Genetic Regulation of Redox Balance in β-Thalassemia Trait

Autor: Magdalena María Terán, Cecilia Haro, Maria Eugenia Monaco, Blanca Issé, Natalia A Asensio, Sandra Stella Lazarte, Emilse Ledesma Achem

Publikováno v: Hemoglobin. 44:122-127

β-Thalassemia (β-thal) trait is a heterogeneous group of genetic defects leading to decreased β-globin production, ineffective erythropoiesis, and oxidative stress. The aim is to evaluate the cytoprotective response, at transcriptional and systemi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c731655b6fdf5825088339e5b313c7a
https://doi.org/10.1080/03630269.2020.1765794

Erythrocyte Catalase Activity in More Frequent Microcytic Hypochromic Anemia: Beta-Thalassemia Trait and Iron Deficiency Anemia

Autor: Magdalena María Terán, Miryam Emilse Ledesma Achem, Cecilia Jiménez, Blanca Issé, Sandra Stella Lazarte, Maria Eugenia Monaco

Publikováno v: Advances in Hematology
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Advances in Hematology, Vol 2015 (2015)

Most common microcytic hypochromic anemias are iron deficiency anemia (IDA) and β-thalassemia trait (BTT), in which oxidative stress (OxS) has an essential role. Catalase causes detoxification of H2O2 in cells, and it is an indispensable antioxidant

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8060f95e0c87a1da5e69ea93cdc8c24

Foxo3 gene expression and oxidative status in beta-thalassemia minor subjects.

Autor: Lazarte, Sandra Stella¹ slazarte@fbqf.unt.edu.ar, Mónaco, María Eugenia¹, Terán, Magdalena María¹, Haro, Ana Cecilia¹, Ledesma Achem, Miryam Emilse¹, Issé, Blanca Alicia¹

Publikováno v: Brazilian Journal of Hematology & Hemotherapy / Revista Brasileira de Hematologia e Hemoterapia. Jul-Sep2017, Vol. 39 Issue 3, p115-121. 7p.