Pages that link to "Q34547620"
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The following pages link to Familial amyotrophic lateral sclerosis (Q34547620):
Displaying 50 items.
- VEGF: once regarded as a specific angiogenic factor, now implicated in neuroprotection (Q24302846) (← links)
- A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteins (Q24307582) (← links)
- Misfolded CuZnSOD and amyotrophic lateral sclerosis (Q24683677) (← links)
- ALS-associated mutant SOD1G93A causes mitochondrial vacuolation by expansion of the intermembrane space and by involvement of SOD1 aggregation and peroxisomes (Q24792140) (← links)
- Reactive oxygen species in health and disease (Q26851203) (← links)
- Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature (Q28246284) (← links)
- Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor (Q28509300) (← links)
- Oxidative stress and 17-alpha- and 17-beta-estradiol modulate neurofilaments differently (Q28581009) (← links)
- A mouse forward genetics screen identifies LISTERIN as an E3 ubiquitin ligase involved in neurodegeneration (Q28585283) (← links)
- Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery (Q30444138) (← links)
- Redox proteomics in selected neurodegenerative disorders: from its infancy to future applications. (Q30446460) (← links)
- 2-DE and MALDI-TOF-MS for a comparative analysis of proteins expressed in different cellular models of amyotrophic lateral sclerosis (Q33304797) (← links)
- Complex genetics of amyotrophic lateral sclerosis (Q33910597) (← links)
- Reduction in hSOD1 copy number significantly impacts ALS phenotype presentation in G37R (line 29) mice: implications for the assessment of putative therapeutic agents (Q34051858) (← links)
- Role of oxidative stress and antioxidants in neurodegenerative diseases (Q34154938) (← links)
- Targeting cellular energy production in neurological disorders (Q34266266) (← links)
- Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathy (Q34311332) (← links)
- Flightless flies: Drosophila models of neuromuscular disease (Q34708090) (← links)
- Beyond Mendel: an evolving view of human genetic disease transmission (Q34932051) (← links)
- Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects (Q34981294) (← links)
- Progression in primary lateral sclerosis: a prospective analysis (Q35013428) (← links)
- Recent advances in amyotrophic lateral sclerosis research (Q35036503) (← links)
- Amyotrophic lateral sclerosis: progress and prospects for treatment (Q35048032) (← links)
- The production and use of cells as therapeutic agents in neurodegenerative diseases (Q35172250) (← links)
- Disruption of cellular transport: a common cause of neurodegeneration? (Q35172288) (← links)
- Amino acid transporters: roles in amino acid sensing and signalling in animal cells (Q35184476) (← links)
- Neurodegeneration in amyotrophic lateral sclerosis: the role of oxidative stress and altered homeostasis of metals (Q35196302) (← links)
- Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathology (Q35470942) (← links)
- Adaptive and maladaptive motor axonal sprouting in aging and motoneuron disease (Q35741414) (← links)
- Influence of diagnostic categories, age, and gender on antioxidative defense and lipid peroxidation in skeletal muscle of patients with neuromuscular diseases (Q36275094) (← links)
- Mitochondrial uncoupling proteins in the CNS: in support of function and survival. (Q36285974) (← links)
- Management of amyotrophic lateral sclerosis (Q37165524) (← links)
- Dimer destabilization in superoxide dismutase may result in disease-causing properties: structures of motor neuron disease mutants. (Q37646220) (← links)
- Drosophila melanogaster As a Model Organism to Study RNA Toxicity of Repeat Expansion-Associated Neurodegenerative and Neuromuscular Diseases (Q37713198) (← links)
- 4-Hydroxy-2-nonenal, a reactive product of lipid peroxidation, and neurodegenerative diseases: a toxic combination illuminated by redox proteomics studies (Q37960537) (← links)
- Amyotrophic lateral sclerosis: a hormonal condition? (Q38032904) (← links)
- The discovery and development of new potential antioxidant agents for the treatment of neurodegenerative diseases (Q38233270) (← links)
- Strategy for treating motor neuron diseases using a fusion protein of botulinum toxin binding domain and streptavidin for viral vector access: work in progress (Q39446005) (← links)
- Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan. (Q40045594) (← links)
- Effect of Oxidative Damage on the Stability and Dimerization of Superoxide Dismutase 1. (Q40248187) (← links)
- Critical loss of CBP/p300 histone acetylase activity by caspase-6 during neurodegeneration. (Q40323686) (← links)
- Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice (Q43261428) (← links)
- Mitochondriopathy as a differential diagnosis of amyotrophic lateral sclerosis (Q44413482) (← links)
- Early mitochondrial dysfunction occurs in motor cortex and spinal cord at the onset of disease in the Wobbler mouse (Q44535338) (← links)
- Increased persistent Na(+) current and its effect on excitability in motoneurones cultured from mutant SOD1 mice. (Q45223589) (← links)
- VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death (Q45863485) (← links)
- Age dependent penetrance of three different superoxide dismutase 1 (sod 1) mutations (Q47301610) (← links)
- Voltage-dependent sodium channels in spinal cord motor neurons display rapid recovery from fast inactivation in a mouse model of amyotrophic lateral sclerosis (Q48450897) (← links)
- SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis (Q48720144) (← links)
- Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis (Q48881997) (← links)