Viral vectors for gene therapy : methods and protocols /
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| Imprint: | New York : Humana Press : Springer, [2019] ©2019 |
|---|---|
| Description: | 1 online resource (xiv, 328 pages) : illustrations (some color) |
| Language: | English |
| Series: | Methods in molecular biology, 1940-6029 ; v. 1937 Methods in molecular biology (Clifton, N.J.) ; v. 1937. |
| Subject: | |
| URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/11781379 |
Table of Contents:
- Basic concepts in viral vector-mediated gene therapy / Matthew J. Benskey, Ivette M. Sandoval, Kathryn Miller,Rhyomi L. Sellnow, Aysegul Gezer, Nathan C. Kuhn, Roslyn Vashon, and Fredric P. Manfredsson
- Design and assembly of CRISPR/Cas9 lentiviral and rAAV vectors for targeted genome editing / Ivette M. Sandoval, Timothy J. Collier, and Fredric P. Manfredsson
- Design, construction, and application of transcription activation-like effectors / Peter Deng, Sakereh Carter, and Kyle Fink
- Practical considerations for the use of DREADD and other chemogenetic receptors to regulate neuronal activity in the mammalian brain / Patrick Aldrin-Kirk and Tomas Bjo·rklund
- AAV production using baculovirus expression vector system / Quentin Sandro, Karima Relizani, and Rachid Benchaouir
- Multimodal production of adeno-associated virus / Ivette M. Sandoval, Nathan M. Kuhn, and Fredric P. Manfredsson
- Generation of high-titer pseudotyped lentiviral vectors / Shuang Hu, Mingjie Li, and Ramesh Akkina
- Scalable lentiviral vector production and purification method using mustang Q chromatography and tangential flow filtration / Stuart Tinch, Kathy Szczur, William Swaney, Lilith Reeves, and Scott R. Witting
- Current use of adenovirus vectors and their production methods / Ekramy E. Sayedahmed, Rashmi Kumari, and Suresh K. Mittal
- Construction of oncolytic herpes simplex virus with therapeutic genes of interest / Andranik Kahramanian, Toshihiko Kuroda, and Hiroaki Wakimoto
- Poxviruses as gene therapy vectors : generating poxviral vectors expressing therapeutic transgenes / Steven J. Conrad and Jia Liu
- AAV-mediated gene delivery to the mouse liver / Sharon C. Cunningham and Ian E. Alexander
- Surgical methods for inner ear gene delivery in neonatal mouse / Kevin Isgrig and Wade W. Chien
- Gene Transfer to Mouse Kidney In Vivo / C. J. Rocca and S. Cherqui
- Co-delivery of a short-hairpin RNA and a shRNA-resistant replacement gene with adeno-associated virus : an allele-independent strategy for autosomal-dominant retinal disorders / Michael T. Massengill, Brianna M. Young, Alfred S. Lewin, and Cristhian J. Ildefonso
- Localized intra-arterial gene delivery using AAV / Koji Hosaka, Fredric P. Manfredsson, and Brian L. Hoh
- Stable genetic modification of mesenchymal stromal cells using lentiviral vectors / Francisco Martłþn, Marłþa Tristaþn-Manzano, Noelia Maldonado-Peþrez, Sabina Saþnchez-Hernaþ ndez, Karim Benabdellah, and Marieþn Cobo
- Systemic delivery of adeno-associated viral vectors in mice and dogs / Lakmini P. Wasala, Chady H. Hakim, Yongping Yue, N. Nora Yang, and Dongsheng Duan
- Intrathecal delivery of AAV vectors in cynomolgus macaques for CNS gene therapy and gene expression analysis in microdissected motor neurons / Florie Borel, Eric Adams, and Christian Mueller
- Detailed method for intrathecal delivery of gene therapeutics by direct lumbar puncture in mice / Kelsey R. Pflepsen, Cristina D. Peterson, Kelley F. Kitto, Lucy Vulchanova, George L. Wilcox, and Carolyn A. Fairbanks
- Cerebellomedullary cistern injection of viral vectors in nonhuman primates / Lluis Samaranch, Kousaku Ohno, Waldy San Sebastian, and Krystof Bankiewicz.