Related references
Note: Only part of the references are listed.Consensus Paper: Strengths and Weaknesses of Animal Models of Spinocerebellar Ataxias and Their Clinical Implications
Jan Cendelin et al.
CEREBELLUM (2022)
Cholecystokinin 1 receptor activation restores normal mTORC1 signaling and is protective to Purkinje cells of SCA mice
Emily A. L. Wozniak et al.
CELL REPORTS (2021)
Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias
Katherine J. Robinson et al.
FRONTIERS IN NEUROSCIENCE (2020)
Polyglutamine spinocerebellar ataxias - from genes to potential treatments
Henry L. Paulson et al.
NATURE REVIEWS NEUROSCIENCE (2017)
mTORC1 senses stresses: Coupling stress to proteostasis
Kuo-Hui Su et al.
BIOESSAYS (2017)
Impaired mTORC1-Dependent Expression of Homer-3 Influences SCA1 Pathophysiology
Celine Ruegsegger et al.
NEURON (2016)
Cerebellar Transcriptome Profiles of ATXN1 Transgenic Mice Reveal SCA1 Disease Progression and Protection Pathways
Melissa Ingram et al.
NEURON (2016)
mTORC1 and mTORC2 have largely distinct functions in Purkinje cells
Nico Angliker et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2015)
Reinstating Aberrant mTORC1 Activity in Huntington's Disease Mice Improves Disease Phenotypes
John H. Lee et al.
NEURON (2015)
Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia
Conceicao Bettencourt et al.
JAMA NEUROLOGY (2014)
Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2
Stephen T. Hansen et al.
HUMAN MOLECULAR GENETICS (2013)
Deranged Calcium Signaling in Purkinje Cells and Pathogenesis in Spinocerebellar Ataxia 2 (SCA2) and Other Ataxias
Adebimpe Kasumu et al.
CEREBELLUM (2012)
C-terminal Mutations Destabilize SIL1/BAP and Can Cause Marinesco-Sjogren Syndrome
Jennifer Howes et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Cholecystokinin: A Multi-Functional Molecular Switch of Neuronal Circuits
Soo Yeun Lee et al.
DEVELOPMENTAL NEUROBIOLOGY (2011)
Therapeutic potential for novel drugs targeting the type 1 cholecystokinin receptor
Erin E. Cawston et al.
BRITISH JOURNAL OF PHARMACOLOGY (2010)
SCA1-like Disease in Mice Expressing Wild-Type Ataxin-1 with a Serine to Aspartic Acid Replacement at Residue 776
Lisa Duvick et al.
NEURON (2010)
Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types
Joseph P. Doyle et al.
CELL (2008)
Recurrent axon collaterals underlie facilitating synapses between cerebellar Purkinje cells
David Orduz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration
Jeong Woong Lee et al.
NATURE (2006)
Cholecystokinin and gastrin receptors
Marlene Dufresne et al.
PHYSIOLOGICAL REVIEWS (2006)
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
Taichi Hara et al.
NATURE (2006)
Loss of autophagy in the central nervous system causes neurodegeneration in mice
Masaaki Komatsu et al.
NATURE (2006)
TOR signaling in growth and metabolism
S Wullschleger et al.
CELL (2006)
TOR signaling in growth and metabolism
Stephan Wullschleger et al.
CELL (2006)
Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP
LH Zhao et al.
NATURE GENETICS (2005)
Identification of candidate Purkinje cell-specific markers by gene expression profiling in wild-type and pcd3J mice
YQ Rong et al.
MOLECULAR BRAIN RESEARCH (2004)
Mutational analysis of dendritic Ca2+ kinetics in rodent Purkinje cells:: role of parvalbumin and calbindin D28k
H Schmidt et al.
JOURNAL OF PHYSIOLOGY-LONDON (2003)