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Mostrando ítems 11-20 de 624
Perfil de expressão dos genes APEX1, OGG1 e PARP1 em células do sangue periférico de pessoas com a Síndrome de Berardinelli-Seip do Nordeste do Brasil
(Universidade Federal do Rio Grande do NorteBrasilUFRNBiomedicina, 2016)
Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare recessive autosomal disease characterized by nearly complete absence of adipose tissue, resulting in disturbs on carbohydrates and lipids metabolism, insulin ...
Cloning the human pro-apoptotic BAX gene into a high-expression yeast vector designed for overexpressing genes in Yeast 2.0.
(Universidad EAFITBiologíaEscuela de Ciencias. Ciencias BásicasMedellín, 2019)
Caracterización de genes de resistencia en enterobacterias aisladas de bacteriemias
(PUCE, 2016)
Las cepas resistentes a la terapia antibiótica convencional (β-lactámicos, aminoglucósidos y quinolonas) son una importante amenaza para la salud pública en el mundo. La rápida evolución y propagación de la resistencia se ...
Cloning of the opsin genes present in Bothrops atrox (Viperidae) retina
(PUCE, 2017)
The visual system of vertebrates has evolved over millions of years to adapt to
nocturnal or diurnal habits as well as different environments where varying spectral range
and intensity of light are present. Although much ...
Detecci?n de fibrosis aleda?a a quistes producidos por neurocisticercosis mediante t?cnicas de procesamiento de im?genes
(Universidad de Ibagu?.Facultad de Ingenier?a, 2020)
Importância dos genes do Citoesqueleto eritrocitário na modulação do quadro clínico de pacientes com anemia falciforme: um foco no gene DMTN.
(Universidade Federal do Rio Grande do NorteBrasilUFRNFarmáciaDepartamento de Farmácia, 2021-08-27)
Sickle cell anemia is considered the most common inherited monogenic disease in the world. Currently, there are at least 300,000 diagnosed cases. In the disease, erythrocytes that have hemoglobin S undergo a sickling ...
Influência dos moduladores genéticos nos níveis de hemoglobina fetal na anemia falciforme: revisão literária
(Universidade Federal do Rio Grande do NorteBrasilUFRNCENTRO DE CIÊNCIAS DA SAÚDEDEPARTAMENTO DE FARMÁCIA, 2022-01-27)
Sickle cell anemia is a disease of genetic origin in which the individual has chronic hemolysis and pain crises resulting from vaso occlusion. It is caused by a failure in the synthesis of the molecular structure of ...