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Alessandro Malara

Showing results (31-40 of 39) with videos related to

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Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|October 29, 2013
Biocompatibility of functionalized boron phosphate (BPO4) nanoparticles for boron neutron capture therapy (BNCT) applicationCesare Achilli, Stefania Grandi, Annarita Ciana, et al.
Thrombosis and Haemostasis|June 17, 2016
Oxidative stress and thromboxane-dependent platelet activation in inflammatory bowel disease: effects of anti-TNF-α treatmentAntonio Di Sabatino, Francesca Santilli, Marco Guerci, et al.
Stem Cells (Dayton, Ohio)|January 11, 2016
Thrombopoietin/TGF-β1 Loop Regulates Megakaryocyte Extracellular Matrix Component SynthesisVittorio Abbonante, Christian A Di Buduo, Cristian Gruppi, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 29, 2021
The α<sub>2</sub>-adrenergic receptor pathway modulating depression influences the risk of arterial thrombosis associated with BDNFVal66Met polymorphismLeonardo Sandrini, Patrizia Amadio, Alessandro Ieraci, et al.
The Journal of Experimental Medicine|February 9, 2019
EDA fibronectin-TLR4 axis sustains megakaryocyte expansion and inflammation in bone marrow fibrosisAlessandro Malara, Cristian Gruppi, Vittorio Abbonante, et al.
Blood|January 11, 2015
Programmable 3D silk bone marrow niche for platelet generation ex vivo and modeling of megakaryopoiesis pathologiesChristian A Di Buduo, Lindsay S Wray, Lorenzo Tozzi, et al.
Research and Practice in Thrombosis and Haemostasis|April 3, 2025
Illustrated capsules from the Advanced Course in Platelet ResearchChristian Andrea Di Buduo, Vittorio Abbonante, Alessandro Malara, et al.
American Journal of Human Genetics|March 30, 2023
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhageMauro Lecca, Davut Pehlivan, Damià Heine Suñer, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|October 29, 2013
Biocompatibility of functionalized boron phosphate (BPO4) nanoparticles for boron neutron capture therapy (BNCT) applicationCesare Achilli, Stefania Grandi, Annarita Ciana, et al.
Thrombosis and Haemostasis|June 17, 2016
Oxidative stress and thromboxane-dependent platelet activation in inflammatory bowel disease: effects of anti-TNF-α treatmentAntonio Di Sabatino, Francesca Santilli, Marco Guerci, et al.
Stem Cells (Dayton, Ohio)|January 11, 2016
Thrombopoietin/TGF-β1 Loop Regulates Megakaryocyte Extracellular Matrix Component SynthesisVittorio Abbonante, Christian A Di Buduo, Cristian Gruppi, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 29, 2021
The α<sub>2</sub>-adrenergic receptor pathway modulating depression influences the risk of arterial thrombosis associated with BDNFVal66Met polymorphismLeonardo Sandrini, Patrizia Amadio, Alessandro Ieraci, et al.
The Journal of Experimental Medicine|February 9, 2019
EDA fibronectin-TLR4 axis sustains megakaryocyte expansion and inflammation in bone marrow fibrosisAlessandro Malara, Cristian Gruppi, Vittorio Abbonante, et al.
Blood|January 11, 2015
Programmable 3D silk bone marrow niche for platelet generation ex vivo and modeling of megakaryopoiesis pathologiesChristian A Di Buduo, Lindsay S Wray, Lorenzo Tozzi, et al.
Research and Practice in Thrombosis and Haemostasis|April 3, 2025
Illustrated capsules from the Advanced Course in Platelet ResearchChristian Andrea Di Buduo, Vittorio Abbonante, Alessandro Malara, et al.
American Journal of Human Genetics|March 30, 2023
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhageMauro Lecca, Davut Pehlivan, Damià Heine Suñer, et al.
Pageof 4