Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mark A Kay

Showing results (151-160 of 197) with videos related to

Pageof 20
Sort By:
Nature Chemical Biology|April 3, 2019
An orange calcium-modulated bioluminescent indicator for non-invasive activity imagingYounghee Oh, Yunhee Park, Julia H Cho, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 18, 2010
Minicircle DNA-based gene therapy coupled with immune modulation permits long-term expression of α-L-iduronidase in mice with mucopolysaccharidosis type IMark J Osborn, Ron T McElmurry, Christopher J Lees, et al.
Nature Medicine|April 12, 2016
RNA interference-induced hepatotoxicity results from loss of the first synthesized isoform of microRNA-122 in micePaul N Valdmanis, Shuo Gu, Kirk Chu, et al.
Cell Transplantation|November 9, 2010
Immunogenicity and immunomodulatory properties of umbilical cord lining mesenchymal stem cellsTobias Deuse, Mandy Stubbendorff, Karis Tang-Quan, et al.
Molecular Therapy. Methods & Clinical Development|December 14, 2020
AAV vectors engineered to target insulin receptor greatly enhance intramuscular gene deliveryCody B Jackson, Audrey S Richard, Amrita Ojha, et al.
Hepatology (Baltimore, Md.)|January 29, 2008
Hepatic parenchymal replacement in mice by transplanted allogeneic hepatocytes is facilitated by bone marrow transplantation and mediated by CD4 cellsKonrad L Streetz, Regis Doyonnas, Dirk Grimm, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2007
Correction of DNA protein kinase deficiency by spliceosome-mediated RNA trans-splicing and sleeping beauty transposon deliveryHatem Zayed, Lily Xia, Anton Yerich, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2008
The host response to adenovirus, helper-dependent adenovirus, and adeno-associated virus in mouse liverAnton P McCaffrey, Paul Fawcett, Hiroyuki Nakai, et al.
Scientific Reports|January 29, 2015
Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotencySebastian Diecke, Jiamiao Lu, Jaecheol Lee, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 17, 2017
Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin DeficiencyFlorie Borel, Qiushi Tang, Gwladys Gernoux, et al.
Pageof 20

Showing results (151-160 of 197) with videos related to

Sort By:
Pageof 20
Nature Chemical Biology|April 3, 2019
An orange calcium-modulated bioluminescent indicator for non-invasive activity imagingYounghee Oh, Yunhee Park, Julia H Cho, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 18, 2010
Minicircle DNA-based gene therapy coupled with immune modulation permits long-term expression of α-L-iduronidase in mice with mucopolysaccharidosis type IMark J Osborn, Ron T McElmurry, Christopher J Lees, et al.
Nature Medicine|April 12, 2016
RNA interference-induced hepatotoxicity results from loss of the first synthesized isoform of microRNA-122 in micePaul N Valdmanis, Shuo Gu, Kirk Chu, et al.
Cell Transplantation|November 9, 2010
Immunogenicity and immunomodulatory properties of umbilical cord lining mesenchymal stem cellsTobias Deuse, Mandy Stubbendorff, Karis Tang-Quan, et al.
Molecular Therapy. Methods & Clinical Development|December 14, 2020
AAV vectors engineered to target insulin receptor greatly enhance intramuscular gene deliveryCody B Jackson, Audrey S Richard, Amrita Ojha, et al.
Hepatology (Baltimore, Md.)|January 29, 2008
Hepatic parenchymal replacement in mice by transplanted allogeneic hepatocytes is facilitated by bone marrow transplantation and mediated by CD4 cellsKonrad L Streetz, Regis Doyonnas, Dirk Grimm, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2007
Correction of DNA protein kinase deficiency by spliceosome-mediated RNA trans-splicing and sleeping beauty transposon deliveryHatem Zayed, Lily Xia, Anton Yerich, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2008
The host response to adenovirus, helper-dependent adenovirus, and adeno-associated virus in mouse liverAnton P McCaffrey, Paul Fawcett, Hiroyuki Nakai, et al.
Scientific Reports|January 29, 2015
Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotencySebastian Diecke, Jiamiao Lu, Jaecheol Lee, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 17, 2017
Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin DeficiencyFlorie Borel, Qiushi Tang, Gwladys Gernoux, et al.
Pageof 20