Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Marijke, Bryckaert"'
Autor:
Lamia Lamrani, Frédéric Adam, Christelle Soukaseum, Cécile V. Denis, Hana Raslova, Jean‐Philippe Rosa, Marijke Bryckaert
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 6, Iss 2, Pp n/a-n/a (2022)
Abstract Background Filamin (FLN) regulates many cell functions through its scaffolding activity cross‐linking cytoskeleton and integrins. FLN was shown to inhibit integrin activity, but the exact mechanism remains unclear. Objectives The aim of th
Externí odkaz:
https://doaj.org/article/8a66c3162756480ca903cda5b86d834b
Autor:
Caterina Casari, David S. Paul, Sophie Susen, Cécile Lavenu-Bombled, Annie Harroche, Raymond Piatt, Kathryn O. Poe, Robert H. Lee, Marijke Bryckaert, Olivier D. Christophe, Peter J. Lenting, Cécile V. Denis, Wolfgang Bergmeier
Publikováno v:
Blood Advances, Vol 2, Iss 12, Pp 1417-1428 (2018)
Abstract: von Willebrand disease (VWD) type 2B is characterized by gain-of-function mutations in von Willebrand factor (VWF), enhancing its binding affinity for the platelet receptor glycoprotein (GP)Ibα. VWD type 2B patients display a bleeding tend
Externí odkaz:
https://doaj.org/article/1507902593a948d4b4b113e3cb58c34b
Autor:
Annabelle Dupont, Christelle Soukaseum, Mathilde Cheptou, Frédéric Adam, Thomas Nipoti, Marc-Damien Lourenco-Rodrigues, Paulette Legendre, Valérie Proulle, Antoine Rauch, Charlotte Kawecki, Marijke Bryckaert, Jean-Philippe Rosa, Camille Paris, Catherine Ternisien, Pierre Boisseau, Jenny Goudemand, Delphine Borgel, Dominique Lasne, Pascal Maurice, Peter J. Lenting, Cécile V. Denis, Sophie Susen, Alexandre Kauskot
Publikováno v:
Haematologica, Vol 104, Iss 12 (2019)
Patients with type 2B von Willebrand disease (vWD) (caused by gain-of-function mutations in the gene coding for von Willebrand factor) display bleeding to a variable extent and, in some cases, thrombocytopenia. There are several underlying causes of
Externí odkaz:
https://doaj.org/article/c6a2a981946540fc902c3cbea7dc27d8
Autor:
Alexandre Kauskot, Tiffany Pascreau, Frédéric Adam, Arnaud Bruneel, Christelle Reperant, Marc-Damien Lourenco-Rodrigues, Jean-Philippe Rosa, Rachel Petermann, Hélène Maurey, Claire Auditeau, Dominique Lasne, Cécile V. Denis, Marijke Bryckaert, Pascale de Lonlay, Cécile Lavenu-Bombled, Judith Melki, Delphine Borgel
Publikováno v:
Haematologica, Vol 103, Iss 12 (2018)
Externí odkaz:
https://doaj.org/article/1449f4971f1041b4aeca66901242487a
Autor:
Frédéric Adam, Alexandre Kauskot, Lamia Lamrani, Jean Solarz, Christelle Soukaseum, Christelle Repérant, Cécile V. Denis, Hana Raslova, Jean‐Philippe Rosa, Marijke Bryckaert
Publikováno v:
Journal of thrombosis and haemostasis : JTHREFERENCES. 20(11)
Filaminopathies A are rare disorders affecting the brain, intestine, or skeleton, characterized by dominant X-linked filamin A (FLNA) gene mutations. Macrothrombocytopenia with functionally defective platelets is frequent. We have described a filamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d7496cfb3fa16610b0d14309c2ad0c9
https://pubmed.ncbi.nlm.nih.gov/36006037
https://pubmed.ncbi.nlm.nih.gov/36006037
Autor:
Lamia Lamrani, Frédéric Adam, Christelle Soukaseum, Cécile V. Denis, Hana Raslova, Jean‐Philippe Rosa, Marijke Bryckaert
Publikováno v:
Research and practice in thrombosis and haemostasis. 6(2)
Filamin (FLN) regulates many cell functions through its scaffolding activity cross-linking cytoskeleton and integrins. FLN was shown to inhibit integrin activity, but the exact mechanism remains unclear.The aim of this study was to evaluate the role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eabff3041dc8ada07c8215d80c46be2d
https://pubmed.ncbi.nlm.nih.gov/35316942
https://pubmed.ncbi.nlm.nih.gov/35316942
Autor:
Miao Feng, Béatrice Hechler, Frédéric Adam, Christian Gachet, Anita Eckly, Alexandre Kauskot, Cécile V. Denis, Marijke Bryckaert, Régis Bobe, Jean-Philippe Rosa
Publikováno v:
Research and Practice in Thrombosis and Haemostasis. 7:100004
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48b48d807073c303b24fce9cb66fa8f
https://doi.org/10.1016/j.rpth.2022.100004
https://doi.org/10.1016/j.rpth.2022.100004
Autor:
Eliane Berrou, Alexandre Kauskot, Frédéric Adam, Amélie Harel, Paulette Legendre, Cécile Lavenu Bombled, Chantal Rothschild, Nicolas Prevost, Olivier D Christophe, Peter J Lenting, Cécile V Denis, Jean-Philippe Rosa, Marijke Bryckaert
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143896 (2015)
Thrombocytopenia and increased platelet clearance observed in von Willebrand disease-type 2B (VWD-2B) may be explained by platelet apoptosis triggered by the constitutive binding of VWF to its receptor, glycoprotein Ib (GPIb). Apoptosis was assessed
Externí odkaz:
https://doaj.org/article/d8e2b4c2a0aa4289808c2ba24a245f90
Autor:
Cécile V. Denis, Frédéric Adam, Delphine Borgel, Regis Bobe, Jean-Philippe Rosa, Ziane Elaib, Miao Feng, Marijke Bryckaert
Publikováno v:
Circulation Research
Circulation Research, American Heart Association, 2020, 127 (7), pp.e166-e183. ⟨10.1161/CIRCRESAHA.119.316090⟩
Circulation Research, American Heart Association, 2020, 127 (7), pp.e166-e183. ⟨10.1161/CIRCRESAHA.119.316090⟩
Rationale: Ca 2+ signaling is a key and ubiquitous actor of cell organization and its modulation controls many cellular responses. SERCAs (sarco-endoplasmic reticulum Ca 2+ -ATPases) pump Ca 2+ into internal stores that play a major role in the cytos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c54e26d94be7dc042d9ca3cb699d0d2c
https://doi.org/10.1161/circresaha.119.316090
https://doi.org/10.1161/circresaha.119.316090
Autor:
Miao, Feng, Ziane, Elaïb, Delphine, Borgel, Cécile V, Denis, Frédéric, Adam, Marijke, Bryckaert, Jean-Philippe, Rosa, Régis, Bobe
Publikováno v:
Circulation research. 127(7)
CaTo uncover the signaling mechanisms associated with CaUsing platelets from wild-type orUpon activation, an NAADP/SERCA3 Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2659c0104b11952edf3f2f773f3d0e63
https://pubmed.ncbi.nlm.nih.gov/32588751
https://pubmed.ncbi.nlm.nih.gov/32588751