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

Barbara Lunghi

Showing results (31-40 of 35) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 35 results.
Journal of Thrombosis and Haemostasis : JTH|October 22, 2023
In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiencyAlice M Todaro, Claudia M Radu, Maria Ciccone, et al.
Journal of Thrombosis and Haemostasis : JTH|October 9, 2021
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypesAlessio Branchini, Massimo Morfini, Barbara Lunghi, et al.
Frontiers in Genetics|July 13, 2019
<i>C6orf10</i> Low-Frequency and Rare Variants in Italian Multiple Sclerosis PatientsNicole Ziliotto, Giovanna Marchetti, Chiara Scapoli, et al.
Thrombosis and Haemostasis|November 7, 2014
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosisGiovanna Marchetti, Domenico Girelli, Carlotta Zerbinati, et al.
Thrombosis Research|September 12, 2025
Genetic determinants of activated factor VII-antithrombin plasma levels and mortality in patients with coronary artery diseaseNicola Osti, Gerardo Musuraca, Barbara Lunghi, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Thrombosis and Haemostasis : JTH|October 22, 2023
In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiencyAlice M Todaro, Claudia M Radu, Maria Ciccone, et al.
Journal of Thrombosis and Haemostasis : JTH|October 9, 2021
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypesAlessio Branchini, Massimo Morfini, Barbara Lunghi, et al.
Frontiers in Genetics|July 13, 2019
<i>C6orf10</i> Low-Frequency and Rare Variants in Italian Multiple Sclerosis PatientsNicole Ziliotto, Giovanna Marchetti, Chiara Scapoli, et al.
Thrombosis and Haemostasis|November 7, 2014
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosisGiovanna Marchetti, Domenico Girelli, Carlotta Zerbinati, et al.
Thrombosis Research|September 12, 2025
Genetic determinants of activated factor VII-antithrombin plasma levels and mortality in patients with coronary artery diseaseNicola Osti, Gerardo Musuraca, Barbara Lunghi, et al.
Pageof 4