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Neurobiology of Aging|February 26, 2003
Abeta42 generation is toxic to endothelial cells and inhibits eNOS function through an Akt/GSK-3beta signaling-dependent mechanismToshimitsu Suhara, Jordi Magrané, Kenneth Rosen, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 2, 2014
α-Synuclein is localized to mitochondria-associated ER membranesCristina Guardia-Laguarta, Estela Area-Gomez, Cornelia Rüb, et al.Journal of Neurochemistry|October 15, 2013
Autosomal-dominant Alzheimer's disease mutations at the same codon of amyloid precursor protein differentially alter Aβ productionMarc Suárez-Calvet, Olivia Belbin, Marta Pera, et al.Nutrients|August 23, 2020
High-Dose Vitamin D Supplementation Improves Microcirculation and Reduces Inflammation in Diabetic Neuropathy PatientsTatiana Karonova, Anna Stepanova, Anna Bystrova, et al.Biochimica Et Biophysica Acta|June 12, 2016
Differential susceptibility of mitochondrial complex II to inhibition by oxaloacetate in brain and heartAnna Stepanova, Yevgeniya Shurubor, Federica Valsecchi, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 4, 2011
In vivo pathogenic role of mutant SOD1 localized in the mitochondrial intermembrane spaceAnissa Igoudjil, Jordi Magrané, Lindsey R Fischer, et al.BMC Genomics|June 7, 2019
RiboStreamR: a web application for quality control, analysis, and visualization of Ribo-seq dataPatrick Perkins, Serina Mazzoni-Putman, Anna Stepanova, et al.Journal of Neurochemistry|December 25, 2018
The dependence of brain mitochondria reactive oxygen species production on oxygen level is linear, except when inhibited by antimycin AAnna Stepanova, Csaba Konrad, Giovanni Manfredi, et al.Genes|November 25, 2023
A Molecular Genetic Analysis of RPE65-Associated Forms of Inherited Retinal Degenerations in the Russian FederationAnna Stepanova, Natalya Ogorodova, Vitaly Kadyshev, et al.Frontiers in Genetics|June 17, 2022
Case Report: Phenotype-Driven Diagnosis of Atypical Dravet-Like Syndrome Caused by a Novel Splicing Variant in the SCN2A GeneArtem Sharkov, Peter Sparber, Anna Stepanova, et al.Pageof 8