A combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3Jonasz Jeremiasz Weber, Jeannette Hübener‐Schmid, Lüdger Schöls et al.|Brain|2017Cited by 44
Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3Tina Harmuth, Jeannette Hübener‐Schmid, Caroline Prell-Schicker et al.|Frontiers in Molecular Neuroscience|2018Cited by 43
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, John C. Ambrose, Arianna Tucci et al.|Genetics in Medicine|2022Cited by 20
Generation of an induced pluripotent stem cell line from a patient with spinocerebellar ataxia type 3 (SCA3): HIHCNi002-AStefanie N. Hayer, Lüdger Schöls, Yvonne Schelling et al.|Stem Cell Research|2018Cited by 11
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Tobias B. Haack, Arianna Tucci et al.|Genetics in Medicine|2023Cited by 4