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Mostrando ítems 31-40 de 132
How Do We Identify Rhd Variants Using A Practical Molecular Approach?
(Blackwell Publishing Inc., 2014)
Estudo da frequência dos haplótipos do gene JAK2 em pacientes portadores de neoplasias mieloproliferativas crônicasEvaluation of the JAK2 gene haplotype frequency in patients with chronic myeloproliferative neoplasm
(Universidade Estadual de MaringáBrasilDepartamento de Análises Clínicas e BiomedicinaPrograma de Pós-Graduação em Biociências Aplicadas à FarmáciaUEMMaringá, PRCentro de Ciências da Saúde, 2018)
PSA and androgen-related gene (AR, CYP17, and CYP19) polymorphisms and the risk of adenocarcinoma at prostate biopsy
(MARY ANN LIEBERT INC, 2008)
The aim of the present study was to examine the impact of polymorphisms in prostate-specific antigen (PSA) and androgen-related genes (AR, CYP17, and CYP19) on prostate cancer (PCa) risk in selected high-risk patients who ...
G6PD deficiency alleles in a malaria-endemic region in the Western Brazilian Amazon
(BioMed Central, 2017)
Abstract
Background
Plasmodium vivax parasites are the predominant cause of malaria infections in the Brazilian Amazon. Infected individuals ...
Amplificação gênica alelo específica e multiplex no diagnóstico laboratorial de hemoglobinas anormais
(Universidade Estadual Paulista (Unesp), 2005-11-16)
As hemoglobinopatias constituem um grupo de alterações hereditárias prevalentes em muitas regiões do mundo, atingindo a população brasileira de forma significativa; sendo decorrentes de alterações em genes estruturais, ...
Amplificação gênica alelo específica e multiplex no diagnóstico laboratorial de hemoglobinas anormais
(Universidade Estadual Paulista (Unesp), 2005-11-16)
As hemoglobinopatias constituem um grupo de alterações hereditárias prevalentes em muitas regiões do mundo, atingindo a população brasileira de forma significativa; sendo decorrentes de alterações em genes estruturais, ...
Molecular analysis of the eighteen most frequent mutations in the BRCA 1 gene in 63 Chilean breast cancer families
(Society of Biology of Chile, 2004)
BRCA1 gene mutations account for nearly all families with multiple cases of both early onset breast and/or ovarian cancer and about 30% of hereditary breast cancer. Although to date more than 1,237 distinct mutations, ...
HNA-3 gene frequencies in Brazilians and a new polymerase chain reaction-restriction fragment length polymorphism method for HNA-3a/3b genotyping
(Wiley-Blackwell, 2014-06-01)
Background HNA-3 antigens are the result of a rs2288904 single-nucleotide polymorphism (SNP) in the CTL2, and the HNA-3a and HNA-3b variants are encoded by a guanine and adenine at Nucleotide Position 461. Anti-HNA-3 are ...