scispace - formally typeset
Search or ask a question
Institution

University of São Paulo

EducationSão Paulo, Brazil
About: University of São Paulo is a education organization based out in São Paulo, Brazil. It is known for research contribution in the topics: Population & Health care. The organization has 136513 authors who have published 272320 publications receiving 5127869 citations. The organization is also known as: USP & Universidade de São Paulo.


Papers
More filters
Journal ArticleDOI
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
Abstract: In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.

1,129 citations

Journal ArticleDOI
TL;DR: The purpose of this review is to examine current molecular docking strategies used in drug discovery and medicinal chemistry, exploring the advances in the field and the role played by the integration of structure- and ligand-based methods.
Abstract: Pharmaceutical research has successfully incorporated a wealth of molecular modeling methods, within a variety of drug discovery programs, to study complex biological and chemical systems. The integration of computational and experimental strategies has been of great value in the identification and development of novel promising compounds. Broadly used in modern drug design, molecular docking methods explore the ligand conformations adopted within the binding sites of macromolecular targets. This approach also estimates the ligand-receptor binding free energy by evaluating critical phenomena involved in the intermolecular recognition process. Today, as a variety of docking algorithms are available, an understanding of the advantages and limitations of each method is of fundamental importance in the development of effective strategies and the generation of relevant results. The purpose of this review is to examine current molecular docking strategies used in drug discovery and medicinal chemistry, exploring the advances in the field and the role played by the integration of structure- and ligand-based methods.

1,120 citations

Journal ArticleDOI
TL;DR: This work describes an electrochemical neuromorphic organic device (ENODe) operating with a fundamentally different mechanism from existing memristors, opening a path towards extreme interconnectivity comparable to the human brain.
Abstract: A neuromorphic device based on the stable electrochemical fine-tuning of the conductivity of an organic ionic/electronic conductor is realized. These devices show high linearity, low noise and extremely low switching voltage. The brain is capable of massively parallel information processing while consuming only ∼1–100 fJ per synaptic event1,2. Inspired by the efficiency of the brain, CMOS-based neural architectures3 and memristors4,5 are being developed for pattern recognition and machine learning. However, the volatility, design complexity and high supply voltages for CMOS architectures, and the stochastic and energy-costly switching of memristors complicate the path to achieve the interconnectivity, information density, and energy efficiency of the brain using either approach. Here we describe an electrochemical neuromorphic organic device (ENODe) operating with a fundamentally different mechanism from existing memristors. ENODe switches at low voltage and energy ( 500 distinct, non-volatile conductance states within a ∼1 V range, and achieves high classification accuracy when implemented in neural network simulations. Plastic ENODes are also fabricated on flexible substrates enabling the integration of neuromorphic functionality in stretchable electronic systems6,7. Mechanical flexibility makes ENODes compatible with three-dimensional architectures, opening a path towards extreme interconnectivity comparable to the human brain.

1,119 citations

Journal ArticleDOI
TL;DR: The results indicate that left prefrontal anodal stimulation leads to an enhancement of working memory performance, which depends on the stimulation polarity and is specific to the site of stimulation.
Abstract: Previous studies have claimed that weak transcranial direct current stimulation (tDCS) induces persisting excitability changes in the human motor cortex that can be more pronounced than cortical modulation induced by transcranial magnetic stimulation, but there are no studies that have evaluated the effects of tDCS on working memory. Our aim was to determine whether anodal transcranial direct current stimulation, which enhances brain cortical excitability and activity, would modify performance in a sequential-letter working memory task when administered to the dorsolateral prefrontal cortex (DLPFC). Fifteen subjects underwent a three-back working memory task based on letters. This task was performed during sham and anodal stimulation applied over the left DLPFC. Moreover seven of these subjects performed the same task, but with inverse polarity (cathodal stimulation of the left DLPFC) and anodal stimulation of the primary motor cortex (M1). Our results indicate that only anodal stimulation of the left prefrontal cortex, but not cathodal stimulation of left DLPFC or anodal stimulation of M1, increases the accuracy of the task performance when compared to sham stimulation of the same area. This accuracy enhancement during active stimulation cannot be accounted for by slowed responses, as response times were not changed by stimulation. Our results indicate that left prefrontal anodal stimulation leads to an enhancement of working memory performance. Furthermore, this effect depends on the stimulation polarity and is specific to the site of stimulation. This result may be helpful to develop future interventions aiming at clinical benefits.

1,111 citations

Journal ArticleDOI
Vishvanath Nene1, Jennifer R. Wortman1, Daniel Lawson, Brian J. Haas1, Chinnappa D. Kodira2, Zhijian Jake Tu3, Brendan J. Loftus, Zhiyong Xi4, Karyn Megy, Manfred Grabherr2, Quinghu Ren1, Evgeny M. Zdobnov, Neil F. Lobo5, Kathryn S. Campbell6, Susan E. Brown7, Maria de Fatima Bonaldo8, Jingsong Zhu9, Steven P. Sinkins10, David G. Hogenkamp11, Paolo Amedeo1, Peter Arensburger9, Peter W. Atkinson9, Shelby L. Bidwell1, Jim Biedler3, Ewan Birney, Robert V. Bruggner5, Javier Costas, Monique R. Coy3, Jonathan Crabtree1, Matt Crawford2, Becky deBruyn5, David DeCaprio2, Karin Eiglmeier12, Eric Eisenstadt1, Hamza El-Dorry13, William M. Gelbart6, Suely Lopes Gomes13, Martin Hammond, Linda Hannick1, James R. Hogan5, Michael H. Holmes1, David M. Jaffe2, J. Spencer Johnston, Ryan C. Kennedy5, Hean Koo1, Saul A. Kravitz, Evgenia V. Kriventseva14, David Kulp15, Kurt LaButti2, Eduardo Lee1, Song Li3, Diane D. Lovin5, Chunhong Mao3, Evan Mauceli2, Carlos Frederico Martins Menck13, Jason R. Miller1, Philip Montgomery2, Akio Mori5, Ana L. T. O. Nascimento16, Horacio Naveira17, Chad Nusbaum2, Sinéad B. O'Leary2, Joshua Orvis1, Mihaela Pertea, Hadi Quesneville, Kyanne R. Reidenbach11, Yu-Hui Rogers, Charles Roth12, Jennifer R. Schneider5, Michael C. Schatz, Martin Shumway1, Mario Stanke, Eric O. Stinson5, Jose M. C. Tubio, Janice P. Vanzee11, Sergio Verjovski-Almeida13, Doreen Werner18, Owen White1, Stefan Wyder14, Qiandong Zeng2, Qi Zhao1, Yongmei Zhao1, Catherine A. Hill11, Alexander S. Raikhel9, Marcelo B. Soares8, Dennis L. Knudson7, Norman H. Lee, James E. Galagan2, Steven L. Salzberg, Ian T. Paulsen1, George Dimopoulos4, Frank H. Collins5, Bruce W. Birren2, Claire M. Fraser-Liggett, David W. Severson5 
22 Jun 2007-Science
TL;DR: A draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at approximately 1376 million base pairs is about 5 times the size of the genomes of the malaria vector Anopheles gambiae was presented in this paper.
Abstract: We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at approximately 1376 million base pairs is about 5 times the size of the genome of the malaria vector Anopheles gambiae. Nearly 50% of the Ae. aegypti genome consists of transposable elements. These contribute to a factor of approximately 4 to 6 increase in average gene length and in sizes of intergenic regions relative to An. gambiae and Drosophila melanogaster. Nonetheless, chromosomal synteny is generally maintained among all three insects, although conservation of orthologous gene order is higher (by a factor of approximately 2) between the mosquito species than between either of them and the fruit fly. An increase in genes encoding odorant binding, cytochrome P450, and cuticle domains relative to An. gambiae suggests that members of these protein families underpin some of the biological differences between the two mosquito species.

1,107 citations


Authors

Showing all 138091 results

NameH-indexPapersCitations
George M. Whitesides2401739269833
Peter Libby211932182724
Robert C. Nichol187851162994
Paul M. Thompson1832271146736
Terrie E. Moffitt182594150609
Douglas R. Green182661145944
Richard B. Lipton1762110140776
Robin M. Murray1711539116362
George P. Chrousos1691612120752
David A. Bennett1671142109844
Barry M. Popkin15775190453
David H. Adams1551613117783
Joao Seixas1531538115070
Matthias Egger152901184176
Ichiro Kawachi149121690282
Network Information
Related Institutions (5)
Federal University of Rio de Janeiro
89.1K papers, 1.5M citations

98% related

State University of Campinas
104.6K papers, 1.8M citations

97% related

Universidade Federal do Rio Grande do Sul
89.4K papers, 1.4M citations

97% related

Universidade Federal de Minas Gerais
75.6K papers, 1.2M citations

96% related

Sao Paulo State University
100.4K papers, 1.3M citations

96% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
2023331
20222,547
202118,134
202017,960
201916,297