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Martina E Daly

Showing results (1-10 of 19) with videos related to

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Blood Reviews|July 25, 2016
Transcription factor defects causing platelet disordersMartina E Daly
Thrombosis Research|August 16, 2011
Lack of association between polymorphisms in the interleukin-1 gene cluster and familial thrombophiliaLuke Marsden, Angela Cox, Mike Makris, et al.
Journal of the National Cancer Institute|November 20, 2003
Hemostatic regulators of tumor angiogenesis: a source of antiangiogenic agents for cancer treatment?Martina E Daly, Andreas Makris, Malcolm Reed, et al.
British Journal of Haematology|May 19, 2004
The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general populationNicholas J Beauchamp, Anne C Dykes, Nirzari Parikh, et al.
British Journal of Haematology|February 1, 2014
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?Martina E Daly, Vincenzo C Leo, Gillian C Lowe, et al.
Blood|September 23, 2011
An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human plateletsShaista Nisar, Martina E Daly, Augusto B Federici, et al.
Blood|June 7, 2003
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factorGrégoire Michaux, Lindsay J Hewlett, Sarah L Messenger, et al.
Platelets|June 14, 2006
Common sequence variations in the P2Y12 and CYP3A5 genes do not explain the variability in the inhibitory effects of clopidogrel therapySimon M G Smith, Heather M Judge, Gary Peters, et al.
Blood|September 25, 2012
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panelBan B Dawood, Gillian C Lowe, Marie Lordkipanidzé, et al.
Haematologica|January 13, 2022
Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytesJoanne Lacey, Simon J Webster, Paul R Heath, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Blood Reviews|July 25, 2016
Transcription factor defects causing platelet disordersMartina E Daly
Thrombosis Research|August 16, 2011
Lack of association between polymorphisms in the interleukin-1 gene cluster and familial thrombophiliaLuke Marsden, Angela Cox, Mike Makris, et al.
Journal of the National Cancer Institute|November 20, 2003
Hemostatic regulators of tumor angiogenesis: a source of antiangiogenic agents for cancer treatment?Martina E Daly, Andreas Makris, Malcolm Reed, et al.
British Journal of Haematology|May 19, 2004
The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general populationNicholas J Beauchamp, Anne C Dykes, Nirzari Parikh, et al.
British Journal of Haematology|February 1, 2014
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?Martina E Daly, Vincenzo C Leo, Gillian C Lowe, et al.
Blood|September 23, 2011
An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human plateletsShaista Nisar, Martina E Daly, Augusto B Federici, et al.
Blood|June 7, 2003
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factorGrégoire Michaux, Lindsay J Hewlett, Sarah L Messenger, et al.
Platelets|June 14, 2006
Common sequence variations in the P2Y12 and CYP3A5 genes do not explain the variability in the inhibitory effects of clopidogrel therapySimon M G Smith, Heather M Judge, Gary Peters, et al.
Blood|September 25, 2012
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panelBan B Dawood, Gillian C Lowe, Marie Lordkipanidzé, et al.
Haematologica|January 13, 2022
Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytesJoanne Lacey, Simon J Webster, Paul R Heath, et al.
Pageof 2