Resultados da busca - Ramos, Priscila Zonzini

Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping Platform por Martins, Fábio Tadeu Arrojo, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Structural Analysis of Inhibitor Binding to CAMKK1 Identifies Features Necessary for Design of Specific Inhibitors por Santiago, André da Silva, Couñago, Rafael M., Ramos, Priscila Zonzini, Godoi, Paulo H. C., Massirer, Katlin B., Gileadi, Opher, Elkins, Jonathan M.

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Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology por Svidnicki, Maria Carolina CCosta CMelo, Silva-Costa, Sueli Matilde, Ramos, Priscila Zonzini, dos Santos, Nathalia Zocal Pereira, Martins, Fábio Tadeu Arrojo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry por Alves, Rogério Marins, da Silva Costa, Sueli Matilde, do Amôr Divino Miranda, Paulo Mauricio, Ramos, Priscila Zonzini, Marconi, Thiago Gibbin, Santos Oliveira, Gisele, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Structural features and development of an assay platform of the parasite target deoxyhypusine synthase of Brugia malayi and Leishmania major por Silva, Suélen Fernandes, Klippel, Angélica Hollunder, Ramos, Priscila Zonzini, Santiago, André da Silva, Valentini, Sandro Roberto, Bengtson, Mario Henrique, Massirer, Katlin Brauer, Bilsland, Elizabeth, Couñago, Rafael Miguez, Zanelli, Cleslei Fernando

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