fi ocruz.br We declare no confl icts of interest A mutation described as a G-to-A transition has been reported in SDF-1 gene (SDF1-3’A), being prevalent in all ethnic groups, except in Africans. This mutation is associated with the onset of AIDS progression. Our aim was to identify the frequency of this allele in different groups from Brazil: Tiri-yó and Waiampi Amerindian tribes (Asian ancestry); selected blood donors from Joinville (German descendents); and from Salvador (predominance of African and Portuguese mixture). SDF1-3’A was screened by PCR/RFLP with MspI enzyme. Our results showed a high allelic frequency in Tiriyó tribe (0.24) and Joinville population (0.21), and a frequency of 0.17 and 0.05 in the Salvador popu-lation and in th...
This study reports the frequencies of the CCR5D32 mutation of the beta-chemokine 5 gene and discusse...
Mutations in the GJB2 gene are a major cause of congenital deafness. One specific mutation, the 35de...
Texto completo: acesso restrito. p. 293-297Cystic fibrosis (CF) is the most common autosomal recessi...
A mutation described as a G-to-A transition has been reported in SDF-1 gene (SDF1-3'A), being preval...
AbstractA mutation described as a G-to-A transition has been reported in SDF-1 gene (SDF1-3’A), bein...
The main coreceptor gene involved in HIV-1 infection is CCR5 beta chemokine receptor gene for which ...
The frequency distribution of the CCR5- 32, CCR2-64I, and SDF1-3 A alleles was studied in the urban ...
Mutations in the GJB2 gene, which encodes the protein connexin 26, are a major cause of autosomal re...
Texto completo: acesso restrito. p. 102-104We investigated the occurrence of the CCR5Δ32 mutation in...
p.214-217The main coreceptor gene involved in HIV-1 infection is CCR5 b chemokine receptor gene for ...
CCR2 is a member of the superfamily of seven transmembrane domain G protein-coupled receptors, the l...
We have recently described in this journal the distri-bution of CGG repeats of the FMR1 gene, the al...
circulating in other parts of the world, I present the results obtainedCirculating in São Paulo, Br...
A southern Brazilian isolated community of predominantly sub-Saharan African origin, with a total po...
Major mutations associated with HIV-I integrase inhibitors (INI) resistance are rare in INI-naive pa...
This study reports the frequencies of the CCR5D32 mutation of the beta-chemokine 5 gene and discusse...
Mutations in the GJB2 gene are a major cause of congenital deafness. One specific mutation, the 35de...
Texto completo: acesso restrito. p. 293-297Cystic fibrosis (CF) is the most common autosomal recessi...
A mutation described as a G-to-A transition has been reported in SDF-1 gene (SDF1-3'A), being preval...
AbstractA mutation described as a G-to-A transition has been reported in SDF-1 gene (SDF1-3’A), bein...
The main coreceptor gene involved in HIV-1 infection is CCR5 beta chemokine receptor gene for which ...
The frequency distribution of the CCR5- 32, CCR2-64I, and SDF1-3 A alleles was studied in the urban ...
Mutations in the GJB2 gene, which encodes the protein connexin 26, are a major cause of autosomal re...
Texto completo: acesso restrito. p. 102-104We investigated the occurrence of the CCR5Δ32 mutation in...
p.214-217The main coreceptor gene involved in HIV-1 infection is CCR5 b chemokine receptor gene for ...
CCR2 is a member of the superfamily of seven transmembrane domain G protein-coupled receptors, the l...
We have recently described in this journal the distri-bution of CGG repeats of the FMR1 gene, the al...
circulating in other parts of the world, I present the results obtainedCirculating in São Paulo, Br...
A southern Brazilian isolated community of predominantly sub-Saharan African origin, with a total po...
Major mutations associated with HIV-I integrase inhibitors (INI) resistance are rare in INI-naive pa...
This study reports the frequencies of the CCR5D32 mutation of the beta-chemokine 5 gene and discusse...
Mutations in the GJB2 gene are a major cause of congenital deafness. One specific mutation, the 35de...
Texto completo: acesso restrito. p. 293-297Cystic fibrosis (CF) is the most common autosomal recessi...