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Carlos Cepeda

Showing results (111-120 of 141) with videos related to

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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.
Neurobiology of Disease|October 21, 2019
Pathological high frequency oscillations associate with increased GABA synaptic activity in pediatric epilepsy surgery patientsCarlos Cepeda, Simon Levinson, Hiroki Nariai, 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.
Neuron|April 11, 2008
Repeated exposure to methamphetamine causes long-lasting presynaptic corticostriatal depression that is renormalized with drug readministrationNigel S Bamford, Hui Zhang, John A Joyce, 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.
Elife|June 18, 2021
A bidirectional corticoamygdala circuit for the encoding and retrieval of detailed reward memoriesAna C Sias, Ashleigh K Morse, Sherry Wang, et al.
Nature Medicine|May 3, 2014
Neuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington's diseaseNan Wang, Michelle Gray, Xiao-Hong Lu, 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.
Elife|June 9, 2015
Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neuronsSamuel S Pappas, Katherine Darr, Sandra M Holley, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
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.
Neurobiology of Disease|October 21, 2019
Pathological high frequency oscillations associate with increased GABA synaptic activity in pediatric epilepsy surgery patientsCarlos Cepeda, Simon Levinson, Hiroki Nariai, 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.
Neuron|April 11, 2008
Repeated exposure to methamphetamine causes long-lasting presynaptic corticostriatal depression that is renormalized with drug readministrationNigel S Bamford, Hui Zhang, John A Joyce, 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.
Elife|June 18, 2021
A bidirectional corticoamygdala circuit for the encoding and retrieval of detailed reward memoriesAna C Sias, Ashleigh K Morse, Sherry Wang, et al.
Nature Medicine|May 3, 2014
Neuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington's diseaseNan Wang, Michelle Gray, Xiao-Hong Lu, 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.
Elife|June 9, 2015
Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neuronsSamuel S Pappas, Katherine Darr, Sandra M Holley, et al.
Pageof 15