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Journal Articles

Turbulence Enhances Fine-Tuning of Mitochondria Delivery in Megakaryocyte Maturation Contributing to Biogenesis of High Quality Platelets

Emiri Nakamura, Yasuo Harada, Koenraad De Wispelaere, Chantal Thys, Kathleen Freson, Koji Eto

Blood (2023) 142 (Supplement 1): 3964.

https://doi.org/10.1182/blood-2023-181330

Published: 2023

Journal Articles

Ribosome dysfunction underlies SLFN14-related thrombocytopenia

Fabienne Ver Donck, Kato Ramaekers, Chantal Thys, Christine Van Laer, Kathelijne Peerlinck, Chris Van Geet, Koji Eto, Veerle Labarque, Kathleen Freson

Blood (2023) 141 (18): 2261–2274.

https://doi.org/10.1182/blood.2022017712

Published: 2023

Includes: Supplemental data

Journal Articles

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

Blood (2019) 134 (23): 2070–2081.

https://doi.org/10.1182/blood.2019000782

Published: 2019

Includes: Supplemental data

Journal Articles

Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

Blood (2019) 134 (23): 2082–2091.

https://doi.org/10.1182/blood.2018891192

Published: 2019

Includes: Supplemental data

Journal Articles

A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

Blood (2016) 127 (23): 2903–2914.

https://doi.org/10.1182/blood-2015-10-675629

Published: 2016

Includes: Supplemental data

Journal Articles

First Report of Transheterozygosity in a Patient with An Inherited Platelet Bleeding Disorder Due to Mutations in the Thromboxane A2 Receptor ( TBXA2R) and cyclooxygenase1 ( PTGS1) ,

Kathleen Freson, Chantal Thys, Christel Van Geet, MD, PhD

Blood (2011) 118 (21): 3260.

https://doi.org/10.1182/blood.V118.21.3260.3260

Published: 2011

Journal Articles

A Myelodysplastic Syndrome Associated with a Clonal GATA1 Mutation.

Kathleen Freson, Liesbeth De Waele, Chantal Thys, Christine Wittevrongel, Peter Vandenberghe, Rita De Vos, Paresh Vyas, Christel Van Geet

Blood (2008) 112 (11): 1243.

https://doi.org/10.1182/blood.V112.11.1243.1243

Published: 2008

Journal Articles

PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implications

Kathleen Freson, Karen Peeters, Rita De Vos, Christine Wittevrongel, Chantal Thys, Marc F. Hoylaerts, Jos Vermylen, Chris Van Geet

Blood (2008) 111 (4): 1885–1893.

https://doi.org/10.1182/blood-2007-06-098558

Published: 2008

Includes: Supplemental data

Journal Articles

GPVI Mutation and Absent Platelet Collagen Activation in a Patient with a Bleeding Disorder.

Kathleen Freson, PhD, Cedric Hermans, MD, PhD, Chantal Thys, Christel Van Geet, MD, PhD

Blood (2007) 110 (11): 2106.

https://doi.org/10.1182/blood.V110.11.2106.2106

Published: 2007

Journal Articles

Development of Megakaryocyte-Specific Lentiviral Vectors for Gene Therapy of Platelet Disorders.

Liesbeth De Waele, MD, Kathleen Freson, PhD, Chantal Thys, Christel Van Geet, MD, PhD, Désiré Collen, MD, PhD, Thierry VandenDriessche, PhD, Marinee Chuah, PhD

Blood (2007) 110 (11): 5143.

https://doi.org/10.1182/blood.V110.11.5143.5143

Published: 2007

Journal Articles

Inhibition of VPAC1 Signaling Raises Platelet Numbers after Myelosuppressive Therapy and in GATA1 Congenital Thrombocytopenia.

Karen Peeters, Kathleen Freson, PhD, Christine Wittevrongel, Chantal Thys, Jean-Marie Stassen, PhD, Marc F. Hoylaerts, PhD, Chris Van Geet, MD PhD

Blood (2007) 110 (11): 1264.

https://doi.org/10.1182/blood.V110.11.1264.1264

Published: 2007

Journal Articles

Increased Bleeding Tendency in a Patient with Caffey Disease Due to a COL1A1 Mutation and a Defect in Platelet Morphology and Function.

Kathleen Freson, PhD, Veerle Labarque, MD, Chantal Thys, Christine Wittevrongel, Rita De Vos, MD, PhD, Richard Farndale, PhD, Chris Van Geet, MD, PhD

Blood (2005) 106 (11): 736.

https://doi.org/10.1182/blood.V106.11.736.736

Published: 2005

Journal Articles

The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure

Kathleen Freson, Rita De Vos, Christine Wittevrongel, Chantal Thys, Johan Defoor, Luc Vanhees, Jos Vermylen, Kathelijne Peerlinck, Chris Van Geet

Blood (2005) 106 (7): 2356–2362.

https://doi.org/10.1182/blood-2005-02-0723

Published: 2005

Includes: Supplemental data

Journal Articles

Myelodysplastic Syndrome Due to Somatic GATA1 Mutation.

Kathleen Freson, PhD, Paresh Vyas, PhD, MD, Chantal Thys, Christine Wittevrongel, Rita De Vos, PhD, Chris Van Geet, PhD, MD

Blood (2004) 104 (11): 4711.

https://doi.org/10.1182/blood.V104.11.4711.4711

Published: 2004

Journal Articles

VPAC1 Receptor-Mediated Regulation of Megakaryopoiesis.

Kathleen Freson, PhD, Chantal Thys, Christine Wittevrongel, Rita De Vos, PhD, Jos Vermylen, PhD, MD, Marc F. Hoylaerts, PhD, MD, Chris Van Geet, PhD, MD

Blood (2004) 104 (11): 735.

https://doi.org/10.1182/blood.V104.11.735.735

Published: 2004

Journal Articles

Shielding the front-strand β3 of the von Willebrand factor A1 domain inhibits its binding to platelet glycoprotein Ibα

Arnaud Bonnefoy, Hiroshi Yamamoto, Chantal Thys, Morikazu Kito, Jos Vermylen, Marc F. Hoylaerts

Blood (2003) 101 (4): 1375–1383.

https://doi.org/10.1182/blood-2002-06-1818

Published: 2003

Journal Articles

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

Kathleen Freson, Koen Devriendt, Gert Matthijs, Achiel Van Hoof, Rita De Vos, Chantal Thys, Kristien Minner, Marc F. Hoylaerts, Jos Vermylen, Chris Van Geet

Blood (2001) 98 (1): 85–92.

https://doi.org/10.1182/blood.V98.1.85

Published: 2001

Journal Articles

Recurrent Arterial Thrombosis Linked to Autoimmune Antibodies Enhancing von Willebrand Factor Binding to Platelets and Inducing FcγRII Receptor-Mediated Platelet Activation

Marc F. Hoylaerts, Chantal Thys, Jef Arnout, Jos Vermylen

Blood (1998) 91 (8): 2810–2817.

https://doi.org/10.1182/blood.V91.8.2810.2810_2810_2817

Published: 1998

NARROW

Turbulence Enhances Fine-Tuning of Mitochondria Delivery in Megakaryocyte Maturation Contributing to Biogenesis of High Quality Platelets

Ribosome dysfunction underlies SLFN14-related thrombocytopenia

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

First Report of Transheterozygosity in a Patient with An Inherited Platelet Bleeding Disorder Due to Mutations in the Thromboxane A2 Receptor ( TBXA2R) and cyclooxygenase1 ( PTGS1) ,

A Myelodysplastic Syndrome Associated with a Clonal GATA1 Mutation.

PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implications

GPVI Mutation and Absent Platelet Collagen Activation in a Patient with a Bleeding Disorder.

Development of Megakaryocyte-Specific Lentiviral Vectors for Gene Therapy of Platelet Disorders.

Inhibition of VPAC1 Signaling Raises Platelet Numbers after Myelosuppressive Therapy and in GATA1 Congenital Thrombocytopenia.

Increased Bleeding Tendency in a Patient with Caffey Disease Due to a COL1A1 Mutation and a Defect in Platelet Morphology and Function.

The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure

Myelodysplastic Syndrome Due to Somatic GATA1 Mutation.

VPAC1 Receptor-Mediated Regulation of Megakaryopoiesis.

Shielding the front-strand β3 of the von Willebrand factor A1 domain inhibits its binding to platelet glycoprotein Ibα

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

Recurrent Arterial Thrombosis Linked to Autoimmune Antibodies Enhancing von Willebrand Factor Binding to Platelets and Inducing FcγRII Receptor-Mediated Platelet Activation

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American Society of Hematology

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American Society of Hematology

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