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Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
NLRP3 inflammasome activation and altered mitophagy are key pathways in inclusion body myositisElie Naddaf, Thi Kim Oanh Nguyen, Jens O Watzlawik, et al.Journal of Cachexia, Sarcopenia and Muscle|December 26, 2024
NLRP3 Inflammasome Activation and Altered Mitophagy Are Key Pathways in Inclusion Body MyositisElie Naddaf, Thi Kim Oanh Nguyen, Jens O Watzlawik, et al.Autophagy|February 6, 2025
Development and validation of a sensitive sandwich ELISA against human PINK1Zahra Baninameh, Jens O Watzlawik, Bernardo A Bustillos, et al.Genes|August 26, 2023
Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDGAnna N Ligezka, Rohit Budhraja, Yurika Nishiyama, et al.Biorxiv : the Preprint Server for Biology|June 21, 2024
The UFMylation pathway is impaired in Alzheimer's diseaseTingxiang Yan, Michael G Heckman, Emily C Craver, et al.Molecular Neurodegeneration|December 19, 2024
The UFMylation pathway is impaired in Alzheimer's diseaseTingxiang Yan, Michael G Heckman, Emily C Craver, et al.Parkinsonism & Related Disorders|September 18, 2014
Early-onset Parkinson's disease due to PINK1 p.Q456X mutation--clinical and functional studyJoanna Siuda, Barbara Jasinska-Myga, Magdalena Boczarska-Jedynak, et al.Parkinsonism & Related Disorders|June 3, 2014
Three families with Perry syndrome from distinct parts of the worldPawel Tacik, Fabienne C Fiesel, Shinsuke Fujioka, et al.Molecular Neurodegeneration|April 26, 2017
The PINK1 p.I368N mutation affects protein stability and ubiquitin kinase activityMaya Ando, Fabienne C Fiesel, Roman Hudec, et al.Acta Neuropathologica|March 3, 2026
Association of mitochondrial genetic background with pS65-Ub in Lewy body diseaseNgan Le Kim Tran, Xu Hou, Michael G Heckman, et al.Pageof 7