Sergio Emanuel Galembeck

Dr. Sergio Emanuel Galembeck

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Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 February 2003 in Proteomics
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MSMarcus Bustamante Smolka
Marcus Bustamante Smolka
DMDaniel Martins-de-Souza
Daniel Martins-de-Souza
Flavia Vischi WinckFlavia Vischi Winck
Flavia Vischi Winck
CSCarlos Eduardo Santoro
Carlos Eduardo Santoro
RCRafael Ramos Castellari
Rafael Ramos Castellari
JNJose Camillo Novello
Jose Camillo Novello

23 April 2017 in Biochemistry and Molecular Biology Education
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JGJuan Carlos Vega Garzón
Juan Carlos Vega Garzón
MMMarcio Luiz Magrini
Marcio Luiz Magrini
SGSergio Emanuel Galembeck
Sergio Emanuel Galembeck
Understanding metabolism and metabolic pathways constitutes one of the central aims for students of biological sciences. Learning metabolic pathways should be focused on the understanding of general concepts and core principles. New technologies such Augmented Reality (AR) have shown potential to improve assimilation of biochemistry abstract concepts because students can manipulate 3D molecules in real time. Here we describe an application named Augmented Reality Metabolic Pathways (ARMET), which allowed students to visualize the 3D molecular structure of substrates and products, thus perceiving changes in each molecule. The structural modification of molecules shows students the flow and exchange of compounds and energy through metabolism. © 2017 by The International Union of Biochemistry and Molecular Biology, 45(5):417–420, 2017.

1 February 2010 in Journal of Cellular Biochemistry
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RMRenato Milani
Renato Milani
CFCarmen V. Ferreira
Carmen V. Ferreira
JGJose M. Granjeiro
Jose M. Granjeiro
EGEdgar Julian Paredes Gamero
Edgar Julian Paredes Gamero
Rodrigo Augusto Foganholi da SilvaRodrigo Augusto Foganholi da Silva
Rodrigo Augusto Foganholi da Silva
Willian Fernando ZambuzziWillian Fernando Zambuzzi
Willian Fernando Zambuzzi

2 May 2016 in Frontiers in Aging Neuroscience
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GSGesivaldo Santos
Gesivaldo Santos
LGLisandro Diego Giraldez-Alvarez
Lisandro Diego Giraldez-Alvarez
MAMarco Avila-Rodriguez
Marco Avila-Rodriguez
FCFrancisco Capani
Francisco Capani
SGSergio Emanuel Galembeck
Sergio Emanuel Galembeck
Bruno Silva AndradeBruno Silva Andrade
Bruno Silva Andrade
Parkinson’s disease (PD) is one of the most common neurodegenerative disorders. A theoretical approach of our previous experiments reporting the cytoprotective effects of the Valeriana officinalis compounds extract for PD is suggested. In addiction to considering the PD as a result of mitochondrial metabolic imbalance and oxidative stress, such as in our previous in vitro model of rotenone, in the present manuscript we added a genomic approach to evaluate the possible underlying mechanisms of the effect of the plant extract. Microarray of substantia nigra (SN) genome obtained from Allen Brain Institute was analyzed using gene set enrichment analysis to build a network of hub genes implicated in PD. Proteins transcribed from hub genes and their ligands selected by search ensemble approach algorithm were subjected to molecular docking studies, as well as 20 nanoseconds Molecular Dynamics using a MMPBSA protocol. Our results bring a new approach to Valeriana officinalis extract, and suggest that hesperidin, and probably linarin are able to relieve effects of oxidative stress during ATP depletion due to its ability to binding SUR1. In addition, the key role of valerenic acid and apigenin is possibly related to prevent cortical hyperexcitation by inducing neuronal cells from substancia nigra to release GABA on brain stem. Thus, under hyperexcitability, oxidative stress, asphyxia and/or ATP depletion, Valeriana officinalis may trigger different mechanisms to provide neuronal cell protection.

1 May 1998 in Chemico-Biological Interactions
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SGSergio Emanuel Galembeck
Sergio Emanuel Galembeck
AAAntônio Alonso
Antônio Alonso
NMNilce Correa Meirelles
Nilce Correa Meirelles