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Chantal Thys

Showing results (21-30 of 43) with videos related to

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Journal of Proteomics|March 17, 2011
An integrated proteomics and genomics analysis to unravel a heterogeneous platelet secretion defectMichela Di Michele, Chantal Thys, Etienne Waelkens, et al.
Blood Advances|September 21, 2021
The brain-derived neurotrophic factor prompts platelet aggregation and secretionImane Boukhatem, Samuel Fleury, Melanie Welman, et al.
Human Molecular Genetics|September 27, 2012
NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafishSophie Louwette, Luc Régal, Christine Wittevrongel, et al.
Journal of Proteomics|May 18, 2013
Functional studies and proteomics in platelets and fibroblasts reveal a lysosomal defect with increased cathepsin-dependent apoptosis in ATP1A3 defective alternating hemiplegia of childhoodMichela Di Michele, Christophe Goubau, Etienne Waelkens, et al.
Human Molecular Genetics|October 19, 2020
Unravelling the disease mechanism for TSPYL1 deficiencyGunnar Buyse, Michela Di Michele, Anouck Wijgaerts, et al.
JIMD Reports|June 27, 2019
A novel missense variant in <i>SLC18A2</i> causes recessive brain monoamine vesicular transport disease and absent serotonin in plateletsManisha Padmakumar, Jaak Jaeken, Vincent Ramaekers, et al.
The Journal of Clinical Investigation|April 7, 2004
The pituitary adenylate cyclase-activating polypeptide is a physiological inhibitor of platelet activationKathleen Freson, Hitoshi Hashimoto, Chantal Thys, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experienceChristine Van Laer, Marc Jacquemin, Sarissa Baert, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2012
Homozygosity for aquaporin 7 G264V in three unrelated children with hyperglyceroluria and a mild platelet secretion defectChristophe Goubau, Jaak Jaeken, Elena N Levtchenko, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Journal of Proteomics|March 17, 2011
An integrated proteomics and genomics analysis to unravel a heterogeneous platelet secretion defectMichela Di Michele, Chantal Thys, Etienne Waelkens, et al.
Blood Advances|September 21, 2021
The brain-derived neurotrophic factor prompts platelet aggregation and secretionImane Boukhatem, Samuel Fleury, Melanie Welman, et al.
Human Molecular Genetics|September 27, 2012
NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafishSophie Louwette, Luc Régal, Christine Wittevrongel, et al.
Journal of Proteomics|May 18, 2013
Functional studies and proteomics in platelets and fibroblasts reveal a lysosomal defect with increased cathepsin-dependent apoptosis in ATP1A3 defective alternating hemiplegia of childhoodMichela Di Michele, Christophe Goubau, Etienne Waelkens, et al.
Human Molecular Genetics|October 19, 2020
Unravelling the disease mechanism for TSPYL1 deficiencyGunnar Buyse, Michela Di Michele, Anouck Wijgaerts, et al.
JIMD Reports|June 27, 2019
A novel missense variant in <i>SLC18A2</i> causes recessive brain monoamine vesicular transport disease and absent serotonin in plateletsManisha Padmakumar, Jaak Jaeken, Vincent Ramaekers, et al.
The Journal of Clinical Investigation|April 7, 2004
The pituitary adenylate cyclase-activating polypeptide is a physiological inhibitor of platelet activationKathleen Freson, Hitoshi Hashimoto, Chantal Thys, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experienceChristine Van Laer, Marc Jacquemin, Sarissa Baert, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2012
Homozygosity for aquaporin 7 G264V in three unrelated children with hyperglyceroluria and a mild platelet secretion defectChristophe Goubau, Jaak Jaeken, Elena N Levtchenko, et al.
Pageof 5