[HTML][HTML] The role of mitochondria in amyotrophic lateral sclerosis

EF Smith, PJ Shaw, KJ De Vos - Neuroscience letters, 2019 - Elsevier
Mitochondria are unique organelles that are essential for a variety of cellular processes
including energy metabolism, calcium homeostasis, lipid biosynthesis, and apoptosis …

Neuronal calcium signaling: function and dysfunction

M Brini, T Calì, D Ottolini, E Carafoli - Cellular and molecular life sciences, 2014 - Springer
Abstract Calcium (Ca 2+) is an universal second messenger that regulates the most
important activities of all eukaryotic cells. It is of critical importance to neurons as it …

The interplay between inflammation, oxidative stress, DNA damage, DNA repair and mitochondrial dysfunction in depression

P Czarny, P Wigner, P Galecki, T Sliwinski - Progress in Neuro …, 2018 - Elsevier
A growing body of evidence suggests that inflammation, mitochondrial dysfunction and
oxidant-antioxidant imbalance may play a significant role in the development and …

The impact of mitochondrial dysfunction in amyotrophic lateral sclerosis

J Zhao, X Wang, Z Huo, Y Chen, J Liu, Z Zhao, F Meng… - Cells, 2022 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and highly fatal
neurodegenerative disease. Although the pathogenesis of ALS remains unclear, increasing …

Amyotrophic lateral sclerosis

LP Rowland, NA Shneider - New England Journal of Medicine, 2001 - Mass Medical Soc
Charcot described amyotrophic lateral sclerosis (ALS) in 1874. Despite progress, this
creeping paralysis, known colloquially as Lou Gehrig's disease, is still not visibly affected by …

Mitochondrial control of cell death

G Kroemer, JC Reed - Nature medicine, 2000 - nature.com
Mitochondrial control of cell death | Nature Medicine Skip to main content Thank you for visiting
nature.com. You are using a browser version with limited support for CSS. To obtain the best …

[HTML][HTML] Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?

KJ De Vos, M Hafezparast - Neurobiology of disease, 2017 - Elsevier
Intracellular trafficking of cargoes is an essential process to maintain the structure and
function of all mammalian cell types, but especially of neurons because of their extreme …

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 …

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

J Kong, Z Xu - Journal of Neuroscience, 1998 - Soc Neuroscience
Amyotrophic lateral sclerosis (ALS) involves motor neuron degeneration, skeletal muscle
atrophy, paralysis, and death. Mutations in Cu, Zn superoxide dismutase (SOD1) are one …

[HTML][HTML] Oxidative stress in ALS: a mechanism of neurodegeneration and a therapeutic target

SC Barber, RJ Mead, PJ Shaw - … et Biophysica Acta (BBA)-Molecular Basis …, 2006 - Elsevier
The cause (s) of amyotrophic lateral sclerosis (ALS) is not fully understood in the vast
majority of cases and the mechanisms involved in motor neuron degeneration are multi …