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

Saverio Francesco Retta

Showing results (51-60 of 60) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 60 results.
Free Radical Biology & Medicine|November 25, 2017
KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous Malformation diseaseCinzia Antognelli, Eliana Trapani, Simona Delle Monache, et al.
Scientific Reports|August 17, 2017
Up-regulation of NADPH oxidase-mediated redox signaling contributes to the loss of barrier function in KRIT1 deficient endotheliumLuca Goitre, Peter V DiStefano, Andrea Moglia, et al.
Antioxidants (Basel, Switzerland)|January 20, 2019
KRIT1 Loss-Of-Function Associated with Cerebral Cavernous Malformation Disease Leads to Enhanced <i>S</i>-Glutathionylation of Distinct Structural and Regulatory ProteinsLaura Cianfruglia, Andrea Perrelli, Claudia Fornelli, et al.
Brain Pathology (Zurich, Switzerland)|October 30, 2010
Mutation analysis of CCM1, CCM2 and CCM3 genes in a cohort of Italian patients with cerebral cavernous malformationRosalia D'Angelo, Valeria Marini, Carmela Rinaldi, et al.
International Journal of Molecular Sciences|October 9, 2019
KRIT1 Deficiency Promotes Aortic Endothelial DysfunctionFrancesco Vieceli Dalla Sega, Raffaella Mastrocola, Giorgio Aquila, et al.
Nature|June 11, 2013
EndMT contributes to the onset and progression of cerebral cavernous malformationsLuigi Maddaluno, Noemi Rudini, Roberto Cuttano, et al.
EMBO Molecular Medicine|September 30, 2015
Defective autophagy is a key feature of cerebral cavernous malformationsSaverio Marchi, Mariangela Corricelli, Eliana Trapani, et al.
The Journal of Biological Chemistry|January 5, 2002
Integrin-induced epidermal growth factor (EGF) receptor activation requires c-Src and p130Cas and leads to phosphorylation of specific EGF receptor tyrosinesLaura Moro, Laura Dolce, Sara Cabodi, et al.
Circulation|December 10, 2014
Strategy for identifying repurposed drugs for the treatment of cerebral cavernous malformationChristopher C Gibson, Weiquan Zhu, Chadwick T Davis, et al.
Journal of Medical Genetics|June 11, 2013
A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasiaEleonora Di Gregorio, Federico T Bianchi, Alfonso Schiavi, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Free Radical Biology & Medicine|November 25, 2017
KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous Malformation diseaseCinzia Antognelli, Eliana Trapani, Simona Delle Monache, et al.
Scientific Reports|August 17, 2017
Up-regulation of NADPH oxidase-mediated redox signaling contributes to the loss of barrier function in KRIT1 deficient endotheliumLuca Goitre, Peter V DiStefano, Andrea Moglia, et al.
Antioxidants (Basel, Switzerland)|January 20, 2019
KRIT1 Loss-Of-Function Associated with Cerebral Cavernous Malformation Disease Leads to Enhanced <i>S</i>-Glutathionylation of Distinct Structural and Regulatory ProteinsLaura Cianfruglia, Andrea Perrelli, Claudia Fornelli, et al.
Brain Pathology (Zurich, Switzerland)|October 30, 2010
Mutation analysis of CCM1, CCM2 and CCM3 genes in a cohort of Italian patients with cerebral cavernous malformationRosalia D'Angelo, Valeria Marini, Carmela Rinaldi, et al.
International Journal of Molecular Sciences|October 9, 2019
KRIT1 Deficiency Promotes Aortic Endothelial DysfunctionFrancesco Vieceli Dalla Sega, Raffaella Mastrocola, Giorgio Aquila, et al.
Nature|June 11, 2013
EndMT contributes to the onset and progression of cerebral cavernous malformationsLuigi Maddaluno, Noemi Rudini, Roberto Cuttano, et al.
EMBO Molecular Medicine|September 30, 2015
Defective autophagy is a key feature of cerebral cavernous malformationsSaverio Marchi, Mariangela Corricelli, Eliana Trapani, et al.
The Journal of Biological Chemistry|January 5, 2002
Integrin-induced epidermal growth factor (EGF) receptor activation requires c-Src and p130Cas and leads to phosphorylation of specific EGF receptor tyrosinesLaura Moro, Laura Dolce, Sara Cabodi, et al.
Circulation|December 10, 2014
Strategy for identifying repurposed drugs for the treatment of cerebral cavernous malformationChristopher C Gibson, Weiquan Zhu, Chadwick T Davis, et al.
Journal of Medical Genetics|June 11, 2013
A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasiaEleonora Di Gregorio, Federico T Bianchi, Alfonso Schiavi, et al.
Pageof 6