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Home > Clinical Trials of Genetic Therapy with Antisense DNA and DNA Vectors > Distribution and Toxicity of Retroviral Vectors after Intracavitary Delivery in Mouse and Man
Clinical Trials of Genetic Therapy with Antisense DNA and DNA Vectors |
Eric Wickstrom
Routledge
Clinical Trials of Genetic Therapy with Antisense DNA and DNA Vectors
Distribution and Toxicity of Retroviral Vectors after Intracavitary Delivery in Mouse and Man
Authors

Patrice S. Obermiller; Carlos L. Arteaga; Jeffrey T. Holt; Anne M. Pilaro

ARI Id

1665824110496_13858687

Access

Open/Free Access

Pages

239-255

DOI

10.1201/9781003064657-12

Table of Contents of Book
Showing 1 to 20 of 20 entries
Chapters/HeadingsAuthor(s)PagesInfo
A Brief History of Genetic Therapy: Gene Therapy, Antisense Technology, and Genomics
James W. Hawkins
1-38
Preclinical Development of Antisense Oligonucleotide Therapeutics for Cancer: Regulatory Aspect
Chang-Ho Ahn; Joseph J. DeGeorge
39-52
Commercial Scale Manufacturing of Oligonucleotides Under Good Manufacturing Practices
Jose E. Gonzalez; Richard G. Einig; Patricia Puma; Timothy P. Noonan; Paul E. Kennedy; Bruce G. Sturgeon; Bing H. Wang; Jin-yan Tang
53-87
The Regulatory Process and Gene Therapy 1
Suzanne L. Epstein
89-99
Production of Clinical Lots of Gene Therapy Vectors Using Good Manufacturing Practice: Experience in a University Setting
Alan R. Davis; Colleen Baker
101-110
Gene Therapy Clinical Trials for Adenosine Deaminase Deficiency/Severe Combined Immunodeficiency
Eriinda M. Gordon; W. French Anderson
111-131
Development of an Oligodeoxynucleotide Pharmaceutical for the Treatment of Human Leukemia
Alan M. Gewirtz; Deborah Lee Sokol
133-153
Clinical Trials with Anti-p53 DNA, OL(1)p53, in Patients with Acute Myelogenous Leukemia and Myelodysplastic Syndrome
Patrick L. Iversen
155-167
Human Bcl-2 Antisense Therapy for Lymphomas
Finbarr E. Cotter; Andrew Webb; Paul Clarke; David Cunningham
169-189
Retroviral Gene Transfer in Autologous Bone Marrow and Stem Cell Transplantation
Rafat Abonour; Kenneth Cornetta
191-218
Adenoviral Gene Transfer of the Herpes Virus Thymidine Kinase Gene for Treating Gliomas
Jane Β. Alavi; Jason G. Smith; Stephen L. Eck
219-237
Distribution and Toxicity of Retroviral Vectors after Intracavitary Delivery in Mouse and Man
Patrice S. Obermiller; Carlos L. Arteaga; Jeffrey T. Holt; Anne M. Pilaro
239-255
Clinical and Immunologic Responses to Gene Transfer of an Allogeneic Major Histocompatibility Complex Antigen
Alison T. Stopeck; Evan M. Hersh
257-278
Defective Tumor Suppressor Gene Replacement and Oncogene Inactivation for the Treatment of Cancer
Jack Roth
279-294
The Molecular Basis of Bladder Cancer and Prospects for Gene Therapy Using Hammerhead Ribozymes
Eric J. Small; Mohammed Kashani-Sabet; David Y. Bouffard; Kevin J. Scanlon
295-309
In Situ Gene Insertion for Immunotherapy Using Vaccinia Virus Vectors
Edmund C. Lattime; Laurence C. Eisenlohr; Michael J. Mastrangelo
311-330
Antisense Oligonucleotide-Based Therapy for HIV-1 Infection from Laboratory to Clinical Trials
Sudhir Agrawal
331-352
Treatment of Retinitis Induced by Cytomegalovirus Using Intravitreal Fomivirsen (ISIS 2922)
Stanley T. Crooke
353-361
Synthetic DNA-Based Compounds for the Prevention of Coronary Restenosis: Current Status and Future Challenges
Andrew Zalewski; Yi Shi; John D. Mannion; Femando Roqué
363-393
Prevention of Restenosis by Gene Targeting
Michael J. Mann; Victor J. Dzau; Heiko E. von der Leyen
395-412
Chapters/HeadingsAuthor(s)PagesInfo
Showing 1 to 20 of 20 entries
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