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

B J Petrof

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
The American Review of Respiratory Disease|May 1, 1991
Nasal continuous positive airway pressure facilitates respiratory muscle function during sleep in severe chronic obstructive pulmonary diseaseB J Petrof, R J Kimoff, R D Levy, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993
Dystrophin protects the sarcolemma from stresses developed during muscle contractionB J Petrof, J B Shrager, H H Stedman, et al.
Physiological Genomics|October 4, 2000
Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) miceS Ebihara, G H Guibinga, R Gilbert, et al.
The American Journal of Physiology|September 1, 1993
Adaptations in myosin heavy chain expression and contractile function in dystrophic mouse diaphragmB J Petrof, H H Stedman, J B Shrager, et al.
Human Gene Therapy|October 1, 1996
Impairment of force generation after adenovirus-mediated gene transfer to muscle is alleviated by adenoviral gene inactivation and host CD8+ T cell deficiencyB J Petrof, H Lochmüller, B Massie, et al.
Human Gene Therapy|April 11, 2000
Modulation of Starling forces and muscle fiber maturity permits adenovirus-mediated gene transfer to adult dystrophic (mdx) mice by the intravascular routeW K Cho, S Ebihara, J Nalbantoglu, et al.
Human Gene Therapy|January 20, 1996
Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transferG Acsadi, H Lochmüller, A Jani, et al.
American Journal of Respiratory Cell and Molecular Biology|November 1, 1995
Efficiency and functional consequences of adenovirus-mediated in vivo gene transfer to normal and dystrophic (mdx) mouse diaphragmB J Petrof, G Acsadi, A Jani, et al.
American Journal of Respiratory and Critical Care Medicine|November 17, 1998
Diaphragm sarcolemmal injury is induced by sepsis and alleviated by nitric oxide synthase inhibitionM C Lin, S Ebihara, Q El Dwairi, et al.
Human Gene Therapy|September 19, 2001
Dystrophin expression in muscle following gene transfer with a fully deleted ("gutted") adenovirus is markedly improved by trans-acting adenoviral gene productsR Gilbert, J Nalbantoglu, J M Howell, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
The American Review of Respiratory Disease|May 1, 1991
Nasal continuous positive airway pressure facilitates respiratory muscle function during sleep in severe chronic obstructive pulmonary diseaseB J Petrof, R J Kimoff, R D Levy, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993
Dystrophin protects the sarcolemma from stresses developed during muscle contractionB J Petrof, J B Shrager, H H Stedman, et al.
Physiological Genomics|October 4, 2000
Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) miceS Ebihara, G H Guibinga, R Gilbert, et al.
The American Journal of Physiology|September 1, 1993
Adaptations in myosin heavy chain expression and contractile function in dystrophic mouse diaphragmB J Petrof, H H Stedman, J B Shrager, et al.
Human Gene Therapy|October 1, 1996
Impairment of force generation after adenovirus-mediated gene transfer to muscle is alleviated by adenoviral gene inactivation and host CD8+ T cell deficiencyB J Petrof, H Lochmüller, B Massie, et al.
Human Gene Therapy|April 11, 2000
Modulation of Starling forces and muscle fiber maturity permits adenovirus-mediated gene transfer to adult dystrophic (mdx) mice by the intravascular routeW K Cho, S Ebihara, J Nalbantoglu, et al.
Human Gene Therapy|January 20, 1996
Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transferG Acsadi, H Lochmüller, A Jani, et al.
American Journal of Respiratory Cell and Molecular Biology|November 1, 1995
Efficiency and functional consequences of adenovirus-mediated in vivo gene transfer to normal and dystrophic (mdx) mouse diaphragmB J Petrof, G Acsadi, A Jani, et al.
American Journal of Respiratory and Critical Care Medicine|November 17, 1998
Diaphragm sarcolemmal injury is induced by sepsis and alleviated by nitric oxide synthase inhibitionM C Lin, S Ebihara, Q El Dwairi, et al.
Human Gene Therapy|September 19, 2001
Dystrophin expression in muscle following gene transfer with a fully deleted ("gutted") adenovirus is markedly improved by trans-acting adenoviral gene productsR Gilbert, J Nalbantoglu, J M Howell, et al.
Pageof 4