Implications of glial nitric oxide in neurodegenerative diseases

JE Yuste, E Tarragon, CM Campuzano… - Frontiers in cellular …, 2015 - frontiersin.org
Nitric oxide (NO) is a pleiotropic janus-faced molecule synthesized by nitric oxide synthases
(NOS) which plays a critical role in a number of physiological and pathological processes in …

Cyclophilin A: a key player for human disease

P Nigro, G Pompilio, MC Capogrossi - Cell death & disease, 2013 - nature.com
Cyclophilin A (CyPA) is a ubiquitously distributed protein belonging to the immunophilin
family. CyPA has peptidyl prolyl cis-trans isomerase (PPIase) activity, which regulates …

Oxidative stress in ALS: key role in motor neuron injury and therapeutic target

SC Barber, PJ Shaw - Free Radical Biology and Medicine, 2010 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder
characterized by death of motor neurons leading to muscle wasting, paralysis, and death …

The proteasomal system

T Jung, B Catalgol, T Grune - Molecular aspects of medicine, 2009 - Elsevier
Rising interest in the mechanism and function of the proteasomes and the ubiquitin system
revealed that it is hard to find any aspect of the cellular metabolic network that is not directly …

Clinical efficacy of edaravone for the treatment of amyotrophic lateral sclerosis

H Sawada - Expert opinion on pharmacotherapy, 2017 - Taylor & Francis
Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive, fatal, neurodegenerative
disease. Although the pathogenesis remains unresolved, oxidative stress is known to play a …

Molecular and cellular pathways of neurodegeneration in motor neurone disease

PJ Shaw - Journal of Neurology, Neurosurgery & Psychiatry, 2005 - jnnp.bmj.com
The process of neuronal degeneration in motor neurone disease is complex. Several
genetic alterations may be involved in motor neurone injury in familial amyotrophic lateral …

Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III

P Kaufmann, JLP Thompson, G Levy… - Annals of Neurology …, 2009 - Wiley Online Library
Objective Amyotrophic lateral sclerosis (ALS) is a devastating, and currently incurable,
neuromuscular disease in which oxidative stress and mitochondrial impairment are …

Adaptive and maladaptive motor axonal sprouting in aging and motoneuron disease

T Gordon, J Hegedus, SL Tam - Neurological research, 2004 - Taylor & Francis
Motor unit (MU) enlargement by sprouting is an important compensatory mechanism for loss
of functional MUs during normal aging and neuromuscular disease. Perisynaptic Schwann …

Dose-dependent functionality and toxicity of green tea polyphenols in experimental rodents

A Murakami - Archives of biochemistry and biophysics, 2014 - Elsevier
A large number of physiologically functional foods are comprised of plant polyphenols. Their
antioxidative activities have been intensively studied for a long period and proposed to be …

Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS

J Kirby, E Halligan, MJ Baptista, S Allen, PR Heath… - Brain, 2005 - academic.oup.com
Familial amyotrophic lateral sclerosis (FALS) is caused, in 20% of cases, by mutations in the
Cu/Zn superoxide dismutase gene (SOD1). Although motor neuron injury occurs through a …