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

M Fabbrini

Showing results (11-20 of 13) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 13 results.
NPJ Vaccines|October 31, 2025
Contribution of the different Neisseria gonorrhoeae lipooligosaccharide structural variants to functional responses elicited by GMMA outer membrane vesiclesR Cuffaro, G Buffi, G Romagnoli, et al.
International Journal of Molecular Sciences|June 29, 2019
Nuclear Phosphoinositides: Their Regulation and Roles in Nuclear FunctionsR Fiume, I Faenza, B Sheth, et al.
Journal of Medicinal Chemistry|July 21, 2001
Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agentG Campiani, F Aiello, M Fabbrini, et al.
Pageof 2

Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
NPJ Vaccines|October 31, 2025
Contribution of the different Neisseria gonorrhoeae lipooligosaccharide structural variants to functional responses elicited by GMMA outer membrane vesiclesR Cuffaro, G Buffi, G Romagnoli, et al.
International Journal of Molecular Sciences|June 29, 2019
Nuclear Phosphoinositides: Their Regulation and Roles in Nuclear FunctionsR Fiume, I Faenza, B Sheth, et al.
Journal of Medicinal Chemistry|July 21, 2001
Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agentG Campiani, F Aiello, M Fabbrini, et al.
Pageof 2