Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
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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 examplesRole of apoptosis in diseaseHuman endogenous retroviruses and the nervous systemGene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases.Saturation of the human phenomeAmyotrophic lateral sclerosis: a focus on disease progressionExpression of zinc-deficient human superoxide dismutase in Drosophila neurons produces a locomotor defect linked to mitochondrial dysfunction.Omental transplantation for neurodegenerative diseasesMesenchymal stem cells for the treatment of neurodegenerative disease.Vitamin D(3) at 50x AI attenuates the decline in paw grip endurance, but not disease outcomes, in the G93A mouse model of ALS, and is toxic in females.Identification of active loci of a human endogenous retrovirus in neurons of patients with amyotrophic lateral sclerosis.Dissecting the mechanisms underlying short-interval intracortical inhibition using exercise.Spin hamiltonian parameters for Cu(II)-prion peptide complexes from L-band electron paramagnetic resonance spectroscopyTriheptanoin Protects Motor Neurons and Delays the Onset of Motor Symptoms in a Mouse Model of Amyotrophic Lateral SclerosisA Perspective on Roles Played by Innate and Adaptive Immunity in the Pathobiology of Neurodegenerative DisordersInducing Chronic Excitotoxicity in the Mouse Spinal Cord to Investigate Lower Motor Neuron Degeneration.Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders.Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights.Mitochondrial quality control and communications with the nucleus are important in maintaining mitochondrial function and cell health.Control of intracellular calcium signaling as a neuroprotective strategyIs there a case for diaphragm pacing for amyotrophic lateral sclerosis patients?Vitamin D as a potential therapy in amyotrophic lateral sclerosis.EPR Methods for Biological Cu(II): L-Band CW and NARS.Fermented Brown Rice Extract Stimulates BDNF Gene Transcription in C6 Glioma Cells: Possible Connection with HO-1 Expression.Spirulina non-protein components induce BDNF gene transcription via HO-1 activity in C6 glioma cells.Amyotrophic lateral sclerosis: a dying motor unit?Trichostatin A enhances glutamate transporter GLT-1 mRNA levels in C6 glioma cells via neurosteroid-mediated cell differentiation.Neuroprotective Effects of Exercise Treatments After Injury: The Dual Role of Neurotrophic Factors.Tragic choices.Apparent anticipation in SOD1 familial amyotrophic lateral sclerosis.Vitamin D and Neurological Diseases: An Endocrine View.Riluzole exerts central and peripheral modulating effects in amyotrophic lateral sclerosis.Maladaptation of cortical circuits underlies fatigue and weakness in ALS.Lotus Root Extract Stimulates BDNF Gene Expression Through Potential Mechanism Depending on HO-1 Activity in C6 Glioma Cells.The effects of dexpramipexole (KNS-760704) in individuals with amyotrophic lateral sclerosis
P2860
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P2860
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@en
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@nl
type
label
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@en
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@nl
prefLabel
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@en
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@nl
P1476
Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.
@en
P304
P356
10.2174/156652409787847173
P577
2009-04-01T00:00:00Z