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Methods in Molecular Biology (Clifton, N.J.)|November 24, 2020
Quantitative Proteomics in Drosophila with Holidic Stable-Isotope Labeling of Amino Acids in Fruit Flies (SILAF)Florian A Schober, Ilian Atanassov, Christoph Freyer, et al.Frontiers in Neurology|April 12, 2021
Case Report: A Novel Mutation in the Mitochondrial <i>MT-ND5</i> Gene Is Associated With Leber Hereditary Optic Neuropathy (LHON)Martin Engvall, Aki Kawasaki, Valerio Carelli, et al.EMBO Molecular Medicine|June 12, 2020
FBXL4 deficiency increases mitochondrial removal by autophagyDavid Alsina, Oleksandr Lytovchenko, Aleksandra Schab, 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.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.Stem Cell Reports|March 5, 2019
SQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal NeurodifferentiationJavier Calvo-Garrido, Camilla Maffezzini, Florian A Schober, et al.Nucleic Acids Research|August 10, 2019
C6orf203 is an RNA-binding protein involved in mitochondrial protein synthesisShreekara Gopalakrishna, Sarah F Pearce, Adam M Dinan, et al.Human Mutation|January 27, 2021
Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7Sandrina P Correia, Marco F Moedas, Karin Naess, et al.Human Molecular Genetics|April 22, 2017
A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gammaTriinu Siibak, Paula Clemente, Ana Bratic, et al.Nature Communications|September 30, 2022
ANGEL2 phosphatase activity is required for non-canonical mitochondrial RNA processingPaula Clemente, Javier Calvo-Garrido, Sarah F Pearce, et al.Pageof 2