153 related articles for article (PubMed ID: 19478559)
1. Intracellular amyloid beta interacts with SOD1 and impairs the enzymatic activity of SOD1: implications for the pathogenesis of amyotrophic lateral sclerosis.
Yoon EJ; Park HJ; Kim GY; Cho HM; Choi JH; Park HY; Jang JY; Rhim HS; Kang SM
Exp Mol Med; 2009 Sep; 41(9):611-7. PubMed ID: 19478559
[TBL] [Abstract][Full Text] [Related]
2. ALS-linked mutant SOD1 proteins promote Aβ aggregates in ALS through direct interaction with Aβ.
Jang JY; Cho H; Park HY; Rhim H; Kang S
Biochem Biophys Res Commun; 2017 Nov; 493(1):697-707. PubMed ID: 28864422
[TBL] [Abstract][Full Text] [Related]
3. Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.
Li QX; Mok SS; Laughton KM; McLean CA; Volitakis I; Cherny RA; Cheung NS; White AR; Masters CL
Aging Cell; 2006 Apr; 5(2):153-65. PubMed ID: 16626394
[TBL] [Abstract][Full Text] [Related]
4. Brain beta-amyloid accumulation in transgenic mice expressing mutant superoxide dismutase 1.
Turner BJ; Li QX; Laughton KM; Masters CL; Lopes EC; Atkin JD; Cheema SS
Neurochem Res; 2004 Dec; 29(12):2281-6. PubMed ID: 15672551
[TBL] [Abstract][Full Text] [Related]
5. Expression of a Cu,Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of neuroblastoma cells to infectious injury.
Goos M; Zech WD; Jaiswal MK; Balakrishnan S; Ebert S; Mitchell T; Carrì MT; Keller BU; Nau R
BMC Infect Dis; 2007 Nov; 7():131. PubMed ID: 17997855
[TBL] [Abstract][Full Text] [Related]
6. Familial amyotrophic lateral sclerosis-linked mutant SOD1 aberrantly interacts with tubulin.
Kabuta T; Kinugawa A; Tsuchiya Y; Kabuta C; Setsuie R; Tateno M; Araki T; Wada K
Biochem Biophys Res Commun; 2009 Sep; 387(1):121-6. PubMed ID: 19576169
[TBL] [Abstract][Full Text] [Related]
7. Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells.
Oh YK; Shin KS; Yuan J; Kang SJ
J Neurochem; 2008 Feb; 104(4):993-1005. PubMed ID: 18233996
[TBL] [Abstract][Full Text] [Related]
8. Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.
Zhang F; Ström AL; Fukada K; Lee S; Hayward LJ; Zhu H
J Biol Chem; 2007 Jun; 282(22):16691-9. PubMed ID: 17403682
[TBL] [Abstract][Full Text] [Related]
9. Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis.
Beqollari D; Romberg CF; Dobrowolny G; Martini M; Voss AA; Musarò A; Bannister RA
Skelet Muscle; 2016; 6():24. PubMed ID: 27340545
[TBL] [Abstract][Full Text] [Related]
10. Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stress.
Cookson MR; Menzies FM; Manning P; Eggett CJ; Figlewicz DA; McNeil CJ; Shaw PJ
Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):75-85. PubMed ID: 12215229
[TBL] [Abstract][Full Text] [Related]
11. Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice.
Fukada K; Nagano S; Satoh M; Tohyama C; Nakanishi T; Shimizu A; Yanagihara T; Sakoda S
Eur J Neurosci; 2001 Dec; 14(12):2032-6. PubMed ID: 11860498
[TBL] [Abstract][Full Text] [Related]
12. Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Bryson JB; Hobbs C; Parsons MJ; Bosch KD; Pandraud A; Walsh FS; Doherty P; Greensmith L
Hum Mol Genet; 2012 Sep; 21(17):3871-82. PubMed ID: 22678056
[TBL] [Abstract][Full Text] [Related]
13. The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).
Crippa V; Sau D; Rusmini P; Boncoraglio A; Onesto E; Bolzoni E; Galbiati M; Fontana E; Marino M; Carra S; Bendotti C; De Biasi S; Poletti A
Hum Mol Genet; 2010 Sep; 19(17):3440-56. PubMed ID: 20570967
[TBL] [Abstract][Full Text] [Related]
14. Mutant copper-zinc superoxide dismutase associated with amyotrophic lateral sclerosis binds to adenine/uridine-rich stability elements in the vascular endothelial growth factor 3'-untranslated region.
Li X; Lu L; Bush DJ; Zhang X; Zheng L; Suswam EA; King PH
J Neurochem; 2009 Feb; 108(4):1032-44. PubMed ID: 19196430
[TBL] [Abstract][Full Text] [Related]
15. Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.
Atkin JD; Farg MA; Turner BJ; Tomas D; Lysaght JA; Nunan J; Rembach A; Nagley P; Beart PM; Cheema SS; Horne MK
J Biol Chem; 2006 Oct; 281(40):30152-65. PubMed ID: 16847061
[TBL] [Abstract][Full Text] [Related]
16. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Milanese M; Giribaldi F; Melone M; Bonifacino T; Musante I; Carminati E; Rossi PI; Vergani L; Voci A; Conti F; Puliti A; Bonanno G
Neurobiol Dis; 2014 Apr; 64():48-59. PubMed ID: 24361555
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Immunodetection of disease-associated conformers of mutant cu/zn superoxide dismutase 1 selectively expressed in degenerating neurons in amyotrophic lateral sclerosis.
Sábado J; Casanovas A; Hernández S; Piedrafita L; Hereu M; Esquerda JE
J Neuropathol Exp Neurol; 2013 Jul; 72(7):646-61. PubMed ID: 23771221
[TBL] [Abstract][Full Text] [Related]
19. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.
Tokuda E; Okawa E; Watanabe S; Ono S
Hum Mol Genet; 2014 Mar; 23(5):1271-85. PubMed ID: 24163136
[TBL] [Abstract][Full Text] [Related]
20. TDP-43 physically interacts with amyotrophic lateral sclerosis-linked mutant CuZn superoxide dismutase.
Higashi S; Tsuchiya Y; Araki T; Wada K; Kabuta T
Neurochem Int; 2010 Dec; 57(8):906-13. PubMed ID: 20933032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]