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Life Science Alliance|April 24, 2020
Microtubule-dependent and independent roles of spastin in lipid droplet dispersion and biogenesisNimesha Tadepalle, Lennart Robers, Matteo Veronese, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 12, 2025
Pathogenesis of mtDNA point mutation m.10191T>C affecting complex I function is a multifactorial process leading to metabolic remodeling of mitochondriaZeinab Alsadat Ahmadi, Alfredo Cabrera-Orefice, Marta Zaninello, et al.
The Journal of Clinical Investigation|October 9, 2012
AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survivalEva R Almajan, Ricarda Richter, Lars Paeger, et al.
The Journal of Cell Biology|October 29, 2014
CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteinsJie Gao, Désirée Schatton, Paola Martinelli, et al.
The Journal of Cell Biology|January 20, 2016
Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondriaAnne Korwitz, Carsten Merkwirth, Ricarda Richter-Dennerlein, et al.
Nature Communications|April 7, 2019
The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPARαAnton Iershov, Ivan Nemazanyy, Chantal Alkhoury, et al.
Brain : a Journal of Neurology|April 22, 2023
SARM1 deletion delays cerebellar but not spinal cord degeneration in an enhanced mouse model of SPG7 deficiencyCarolina Montoro-Gámez, Hendrik Nolte, Thibaut Molinié, et al.
Life Science Alliance|May 23, 2024
ERLIN1/2 scaffolds bridge TMUB1 and RNF170 and restrict cholesterol esterification to regulate the secretory pathwayMatteo Veronese, Sebastian Kallabis, Alexander Tobias Kaczmarek, et al.
EMBO Molecular Medicine|November 4, 2018
Loss of the mitochondrial <i>i</i>-AAA protease YME1L leads to ocular dysfunction and spinal axonopathyHans-Georg Sprenger, Gulzar Wani, Annika Hesseling, et al.
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