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Platelets|June 28, 2016
Inherited platelet disorders: Insight from platelet genomics using next-generation sequencingAnnabel Maclachlan, Steve P Watson, Neil V MorganPlatelets|March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet functionAnnabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.Platelets|December 7, 2018
Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleedingGillian C Lowe, Roksana Fickowska, Rashid Al Ghaithi, 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.Platelets|October 27, 2018
Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysisRashid Al Ghaithi, Jun Mori, Zoltan Nagy, et al.Current Pharmaceutical Design|April 10, 2009
Platelet activation by extracellular matrix proteins in haemostasis and thrombosisSteve P WatsonHaematologica|December 17, 2020
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and functionAbdullah O Khan, Alexandre Slater, Annabel Maclachlan, et al.Blood|March 22, 2003
Platelet-collagen interaction: is GPVI the central receptor?Bernhard Nieswandt, Steve P WatsonBlood Advances|January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitmentRachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.Pageof 33