Hyperactive GPIb-von Willebrand factor interaction as cause of thrombocytopenia: altered platelet formation versus clearance by Kathleen Freson

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Loss of APOLD1: a new vascular bleeding disorder? by Kathleen Freson

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The (Patho)Biology of SRC Kinase in Platelets and Megakaryocytes by Lore De Kock, Kathleen Freson

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Hemostatic phenotypes and genetic disorders by Fabienne Ver Donck, Veerle Labarque, Kathleen Freson

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GATA1 gene variants associated with thrombocytopenia and anemia by Kathleen Freson, Anouck Wijgaerts, Chris Van Geet

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Effect of VPAC1 Blockade on Adipose Tissue Formation and Composition in Mouse Models of Nutritionally Induced Obesity by H. Roger Lijnen, Kathleen Freson, Marc F. Hoylaerts

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Thrombophilia Testing: from Genetic Predisposition to Discrimination by Andreas Verstraete, Kathleen Freson, Peter Verhamme, Thomas Vanassche

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Blood platelet research in autism spectrum disorders: In search of biomarkers by Manisha Padmakumar, Eveline Van Raes, Chris Van Geet, Kathleen Freson

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De novo variant in tyrosine kinase SRC causes thrombocytopenia: case report of a second family by Lore De Kock, Chantal Thys, Kate Downes, Daniel Duarte, Karyn Megy, Chris Van Geet, Kathleen Freson

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Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes by Lore De Kock, Fabienne Ver Donck, Chantal Thys, Anouck Wijgaerts, Koji Eto, Chris Van Geet, Kathleen Freson

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The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer by Anouck Wijgaerts, Christine Wittevrongel, Chantal Thys, Timothy Devos, Kathelijne Peerlinck, Marloes R. Tijssen, Chris Van Geet, Kathleen Freson

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Dietary and supplemental maternal methyl-group donor intake and cord blood DNA methylation by Sara Pauwels, Manosij Ghosh, Radu Corneliu Duca, Bram Bekaert, Kathleen Freson, Inge Huybrechts, Sabine A. S. Langie, Gudrun Koppen, Roland Devlieger, Lode Godderis

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A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder by Ibrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, Kate Downes, Kathleen Freson, Joanne Mason, Paula Page, Kim Reay, Bethan Myers, Neil V Morgan

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Glanzmann thrombasthenia: genetic basis and clinical correlates by Juliana Perez Botero, Kristy Lee, Brian R Branchford, Paul F Bray, Kathleen Freson, Michele P. Lambert, Minjie Luo, Shruthi Mohan, Justyne E. Ross, Wolfgang Bergmeier, Jorge Di Paola

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A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger by José M. Bastida, Stefano Malvestiti, Doris Boeckelmann, Verónica Palma-Barqueros, Mira Wolter, María L. Lozano, Hannah Glonnegger, Rocío Benito, Carlo Zaninetti, Felix Sobotta, Freimut H. Schilling, Neil V. Morgan, Kathleen Freson, José Rivera, Barbara Zieger

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Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia by Tadbir K. Bariana, Veerle Labarque, Jessica Heremans, Chantal Thys, Mara De Reys, Daniel Greene, Benjamin Jenkins, Luigi Grassi, Denis Seyres, Frances Burden, Deborah Whitehorn, Olga Shamardina, Sofia Papadia, Keith Gomez, NIHR BioResource, Chris Van Geet, Albert Koulman, Willem H. Ouwehand, Cedric Ghevaert, Mattia Frontini, Ernest Turro, Kathleen Freson

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The EHA Research Roadmap: Platelet Disorders by Carlo Balduini, Kathleen Freson, Andreas Greinacher, Paolo Gresele, Thomas Kühne, Marie Scully, Tamam Bakchoul, Paul Coppo, Tadeja Dovc Drnovsek, Bertrand Godeau, Yves Gruel, A. Koneti Rao, Johanna A. Kremer Hovinga, Michael Makris, Axel Matzdorff, Andrew Mumford, Alessandro Pecci, Hana Raslova, José Rivera, Irene Roberts, Rüdiger E. Scharf, John W. Semple, Christel Van Geet

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Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses by Rinske van Oorschot, Anna E. Marneth, Saskia M. Bergevoet, Maaike G.J.M. van Bergen, Kathelijne Peerlinck, Claire E. Lentaigne, Carolyn M. Millar, Sarah K. Westbury, Remi Favier, Wendy N. Erber, Ernest Turro, Joop H. Jansen, Willem H. Ouwehand, Harriet L. McKinney, NIHR BioResource Collaborative Group, Kate Downes, Kathleen Freson, Bert A. van der Reijden

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Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors by Marjorie Poggi, Matthias Canault, Marie Favier, Ernest Turro, Paul Saultier, Dorsaf Ghalloussi, Veronique Baccini, Lea Vidal, Anna Mezzapesa, Nadjim Chelghoum, Badreddine Mohand-Oumoussa, Céline Falaise, Rémi Favier, Willem H. Ouwehand, Mathieu Fiore, Franck Peiretti, Pierre Emmanuel Morange, Noémie Saut, Denis Bernot, Andreas Greinacher, NIHR BioResource, Alan T. Nurden, Paquita Nurden, Kathleen Freson, David-Alexandre Trégouët, Hana Raslova, Marie-Christine Alessi

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Identification of a homozygous recessive variant in <i>PTGS1</i> resulting in a congenital aspirin-like defect in platelet function by Melissa V. Chan, Melissa A. Hayman, Suthesh Sivapalaratnam, Marilena Crescente, Harriet E. Allan, Matthew L. Edin, Darryl C. Zeldin, Ginger L. Milne, Jonathan Stephens, Daniel Greene, Moghees Hanif, Valerie B. O'Donnell, Liang Dong, Michael G. Malkowski, Claire Lentaigne, Katherine Wedderburn, Matthew Stubbs, Kate Downes, Willem H. Ouwehand, Ernest Turro, NIHR BioResource, Daniel P. Hart, Kathleen Freson, Michael A. Laffan, Timothy D. Warner

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