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Silvia Ferrari

Showing results (61-70 of 246) with videos related to

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British Journal of Haematology|June 26, 2024
The compound pathogenic effects of a homozygous frameshift variant in the transmembrane region of GP9, causing Bernard-Soulier syndrome, with a missense variant in GP1BBSilvia Ferrari, Daniela Regazzo, Anna Cerbo, et al.
Biomolecules|October 10, 2020
Harnessing Mechanosensation in Next Generation Cardiovascular Tissue EngineeringGloria Garoffolo, Silvia Ferrari, Stefano Rizzi, et al.
Molecular and Cellular Biology|August 26, 2009
HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by gemininValentina Salsi, Silvia Ferrari, Roberta Ferraresi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 2017
Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up studyAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
European Journal of Haematology|April 29, 2016
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)Antonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Neuroimage|September 9, 2017
Probabilistic inference under time pressure leads to a cortical-to-subcortical shift in decision evidence integrationHanna Oh-Descher, Jeffrey M Beck, Silvia Ferrari, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 12, 2017
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)Antonio Girolami, Salvador Minoldo, Silvia Ferrari, et al.
Blood Cells, Molecules & Diseases|April 10, 2017
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemiaAnna Maria Lombardi, Silvia Ferrari, Isabella Barzon, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 30, 2016
Factor X Friuli Coagulation Disorder: Almost 50 Years LaterAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Frontiers in Robotics and AI|November 27, 2024
Heuristic satisficing inferential decision making in human and robot active perceptionYucheng Chen, Pingping Zhu, Anthony Alers, et al.
Pageof 25

Showing results (61-70 of 246) with videos related to

Sort By:
Pageof 25
British Journal of Haematology|June 26, 2024
The compound pathogenic effects of a homozygous frameshift variant in the transmembrane region of GP9, causing Bernard-Soulier syndrome, with a missense variant in GP1BBSilvia Ferrari, Daniela Regazzo, Anna Cerbo, et al.
Biomolecules|October 10, 2020
Harnessing Mechanosensation in Next Generation Cardiovascular Tissue EngineeringGloria Garoffolo, Silvia Ferrari, Stefano Rizzi, et al.
Molecular and Cellular Biology|August 26, 2009
HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by gemininValentina Salsi, Silvia Ferrari, Roberta Ferraresi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 2017
Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up studyAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
European Journal of Haematology|April 29, 2016
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)Antonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Neuroimage|September 9, 2017
Probabilistic inference under time pressure leads to a cortical-to-subcortical shift in decision evidence integrationHanna Oh-Descher, Jeffrey M Beck, Silvia Ferrari, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 12, 2017
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)Antonio Girolami, Salvador Minoldo, Silvia Ferrari, et al.
Blood Cells, Molecules & Diseases|April 10, 2017
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemiaAnna Maria Lombardi, Silvia Ferrari, Isabella Barzon, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 30, 2016
Factor X Friuli Coagulation Disorder: Almost 50 Years LaterAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Frontiers in Robotics and AI|November 27, 2024
Heuristic satisficing inferential decision making in human and robot active perceptionYucheng Chen, Pingping Zhu, Anthony Alers, et al.
Pageof 25