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Do oxidatively modified proteins cause ALS?
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Do oxidatively modified proteins cause ALS?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
main subject
amyotrophic lateral sclerosis
1 reference
based on heuristic
inferred from title
author name string
Joan Selverstone Valentine
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
publication date
1 November 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
published in
Free Radical Biology and Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
volume
33
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
issue
10
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
page(s)
1314-1320
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
cites work
Amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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A low expressor line of transgenic mice carrying a mutant human Cu,Zn superoxide dismutase (SOD1) gene develops pathological changes that most closely resemble those in human amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Transgenic animal models of familial amyotrophic lateral sclerosis
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Crossref
reference URL
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7 January 2021
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ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Loss of in vitro metal ion binding specificity in mutant copper-zinc superoxide dismutases associated with familial amyotrophic lateral sclerosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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inferred from DOI database lookup
Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Reactions of hydrogen peroxide with familial amyotrophic lateral sclerosis mutant human copper-zinc superoxide dismutases studied by pulse radiolysis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Familial amyotrophic lateral sclerosis-associated mutations decrease the thermal stability of distinctly metallated species of human copper/zinc superoxide dismutase
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Copper(2+) binding to the surface residue cysteine 111 of His46Arg human copper-zinc superoxide dismutase, a familial amyotrophic lateral sclerosis mutant
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Aberrant protein deposition and neurological disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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inferred from DOI database lookup
Formation of granular cytoplasmic aggregates in COS7 cells expressing mutant Cu/Zn superoxide dismutase associated with familial amyotrophic lateral sclerosis.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Immunohistochemical study on superoxide dismutases in spinal cords from autopsied patients with amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Cu/Zn superoxide dismutase-like immunoreactivity in Lewy body-like inclusions of sporadic amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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The neuronal Golgi apparatus is fragmented in transgenic mice expressing a mutant human SOD1, but not in mice expressing the human NF-H gene
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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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
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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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.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Morphological evidence for lipid peroxidation and protein glycoxidation in spinal cords from sporadic amyotrophic lateral sclerosis patients
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Nonoxidative protein glycation is implicated in familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Enhanced oxygen radical production in a transgenic mouse model of familial amyotrophic lateral sclerosis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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Elevated "hydroxyl radical" generation in vivo in an animal model of amyotrophic lateral sclerosis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in copper-zinc superoxide dismutase that cause amyotrophic lateral sclerosis alter the zinc binding site and the redox behavior of the protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of wild-type and amyotrophic lateral sclerosis-related mutant Cu,Zn-superoxide dismutases overproduced in baculovirus-infected insect cells.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Gain in functions of mutant Cu,Zn-superoxide dismutases as a causative factor in familial amyotrophic lateral sclerosis: less reactive oxidant formation but high spontaneous aggregation and precipitation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
ALS, SOD and peroxynitrite
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo peroxidative activity of FALS-mutant human CuZnSODs expressed in yeast
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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A familial amyotrophic lateral sclerosis-associated A4V Cu, Zn-superoxide dismutase mutant has a lower Km for hydrogen peroxide. Correlation between clinical severity and the Km value.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Bicarbonate enhances the hydroxylation, nitration, and peroxidation reactions catalyzed by copper, zinc superoxide dismutase. Intermediacy of carbonate anion radical
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Bicarbonate is required for the peroxidase function of Cu, Zn-superoxide dismutase at physiological pH
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Reexamination of the mechanism of hydroxyl radical adducts formed from the reaction between familial amyotrophic lateral sclerosis-associated Cu,Zn superoxide dismutase mutants and H2O2.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1
1 reference
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https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Oxidation versus aggregation - how do SOD1 mutants cause ALS?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
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From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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SOD1 aggregates in ALS: cause, correlate or consequence?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
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Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
A proposed mechanism of ALS fails the test in vivo
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Do posttranslational modifications of CuZnSOD lead to sporadic amyotrophic lateral sclerosis?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Toxic proteins in neurodegenerative disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0891-5849%2802%2901080-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0891-5849(02)01080-8
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
PubMed ID
12419463
1 reference
stated in
Europe PubMed Central
PubMed ID
12419463
retrieved
5 August 2017
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