Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cecilia P. Marin Oyarzún"'
Autor:
Ana C. Glembotsky, Cecilia P. Marin Oyarzún, Geraldine De Luca, Christophe Marzac, Nathalie Auger, Nora P. Goette, Rosana F. Marta, Hana Raslova, Paula G. Heller
Publikováno v:
Haematologica, Vol 105, Iss 10 (2020)
Externí odkaz:
https://doaj.org/article/a61daa6f8d7444bebdd2a4aca751d131
Autor:
Juan P. Salim, Ana C. Glembotsky, Paola R. Lev, Cecilia P. Marin Oyarzún, Nora P. Goette, Felisa C. Molinas, Rosana F. Marta, Paula G. Heller
Publikováno v:
Platelets, Vol 28, Iss 6, Pp 602-606 (2017)
The SDF-1-CXCR4 axis plays an essential role in the regulation of platelet production, by directing megakaryocyte (MK) migration toward the vascular niche, thus allowing terminal maturation and proplatelet formation, and also regulates platelet funct
Externí odkaz:
https://doaj.org/article/9930007e5cf5435d86432ae6f12f066b
Autor:
Ana C. Glembotsky, Dominika Sliwa, Dominique Bluteau, Nathalie Balayn, Cecilia P. Marin Oyarzún, Anna Raimbault, Marie Bordas, Nathalie Droin, Iryna Pirozhkova, Valance Washington, Nora P. Goette, Rosana F. Marta, Rémi Favier, Hana Raslova, Paula G. Heller
Publikováno v:
Haematologica, Vol 104, Iss 6 (2019)
Germline RUNX1 mutations lead to thrombocytopenia and platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia (AML). Multiple aspects of platelet function are impaired in these patients, associated with al
Externí odkaz:
https://doaj.org/article/339e7f5175834da7a016b084f1a82957
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Chronic myeloproliferative neoplasms (MPN) are stem cell disorders driven by mutations in JAK2, CALR, or MPL genes and characterized by myeloid proliferation and increased blood cell counts. They encompass three closely related conditions, including
Externí odkaz:
https://doaj.org/article/8e4f7d59a94e4580bf1061960e2d861f
Autor:
Ana C, Glembotsky, Dominika, Sliwa, Dominique, Bluteau, Nathalie, Balayn, Cecilia P, Marin Oyarzún, Anna, Raimbault, Marie, Bordas, Nathalie, Droin, Iryna, Pirozhkova, Valance, Washington, Nora P, Goette, Rosana F, Marta, Rémi, Favier, Hana, Raslova, Paula G, Heller
Publikováno v:
Haematologica
Germline RUNX1 mutations lead to thrombocytopenia and platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia (AML). Multiple aspects of platelet function are impaired in these patients, associated with al
Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus
Autor:
M. Constanza Baroni Pietto, Paola R. Lev, Ana C. Glembotsky, Cecilia P. Marín Oyarzún, Graciela Gomez, Victoria Collado, Cecilia Pisoni, Ramiro A. Gomez, Matías Grodzielski, Jacqueline Gonzalez, Karina V. Mariño, Paula G. Heller, Nora P. Goette, Rosana F. Marta
Publikováno v:
Platelets, Vol 33, Iss 5, Pp 743-754 (2022)
Systemic lupus erythematosus (SLE) is an autoimmune condition developing thrombocytopenia in about 10–15% of cases, however, mechanisms leading to low platelet count were not deeply investigated in this illness. Here we studied possible causes of t
Externí odkaz:
https://doaj.org/article/6b513b6ff98045f69f1dba0a75e76380
Autor:
Cecilia P. Marín Oyarzún, Ana C. Glembotsky, Nora P. Goette, Paola R. Lev, Geraldine De Luca, María C. Baroni Pietto, Beatriz Moiraghi, Miguel A. Castro Ríos, Angeles Vicente, Rosana F. Marta, Mirta Schattner, Paula G. Heller
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Essential thrombocythemia (ET) is comprised among chronic myeloproliferative neoplasms (MPN) and is caused by driver mutations in JAK2, CALR, and MPL, which lead to megakaryocyte proliferation and prominent thrombocytosis. Thrombosis remains the main
Externí odkaz:
https://doaj.org/article/c645814c0eff4aa58503e674a2eb6b47