Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Igor F Domingos"'
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:
Adekunle E. Alagbe, Igor F. Domingos, Adekunle D. Adekile, Maria H. S. L. Blotta, Magnun N. N. Santos
Publikováno v:
Molecular Biology Reports. 49:2433-2442
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee594057aaca0332525df0e7a6a4ba2e
https://doi.org/10.1007/s11033-021-07009-1
https://doi.org/10.1007/s11033-021-07009-1
Autor:
Thais H. C. Batista, Rodrigo M. Santana, Marcondes J. Sobreira, Gabriela S. Arcanjo, Igor F. Domingos, Diego A. Pereira‐Martins, Diego A. Falcão, Jéssica M. F. Oliveira, Jéssica V. G. F. Batista, Isabel Weinhӓuser, Betânia L. Hatzlhofer, Walter L. B. Júnior, Aderson S. Araujo, Ana C. dos Anjos, Fernando F. Costa, Mario J. A. Saad, Bruno M. Carvalho, Luydson R. S. Vasconcelos, Antonio R. Lucena‐Araujo, Marcos A. Bezerra
Publikováno v:
British Journal of Haematology. 197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5261a3219371dd36165f0d10cb3bf46b
https://doi.org/10.1111/bjh.18018
https://doi.org/10.1111/bjh.18018
Autor:
Diego A, Pereira-Martins, Juan L, Coelho-Silva, Igor F, Domingos, Isabel, Weinhäuser, Pedro L, Franca-Neto, Aderson S, Araujo, Rafael F, Franca, Marcos A, Bezerra, Antonio R, Lucena-Araujo
Publikováno v:
Annals of hematology. 101(2)
One of the physiologic mechanisms responsible to maintain asymmetric phospholipid distribution (in particular phosphatidylserine, PS) in human erythrocyte membranes is orchestrated by the balance between enzymes responsible for active transport of PS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d5e293598ed1b35baa4c2b1a92d17ed
https://pubmed.ncbi.nlm.nih.gov/34651249
https://pubmed.ncbi.nlm.nih.gov/34651249
Autor:
Jéssica V G F, Batista, Gabriela S, Arcanjo, Thais H C, Batista, Marcondes J, Sobreira, Rodrigo M, Santana, Igor F, Domingos, Betânia L, Hatzlhofer, Diego A, Falcão, Diego A, Pereira-Martins, Jéssica M, Oliveira, Amanda S, Araujo, Luana P M, Laranjeira, Fernanda S, Medeiros, Flávia P, Albuquerque, Dulcinéia M, Albuquerque, Magnun N, Santos, Manuela F, Hazin, Ana C, Dos Anjos, Fernando F, Costa, Aderson S, Araujo, Antonio R, Lucena-Araujo, Marcos A, Bezerra
Publikováno v:
Annals of hematology. 100(4)
Hyperbilirubinemia in patients with sickle cell anemia (SCA) as a result of enhanced erythrocyte destruction, lead to cholelithiasis development in a subset of patients. Evidence suggests that hyperbilirubinemia may be related to genetic variations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab5c0c999aaa0fc6412b3440e44768ab
https://pubmed.ncbi.nlm.nih.gov/33523291
https://pubmed.ncbi.nlm.nih.gov/33523291
Autor:
Igor F, Domingos, Diego A, Pereira-Martins, Marcondes J V C, Sobreira, Romulo T D, Oliveira, Adekunle E, Alagbe, Carolina, Lanaro, Dulcineia M, Albuquerque, Maria H S L, Blotta, Aderson S, Araujo, Fernando F, Costa, Antonio R, Lucena-Araujo, Maria F, Sonati, Marcos A C, Bezerra, Magnun N N, Santos
Publikováno v:
Annals of hematology. 99(5)
Sickle cell anemia (SCA) pathophysiology is characterized by the activation of sickle red blood cells, reticulocytes, leukocytes, platelets, and endothelial cells, and with the expression of several inflammatory molecules. Therefore, it is conceivabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e53e9e02f1136048c13ce73239be340
https://pubmed.ncbi.nlm.nih.gov/32140892
https://pubmed.ncbi.nlm.nih.gov/32140892
Autor:
Diego A. Pereira-Martins, Igor F. Domingos, Edis Belini-Junior, Juan L. Coelho-Silva, Isabel Weinhäuser, Aderson S. Araújo, Clarisse L. Lobo, Claudia R. Bonini-Domingos, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 243-248 (2021)
Introduction: Sickle cell anemia (SCA) is a Mendelian disorder with a heterogeneous clinical course. The reasons for this phenotypic diversity are not entirely established, but it is known that high fetal hemoglobin levels lead to a milder course of
Externí odkaz:
https://doaj.org/article/b4f7b9e9364742d191c10f93c9d5a4c7