Viral vectors for gene therapy : methods and protocols /

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Bibliographic Details
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
Hidden Bibliographic Details
Other authors / contributors:Manfredsson, Fredric P., editor.
Benskey, Matthew J., editor.
ISBN:9781493990658
1493990659
9781493990641
1493990640
Digital file characteristics:text file PDF
Notes:Includes bibliographical references and index.
Online resource; title from PDF title page (SpringerLink, viewed January 31, 2019).
Other form:Print version: Viral vectors for gene therapy. New York : Humana Press ; Springer, 2019 9781493990474
Standard no.:10.1007/978-1-4939-9065-8

MARC

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245 0 0 |a Viral vectors for gene therapy :  |b methods and protocols /  |c edited by Fredric P. Manfredsson, Matthew J. Benskey. 
264 1 |a New York :  |b Humana Press :  |b Springer,  |c [2019] 
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490 1 |a Methods in molecular biology,  |x 1940-6029 ;  |v v. 1937 
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588 0 |a Online resource; title from PDF title page (SpringerLink, viewed January 31, 2019). 
505 0 0 |t Basic concepts in viral vector-mediated gene therapy /  |r Matthew J. Benskey, Ivette M. Sandoval, Kathryn Miller,Rhyomi L. Sellnow, Aysegul Gezer, Nathan C. Kuhn, Roslyn Vashon, and Fredric P. Manfredsson --  |t Design and assembly of CRISPR/Cas9 lentiviral and rAAV vectors for targeted genome editing /  |r Ivette M. Sandoval, Timothy J. Collier, and Fredric P. Manfredsson --  |t Design, construction, and application of transcription activation-like effectors /  |r Peter Deng, Sakereh Carter, and Kyle Fink --  |t Practical considerations for the use of DREADD and other chemogenetic receptors to regulate neuronal activity in the mammalian brain /  |r Patrick Aldrin-Kirk and Tomas Bjo·rklund --  |t AAV production using baculovirus expression vector system /  |r Quentin Sandro, Karima Relizani, and Rachid Benchaouir --  |t Multimodal production of adeno-associated virus /  |r Ivette M. Sandoval, Nathan M. Kuhn, and Fredric P. Manfredsson --  |t Generation of high-titer pseudotyped lentiviral vectors /  |r Shuang Hu, Mingjie Li, and Ramesh Akkina --  |t Scalable lentiviral vector production and purification method using mustang Q chromatography and tangential flow filtration /  |r Stuart Tinch, Kathy Szczur, William Swaney, Lilith Reeves, and Scott R. Witting --  |t Current use of adenovirus vectors and their production methods /  |r Ekramy E. Sayedahmed, Rashmi Kumari, and Suresh K. Mittal --  |t Construction of oncolytic herpes simplex virus with therapeutic genes of interest /  |r Andranik Kahramanian, Toshihiko Kuroda, and Hiroaki Wakimoto --  |t Poxviruses as gene therapy vectors : generating poxviral vectors expressing therapeutic transgenes /  |r Steven J. Conrad and Jia Liu --  |t AAV-mediated gene delivery to the mouse liver /  |r Sharon C. Cunningham and Ian E. Alexander --  |t Surgical methods for inner ear gene delivery in neonatal mouse /  |r Kevin Isgrig and Wade W. Chien --  |t Gene Transfer to Mouse Kidney In Vivo /  |r C. J. Rocca and S. Cherqui --  |t 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 /  |r Michael T. Massengill, Brianna M. Young, Alfred S. Lewin, and Cristhian J. Ildefonso --  |t Localized intra-arterial gene delivery using AAV /  |r Koji Hosaka, Fredric P. Manfredsson, and Brian L. Hoh --  |t Stable genetic modification of mesenchymal stromal cells using lentiviral vectors /  |r Francisco Martłþn, Marłþa Tristaþn-Manzano, Noelia Maldonado-Peþrez, Sabina Saþnchez-Hernaþ ndez, Karim Benabdellah, and Marieþn Cobo --  |t Systemic delivery of adeno-associated viral vectors in mice and dogs /  |r Lakmini P. Wasala, Chady H. Hakim, Yongping Yue, N. Nora Yang, and Dongsheng Duan --  |t Intrathecal delivery of AAV vectors in cynomolgus macaques for CNS gene therapy and gene expression analysis in microdissected motor neurons /  |r Florie Borel, Eric Adams, and Christian Mueller --  |t Detailed method for intrathecal delivery of gene therapeutics by direct lumbar puncture in mice /  |r Kelsey R. Pflepsen, Cristina D. Peterson, Kelley F. Kitto, Lucy Vulchanova, George L. Wilcox, and Carolyn A. Fairbanks --  |t Cerebellomedullary cistern injection of viral vectors in nonhuman primates /  |r Lluis Samaranch, Kousaku Ohno, Waldy San Sebastian, and Krystof Bankiewicz. 
650 0 |a Gene therapy  |v Laboratory manuals. 
650 0 |a Viral genetics  |v Laboratory manuals. 
650 2 |a Genetic Vectors. 
650 2 |a Viruses. 
650 1 2 |a Genetic Therapy. 
650 2 |a Genes, Viral. 
650 2 2 |a Gene Transfer Techniques. 
650 7 |a Gene therapy.  |2 fast  |0 (OCoLC)fst00939638 
650 7 |a Viral genetics.  |2 fast  |0 (OCoLC)fst01167607 
655 2 |a Laboratory Manual. 
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700 1 |a Benskey, Matthew J.,  |e editor. 
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