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Peter Colosi

Showing results (21-30 of 25) with videos related to

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Stroke|March 23, 2017
Soluble FLT1 Gene Therapy Alleviates Brain Arteriovenous Malformation SeverityWan Zhu, Fanxia Shen, Lei Mao, et al.
Molecular Therapy. Methods & Clinical Development|July 5, 2022
Application of <i>in</i>-<i>vitro</i>-cultured primary hepatocytes to evaluate species translatability and AAV transduction mechanisms of actionSu Liu, Lisa Razon, Olivia Ritchie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 3, 2018
Gene Therapy with BMN 270 Results in Therapeutic Levels of FVIII in Mice and Primates and Normalization of Bleeding in Hemophilic MiceStuart Bunting, Lening Zhang, Lin Xie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2018
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal DeliveryCatherine Cukras, Henry E Wiley, Brett G Jeffrey, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
PDGF-CC blockade inhibits pathological angiogenesis by acting on multiple cellular and molecular targetsXu Hou, Anil Kumar, Chunsik Lee, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Stroke|March 23, 2017
Soluble FLT1 Gene Therapy Alleviates Brain Arteriovenous Malformation SeverityWan Zhu, Fanxia Shen, Lei Mao, et al.
Molecular Therapy. Methods & Clinical Development|July 5, 2022
Application of <i>in</i>-<i>vitro</i>-cultured primary hepatocytes to evaluate species translatability and AAV transduction mechanisms of actionSu Liu, Lisa Razon, Olivia Ritchie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 3, 2018
Gene Therapy with BMN 270 Results in Therapeutic Levels of FVIII in Mice and Primates and Normalization of Bleeding in Hemophilic MiceStuart Bunting, Lening Zhang, Lin Xie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2018
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal DeliveryCatherine Cukras, Henry E Wiley, Brett G Jeffrey, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
PDGF-CC blockade inhibits pathological angiogenesis by acting on multiple cellular and molecular targetsXu Hou, Anil Kumar, Chunsik Lee, et al.
Pageof 3