Priscila Zonzini Ramos

Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology

Maria Carolina CCosta CMelo Svidnicki, Sueli Matilde da Silva-Costa, Priscila Zonzini Ramos et al. · BMC Medical Genetics · 2015 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Hinge Binder Scaffold Hopping Identifies Potent Calcium/Calmodulin-Dependent Protein Kinase Kinase 2 (CAMKK2) Inhibitor Chemotypes

Benjamin J. Eduful, Sean O’Byrne, Louisa Temme et al. · Journal of Medicinal Chemistry · 2021 · 33 citations · Full text

Pharmacy, Medicinal Chemistry, Pharmacology +17

Binding and structural analyses of potent inhibitors of the human Ca2+/calmodulin dependent protein kinase kinase 2 (CAMKK2) identified from a collection of commercially-available kinase inhibitors

Gerson S. Profeta, C.V. dos Reis, André da Silva Santiago et al. · Scientific Reports · 2019 · 25 citations · Full text

Life Sciences, Biochemistry, Medicinal Chemistry +17

Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping Platform

Fábio Tadeu Arrojo Martins, Priscila Zonzini Ramos, Maria Carolina Costa Melo Svidnicki et al. · BMC Medical Genetics · 2013 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Structural Analysis of Inhibitor Binding to CAMKK1 Identifies Features Necessary for Design of Specific Inhibitors

André da Silva Santiago, Rafael M. Couñago, Priscila Zonzini Ramos et al. · Scientific Reports · 2018 · 21 citations · Full text

Pharmacy, Medicinal Chemistry, Molecular Biology +17