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Ernest Turro

Showing results (31-40 of 81) with videos related to

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Blood|May 29, 2026
Reduced platelet formation associated with serine metabolic dysregulation in integrin αIIbβ3-deficient megakaryocytesKato Ramaekers, My Tran, Marco Lunghi, et al.
Transfusion|July 16, 2015
A multicenter validation of recombinant β3 integrin-coupled beads to detect human platelet antigen-1 alloantibodies in 498 cases of fetomaternal alloimmune thrombocytopeniaWinnie Chong, Ernest Turro, Paul Metcalfe, et al.
The Journal of Clinical Investigation|July 15, 2020
A coagulation defect arising from heterozygous premature termination of tissue factorSol Schulman, Emale El-Darzi, Mary Hc Florido, et al.
Blood|June 24, 2020
Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasiaClaire L Shovlin, Ilenia Simeoni, Kate Downes, et al.
Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Blood|September 15, 2018
A mutation of the human Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
Haematologica|March 12, 2026
Thyroid hormones induce an acute platelet release mechanism via integrin αVβ3Holly R Foster, Nina Herbert, Christian A Di Buduo, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|January 20, 2026
Understanding how a highly prevalent GRK5 polymorphism affects platelets and enhances thrombotic riskYanki Yarman, Xuefei Zhao, Hyunsook Ahn, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
Blood|May 29, 2026
Reduced platelet formation associated with serine metabolic dysregulation in integrin αIIbβ3-deficient megakaryocytesKato Ramaekers, My Tran, Marco Lunghi, et al.
Transfusion|July 16, 2015
A multicenter validation of recombinant β3 integrin-coupled beads to detect human platelet antigen-1 alloantibodies in 498 cases of fetomaternal alloimmune thrombocytopeniaWinnie Chong, Ernest Turro, Paul Metcalfe, et al.
The Journal of Clinical Investigation|July 15, 2020
A coagulation defect arising from heterozygous premature termination of tissue factorSol Schulman, Emale El-Darzi, Mary Hc Florido, et al.
Blood|June 24, 2020
Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasiaClaire L Shovlin, Ilenia Simeoni, Kate Downes, et al.
Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Blood|September 15, 2018
A mutation of the human Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
Haematologica|March 12, 2026
Thyroid hormones induce an acute platelet release mechanism via integrin αVβ3Holly R Foster, Nina Herbert, Christian A Di Buduo, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|January 20, 2026
Understanding how a highly prevalent GRK5 polymorphism affects platelets and enhances thrombotic riskYanki Yarman, Xuefei Zhao, Hyunsook Ahn, et al.
Pageof 9