Pages that link to "Q28131805"
The following pages link to Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis (Q28131805):
Displaying 50 items.
- amyotrophic lateral sclerosis (Q206901) (← links)
- SOD1 and amyotrophic lateral sclerosis: mutations and oligomerization (Q21090100) (← links)
- Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis (Q21136374) (← links)
- Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion (Q21195686) (← links)
- A retrospective study of the prevalence of the canine degenerative myelopathy associated superoxide dismutase 1 mutation (SOD1:c.118G > A) in a referral population of German Shepherd dogs from the UK (Q21195749) (← links)
- Sporadic ALS is not associated with VAPB gene mutations in Southern Italy (Q21245641) (← links)
- Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD (Q21261387) (← links)
- A ketogenic diet as a potential novel therapeutic intervention in amyotrophic lateral sclerosis (Q21262053) (← links)
- Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease (Q21262978) (← links)
- Mechanisms of the noxious inflammatory cycle in cystic fibrosis (Q21284420) (← links)
- Ketogenic diet in neuromuscular and neurodegenerative diseases (Q21284703) (← links)
- Dysregulation of the autophagy-endolysosomal system in amyotrophic lateral sclerosis and related motor neuron diseases (Q21285051) (← links)
- SOD1 Transcriptional and Posttranscriptional Regulation and Its Potential Implications in ALS (Q21296781) (← links)
- Different human copper-zinc superoxide dismutase mutants, SOD1G93A and SOD1H46R, exert distinct harmful effects on gross phenotype in mice (Q21560962) (← links)
- Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA) (Q22007950) (← links)
- Development and characterization of human and mouse specific antibodies to CuZn-superoxide dismutase (SOD1) (Q22254203) (← links)
- The genetic epidemiology of neurodegenerative disease (Q22306301) (← links)
- The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: from respiration to apoptosis (Q23917508) (← links)
- Transcriptional responses to oxidative stress: pathological and toxicological implications (Q23919656) (← links)
- Creatine for amyotrophic lateral sclerosis/motor neuron disease (Q24202577) (← links)
- Creatine for amyotrophic lateral sclerosis/motor neuron disease (Q24234800) (← links)
- Antioxidant treatment for amyotrophic lateral sclerosis or motor neuron disease (Q24243199) (← links)
- Creatine for amyotrophic lateral sclerosis/motor neuron disease (Q24244631) (← links)
- Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease (Q24244879) (← links)
- Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples (Q24289511) (← links)
- A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (Q24291755) (← links)
- Mitochondrial damage due to SOD1 deficiency in SH-SY5Y neuroblastoma cells: a rationale for the redundancy of SOD1 (Q24294416) (← links)
- Expression and localization of cyclooxygenase‐1 and ‐2 in human sporadic amyotrophic lateral sclerosis (Q24295307) (← links)
- Tumor necrosis factor-alpha down-regulates human Cu/Zn superoxide dismutase 1 promoter via JNK/AP-1 signaling pathway (Q24299266) (← links)
- Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis (Q24299487) (← links)
- Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia (Q24299953) (← links)
- XIAP: cell death regulation meets copper homeostasis (Q24300814) (← links)
- A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis (Q24304337) (← links)
- Mutation of SOD1 in ALS: a gain of a loss of function (Q24305971) (← links)
- SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model (Q24307703) (← links)
- Altered localization, abnormal modification and loss of function of Sigma receptor-1 in amyotrophic lateral sclerosis (Q24308696) (← links)
- ALS2/Alsin regulates Rac-PAK signaling and neurite outgrowth (Q24310305) (← links)
- The Copper Chaperone CCS Directly Interacts with Copper/Zinc Superoxide Dismutase (Q24310363) (← links)
- The Copper Chaperone for Superoxide Dismutase (Q24311669) (← links)
- Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis (Q24312170) (← links)
- Alsin is partially associated with centrosome in human cells (Q24313283) (← links)
- Mitochondrial ubiquitin ligase MITOL ubiquitinates mutant SOD1 and attenuates mutant SOD1-induced reactive oxygen species generation (Q24314962) (← links)
- Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport (Q24315910) (← links)
- A mutation in sigma‐1 receptor causes juvenile amyotrophic lateral sclerosis (Q24322790) (← links)
- HDAC6 regulates mutant SOD1 aggregation through two SMIR motifs and tubulin acetylation (Q24338404) (← links)
- Neurogenetics. Triumphs and challenges (Q24514894) (← links)
- Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments (Q24518243) (← links)
- The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype (Q24531747) (← links)
- DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4) (Q24533845) (← links)
- Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34 (Q24538838) (← links)