© 2020 Elsevier Inc. All rights reserved.We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in pediatric sickle cell anemia (SCA) patients of sub-Saharan African ancestry. We found that one VCAM1 promoter haplotype (haplotype 7) and VCAM1 single nucleotide variant rs1409419_T were associated with stroke events, stroke risk, as measured by time-averaged mean of maximum velocity in the middle cerebral artery, and with high serum levels of the hemolysis biomarker lactate dehydrogenase. Furthermore, VCAM-1 ligand coding gene ITGA4 variants rs113276800_A and rs3770138_T showed a positive association with stroke events. An additional positive relationship between a genetic variant and stroke risk was ...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
Sickle cell anaemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene. Howeve...
Palestras de difusão da cultura científica dirigidas aos colaboradores internos do INSA, podendo inc...
Sickle cell disease (SCD) is a genetic disorder with recessive transmission, caused by the mutation ...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity f...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of h...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
A drepanocitose é uma doença genética causada pela mutação c.20A>T, em homozigotia, no gene da beta...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
We investigated biomarkers and genetic modulators of the cerebral vasculopathy (CV) subphenotype in ...
Sickle cell anaemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene. Howeve...
Palestras de difusão da cultura científica dirigidas aos colaboradores internos do INSA, podendo inc...
Sickle cell disease (SCD) is a genetic disorder with recessive transmission, caused by the mutation ...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity f...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of h...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
A drepanocitose é uma doença genética causada pela mutação c.20A>T, em homozigotia, no gene da beta...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...