Transplanted Fetal Striatum in Huntington's Disease: Phenotypic Development and Lack of Pathology
Transplanted Fetal Striatum in Huntington's Disease: Phenotypic Development and Lack of Pathology
About this item
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Author / Creator
Freeman, T B , Cicchetti, F , Hauser, R A , Deacon, T W , Li, X J , Hersch, S M , Nauert, G M , Sanberg, P R , Kordower, J H , Saporta, S and Isacson, O
Publisher
United States: National Academy of Sciences of the United States of America
Journal title
Language
English
Formats
Publication information
Publisher
United States: National Academy of Sciences of the United States of America
Subjects
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Scope and Contents
Contents
Neural and stem cell transplantation is emerging as a potential treatment for neurodegenerative diseases. Transplantation of specific committed neuroblasts (fetal neurons) to the adult brain provides such scientific exploration of these new potential therapies. Huntington's disease (HD) is a fatal, incurable autosomal dominant (CAG repeat expansion...
Alternative Titles
Full title
Transplanted Fetal Striatum in Huntington's Disease: Phenotypic Development and Lack of Pathology
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_17742555
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_17742555
Other Identifiers
ISSN
0027-8424
E-ISSN
1091-6490
DOI
10.1073/pnas.97.25.13877
