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Cell Reports Methods|July 9, 2024
Antibody-assisted selective isolation of Purkinje cell nuclei from mouse cerebellar tissueLuke C Bartelt, Mouad Fakhri, Grazyna Adamek, et al.Disease Models & Mechanisms|June 23, 2021
Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7Anna F Fusco, Logan A Pucci, Pawel M Switonski, et al.Journal of Applied Genetics|April 29, 2025
Spinocerebellar ataxia 27B (SCA27B)-a systematic review and a case report of a Polish familyAdam S Hirschfeld, Julia O Misiorek, Magdalena Dabrowska, et al.Cell Reports|December 1, 2021
Altered H3 histone acetylation impairs high-fidelity DNA repair to promote cerebellar degeneration in spinocerebellar ataxia type 7Pawel M Switonski, Joe R Delaney, Luke C Bartelt, et al.Biorxiv : the Preprint Server for Biology|May 22, 2023
Purkinje-Enriched snRNA-seq in SCA7 Cerebellum Reveals Zebrin Identity Loss as a Central Feature of Polyglutamine AtaxiasLuke C Bartelt, Pawel M Switonski, Grażyna Adamek, et al.Science Translational Medicine|November 6, 2024
Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patientsLuke C Bartelt, Pawel M Switonski, Grażyna Adamek, et al.Neuron|December 21, 2019
Nicotinamide Pathway-Dependent Sirt1 Activation Restores Calcium Homeostasis to Achieve Neuroprotection in Spinocerebellar Ataxia Type 7Colleen A Stoyas, David D Bushart, Pawel M Switonski, et al.Cell Reports|January 31, 2019
Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial DiseaseJacqueline M Ward, Colleen A Stoyas, Pawel M Switonski, et al.Pageof 2