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Identificación y caracterización serológica de variantes antigénicas de Virus Influenza A pH1N109 en planteles de producción intensiva de cerdos
(Universidad de Chile, 2019)
El virus de influenza A, es un virus ampliamente distribuido alrededor del mundo y es una de las causas principales de aparición de brotes respiratorios en cerdos. Este virus posee, una gran variabilidad antigénica, que ...
Profiling of WDR36 Missense Variants in German Patients with Glaucoma
(2008-02)
PURPOSE. Mutations in WDR36 were recently reported in patients with adult-onset primary open-angle glaucoma (POAG). In this study, the prevalence of WDR36 variants was investigated in patients with glaucoma who were of ...
Perfil eletroforético e cromatográfico das hemoglobinas S-like
(Universidade Estadual Paulista (Unesp), 2005-08-29)
As hemoglobinas (Hb) variantes, originadas em sua maioria por simples substituições de aminoácidos, resultam de mudanças na seqüência de nucleotídeos. Atualmente, o número de Hb anormais identificadas tem aumentado devido ...
Perfil eletroforético e cromatográfico das hemoglobinas S-like
(Universidade Estadual Paulista (Unesp), 2005-08-29)
As hemoglobinas (Hb) variantes, originadas em sua maioria por simples substituições de aminoácidos, resultam de mudanças na seqüência de nucleotídeos. Atualmente, o número de Hb anormais identificadas tem aumentado devido ...
Electrophoretic and chromatographic profile for S-like hemoglobin
(Funpec-editora, 2006-01-01)
Hemoglobin variants originate mainly by simple amino acid substitutions, the result of nucleotide sequence changes. Recently, the number of known abnormal hemoglobins has increased due to improvement in analysis methodologies; ...
Electrophoretic and chromatographic profile for S-like hemoglobin
(Funpec-editora, 2006-01-01)
Hemoglobin variants originate mainly by simple amino acid substitutions, the result of nucleotide sequence changes. Recently, the number of known abnormal hemoglobins has increased due to improvement in analysis methodologies; ...
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paraganglioma
(British Medical Association, 2023)
Variantes del gen CFTR en pacientes con diagnóstico de fibrosis quística de la Fundación Fundafiq Cuenca-Ecuador
(Universidad Peruana Cayetano HerediaPE, 2020)
Cystic Fibrosis is an autosomal recessive disease caused by loss of function variants in the CFTR gene. Knowing the genetics of the disease is difficult, because at present more than 2000 different genetic variants have ...