Browsing by Author "Gonçalves, Marilda de Souza"
Now showing items 91-110 of 182
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Genetic characterisation of Langerin gene in human immunodeficiency virus-1-infected women from Bahia, Brazil
Costa, Giselle Calasans de Souza et al. | Date Issued: 2014 -
Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia
Aleluia, Milena Magalhães et al. | Date Issued: 2017 -
Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia
Barbosa, Cynara Gomes et al. | Date Issued: 2013 -
Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children
Oliveira, Rodrigo Mota de et al. | Date Issued: 2018 -
Genetic variability of platelet glycoprotein Ibalpha gene
Ozelo, Margareth Castro et al. | Date Issued: 2004 -
A genome survey of Moniliophthora perniciosa gives new insights into Witches' Broom Disease of cacao
Mondego, Jorge Mauricio Costa et al. | Date Issued: 2008 -
Globin haplotypes of human T-cell lymphotropic virus type I-infected individuals in Salvador, Bahia, Brazil, suggest a post-Columbian African origin of this virus.
Alcantara, Luiz Carlos Júnior et al. | Date Issued: 2003 -
Glutathione S-transferase, catalase, and mitochondrial superoxide dismutase gene polymorphisms modulate redox potential in systemic lupus erythematosus patients from Manaus, Amazonas, Brazil
Oliveira, Marco Aurélio Almeida de et al. | Date Issued: 2021 -
Haplotype analysis and Agamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin
Bordin, Silvana et al. | Date Issued: 1998 -
Heme Drives Oxidative Stress-Associated Cell Death in Human Neutrophils Infected with Leishmania infantum
Carvalho, Graziele Quintela et al. | Date Issued: 2017 -
Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia
Guarda, Caroline Conceição da et al. | Date Issued: 2017 -
Hemoglobin Variant Profiles among Brazilian Quilombola Communities
Santiago, Rayra Pereira et al. | Date Issued: 2017 -
Hemoglobinopathies in newborns from Salvador, Bahia, Northeast Brazil.
Adorno, Elisângela Vitória et al. | Date Issued: 2005Hemoglobinopatias são alterações hereditárias na molécula de hemoglobina com prevalência mundial elevada. O Brasil apresenta prevalência de 0,1 a 0,3% para recém-nascidos com anemia falciforme e freqüência de 20,0 a ... -
Hemoglobinopatias em trabalhadores expostos à riscos ocupacionais
Silva Filho, Isaac L et al. | Date Issued: 2002 -
Hidroxiureia na doença falciforme: influência de polimorfismos nos genes MPO e SERPINA1 e implicações nas vias dos receptores tipo Toll e do Inflamassoma
Pitanga, Thassila Nogueira | Date Issued: 2015Introdução: A doença falciforme (DF) é uma condição inflamatória associada a crises vaso-oclusivas e hemólise intravascular. Os polimorfismos nos genes SERPINA1 e mieloperoxidase (MPO) -463G>A estão associados a complicações ... -
HPA-3 and C807T polymorphisms are associated with laboratory biomarkers of coronary artery disease in Brazilian women
Valverde, Suellen Pinheiro Carvalho et al. | Date Issued: 2022 -
HTLV type 1 molecular study in Brazilian villages with African characteristics giving support to the post-Columbian introduction hypothesis.
Rego, Filipe Ferreira de Almeida et al. | Date Issued: 2008 -
HTLV-1aA introduction into Brazil and its association with the trans-Atlantic slave trade
Amoussa, Adjile Edjide Roukiyath et al. | Date Issued: 2017 -
Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
Guarda, Caroline Conceição da et al. | Date Issued: 2019 -
Hydroxyurea in the management of sickle cell disease: pharmacogenomics and enzymatic metabolism
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2018