Cleo M. Smeets
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 11 publications
Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 15, 2022
Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23.
Journal: Brain pathology (Zurich, Switzerland)
Published: May 28, 2020
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Journal: Brain : a journal of neurology
Published: March 20, 2017
Reply: SCA23 and prodynorphin: is it time for gene retraction?
Journal: Brain : a journal of neurology
Published: May 18, 2016
Altered secondary structure of Dynorphin A associates with loss of opioid signalling and NMDA-mediated excitotoxicity in SCA23.
Journal: Human molecular genetics
Published: December 02, 2015
Climbing fibers in spinocerebellar ataxia: A mechanism for the loss of motor control.
Journal: Neurobiology of disease
Published: August 18, 2015
Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23.
Journal: Brain : a journal of neurology
Published: December 22, 2014
HDAC4-myogenin axis as an important marker of HD-related skeletal muscle atrophy.
Journal: PLoS genetics
Published: November 12, 2014
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.
Journal: Cellular and molecular life sciences : CMLS
Published: July 31, 2014
Cerebellar ataxia and functional genomics: Identifying the routes to cerebellar neurodegeneration.
Journal: Biochimica et biophysica acta
Published: November 25, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026