Pages that link to "Q37085354"

The following pages link to Molecular Approaches to Hereditary Diseases of the Nervous System: Huntington's Disease as a Paradigm (Q37085354):

Displaying 19 items.

• Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons (Q24317574) (← links)
• Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors (Q24324769) (← links)
• Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brain (Q24337133) (← links)
• Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene (Q28181555) (← links)
• Expression of normal and mutant huntingtin in the developing brain (Q28508248) (← links)
• Synchrotron Infrared Microspectroscopy Detecting the Evolution of Huntington’s Disease Neuropathology and Suggesting Unique Correlates of Dysfunction in White versus Gray Brain Matter (Q30406678) (← links)
• Molecular biology of neurological diseases (Q30493405) (← links)
• Dopamine receptor genes: new tools for molecular psychiatry. (Q33921096) (← links)
• Electroconvulsive shock ameliorates disease processes and extends survival in huntingtin mutant mice. (Q34505628) (← links)
• The paradigm of Huntington's disease: therapeutic opportunities in neurodegeneration (Q36045254) (← links)
• Transcriptional signatures in Huntington's disease (Q36752799) (← links)
• Expression of NMDA Receptor-1 (NR1) and Huntingtin in Striatal Neurons Which Colocalize Somatostatin, Neuropeptide Y, and NADPH Diaphorase: A Double-Label Histochemical and Immunohistochemical Study (Q36870168) (← links)
• A large number of protein expression changes occur early in life and precede phenotype onset in a mouse model for huntington disease (Q37154448) (← links)
• Factors associated with HD CAG repeat instability in Huntington disease (Q37248874) (← links)
• The elimination of accumulated and aggregated proteins: a role for aggrephagy in neurodegeneration (Q37781878) (← links)
• Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. (Q40537014) (← links)
• Testing for Huntington's disease (Q42764980) (← links)
• Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene (Q45302128) (← links)
• Apolipoprotein E and Alzheimer's disease: the implications of progress in molecular medicine (Q52013897) (← links)