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

Zweier

Showing results (371-380 of 677) with videos related to

Pageof 68
Sort By:
European Journal of Medical Genetics|September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1Bernt Popp, Regina Trollmann, Christian Büttner, et al.
British Journal of Pharmacology|October 3, 2003
On the selectivity of superoxide dismutase mimetics and its importance in pharmacological studiesCarolina Muscoli, Salvatore Cuzzocrea, Dennis P Riley, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2007
Myocardial ischemia results in tetrahydrobiopterin (BH4) oxidation with impaired endothelial function ameliorated by BH4Cristian Dumitrescu, Roberto Biondi, Yong Xia, et al.
American Journal of Physiology. Cell Physiology|September 16, 2005
Heat shock-induced attenuation of hydroxyl radical generation and mitochondrial aconitase activity in cardiac H9c2 cellsGovindasamy Ilangovan, C D Venkatakrishnan, Anna Bratasz, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Overexpression of human copper, zinc-superoxide dismutase (SOD1) prevents postischemic injuryP Wang, H Chen, H Qin, et al.
Clinical Genetics|June 6, 2022
Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6Céline B Gerber, Anna Fliedner, Oliver Bartsch, et al.
Human Mutation|June 1, 2010
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expressionMarkus Zweier, Anne Gregor, Christiane Zweier, et al.
Nitric Oxide : Biology and Chemistry|September 22, 2010
Application of carbon fiber composite minielectrodes for measurement of kinetic constants of nitric oxide decay in solutionXiaoping Liu, Gamal A El-Sherbiny, Eric Collard, et al.
Genetics Research|October 7, 2015
A de novo microdeletion in NRXN1 in a Dutch patient with mild intellectual disability, microcephaly and gonadal dysgenesisZehra Agha, Zafar Iqbal, Tjitske Kleefstra, et al.
Biochemistry|June 17, 2008
Regulation of eNOS-derived superoxide by endogenous methylargininesLawrence J Druhan, Scott P Forbes, Arthur J Pope, et al.
Pageof 68

Showing results (371-380 of 677) with videos related to

Sort By:
Pageof 68
European Journal of Medical Genetics|September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1Bernt Popp, Regina Trollmann, Christian Büttner, et al.
British Journal of Pharmacology|October 3, 2003
On the selectivity of superoxide dismutase mimetics and its importance in pharmacological studiesCarolina Muscoli, Salvatore Cuzzocrea, Dennis P Riley, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2007
Myocardial ischemia results in tetrahydrobiopterin (BH4) oxidation with impaired endothelial function ameliorated by BH4Cristian Dumitrescu, Roberto Biondi, Yong Xia, et al.
American Journal of Physiology. Cell Physiology|September 16, 2005
Heat shock-induced attenuation of hydroxyl radical generation and mitochondrial aconitase activity in cardiac H9c2 cellsGovindasamy Ilangovan, C D Venkatakrishnan, Anna Bratasz, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Overexpression of human copper, zinc-superoxide dismutase (SOD1) prevents postischemic injuryP Wang, H Chen, H Qin, et al.
Clinical Genetics|June 6, 2022
Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6Céline B Gerber, Anna Fliedner, Oliver Bartsch, et al.
Human Mutation|June 1, 2010
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expressionMarkus Zweier, Anne Gregor, Christiane Zweier, et al.
Nitric Oxide : Biology and Chemistry|September 22, 2010
Application of carbon fiber composite minielectrodes for measurement of kinetic constants of nitric oxide decay in solutionXiaoping Liu, Gamal A El-Sherbiny, Eric Collard, et al.
Genetics Research|October 7, 2015
A de novo microdeletion in NRXN1 in a Dutch patient with mild intellectual disability, microcephaly and gonadal dysgenesisZehra Agha, Zafar Iqbal, Tjitske Kleefstra, et al.
Biochemistry|June 17, 2008
Regulation of eNOS-derived superoxide by endogenous methylargininesLawrence J Druhan, Scott P Forbes, Arthur J Pope, et al.
Pageof 68