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Molecular & Cellular Proteomics : MCP|February 28, 2021
Stable Isotope Labeling of Amino Acids in Flies (SILAF) Reveals Differential Phosphorylation of Mitochondrial Proteins Upon Loss of OXPHOS SubunitsFlorian A Rosenberger, Ilian Atanassov, David Moore, et al.Autophagy|July 7, 2010
Autophagy in Dictyostelium: genes and pathways, cell death and infectionJavier Calvo-Garrido, Sergio Carilla-Latorre, Yuzuru Kubohara, et al.BMC Microbiology|July 2, 2008
Dictyostelium transcriptional responses to Pseudomonas aeruginosa: common and specific effects from PAO1 and PA14 strainsSergio Carilla-Latorre, Javier Calvo-Garrido, Gareth Bloomfield, et al.Journal of Alzheimer'S Disease : JAD|December 31, 2016
Apolipoprotein E4 Elicits Lysosomal Cathepsin D Release, Decreased Thioredoxin-1 Levels, and ApoptosisTorbjörn Persson, Francesca Lattanzio, Javier Calvo-Garrido, et al.Molecular Psychiatry|September 15, 2019
Thioredoxin-80 protects against amyloid-beta pathology through autophagic-lysosomal pathway regulationGorka Gerenu, Torbjörn Persson, Julen Goikolea, et al.Molecular Genetics & Genomic Medicine|March 29, 2019
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathyCamilla Maffezzini, Isabelle Laine, Cristina Dallabona, et al.Neuroscience Letters|April 6, 2015
5-HT1B and other related serotonergic proteins are altered in APPswe mutationWalid Tajeddinn, Torbjörn Persson, Silvia Maioli, et al.Neurology. Genetics|March 18, 2021
Novel Mutation m.10372A>G in <i>MT-ND3</i> Causing Sensorimotor Axonal PolyneuropathyHelene Bruhn, Kristin Samuelsson, Florian A Schober, et al.Journal of Cell Science|April 22, 2010
MidA is a putative methyltransferase that is required for mitochondrial complex I functionSergio Carilla-Latorre, M Esther Gallardo, Sarah J Annesley, et al.Plos Genetics|August 1, 2019
Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivoAleksandra Pajak, Isabelle Laine, Paula Clemente, et al.Pageof 3