Browsing by Author "Costa, Fernando Ferreira"
Now showing items 1-9 of 9
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Anemia falciforme em Salvador-Bahia: caracterização fenotípica, molecular e de sequências gênicas potencialmente importantes na expressão dos genes gama da hemoglobina fetal
Adorno, Elisângela Vitória | Date Issued: 2005do gene da globina p, levando à substituição do ácido glutâmico por valina na cadeia da globina p. A anemia falciforme ou a homozigose para a HbS, freqüentemente apresenta manifestações clínicas heterogêneas, fortemente ... -
Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients from two different cities in Brazil
Lyra, Isa Menezes et al. | Date Issued: 2005O objetivo desse estudo foi avaliar aspectos clínicos, hematológicos e moleculares de pacientes pediátricos portadores de anemia falciforme em duas cidades brasileiras: Salvador e São Paulo. Foram estudados 71 pacientes ... -
Frequencies of platelet-specific alloantigen systems 1–5 in three distinct ethnic groups in Brazil
Castro, Vagner de et al. | Date Issued: 1999 -
Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil
Fertrin, Kleber Yotsumoto et al. | Date Issued: 2002 -
Increasing seroprevalence of human herpesvirus 8 (HHV-8) with age confirms HHV-8 endemicity in Amazon Amerindians from Brazil.
Cunha, Andréa Mendonça Gusmão et al. | Date Issued: 2005 -
Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia
Rodriguez, David Enrique Aguilar et al. | Date Issued: 2005 -
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?
Arruda, Valder Roberval et al. | Date Issued: 1998 -
The Ay-195 (C®G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
Schreiber, R et al. | Date Issued: 2001 -
Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients
Siqueira, Gabriela Queila de Carvalho et al. | Date Issued: 2019