219 related articles for article (PubMed ID: 20871097)
1. An examination of wild-type SOD1 in modulating the toxicity and aggregation of ALS-associated mutant SOD1.
Prudencio M; Durazo A; Whitelegge JP; Borchelt DR
Hum Mol Genet; 2010 Dec; 19(24):4774-89. PubMed ID: 20871097
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Modulation of mutant superoxide dismutase 1 aggregation by co-expression of wild-type enzyme.
Prudencio M; Durazo A; Whitelegge JP; Borchelt DR
J Neurochem; 2009 Feb; 108(4):1009-18. PubMed ID: 19077113
[TBL] [Abstract][Full Text] [Related]
4. An analysis of interactions between fluorescently-tagged mutant and wild-type SOD1 in intracellular inclusions.
Qualls DA; Crosby K; Brown H; Borchelt DR
PLoS One; 2013; 8(12):e83981. PubMed ID: 24391857
[TBL] [Abstract][Full Text] [Related]
5. Superoxide dismutase 1 encoding mutations linked to ALS adopts a spectrum of misfolded states.
Prudencio M; Borchelt DR
Mol Neurodegener; 2011 Nov; 6():77. PubMed ID: 22094223
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Direct and indirect mechanisms for wild-type SOD1 to enhance the toxicity of mutant SOD1 in bigenic transgenic mice.
Xu G; Ayers JI; Roberts BL; Brown H; Fromholt S; Green C; Borchelt DR
Hum Mol Genet; 2015 Feb; 24(4):1019-35. PubMed ID: 25305079
[TBL] [Abstract][Full Text] [Related]
8. Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis.
Turner BJ; Atkin JD; Farg MA; Zang DW; Rembach A; Lopes EC; Patch JD; Hill AF; Cheema SS
J Neurosci; 2005 Jan; 25(1):108-17. PubMed ID: 15634772
[TBL] [Abstract][Full Text] [Related]
9. Characterization of the activity, aggregation, and toxicity of heterodimers of WT and ALS-associated mutant Sod1.
Brasil AA; de Carvalho MDC; Gerhardt E; Queiroz DD; Pereira MD; Outeiro TF; Eleutherio ECA
Proc Natl Acad Sci U S A; 2019 Dec; 116(51):25991-26000. PubMed ID: 31796595
[TBL] [Abstract][Full Text] [Related]
10. Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis.
Ekhtiari Bidhendi E; Bergh J; Zetterström P; Forsberg K; Pakkenberg B; Andersen PM; Marklund SL; Brännström T
Acta Neuropathol; 2018 Dec; 136(6):939-953. PubMed ID: 30284034
[TBL] [Abstract][Full Text] [Related]
11. Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosis.
Medinas DB; Rozas P; Martínez Traub F; Woehlbier U; Brown RH; Bosco DA; Hetz C
Proc Natl Acad Sci U S A; 2018 Aug; 115(32):8209-8214. PubMed ID: 30038021
[TBL] [Abstract][Full Text] [Related]
12. An examination of alpha B-crystallin as a modifier of SOD1 aggregate pathology and toxicity in models of familial amyotrophic lateral sclerosis.
Karch CM; Borchelt DR
J Neurochem; 2010 Jun; 113(5):1092-100. PubMed ID: 20067574
[TBL] [Abstract][Full Text] [Related]
13. Features of wild-type human SOD1 limit interactions with misfolded aggregates of mouse G86R Sod1.
Qualls DA; Prudencio M; Roberts BL; Crosby K; Brown H; Borchelt DR
Mol Neurodegener; 2013 Dec; 8():46. PubMed ID: 24341866
[TBL] [Abstract][Full Text] [Related]
14. Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model.
Okamoto Y; Shirakashi Y; Ihara M; Urushitani M; Oono M; Kawamoto Y; Yamashita H; Shimohama S; Kato S; Hirano A; Tomimoto H; Ito H; Takahashi R
PLoS One; 2011; 6(5):e20427. PubMed ID: 21655264
[TBL] [Abstract][Full Text] [Related]
15. Mutation-dependent polymorphism of Cu,Zn-superoxide dismutase aggregates in the familial form of amyotrophic lateral sclerosis.
Furukawa Y; Kaneko K; Yamanaka K; Nukina N
J Biol Chem; 2010 Jul; 285(29):22221-31. PubMed ID: 20404329
[TBL] [Abstract][Full Text] [Related]
16. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD
Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389
[TBL] [Abstract][Full Text] [Related]
17. Adherent monomer-misfolded SOD1.
Watanabe Y; Morita E; Fukada Y; Doi K; Yasui K; Kitayama M; Nakano T; Nakashima K
PLoS One; 2008; 3(10):e3497. PubMed ID: 18946506
[TBL] [Abstract][Full Text] [Related]
18. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
Kato S; Sumi-Akamaru H; Fujimura H; Sakoda S; Kato M; Hirano A; Takikawa M; Ohama E
Acta Neuropathol; 2001 Sep; 102(3):233-8. PubMed ID: 11585247
[TBL] [Abstract][Full Text] [Related]
19. Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis.
Urushitani M; Kurisu J; Tsukita K; Takahashi R
J Neurochem; 2002 Dec; 83(5):1030-42. PubMed ID: 12437574
[TBL] [Abstract][Full Text] [Related]
20. Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.
Wang J; Xu G; Slunt HH; Gonzales V; Coonfield M; Fromholt D; Copeland NG; Jenkins NA; Borchelt DR
Neurobiol Dis; 2005 Dec; 20(3):943-52. PubMed ID: 16046140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
