Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Sandrine Laurance"'
Autor:
Maria Y. Najem, Ryan N. Rys, Sandrine Laurance, François‐René Bertin, Virginie Gourdou‐Latyszenok, Lénaïck Gourhant, Lauriane Le Gall, Rozenn Le Corre, Francis Couturaud, Mark D. Blostein, Catherine A. Lemarié
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 15 (2024)
Background Venous thromboembolism is associated with endothelial cell activation that contributes to the inflammation‐dependent activation of the coagulation system. Cellular damage is associated with the release of different species of extracellul
Externí odkaz:
https://doaj.org/article/67f57dfc8de74c6982911de9874d5841
Autor:
Florencia Orrico, Sandrine Laurance, Ana C. Lopez, Sophie D. Lefevre, Leonor Thomson, Matias N. Möller, Mariano A. Ostuni
Publikováno v:
Biomolecules, Vol 13, Iss 8, p 1262 (2023)
Red cell diseases encompass a group of inherited or acquired erythrocyte disorders that affect the structure, function, or production of red blood cells (RBCs). These disorders can lead to various clinical manifestations, including anemia, hemolysis,
Externí odkaz:
https://doaj.org/article/6b020c8550ec4a36ab03313ead6c3b1a
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1072 (2023)
Central retinal vein occlusion (CRVO) is a frequent retinal disorder inducing blindness due to the occlusion of the central vein of the retina. The primary cause of the occlusion remains to be identified leading to the lack of treatment. To date, cur
Externí odkaz:
https://doaj.org/article/2c7b385c34ec44a998eebb9723baedbb
Autor:
Sara El Hoss, Sylvie Cochet, Auria Godard, Hongxia Yan, Michaël Dussiot, Giacomo Frati, Bénédicte Boutonnat-Faucher, Sandrine Laurance, Olivier Renaud, Laure Joseph, Annarita Miccio, Valentine Brousse, Mohandas Narla, Wassim El Nemer
Publikováno v:
Haematologica, Vol 106, Iss 10 (2020)
While ineffective erythropoiesis has long been recognized as a key contributor to anemia in thalassemia, its role in anemia of sickle cell disease (SCD) has not been critically explored. Using in vitro and in vivo derived human erythroblasts we asses
Externí odkaz:
https://doaj.org/article/aaaa847b38394956a803db1d63a540dd
Autor:
Sandrine Laurance, Pauline Lansiaux, François-Xavier Pellay, Michelle Hauchecorne, Arndt Benecke, Jacques Elion, Claudine Lapoumeroulie
Publikováno v:
Haematologica, Vol 96, Iss 4 (2011)
Background All the cellular partners of the vascular system and especially endothelial cells are involved in the pathophysiology of the vasoocclusive crises associated with sickle cell disease. In sickle cell disease, circulating cells adhere abnorma
Externí odkaz:
https://doaj.org/article/1ae5be375b4c4547b085d9762d9bb84b
Autor:
Charlotte Pourdieu, Sara El Hoss, Enora Le Roux, Justine Pages, Bérengère Koehl, Florence Missud, Laurent Holvoet, Ghislaine Ithier, Malika Benkerrou, Zinedine Haouari, Lydie Da Costa, Wassim El Nemer, Sandrine Laurance, Yves Colin Aronovicz, Caroline Le Van Kim, Odile Fenneteau, Elodie Lainey, Valentine Brousse
Publikováno v:
American Journal of Hematology
American Journal of Hematology, 2023, ⟨10.1002/ajh.26879⟩
American Journal of Hematology, 2023, ⟨10.1002/ajh.26879⟩
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949c3cab62b6845be5761d697e99542c
https://hal.science/hal-03997176
https://hal.science/hal-03997176
Publikováno v:
International Journal of Molecular Sciences. 24:1072
Central retinal vein occlusion (CRVO) is a frequent retinal disorder inducing blindness due to the occlusion of the central vein of the retina. The primary cause of the occlusion remains to be identified leading to the lack of treatment. To date, cur
Autor:
Catherine A. Lemarié, Ryan N Rys, C. Mathieu, Francois-Rene Bertin, Mark Blostein, Sandrine Laurance
Publikováno v:
Journal of Thrombosis and Haemostasis. 17:403-414
Essentials Neutrophil extracellular traps (NETs) are generated during deep vein thrombosis (DVT). The role of interferon γ (IFNγ) and natural killer (NK) cells in NET formation was studied. IFNγ promote venous thrombosis through NET formation. NK
Autor:
Benedicte Boutonnat-Faucher, Sylvie Cochet, Sara El Hoss, Mickael Dussiot, Annarita Miccio, Sandrine Laurance, Hongxia Yan, Olivier Renaud, Wassim El Nemer, Laure Joseph, Narla Mohandas, Valentine Brousse, Giacomo Frati, Auria Godard
Publikováno v:
Transfusion Clinique et Biologique. 28:S47
Autor:
Hongxia Yan, Mohandas Narla, Sylvie Cochet, Sandrine Laurance, Giacomo Frati, Olivier Renaud, Laure Joseph, Annarita Miccio, Auria Godard, Benedicte Boutonnat-Faucher, Wassim El Nemer, Valentine Brousse, Michael Dussiot, Sara El Hoss
Publikováno v:
Blood. 136:14-15
Sickle cell disease (SCD) is an autosomal hereditary recessive disorder caused by a point mutation in the β globin gene resulting in a Glu-to-Val substitution at the 6th position of the β globin protein. The resulting abnormal hemoglobin (HbS) poly