These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
443 related articles for article (PubMed ID: 19104447)
1. 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]
2. 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]
3. 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]
4. TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations. Maekawa S; Leigh PN; King A; Jones E; Steele JC; Bodi I; Shaw CE; Hortobagyi T; Al-Sarraj S Neuropathology; 2009 Dec; 29(6):672-83. PubMed ID: 19496940 [TBL] [Abstract][Full Text] [Related]
5. Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS. Shan X; Vocadlo D; Krieger C Neurosci Lett; 2009 Jul; 458(2):70-4. PubMed ID: 19379791 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis. Lu Y; Tang C; Zhu L; Li J; Liang H; Zhang J; Xu R Int J Biol Sci; 2016; 12(9):1140-9. PubMed ID: 27570488 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations. Jeon GS; Shim YM; Lee DY; Kim JS; Kang M; Ahn SH; Shin JY; Geum D; Hong YH; Sung JJ Mol Neurobiol; 2019 Mar; 56(3):2007-2021. PubMed ID: 29982983 [TBL] [Abstract][Full Text] [Related]
14. Rab1-dependent ER-Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS. Soo KY; Halloran M; Sundaramoorthy V; Parakh S; Toth RP; Southam KA; McLean CA; Lock P; King A; Farg MA; Atkin JD Acta Neuropathol; 2015 Nov; 130(5):679-97. PubMed ID: 26298469 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. TDP-43 in differential diagnosis of motor neuron disorders. Dickson DW; Josephs KA; Amador-Ortiz C Acta Neuropathol; 2007 Jul; 114(1):71-9. PubMed ID: 17569066 [TBL] [Abstract][Full Text] [Related]
18. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Deng HX; Zhai H; Bigio EH; Yan J; Fecto F; Ajroud K; Mishra M; Ajroud-Driss S; Heller S; Sufit R; Siddique N; Mugnaini E; Siddique T Ann Neurol; 2010 Jun; 67(6):739-48. PubMed ID: 20517935 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology. Nishihira Y; Tan CF; Hoshi Y; Iwanaga K; Yamada M; Kawachi I; Tsujihata M; Hozumi I; Morita T; Onodera O; Nishizawa M; Kakita A; Takahashi H Acta Neuropathol; 2009 Jan; 117(1):45-53. PubMed ID: 18923836 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]