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Evaluación de la mutación a3243g en mtDNA, en familias de pacientes diagnosticados con el síndrome Melas
(Universidad de Antioquia, Facultad de MedicinaMedellín, Colombia, 2022)
Use of the SSCP technique to detect point mutations on human mtDNAUso de la técnica SSCP para detectar mutaciones puntuales del ADN mitocondrial humano
(Universidad Nacional Mayor de San Marcos, Facultad de Ciencias Biológicas, 2005)
Internucleotide correlations and nucleotide periodicity in drosophila mtDNA: New evidence for panselective evolution
(Society of Biology of Chile, 2010)
Analysis for the homogeneity of the distribution of the second base of dinucleotides in relation to the first, whose bases are separated by 0, 1, 2, 21 nucleotide sites, was performed with the VIH-1 genome (cDNA), the ...
Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy
(Molecular VisionAtlantaEUA, 2011)
Aedes aegypti on Madeira Island (Portugal): genetic variation of a recently introduced dengue vector
(Instituto Oswaldo Cruz, Ministério da Saúde, 2013)
The increasing population of Aedes aegypti mosquitoes on Madeira Island (Portugal) resulted in the first autochthonous dengue outbreak, which occurred in October 2012. Our study establishes the first genetic evaluation ...