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Mor Cohen

Showing results (21-30 of 41) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 9, 2007
Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrationsRonit Mor-Cohen, Ariella Zivelin, Yonit Fromovich-Amit, et al.
Frontiers in Public Health|March 18, 2026
Implementation of an innovative virtual selective screening program for early detection of cerebral palsy in British ColumbiaKeith O'Connor, Nandy Fajardo, Carol Lai, et al.
Experimental Cell Research|May 3, 2019
Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomeraseNurit Rosenberg, Ronit Mor-Cohen, Vera Hazan Sheptovitsky, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
Thrombosis Research|October 31, 2015
The role of protein disulfide isomerase in the post-ligation phase of β3 integrin-dependent cell adhesionAvi Leader, Ronit Mor-Cohen, Ron Ram, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 26, 2015
Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndromeHagit Hauschner, Ronit Mor-Cohen, Stefania Messineo, et al.
Thrombosis and Haemostasis|December 8, 2007
Disulfide bond disruption by a beta 3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active alpha IIb beta 3Ronit Mor-Cohen, Nurit Rosenberg, Hava Peretz, et al.
Acta Haematologica|January 22, 2011
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type IIAchiya Amir, Orly Dgany, Tanya Krasnov, et al.
The Journal of Biological Chemistry|February 7, 2012
Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different mannerRonit Mor-Cohen, Nurit Rosenberg, Yulia Einav, et al.
Journal of Medical Internet Research|August 6, 2025
Monitoring Ovarian Stimulation for Assisted Reproduction With Patient Self-Scans Using a Home Vaginal Ultrasound Device: A Single-Center Interventional, Prospective StudyYoel Shufaro, Mor Cohen, Avital Wertheimer, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 9, 2007
Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrationsRonit Mor-Cohen, Ariella Zivelin, Yonit Fromovich-Amit, et al.
Frontiers in Public Health|March 18, 2026
Implementation of an innovative virtual selective screening program for early detection of cerebral palsy in British ColumbiaKeith O'Connor, Nandy Fajardo, Carol Lai, et al.
Experimental Cell Research|May 3, 2019
Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomeraseNurit Rosenberg, Ronit Mor-Cohen, Vera Hazan Sheptovitsky, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
Thrombosis Research|October 31, 2015
The role of protein disulfide isomerase in the post-ligation phase of β3 integrin-dependent cell adhesionAvi Leader, Ronit Mor-Cohen, Ron Ram, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 26, 2015
Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndromeHagit Hauschner, Ronit Mor-Cohen, Stefania Messineo, et al.
Thrombosis and Haemostasis|December 8, 2007
Disulfide bond disruption by a beta 3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active alpha IIb beta 3Ronit Mor-Cohen, Nurit Rosenberg, Hava Peretz, et al.
Acta Haematologica|January 22, 2011
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type IIAchiya Amir, Orly Dgany, Tanya Krasnov, et al.
The Journal of Biological Chemistry|February 7, 2012
Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different mannerRonit Mor-Cohen, Nurit Rosenberg, Yulia Einav, et al.
Journal of Medical Internet Research|August 6, 2025
Monitoring Ovarian Stimulation for Assisted Reproduction With Patient Self-Scans Using a Home Vaginal Ultrasound Device: A Single-Center Interventional, Prospective StudyYoel Shufaro, Mor Cohen, Avital Wertheimer, et al.
Pageof 5