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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 7, 2002
Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stressMark R Cookson, Fiona M Menzies, Philip Manning, et al.
The Journal of Biological Chemistry|January 7, 2009
Formation of a stabilized cysteine sulfinic acid is critical for the mitochondrial function of the parkinsonism protein DJ-1Jeff Blackinton, Mahadevan Lakshminarasimhan, Kelly J Thomas, et al.
European Journal of Nutrition|September 3, 2021
Digestible indispensable amino acid score (DIAAS) is greater in animal-based burgers than in plant-based burgers if determined in pigsNatalia S Fanelli, Hannah M Bailey, Tyler W Thompson, et al.
The FEBS Journal|August 12, 2009
Parkin deficiency disrupts calcium homeostasis by modulating phospholipase C signallingAnna Sandebring, Nodi Dehvari, Monica Perez-Manso, et al.
Nature Communications|August 5, 2025
14-3-3 binding maintains the Parkinson's associated kinase LRRK2 in an inactive stateJuliana A Martinez Fiesco, Alexandra Beilina, Astrid Alvarez de la Cruz, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
14-3-3 binding maintains the Parkinson's associated kinase LRRK2 in an inactive stateJuliana A Martinez Fiesco, Ning Li, Astrid Alvarez de la Cruz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 15, 2002
An in vitro model of Parkinson's disease: linking mitochondrial impairment to altered alpha-synuclein metabolism and oxidative damageTodd B Sherer, Ranjita Betarbet, Amy K Stout, et al.
Journal of Cellular and Molecular Medicine|August 23, 2018
Reduction of PINK1 or DJ-1 impair mitochondrial motility in neurites and alter ER-mitochondria contactsCristina Parrado-Fernández, Bernadette Schneider, Maria Ankarcrona, et al.
The Biochemical Journal|May 23, 2012
The G2385R variant of leucine-rich repeat kinase 2 associated with Parkinson's disease is a partial loss-of-function mutationIakov N Rudenko, Alice Kaganovich, David N Hauser, et al.
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