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A hypothesis about the role of fetal hemoglobin in COVID-19
COVID-19 infection is less common in children (with higher fetal hemoglobin levels). In our preliminary study, we also observed a low prevalence and fatality of
COVID-19 in countries with high rate of hemoglobinopathy ...
The Agamma-195 (C->G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
(Associação Brasileira de Divulgação Científica, 2001)
The Ay-195 (C®G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
(Associação Brasileira de Divulgação Científica, 2017)
Molecular identification of Sicilian (8 beta)degrees-thalassemia associated with beta-thalassemia and hemoglobin S in Brazil
(Assoc Bras Divulg CientificaSao PauloBrasil, 2002)
What influences Hb fetal production in adulthood?
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2011-06-01)
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respectively. Different types of hemoglobin are synthesized according to the stage of development with fetal hemoglobin (α2γ2) ...
What influences Hb fetal production in adulthood?
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2011-06-01)
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respectively. Different types of hemoglobin are synthesized according to the stage of development with fetal hemoglobin (α2γ2) ...
Contribuição para a estimativa da freqüência populacional da Persistência Hereditária da Hemoglobina Fetal no BrasilEstimation of the frequency of Hereditary Persistence of Fetal Hemoglobin in Brazil
(Escola Nacional de Saúde Pública Sergio Arouca, Fundação Oswaldo Cruz, 2002)
Recent Insights on the Medicinal Chemistry of Sickle Cell Disease
(Bentham Science Publ Ltd, 2011-05-01)
Sickle Cell Disease (SCD) is one of the most prevalent hematological diseases in the world. SCD is a genetic disease characterized by punctual mutation that basis on the exchange of glutamic acid to valine in a beta chain ...