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Journal of Neurophysiology|December 31, 2004
Striatal potassium channel dysfunction in Huntington's disease transgenic miceMarjorie A Ariano, Carlos Cepeda, Christopher R Calvert, et al.
Journal of Neurophysiology|November 11, 2011
A critical window of CAG repeat-length correlates with phenotype severity in the R6/2 mouse model of Huntington's diseaseDamian M Cummings, Yasaman Alaghband, Miriam A Hickey, et al.
Neurobiology of Disease|September 6, 2011
Enhanced GABAergic network and receptor function in pediatric cortical dysplasia Type IIB compared with Tuberous Sclerosis ComplexCarlos Cepeda, Véronique M André, Jason S Hauptman, et al.
Free Radical Biology & Medicine|October 13, 2015
Beyond the redox imbalance: Oxidative stress contributes to an impaired GLUT3 modulation in Huntington's diseaseAdriana Covarrubias-Pinto, Pablo Moll, Macarena Solís-Maldonado, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2009
Age-dependent alterations of corticostriatal activity in the YAC128 mouse model of Huntington diseasePrasad R Joshi, Nan-Ping Wu, Véronique M André, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 14, 2008
Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD miceMichelle Gray, Dyna I Shirasaki, Carlos Cepeda, et al.
Nature Communications|December 17, 2013
A failure in energy metabolism and antioxidant uptake precede symptoms of Huntington's disease in miceAníbal I Acuña, Magdalena Esparza, Carlos Kramm, et al.
Research Square|May 9, 2025
Neural Networks of the Mouse Primary Visceromotor CortexHong-Wei Dong, Houri Hintiryan, Muye Zhu, et al.
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