Monica Santos de Freitas
Instituição:
Universidade Federal do Rio de Janeiro
Centro:
Centro de Ciências da Saúde
Unidade:
Instituto de Bioquímica Médica
Departamento:
Programa de Biologia Celular e Biofisica
e-mail:
msfreitas@ufrj.br
Linkedin:
Google Scholar:
ORCID:
http://orcid.org/0000-0003-3105-7918
Formação:
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Leibniz-Institut für Molekulare Pharmakologie
| Pós-Doutorado | 2008 - 2010
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Universidade Federal do Rio de Janeiro
| Pós-Doutorado | 2008 - 2008
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Universidade Federal do Rio de Janeiro
| Pós-Doutorado | 2007 - 2008
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Universidade Federal do Rio de Janeiro
Química Biológica | Doutorado | 2003 - 2007
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Universidade Federal do Rio de Janeiro
Química Biológica | Mestrado | 2002 - 2003
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Universidade Federal do Rio de Janeiro
Ciencias Biológicas Modalidade Médica | Graduação | 1998 - 2001
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Colégio Bezerra de Araújo
| Ensino Médio (2o grau) | 1993 - 1995
Laboratórios:
Nenhum laboratório cadastrado
Nuvens de Palavras:
Artigos:
(94.12% artigos com DOI)
Titulo | DOI | Ano |
---|---|---|
The protofilament architecture of a de novo designed coiled coil-based amyloidogenic peptide | 10.1016/j.jsb.2018.05.009 | 2018 |
Structural basis for the dissociation of α-synuclein fibrils triggered by pressure perturbation of the hydrophobic core | 10.1038/srep37990 | 2016 |
Backbone resonance assignments of the human p73 DNA binding domain | 10.1007/s12104-015-9635-x | 2015 |
Structural and Molecular Modeling Features of P2X Receptors | 10.3390/ijms15034531 | 2014 |
The P2X7 receptor: Shifting from a low- to a high-conductance channel - An enigmatic phenomenon? | 10.1016/j.bbamem.2014.05.015 | 2014 |
Vitamins K interact with N-terminus α-synuclein and modulate the protein fibrillization in vitro. Exploring the interaction between quinones and α-synuclein | 10.1016/j.neuint.2012.10.001 | 2013 |
The Anti-Parkinsonian Drug Selegiline Delays the Nucleation Phase of ?-Synuclein Aggregation Leading to the Formation of Nontoxic Species | 10.1016/j.jmb.2010.10.027 | 2011 |
Measuring the Strength of Interaction between the Ebola Fusion Peptide and Lipid Rafts: Implications for Membrane Fusion and Virus Infection | 10.1371/journal.pone.0015756 | 2011 |
Ligand Binding and Hydration in Protein Misfolding: Insights from Studies of Prion and p53 Tumor Suppressor Proteins | 10.1021/ar900179t | 2010 |
The p53 Core Domain Is a Molten Globule at Low pH: FUNCTIONAL IMPLICATIONS OF A PARTIALLY UNFOLDED STRUCTURE | 10.1074/jbc.M109.075861 | 2010 |
Positive response to imatinib mesylate therapy for childhood chronic myeloid leukemia | 10.1590/S0100-879X2010007500026 | 2010 |
Predictions Suggesting a Participation of ?-Sheet Configuration in the M2 Domain of the P2X7 Receptor: A Novel Conformation? | 10.1016/j.bpj.2008.10.043 | 2009 |
Membrane-disruptive properties of the bioinsecticide Jaburetox-2Ec: Implications to the mechanism of the action of insecticidal peptides derived from ureases | 10.1016/j.bbapap.2009.09.001 | 2009 |
Structure of the Ebola Fusion Peptide in a Membrane-mimetic Environment and the Interaction with Lipid Rafts | 10.1074/jbc.m611864200 | 2007 |
Structure of a Membrane-binding Domain from a Non-enveloped Animal Virus: INSIGHTS INTO THE MECHANISM OF MEMBRANE PERMEABILITY AND CELLULAR ENTRY | 10.1074/jbc.m604689200 | 2006 |
The Fusogenic State of Mayaro Virus Induced by Low pH and by Hydrostatic Pressure | 10.1385/cbb:44:3:325 | 2006 |
Hidrostatic Pressure induces the fusion-active state of enveloped viruses | 2002 |
Eventos:
(0.00% eventos com DOI)