Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Carolina Lanaro"'
Autor:
Sueli Matilde da Silva Costa, Mirta Tomie Ito, Pedro Rodrigues Sousa da Cruz, Bruno Batista De Souza, Vinicius Mandolesi Rios, Victor de Haidar e Bertozzo, Ana Carolina Lima Camargo, Marina Gonçalves Monteiro Viturino, Carolina Lanaro, Dulcinéia Martins de Albuquerque, Amanda Morato do Canto, Sara Teresinha Olalla Saad, Stephanie Ospina-Prieto, Margareth Castro Ozelo, Fernando Ferreira Costa, Mônica Barbosa de Melo
Publikováno v:
Experimental Biology and Medicine, Vol 249 (2024)
HbSC disease, a less severe form of sickle cell disease, affects the retina more frequently and patients have higher rates of proliferative retinopathy that can progress to vision loss. This study aimed to identify differences in the expression of en
Externí odkaz:
https://doaj.org/article/fa1706a357894d4bbcbdf5ba1859ce6d
Autor:
Ana Carolina Toreli, Paula De Melo Campos, Isabella Toni, Daniela Pinheiro Leonardo, Carolina Lanaro, Dulcineia Martins de Albuquerque, Kleber Yotsumoto Fertrin, Fernando F Costa
Publikováno v:
HemaSphere, Vol 7, p e80012a1 (2023)
Externí odkaz:
https://doaj.org/article/b0f272e0af4e4577942d382d1ca15afb
Autor:
Renata Sesti-Costa, Marina Dorigatti Borges, Carolina Lanaro, Dulcinéia Martins de Albuquerque, Sara Terezinha Olalla Saad, Fernando Ferreira Costa
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
Sickle cell disease (SCD), one of the most common hemoglobinopathies worldwide, is characterized by a chronic inflammatory component, with systemic release of inflammatory cytokines, due to hemolysis and vaso-occlusive processes. Patients with SCD de
Externí odkaz:
https://doaj.org/article/09a63da267c24f1e98272b46ae8e1753
Autor:
Karen S Romanello, Karina K L Teixeira, João Pedro M O Silva, Sheila T Nagamatsu, Marcos André C Bezerra, Igor F Domingos, Diego A P Martins, Aderson S Araujo, Carolina Lanaro, Carlos A Breyer, Regiane A Ferreira, Carla Franco-Penteado, Fernando F Costa, Iran Malavazi, Luis E S Netto, Marcos A de Oliveira, Anderson F Cunha
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0208316 (2018)
β-thalassemia is a worldwide distributed monogenic red cell disorder, characterized by an absent or reduced beta globin chain synthesis. The unbalance of alpha-gamma chain and the presence of pathological free iron promote severe oxidative damage, p
Externí odkaz:
https://doaj.org/article/4b78522957f34bf29516daf39d4e0b8c
Autor:
Daniela P Leonardo, Dulcinéia M Albuquerque, Carolina Lanaro, Letícia C Baptista, José G Cecatti, Fernanda G Surita, Mary A Parpinelli, Fernando F Costa, Carla F Franco-Penteado, Kleber Y Fertrin, Maria Laura Costa
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136693 (2015)
Preeclampsia is one of the leading causes of maternal and neonatal morbidity and mortality in the world, but its appearance is still unpredictable and its pathophysiology has not been entirely elucidated. Genetic studies have associated single nucleo
Externí odkaz:
https://doaj.org/article/2c2ce5b846c74c2a90a260123d6c6f76
Autor:
Daniela Pinheiro Leonardo, Myriam Salazar-Terreros, Stephan Menzel, Carolina Lanaro, Dulcinéia Martins de Albuquerque, Sara T Olalla Saad, Kleber Yotsumoto Fertrin, Fernando Ferreira Costa
Publikováno v:
Blood. 140:2510-2511
Autor:
Bidossessi Wilfried Hounkpe, Carla Roberta Peachazepi Moraes, Carolina Lanaro, Magnun Nueldo Nunes Santos, Fernando Ferreira Costa, Erich Vinicius De Paula
Publikováno v:
Exp Biol Med (Maywood)
Hemolytic diseases such as Sickle Cell Disease (SCD) are characterized by a natural propensity for both arterial and venous thrombosis. The ability of heme to induce tissue factor (TF) activation has been shown both in animal models of SCD, and in hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca5942125f247af9cd66472ce41b2d05
https://europepmc.org/articles/PMC9554166/
https://europepmc.org/articles/PMC9554166/
Autor:
Victor de Haidar e Bertozzo, Sueli Matilde da Silva Costa, Mirta Tomie Ito, Pedro Rodrigues Sousa da Cruz, Bruno Batista Souza, Vinicius Mandolesi Rios, Marina Gonçalves Monteiro Viturino, Júlia Nicoliello Pereira de Castro, Thiago Adalton Rosa Rodrigues, Carolina Lanaro, Dulcinéia Martins de Albuquerque, Roberta Casagrande Saez, Sara Teresinha Olalla Saad, Margareth Castro Ozelo, Fernando Ferreira Costa, Mônica Barbosa de Melo
Publikováno v:
Experimental Biology and Medicine. :153537022311579
Among sickle cell anemia (SCA) complications, proliferative sickle cell retinopathy (PSCR) is one of the most important, being responsible for visual impairment in 10–20% of affected eyes. The aim of this study was to identify differentially expres
Autor:
Thais Regina Ferreira de Melo, Guilherme Felipe dos Santos Fernandes, Brian M. Dulmovits, Cristiane Maria de Souza, Lionel Blanc, Yousef Al Abed, Jean Leandro dos Santos, Minghzu He, Carolina Lanaro, Fernando Ferreira Costa, Man Chin Chung
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Bioorg Chem
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Bioorg Chem
Made available in DSpace on 2021-06-25T10:32:36Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-09-01 Fetal hemoglobin (HbF) induction constitutes a valuable and validated approach to treat the symptoms of sickle cell disease (SCD). Here, we s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489327c495a5f43c4ab434e4120014a8
Autor:
Fernando Ferreira Costa, Oladele Simeon Olatunya, Carolina Lanaro, Adekunle Adekile, Carla Fernanda Franco Penteado, Ana Leda F. Longhini, Kleber Yotsumoto Fertrin, Sara T.O. Saad
Publikováno v:
Annals of Hematology. 98:2507-2521
Microparticles are sub-micron vesicles possessing protein and other materials derived from the plasma membrane of their parent cells, and literature suggests that they may have a role in the pathophysiology and downstream manifestations of sickle cel