87 related articles for article (PubMed ID: 23414135)
1. Apparent anticipation in SOD1 familial amyotrophic lateral sclerosis.
Vucic S; Nicholson GA; Chio A; Kiernan MC
Amyotroph Lateral Scler Frontotemporal Degener; 2013 Sep; 14(5-6):452-6. PubMed ID: 23414135
[TBL] [Abstract][Full Text] [Related]
2. The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.
Syriani E; Morales M; Gamez J
J Neurol Sci; 2009 Oct; 285(1-2):46-53. PubMed ID: 19524271
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.
Wang Z; Cai W; Cui F; Cai T; Chen Z; Mao F; Teng H; Chen L; Wang J; Sun Z; Huang X; Yu P
Neurobiol Aging; 2014 Mar; 35(3):725.e11-5. PubMed ID: 24094577
[TBL] [Abstract][Full Text] [Related]
4. Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
Arisato T; Okubo R; Arata H; Abe K; Fukada K; Sakoda S; Shimizu A; Qin XH; Izumo S; Osame M; Nakagawa M
Acta Neuropathol; 2003 Dec; 106(6):561-8. PubMed ID: 14517684
[TBL] [Abstract][Full Text] [Related]
5. Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis.
Valentine JS; Doucette PA; Zittin Potter S
Annu Rev Biochem; 2005; 74():563-93. PubMed ID: 15952898
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Different clinical phenotypes of siblings with familial amyotrophic lateral sclerosis showing Cys146Arg point mutation of superoxide dismutase 1 gene].
Ito K; Uchiyama T; Fukutake T; Arai K; Kanesaka T; Hattori T
Rinsho Shinkeigaku; 2002 Feb; 42(2):175-7. PubMed ID: 12424972
[TBL] [Abstract][Full Text] [Related]
8. A novel SOD1 mutation in amyotrophic lateral sclerosis with a distinct clinical phenotype.
Hu J; Chen K; Ni B; Li L; Chen G; Shi S
Amyotroph Lateral Scler; 2012 Jan; 13(1):149-54. PubMed ID: 22185396
[TBL] [Abstract][Full Text] [Related]
9. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
Tsai CP; Soong BW; Lin KP; Tu PH; Lin JL; Lee YC
Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325
[TBL] [Abstract][Full Text] [Related]
10. In-cell NMR reveals potential precursor of toxic species from SOD1 fALS mutants.
Luchinat E; Barbieri L; Rubino JT; Kozyreva T; Cantini F; Banci L
Nat Commun; 2014 Nov; 5():5502. PubMed ID: 25429517
[TBL] [Abstract][Full Text] [Related]
11. [Familial amyotrophic lateral sclerosis (FALS) with a novel SOD1 gene mutation: a clinicopathological study].
Kawamata C; Morita M; Shibata N; Nakano I
Rinsho Shinkeigaku; 2007 May; 47(5):211-6. PubMed ID: 17585602
[TBL] [Abstract][Full Text] [Related]
12. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
Jaarsma D; Haasdijk ED; Grashorn JA; Hawkins R; van Duijn W; Verspaget HW; London J; Holstege JC
Neurobiol Dis; 2000 Dec; 7(6 Pt B):623-43. PubMed ID: 11114261
[TBL] [Abstract][Full Text] [Related]
13. High metabolic level in patients with familial amyotrophic lateral sclerosis.
Funalot B; Desport JC; Sturtz F; Camu W; Couratier P
Amyotroph Lateral Scler; 2009 Apr; 10(2):113-7. PubMed ID: 18792852
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase].
Mochizuki Y; Mizutani T; Nakano R; Fukushima T; Honma T; Nemoto N; Takei K
Rinsho Shinkeigaku; 2003 Aug; 43(8):491-5. PubMed ID: 14658402
[TBL] [Abstract][Full Text] [Related]
16. Misfolded SOD1 forms high-density molecular complexes with synaptic molecules in mutant SOD1-linked familial amyotrophic lateral sclerosis cases.
Araki T; Nagano S; Tateno M; Kaido M; Ogata K; Arima K
J Neurol Sci; 2012 Mar; 314(1-2):92-6. PubMed ID: 22088212
[TBL] [Abstract][Full Text] [Related]
17. Familial amyotrophic lateral sclerosis in Alberta, Canada.
Pfister T; Sekhon R; White M; Scott P; Munro S; Johnston M; Kalra S; Korngut L
Amyotroph Lateral Scler Frontotemporal Degener; 2013 May; 14(4):273-7. PubMed ID: 23286750
[TBL] [Abstract][Full Text] [Related]
18. Familial amyotrophic lateral sclerosis (FALS)-linked SOD1 mutation accelerates neuronal cell death by activating cleavage of caspase-4 under ER stress in an in vitro model of FALS.
Koyama Y; Hiratsuka T; Matsuzaki S; Yamagishi S; Kato S; Katayama T; Tohyama M
Neurochem Int; 2010 Dec; 57(7):838-43. PubMed ID: 20816908
[TBL] [Abstract][Full Text] [Related]
19. Small-molecule-mediated stabilization of familial amyotrophic lateral sclerosis-linked superoxide dismutase mutants against unfolding and aggregation.
Ray SS; Nowak RJ; Brown RH; Lansbury PT
Proc Natl Acad Sci U S A; 2005 Mar; 102(10):3639-44. PubMed ID: 15738401
[TBL] [Abstract][Full Text] [Related]
20. Expression of the copper-zinc superoxide dismutase gene in amyotrophic lateral sclerosis.
Nishiyama K; Murayama S; Kwak S; Kanazawa I
Ann Neurol; 1997 Apr; 41(4):551-6. PubMed ID: 9124814
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
