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Ian E Alexander

Showing results (81-90 of 131) with videos related to

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Molecular Therapy. Methods & Clinical Development|November 5, 2024
AAVolve: Concatenated long-read deep sequencing enables whole capsid tracking during shuffled AAV library selectionSuzanne Scott, Adrian Westhaus, Deborah Nazareth, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|January 30, 2009
Overexpression of indoleamine dioxygenase in rat liver allografts using a high-efficiency adeno-associated virus vector does not prevent acute rejectionJerome M Laurence, Chuanmin Wang, Maolin Zheng, et al.
Stem Cells (Dayton, Ohio)|May 6, 2009
Methylguanine DNA methyltransferase-mediated drug resistance-based selective enrichment and engraftment of transplanted stem cells in skeletal muscleAntonio S J Lee, Prathibha Kahatapitiya, Belinda Kramer, et al.
Nature Structural & Molecular Biology|October 6, 2014
A genome-wide map of adeno-associated virus-mediated human gene targetingDavid R Deyle, R Scott Hansen, Anda M Cornea, et al.
Hepatology (Baltimore, Md.)|May 27, 2015
Modeling correction of severe urea cycle defects in the growing murine liver using a hybrid recombinant adeno-associated virus/piggyBac transposase gene delivery systemSharon C Cunningham, Susan M Siew, Claus V Hallwirth, et al.
Human Molecular Genetics|September 13, 2019
Systemic AAV8-mediated delivery of a functional copy of muscle glycogen phosphorylase (Pygm) ameliorates disease in a murine model of McArdle diseaseElyshia L McNamara, Rhonda L Taylor, Joshua S Clayton, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 1, 2010
Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpressionSamantha L Ginn, Sophia H Y Liao, Allison P Dane, et al.
Molecular Therapy. Methods & Clinical Development|November 16, 2022
Intrabiliary infusion of naked DNA vectors targets periportal hepatocytes in miceSereina Deplazes, Andrea Schlegel, Zhuolun Song, et al.
The Journal of Gene Medicine|August 20, 2024
Stable transduction of the neonatal mouse liver using a hybrid rAAV/sleeping beauty transposon gene delivery systemSharon C Cunningham, Philip M Zakas, Natsuki Sasaki, et al.
Gene Therapy|July 19, 2025
High-throughput evaluation of cardiac-specific promoters for adeno-associated virus mediated cardiac gene therapyDhanya Ravindran, Renuka Rao, Juan Mundisugih, et al.
Pageof 14

Showing results (81-90 of 131) with videos related to

Sort By:
Pageof 14
Molecular Therapy. Methods & Clinical Development|November 5, 2024
AAVolve: Concatenated long-read deep sequencing enables whole capsid tracking during shuffled AAV library selectionSuzanne Scott, Adrian Westhaus, Deborah Nazareth, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|January 30, 2009
Overexpression of indoleamine dioxygenase in rat liver allografts using a high-efficiency adeno-associated virus vector does not prevent acute rejectionJerome M Laurence, Chuanmin Wang, Maolin Zheng, et al.
Stem Cells (Dayton, Ohio)|May 6, 2009
Methylguanine DNA methyltransferase-mediated drug resistance-based selective enrichment and engraftment of transplanted stem cells in skeletal muscleAntonio S J Lee, Prathibha Kahatapitiya, Belinda Kramer, et al.
Nature Structural & Molecular Biology|October 6, 2014
A genome-wide map of adeno-associated virus-mediated human gene targetingDavid R Deyle, R Scott Hansen, Anda M Cornea, et al.
Hepatology (Baltimore, Md.)|May 27, 2015
Modeling correction of severe urea cycle defects in the growing murine liver using a hybrid recombinant adeno-associated virus/piggyBac transposase gene delivery systemSharon C Cunningham, Susan M Siew, Claus V Hallwirth, et al.
Human Molecular Genetics|September 13, 2019
Systemic AAV8-mediated delivery of a functional copy of muscle glycogen phosphorylase (Pygm) ameliorates disease in a murine model of McArdle diseaseElyshia L McNamara, Rhonda L Taylor, Joshua S Clayton, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 1, 2010
Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpressionSamantha L Ginn, Sophia H Y Liao, Allison P Dane, et al.
Molecular Therapy. Methods & Clinical Development|November 16, 2022
Intrabiliary infusion of naked DNA vectors targets periportal hepatocytes in miceSereina Deplazes, Andrea Schlegel, Zhuolun Song, et al.
The Journal of Gene Medicine|August 20, 2024
Stable transduction of the neonatal mouse liver using a hybrid rAAV/sleeping beauty transposon gene delivery systemSharon C Cunningham, Philip M Zakas, Natsuki Sasaki, et al.
Gene Therapy|July 19, 2025
High-throughput evaluation of cardiac-specific promoters for adeno-associated virus mediated cardiac gene therapyDhanya Ravindran, Renuka Rao, Juan Mundisugih, et al.
Pageof 14