Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cecilia Paola Marin Oyarzún"'
Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus
Autor:
Cecilia Paola Marin Oyarzún, Jacqueline Gonzalez, Graciela Gómez, Karina Mariño, M. Constanza Baroni Pietto, Paula G. Heller, Victoria Collado, Paola Roxana Lev, Ana C. Glembotsky, Ramiro Gomez, Cecilia Pisoni, Matías Grodzielski, Nora Paula Goette, Rosana F. Marta
Publikováno v:
Platelets. 33:743-754
SummarySystemic 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
Autor:
Geraldine De Luca, Rosana F. Marta, Cecilia Paola Marin Oyarzún, Nathalie Auger, Hana Raslova, Ana C. Glembotsky, Paula G. Heller, Christophe Marzac, Nora Paula Goette
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Haematologica
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Haematologica
Familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML) is an autosomal dominant condition characterized by abnormal platelet number and function and 30-60% risk of hematologic malignancies, including myelodysplastic sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7a6fa85ec507515f613d4b21b67935
http://www.haematologica.org/lookup/doi/10.3324/haematol.2020.253070
http://www.haematologica.org/lookup/doi/10.3324/haematol.2020.253070
Autor:
Angeles Vicente, Maria Constanza Baroni Pietto, Rosana F. Marta, Paula G. Heller, Nora Paula Goette, Miguel Castro Rios, Mirta Schattner, Geraldine De Luca, Paola Roxana Lev, Ana C. Glembotsky, Beatriz Moiraghi, Cecilia Paola Marin Oyarzún
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2020)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Immunology
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
Autor:
Paula G. Heller, Nora Paula Goette, Rosana F. Marta, Juan P. Salim, Paola Roxana Lev, Ana C. Glembotsky, Cecilia Paola Marin Oyarzún, Felisa C. Molinas
Publikováno v:
Platelets. 28:602-606
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
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
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
Autor:
Miguel Castro Rios, Felisa C. Molinas, Ana C. Glembotsky, Agostina Carestia, Rosana F. Marta, Mirta Schattner, Cecilia Paola Marin Oyarzún, Paola Roxana Lev, Beatriz Moiraghi, Paula G. Heller
Publikováno v:
Scientific Reports
The mechanisms underlying increased thrombotic risk in chronic myeloproliferative neoplasms (MPN) are incompletely understood. We assessed whether neutrophil extracellular traps (NETs), which promote thrombosis, contribute to the procoagulant state i
Autor:
Francesca Basso-Valentina, Alessandro Donada, Vladimir T Manchev, Manuel Lisetto, Nathalie Balayn, Jean Edouard Martin, Delphine Muller, Cecilia Paola Marin Oyarzun, Hélène Duparc, Brahim Arkoun, Alessandro Cumin, Lionel Faivre, Nathalie Droin, Ida Biunno, Alessandro Pecci, Alessandra Balduini, Najet Debili, Iléana Antony-Debré, Caroline Marty, William Vainchenker, Isabelle Plo, Remi Favier, Hana Raslova
Publikováno v:
Haematologica, Vol 108, Iss 8 (2023)
Sustained ANKRD26 expression associated with germline ANKRD26 mutations causes thrombocytopenia 2 (THC2), an inherited platelet disorder associated with a predisposition to leukemia. Some patients also present with erythrocytosis and/or leukocytosis.
Externí odkaz:
https://doaj.org/article/ea73fe6f815643c19db0d298819699a2