Mutant Superoxide Dismutase1Linked Familial Amyotrophic Lateral Sclerosis: Molecular Mechanisms of Neuronal Death and Protection (original) (raw)
Mutant Cu/Zn-Superoxide Dismutase Induced Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis
Gundars Goldsteins
Amyotrophic Lateral Sclerosis, 2012
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Mutant Cu,Zn superoxide dismutase in motor neuron disease
John Althaus
AGE, 1998
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Copper, zinc superoxide dismutase (SODI) and its role in neuronal function and disease with particular relevance to motor neurone disease/amyotrophic lateral sclerosis
James Habgood
Biochemical Society Transactions, 1998
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Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
Michael Guarnieri
Proceedings of the National Academy of Sciences, 1994
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Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca 2+ concentration in transfected neuroblastoma SH-SY5Y cells
Andrea Battistoni
Febs Letters, 1997
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Down-regulation of copper/zinc superoxide dismutase causes apoptotic death in PC12 neuronal cells
Michael Shelanski
Proceedings of the National Academy of Sciences, 1994
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Motor neuron-astrocyte interactions and levels of Cu, Zn superoxide dismutase in sporadic amyotrophic lateral sclerosis
dea nagy
Experimental Neurology, 1995
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Expression of a Cu,Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of neuroblastoma cells to infectious injury
Andrea Battistoni
BMC Infectious Diseases, 2007
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Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis
Ali Naini
Journal of the Neurological Sciences, 2002
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Inhibition of Chaperone Activity Is a Shared Property of Several Cu,Zn-Superoxide Dismutase Mutants That Cause Amyotrophic Lateral Sclerosis
ashutosh tiwari
Journal of Biological Chemistry, 2005
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Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis
M. Dib
American journal of human genetics, 1995
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Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis
Janine Kirby
Journal of Neurochemistry, 2004
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Cu/Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of mitochondria and perturbs Ca2+ homeostasis in SOD1G93A mice
Manoj Kumar Jaiswal
Molecular pharmacology, 2009
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Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine
Carlo Ferrarese
Neurobiology of Disease, 2003
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Glycation proceeds faster in mutated Cu, Zn-superoxide dismutases related to familial amyotrophic lateral sclerosis
Theingi Myint
The FASEB Journal, 2003
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Superoxide Dismutase and Oxidative Stress in Amyotrophic Lateral Sclerosis
Alvaro Estevez
Current Advances in Amyotrophic Lateral Sclerosis, 2013
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An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1
Stefania Guareschi, Cristina Cereda
Proceedings of the National Academy of Sciences, 2012
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The metabolic hypothesis in amyotrophic lateral sclerosis: insights from mutant Cu/Zn-superoxide dismutase mice
Luc Dupuis
Biomedicine & Pharmacotherapy, 2005
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Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene
Pamela Shaw
Acta Neuropathologica, 1994
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Transgenic Mice Carrying a Human Mutant Superoxide Dismutase Transgene Develop Neuronal Cytoskeletal Pathology Resembling Human Amyotrophic Lateral Sclerosis Lesions
Pramod Raju
Proceedings of The National Academy of Sciences, 1996
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Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis: Selective loss of neurofilaments in ALS
Mark Cookson
Journal of Neurochemistry, 2004
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Synthetic superoxide dismutase/catalase mimetics reduce oxidative stress and prolong survival in a mouse amyotrophic lateral sclerosis model
Michel Baudry
Neuroscience Letters, 2001
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Cu/Zn superoxide dismutase activity at different ages in sporadic amyotrophic lateral sclerosis
olga paulina sanz
Journal of the Neurological Sciences, 1999
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Decrease in and Mn-superoxide dismutase activities in brain and spinal cord of patients with amyotrophic lateral sclerosis
Makoto Uchino
Journal of the Neurological Sciences, 1994
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Immunodetection of Disease-Associated Conformers of Mutant Cu/Zn Superoxide Dismutase 1 Selectively Expressed in Degenerating Neurons in Amyotrophic Lateral Sclerosis
J. Esquerda
Journal of Neuropathology & Experimental Neurology, 2013
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Strategies for stabilizing superoxide dismutase (SOD1), the protein destabilized in the most common form of familial amyotrophic lateral sclerosis
Gregory Petsko
Proceedings of the National Academy of Sciences, 2010
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Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium
Tania Aguirre
European Journal of Human Genetics, 1999
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Loss of in Vitro Metal Ion Binding Specificity in Mutant Copper-Zinc Superoxide Dismutases Associated with Familial Amyotrophic Lateral Sclerosis
Edith Gralla
Journal of Biological Chemistry, 2000
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Mutant superoxide dismutase 1 forms aggregates in the brain mitochondrial matrix of amyotrophic lateral sclerosis mice
Chetan Vijayvergiya
The Journal of …, 2005
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