Correction of a Rat Model of Parkinson's Disease by Coexpression of Tyrosine Hydroxylase and Aromatic Amino Acid Decarboxylase from a Helper Virus-Free Herpes Simplex Virus Type 1 Vector-Reference-Cited by-同舟云学术

Correction of a Rat Model of Parkinson's Disease by Coexpression of Tyrosine Hydroxylase and Aromatic Amino Acid Decarboxylase from a Helper Virus-Free Herpes Simplex Virus Type 1 Vector

Published:2003-03-20 Issue:5 Volume:14 Page:415-424
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Sun Mei¹,Zhang Guo-Rong¹,Kong Lingxin¹,Holmes Courtney²,Wang Xiaodan¹,Zhang Wei¹,Goldstein David S.²,Geller Alfred I.¹

Affiliation:

1. Department of Neurology, West Roxbury VA Hospital/Harvard Medical School, West Roxbury, MA 02132

2. Clinical Neurocardiology Section, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/104303403321467180

Reference36 articles.

1. Double Transduction with GTP Cyclohydrolase I and Tyrosine Hydroxylase Is Necessary for Spontaneous Synthesis ofl-DOPA by Primary Fibroblasts

2. Long-term doxycycline-controlled expression of human tyrosine hydroxylase after direct adenovirus-mediated gene transfer to a rat model of Parkinson's disease

3. Long-Term Behavioral Recovery in Parkinsonian Rats by an HSV Vector Expressing Tyrosine Hydroxylase

4. Helper virus-free transfer of herpes simplex virus type 1 plasmid vectors into neural cells

5. HSV-1 vector mediated neuronal gene delivery strategies for molecular neuroscience and neurology

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