Genetic Manipulation of the Nervous System

Front Cover
Elsevier, Nov 24, 1995 - Science - 276 pages
Neuroscience Perspectives provides multidisciplinary reviews of topics in one of the most diverse and rapidly advancing fields in the life sciences.
Whether you are a new recruit to neuroscience, or an established expert, look to this series for 'one-stop' sources of the historical, physiological, pharmacological, biochemical, molecular biological and therapeutic aspects of chosen research areas.
The recent development of Gene Therapy procedures which allow specific genes to be delivered to human patients who lack functional copies of them is of major therapeutic importance. In addition such gene delivery methods can be used in other organisms to define the function of particular genes. These studies are of particular interest in the nervous system where there are many incurable diseases like Alzheimer's and Parkinson's diseases which may benefit from therapies of this kind. Unfortunately gene delivery methods for use in the nervous system have lagged behind those in other systems due to the fact that the methods developed in other systems are often not applicable to cells like neurons which do not divide. This book discusses a wide range of methods which have now been developed to overcome these problems and allow safe and efficient delivery of particular genes to the brain. Methods discussed include virological methods, physical methods (such as liposomes) and the transplantation of genetically modified cells. In a single volume therefore this book provides a complete view of these methods and indicates how they can be applied to the development of therapies for treating previously incurable neurological disorders.

From inside the book

Contents

an overview
1
a vector for gene transfer to the brain and possible gene therapy of neurological disorders
11
a new tool to transfer genes into the central nervous system for treatment o f neurodegenerative disorders
41
Chapter 4 Adenovirusmediated gene therapy of tumors in the central nervous system
53
Chapter 5 Gene delivery using adenoassociated virus
73
Chapter 6 Herpes simplex virusbased vectors
99
Chapter 7 Gene delivery using herpes simplex virus type 1 plasmid vectors
115
Chapter 8 Problems in the use of herpes simplex virus as a vector
127
Chapter 10 Gene delivery to the nervous system using retroviral vectors
149
Chapter 11 Transplantation of genetically modified nonneuronal cells in the central nervous system
181
Chapter 12 Genetic animal models for Alzheimers disease
203
biology and applications
221
Chapter 14 Direct injection of plasmid DNA into the brain
235
Chapter 15 Antlsense oligodeoxynucleotides as novel neuropharmacological tools for selective expression blockade in the brain
249
Index
269
Color Plate Section
277

Chapter 9 Gene delivery to the nervous system by direct injection of retroviral vector
135

Common terms and phrases

Popular passages

Page 247 - Feigner, PL, Gadek, TR, Holm, M., Roman, R., Chan, HW, Wenz, M., Northrop, JP, Ringold, GM, and Danielsen, M.
Page 50 - Lindvall O, Brundin P, Widner H, Rehncrona S, Gustavii B, Frackowiak R, Leenders KL, Sawle G, Rothwell JC, Marsden CD et al (1990) Grafts of fetal dopamine neurons survive and improve motor function in Parkinson's disease.
Page 180 - Xl.BA (1986) Cellular localization of human immunodeficiency virus infection within the brains of acquired immune deficiency syndrome patients. Proc. Natl Acad Sci USA 83, 7089-7093.
Page 231 - J. (1969). Autoradiographic and histological studies of postnatal neurogenesis. IV. Cell proliferation and migration in the anterior forebrain, with special reference to persisting neurogenesis in the olfactory bulb. J.
Page 71 - Isolation of a cytopathogenic agent from human adenoids undergoing spontaneous degeneration in tissue culture.
Page 268 - Zamecnik PC, Stephenson ML ( 1978) Inhibition of Rous sarcoma virus replication and cell transformation by a specific oligodeoxynucleotide. Proc Natl Acad Sci USA 75:289-294 Zamccnik PC.
Page 38 - P. (1990) Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector. Hum. Gene Ther.
Page 177 - JA (1992) Efficient transfer and sustained high expression of the human glucocerebrosidase gene in mice and their functional macrophages following transplantation of bone marrow transduced by a retroviral vector. Proc.
Page 34 - Graham, FL, Smiley, J., Russell, WC, and Nairn, R. (1977) Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J. Gen. Virol. 36, 59-74.

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