A; Takahashi H
Neuropathology; 2012 Aug; 32(4):373-84. PubMed ID: 22098653
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Linear Polyubiquitin Chain Modification of TDP-43-Positive Neuronal Cytoplasmic Inclusions in Amyotrophic Lateral Sclerosis.
Nakayama Y; Tsuji K; Ayaki T; Mori M; Tokunaga F; Ito H
J Neuropathol Exp Neurol; 2020 Mar; 79(3):256-265. PubMed ID: 31951008
[TBL] [Abstract][Full Text] [Related]
38. Characterization of human sporadic ALS biomarkers in the familial ALS transgenic mSOD1(G93A) mouse model.
Lilo E; Wald-Altman S; Solmesky LJ; Ben Yaakov K; Gershoni-Emek N; Bulvik S; Kassis I; Karussis D; Perlson E; Weil M
Hum Mol Genet; 2013 Dec; 22(23):4720-5. PubMed ID: 23836781
[TBL] [Abstract][Full Text] [Related]
39. Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis.
Tada M; Doi H; Koyano S; Kubota S; Fukai R; Hashiguchi S; Hayashi N; Kawamoto Y; Kunii M; Tanaka K; Takahashi K; Ogawa Y; Iwata R; Yamanaka S; Takeuchi H; Tanaka F
Am J Pathol; 2018 Feb; 188(2):507-514. PubMed ID: 29128563
[TBL] [Abstract][Full Text] [Related]
40. Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.
González-Pérez P; Cirulli ET; Drory VE; Dabby R; Nisipeanu P; Carasso RL; Sadeh M; Fox A; Festoff BW; Sapp PC; McKenna-Yasek D; Goldstein DB; Brown RH; Blumen SC
Neurology; 2012 Nov; 79(22):2201-8. PubMed ID: 23152587
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
