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Chantal Thys

Showing results (11-20 of 43) with videos related to

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Blood|November 15, 2007
PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implicationsKathleen Freson, Karen Peeters, Rita De Vos, et al.
Human Molecular Genetics|November 6, 2007
Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgeryVeerle Labarque, Kathleen Freson, Chantal Thys, et al.
Pediatric Research|November 20, 2009
Severe gastrointestinal bleeding and thrombocytopenia in a child with an anti-GATA1 autoantibodyLiesbeth de Waele, Kathleen Freson, Sophie Louwette, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Compound heterozygous mutations in the GNAS gene of a boy with morbid obesity, thyroid-stimulating hormone resistance, pseudohypoparathyroidism, and a prothrombotic stateKathleen Freson, Benedetta Izzi, Jaak Jaeken, et al.
Molecular Autism|October 27, 2015
Platelet studies in autism spectrum disorder patients and first-degree relativesNora Bijl, Chantal Thys, Christine Wittevrongel, et al.
Blood|June 16, 2005
The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structureKathleen Freson, Rita De Vos, Christine Wittevrongel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 7, 2012
Regulator of G-protein signaling 18 controls megakaryopoiesis and the cilia-mediated vertebrate mechanosensory systemSophie Louwette, Veerle Labarque, Christine Wittevrongel, et al.
Journal of Human Genetics|January 27, 2012
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activityBenedetta Izzi, Francis de Zegher, Inge Francois, et al.
Blood|February 15, 2023
Ribosome dysfunction underlies SLFN14-related thrombocytopeniaFabienne Ver Donck, Kato Ramaekers, Chantal Thys, et al.
Human Molecular Genetics|April 30, 2003
Functional polymorphisms in the paternally expressed XLalphas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formationKathleen Freson, Jaak Jaeken, Monique Van Helvoirt, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Blood|November 15, 2007
PACAP and its receptor VPAC1 regulate megakaryocyte maturation: therapeutic implicationsKathleen Freson, Karen Peeters, Rita De Vos, et al.
Human Molecular Genetics|November 6, 2007
Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgeryVeerle Labarque, Kathleen Freson, Chantal Thys, et al.
Pediatric Research|November 20, 2009
Severe gastrointestinal bleeding and thrombocytopenia in a child with an anti-GATA1 autoantibodyLiesbeth de Waele, Kathleen Freson, Sophie Louwette, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Compound heterozygous mutations in the GNAS gene of a boy with morbid obesity, thyroid-stimulating hormone resistance, pseudohypoparathyroidism, and a prothrombotic stateKathleen Freson, Benedetta Izzi, Jaak Jaeken, et al.
Molecular Autism|October 27, 2015
Platelet studies in autism spectrum disorder patients and first-degree relativesNora Bijl, Chantal Thys, Christine Wittevrongel, et al.
Blood|June 16, 2005
The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structureKathleen Freson, Rita De Vos, Christine Wittevrongel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 7, 2012
Regulator of G-protein signaling 18 controls megakaryopoiesis and the cilia-mediated vertebrate mechanosensory systemSophie Louwette, Veerle Labarque, Christine Wittevrongel, et al.
Journal of Human Genetics|January 27, 2012
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activityBenedetta Izzi, Francis de Zegher, Inge Francois, et al.
Blood|February 15, 2023
Ribosome dysfunction underlies SLFN14-related thrombocytopeniaFabienne Ver Donck, Kato Ramaekers, Chantal Thys, et al.
Human Molecular Genetics|April 30, 2003
Functional polymorphisms in the paternally expressed XLalphas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formationKathleen Freson, Jaak Jaeken, Monique Van Helvoirt, et al.
Pageof 5