The inositol trisphosphate/calcium signaling pathway in health and disease

MJ Berridge - Physiological reviews, 2016 - journals.physiology.org
Many cellular functions are regulated by calcium (Ca2+) signals that are generated by
different signaling pathways. One of these is the inositol 1, 4, 5-trisphosphate/calcium …

Mutant SOD1 mediated pathogenesis of amyotrophic lateral sclerosis

SJ Kaur, SR McKeown, S Rashid - Gene, 2016 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a neural disorder that causes death of the motor
neurons in the brain and spinal cord; this affects the voluntary muscles and gradually leads …

Cognitive decline in preclinical Alzheimer's disease: amyloid-beta versus tauopathy

CM Huber, C Yee, T May, A Dhanala… - Journal of …, 2017 - journals.sagepub.com
We perform a large-scale meta-analysis of 51 peer-reviewed 3xTg-AD mouse publications
to compare Alzheimer's disease (AD) quantitative clinical outcome measures, including …

Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels

A Moller, CS Bauer, RN Cohen… - Human molecular …, 2017 - academic.oup.com
Defective axonal transport is an early neuropathological feature of amyotrophic lateral
sclerosis (ALS). We have previously shown that ALS-associated mutations in Cu/Zn …

ASCs-Exosomes Recover Coupling Efficiency and Mitochondrial Membrane Potential in an in vitro Model of ALS

E Calabria, I Scambi, R Bonafede… - Frontiers in …, 2019 - frontiersin.org
The amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized
by motoneurons death. Mutations in the superoxide dismutase 1 (SOD1) protein have been …

Machine learning selection of most predictive brain proteins suggests role of sugar metabolism in Alzheimer's disease

R Tandon, AI Levey, JJ Lah… - Journal of …, 2023 - content.iospress.com
Background: The complex and not yet fully understood etiology of Alzheimer's disease (AD)
shows important proteopathic signs which are unlikely to be linked to a single protein …

A metadata analysis of oxidative stress etiology in preclinical amyotrophic lateral sclerosis: benefits of antioxidant therapy

L Bond, K Bernhardt, P Madria, K Sorrentino… - Frontiers in …, 2018 - frontiersin.org
Oxidative stress, induced by an imbalance of free radicals, incites neurodegeneration in
Amyotrophic Lateral Sclerosis (ALS). In fact, a mutation in antioxidant enzyme superoxide …

An assessment of possible neuropathology and clinical relationships in 46 sporadic amyotrophic lateral sclerosis patient autopsies

G Coan, CS Mitchell - Neurodegenerative Diseases, 2015 - karger.com
Background: Recent studies have suggested overlapping pathological features among
motor neuron, cognitive and neurodegenerative diseases. Aims/Methods: Secondary …

Antecedent disease and amyotrophic lateral sclerosis: what is protecting whom?

SK Hollinger, IS Okosun, CS Mitchell - Frontiers in neurology, 2016 - frontiersin.org
Multiple studies have shown that antecedent diseases are less prevalent in amyotrophic
lateral sclerosis (ALS) patients than the general age-matched population, which suggests …

Unraveling the complexity of amyotrophic lateral sclerosis survival prediction

SR Pfohl, RB Kim, GS Coan… - Frontiers in …, 2018 - frontiersin.org
Objective: The heterogeneity of amyotrophic lateral sclerosis (ALS) survival duration, which
varies from< 1 year to> 10 years, challenges clinical decisions and trials. Utilizing data from …