461 related articles for article (PubMed ID: 11585247)
21. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.
Subramaniam JR; Lyons WE; Liu J; Bartnikas TB; Rothstein J; Price DL; Cleveland DW; Gitlin JD; Wong PC
Nat Neurosci; 2002 Apr; 5(4):301-7. PubMed ID: 11889469
[TBL] [Abstract][Full Text] [Related]
22. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
Ince PG; Tomkins J; Slade JY; Thatcher NM; Shaw PJ
J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.
Takehisa Y; Ujike H; Ishizu H; Terada S; Haraguchi T; Tanaka Y; Nishinaka T; Nobukuni K; Ihara Y; Namba R; Yasuda T; Nishibori M; Hayabara T; Kuroda S
Arch Neurol; 2001 May; 58(5):736-40. PubMed ID: 11346368
[TBL] [Abstract][Full Text] [Related]
26. Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.
Jiang H; Shimizu H; Shiga A; Tanaka M; Onodera O; Kakita A; Takahashi H
Neuropathology; 2017 Feb; 37(1):69-77. PubMed ID: 27444855
[TBL] [Abstract][Full Text] [Related]
27. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.
Kato S; Takikawa M; Nakashima K; Hirano A; Cleveland DW; Kusaka H; Shibata N; Kato M; Nakano I; Ohama E
Amyotroph Lateral Scler Other Motor Neuron Disord; 2000 Jun; 1(3):163-84. PubMed ID: 11464950
[TBL] [Abstract][Full Text] [Related]
28. Colocalization of Bunina bodies and TDP-43 inclusions in a case of sporadic amyotrophic lateral sclerosis with Lewy body-like hyaline inclusions.
Miki Y; Mori F; Seino Y; Tanji K; Yoshizawa T; Kijima H; Shoji M; Wakabayashi K
Neuropathology; 2018 Oct; 38(5):521-528. PubMed ID: 29938835
[TBL] [Abstract][Full Text] [Related]
29. Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis.
Wate R; Ito H; Zhang JH; Ohnishi S; Nakano S; Kusaka H
Acta Neuropathol; 2005 Dec; 110(6):557-62. PubMed ID: 16231159
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Mutations in Superoxide Dismutase 1 (Sod1) Linked to Familial Amyotrophic Lateral Sclerosis Can Disrupt High-Affinity Zinc-Binding Promoted by the Copper Chaperone for Sod1 (Ccs).
Boyd SD; Ullrich MS; Calvo JS; Behnia F; Meloni G; Winkler DD
Molecules; 2020 Feb; 25(5):. PubMed ID: 32121118
[TBL] [Abstract][Full Text] [Related]
32. Effect of CCS on the accumulation of FALS SOD1 mutant-containing aggregates and on mitochondrial translocation of SOD1 mutants: implication of a free radical hypothesis.
Kim HK; Chung YW; Chock PB; Yim MB
Arch Biochem Biophys; 2011 May; 509(2):177-85. PubMed ID: 21354101
[TBL] [Abstract][Full Text] [Related]
33. Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.
Kato S; Hayashi H; Nakashima K; Nanba E; Kato M; Hirano A; Nakano I; Asayama K; Ohama E
Am J Pathol; 1997 Aug; 151(2):611-20. PubMed ID: 9273821
[TBL] [Abstract][Full Text] [Related]
34. Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.
Tagawa A; Tan CF; Kikugawa K; Fukase M; Nakano R; Onodera O; Nishizawa M; Takahashi H
Acta Neuropathol; 2007 Feb; 113(2):205-11. PubMed ID: 17036243
[TBL] [Abstract][Full Text] [Related]
35. A molecular chaperone activity of CCS restores the maturation of SOD1 fALS mutants.
Luchinat E; Barbieri L; Banci L
Sci Rep; 2017 Dec; 7(1):17433. PubMed ID: 29234142
[TBL] [Abstract][Full Text] [Related]
36. Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis.
Stieber A; Gonatas JO; Gonatas NK
J Neurol Sci; 2000 Aug; 177(2):114-23. PubMed ID: 10980307
[TBL] [Abstract][Full Text] [Related]
37. Inducible superoxide dismutase 1 aggregation in transgenic amyotrophic lateral sclerosis mouse fibroblasts.
Turner BJ; Lopes EC; Cheema SS
J Cell Biochem; 2004 Apr; 91(5):1074-84. PubMed ID: 15034941
[TBL] [Abstract][Full Text] [Related]
38. Development of a rat model of amyotrophic lateral sclerosis expressing a human SOD1 transgene.
Aoki M; Kato S; Nagai M; Itoyama Y
Neuropathology; 2005 Dec; 25(4):365-70. PubMed ID: 16382787
[TBL] [Abstract][Full Text] [Related]
39. Complete loss of post-translational modifications triggers fibrillar aggregation of SOD1 in the familial form of amyotrophic lateral sclerosis.
Furukawa Y; Kaneko K; Yamanaka K; O'Halloran TV; Nukina N
J Biol Chem; 2008 Aug; 283(35):24167-76. PubMed ID: 18552350
[TBL] [Abstract][Full Text] [Related]
40. α-Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation.
Takei Y; Oguchi K; Koshihara H; Hineno A; Nakamura A; Ohara S
Hum Pathol; 2013 Jun; 44(6):1171-6. PubMed ID: 23352207
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
