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Plos Genetics|August 19, 2015
In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11Rita-Eva Varga, Mukhran Khundadze, Markus Damme, et al.
Plos Genetics|December 25, 2013
A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal systemMukhran Khundadze, Katrin Kollmann, Nicole Koch, et al.
Nature Communications|August 9, 2024
A synthetic peptide mimic kills Candida albicans and synergistically prevents infectionSebastian Schaefer, Raghav Vij, Jakob L Sprague, et al.
Nature|May 24, 2023
Ubiquitination regulates ER-phagy and remodelling of endoplasmic reticulumAlexis González, Adriana Covarrubias-Pinto, Ramachandra M Bhaskara, et al.
The Journal of Clinical Investigation|September 21, 2013
A spastic paraplegia mouse model reveals REEP1-dependent ER shapingChristian Beetz, Nicole Koch, Mukhran Khundadze, et al.
American Journal of Human Genetics|November 19, 2013
Mutations in KPTN cause macrocephaly, neurodevelopmental delay, and seizuresEmma L Baple, Reza Maroofian, Barry A Chioza, et al.
The EMBO Journal|September 20, 2011
Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin IDennis Koch, Isabella Spiwoks-Becker, Victor Sabanov, et al.
Nature|May 24, 2023
Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagyHector Foronda, Yangxue Fu, Adriana Covarrubias-Pinto, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|November 21, 2025
REEP1 Accumulation Disrupts ER Integrity and Drives Spinal Motoneuron Degeneration in Distal Hereditary Motor NeuropathyAndrea Bock, Mona Schurig, Miles Willoughby, et al.
Elife|December 7, 2016
Calcium-mediated actin reset (CaAR) mediates acute cell adaptationsPauline Wales, Christian E Schuberth, Roland Aufschnaiter, et al.
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