Search Results - "Carter, Rebecca J."

Characterization of Progressive Motor Deficits in Mice Transgenic for the Human Huntington's Disease Mutation by Carter, Rebecca J, Lione, Lisa A, Humby, Trevor, Mangiarini, Laura, Mahal, Amarbirpal, Bates, Gillian P, Dunnett, Stephen B, Morton, A. Jennifer

“…Transgenic mice expressing exon 1 of the human Huntington's disease (HD) gene carrying a 141-157 CAG repeat (line R6/2) develop a progressive neurological…”
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Abnormal Synaptic Plasticity and Impaired Spatial Cognition in Mice Transgenic for Exon 1 of the Human Huntington's Disease Mutation by Murphy, Kerry P. S. J, Carter, Rebecca J, Lione, Lisa A, Mangiarini, Laura, Mahal, Amarbirpal, Bates, Gillian P, Dunnett, Stephen B, Morton, A. Jennifer

“…Huntington's disease (HD) is an autosomal dominant progressive and fatal neurodegenerative brain disorder caused by an expanded CAG/polyglutamine repeat in the…”
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Selective Discrimination Learning Impairments in Mice Expressing the Human Huntington's Disease Mutation by Lione, Lisa A, Carter, Rebecca J, Hunt, Mark J, Bates, Gillian P, Morton, A. Jennifer, Dunnett, Stephen B

“…Cognitive decline is apparent in the early stages of Huntington's disease and progressively worsens throughout the course of the disease. Expression of the…”
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RAGE is expressed in pyramidal cells of the hippocampus following moderate hypoxic–ischemic brain injury in rats by Ma, Li, Carter, Rebecca J, Morton, A.Jennifer, Nicholson, Louise F.B

“…The receptor for advanced glycation end products (RAGE) is a multi-ligand member of the immunoglobulin superfamily of cell surface molecules. The RAGE–ligand…”
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Motor coordination and balance in rodents by Carter, R J, Morton, J, Dunnett, S B

“…Measurement of motor coordination and balance can be used not only to assess the effect of drugs or other experimental manipulations on mice and rats, but also…”
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Environmental stimulation increases survival in mice transgenic for exon 1 of the Huntington's disease gene by Carter, Rebecca J., Hunt, Mark J., Morton, A. Jennifer

“…Mice transgenic for the first exon of the human Huntington's disease (HD) gene carrying an expanded CAG repeat expansion (R6/2 line) develop a progressive…”
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Dopamine Modulates the Susceptibility of Striatal Neurons to 3-Nitropropionic Acid in the Rat Model of Huntington's Disease by Reynolds, David S, Carter, Rebecca J, Morton, A. Jennifer

“…Huntington's disease (HD) is a progressive neurodegenerative disorder characterized by chorea, psychiatric disturbances, and dementia. The striatum is the…”
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Life-threatening dystonia-dyskinesias in a child: Successful treatment with bilateral pallidal stimulation by Angelini, Lucia, Nardocci, Nardo, Estienne, Margherita, Conti, Chiara, Dones, Ivano, Broggi, Giovanni

“…We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The…”
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