Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jéssika V. Okumura"'
Autor:
Flaviene F. Torres, Victoria S. Bernardo, Danilo G.H. Silva, Jéssika V. Okumura, Claudia R. Bonini-Domingos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 2, Pp 156-162 (2022)
Introduction: Studies have shown that the loss of the FOXO3 transcriptional function is involved in the pathophysiology of some chronic erythroid disorders, including beta-thalassemia (β-thal). Therefore, the single nucleotide polymorphism (SNP) rs3
Externí odkaz:
https://doaj.org/article/ca111f8e9f8745f285f2faa993b71e86
Autor:
Lidiane S. Torres, Jéssika V. Okumura, Danilo G. H. Silva, Kallyne K. O. Mimura, Édis Belini-Júnior, Renan G. Oliveira, Clarisse L. C. Lobo, Sonia M. Oliani, Claudia R. Bonini-Domingos
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 2, p e0172659 (2017)
PLoS ONE, Vol 12, Iss 2, p e0172659 (2017)
Sickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive events. Inflammation is a fundamental component in these processes and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c7932d09fcb4c91a9a9c4d92c9b5f70
http://europepmc.org/articles/PMC5313145
http://europepmc.org/articles/PMC5313145
Autor:
Lidiane S Torres, Jéssika V Okumura, Danilo G H Silva, Kallyne K O Mimura, Édis Belini-Júnior, Renan G Oliveira, Clarisse L C Lobo, Sonia M Oliani, Claudia R Bonini-Domingos
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0165833 (2016)
Sickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive events. Inflammation is a fundamental component in these processes and a
Externí odkaz:
https://doaj.org/article/bf0bd5ef2c0b4b3a9b514473238841b2