Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA

Keyphrases

• Transgenic Mice 100%
• Behavioral Abnormalities 100%
• Complementary DNA (cDNA) 100%
• Huntington's Disease 100%
• Selective Neuronal Loss 100%
• Striatum 20%
• Cerebral Cortex 20%
• Gliosis 20%
• Neuron Loss 20%
• CAG Repeat 20%
• Neuropathology 10%
• Progressive Neurodegeneration 10%
• Clinically Significant 10%
• Polyglutamine 10%
• Autosomal Dominant 10%
• Hippocampus 10%
• Cognitive Impairment 10%
• Exon 1 10%
• Clinical Manifestations 10%
• Pathophysiological Mechanisms 10%
• Adult-onset 10%
• Voluntary Movement 10%
• Genetic mutation 10%
• Motor Dysfunction 10%
• Subthalamus 10%
• Chorea 10%
• Involuntary Movement 10%
• Experimental Animal Models 10%
• Triplet Repeat Disorders 10%
• Behavioral Dysfunction 10%
• Pathogenes 10%
• Motor Restlessness 10%
• Movement Impairment 10%
• Protein Products 10%
• Neurodegenerative Disorders 10%
• Mutant Huntingtin (mHTT) 10%
• CAG Trinucleotide Repeats 10%
• Selective Neurodegeneration 10%

Neuroscience

• Complementary DNA 100%
• Huntington's Disease 100%
• Thalamus 20%
• Cerebral Cortex 20%
• Striatum 20%
• Gliosis 20%
• CAG Repeat 20%
• Exon 10%
• Neurodegeneration 10%
• Polyglutamine 10%
• Neurodegenerative Disorder 10%
• Huntingtin 10%
• Cognitive Disorders 10%
• Hippocampus 10%
• Stereotypic Movement Disorder 10%
• Gene Mutation 10%
• Subthalamus 10%
• Chorea 10%
• Trinucleotide Repeat 10%
• Messenger RNA 10%