Joao A. Paulo mostly deals with Cell biology, Biochemistry, Proteome, Proteomics and Mitochondrion. His biological study spans a wide range of topics, including ATG8, Ubiquitin, Ubiquitin ligase and Downregulation and upregulation. Joao A. Paulo interconnects Tandem mass spectrometry, Mass spectrometry, Saccharomyces cerevisiae, Isobaric labeling and Computational biology in the investigation of issues within Proteome.
His Proteomics research focuses on subjects like Bioinformatics, which are linked to Substrate specificity, Ubiquitin-Like Protein Nedd8 and Proteostasis. The Mitochondrion study combines topics in areas such as Parkin and PINK1. Joao A. Paulo has included themes like Receptor, Function and Protein–protein interaction in his Membrane protein study.
Joao A. Paulo focuses on Cell biology, Proteomics, Proteome, Biochemistry and Computational biology. His Cell biology study integrates concerns from other disciplines, such as Receptor, Cell and Ubiquitin, Ubiquitin ligase. His Ubiquitin research includes elements of PINK1 and Mitophagy.
The concepts of his Proteomics study are interwoven with issues in Sample preparation, Pancreatic juice and Mass spectrometry. His Proteome study incorporates themes from Saccharomyces cerevisiae, Tandem mass tag, Quantitative proteomics, Pancreas and Molecular biology. His studies in Computational biology integrate themes in fields like Human interactome and Function.
Joao A. Paulo spends much of his time researching Cell biology, Proteome, Proteomics, Computational biology and Quantitative proteomics. His Cell biology research integrates issues from Ubiquitin, Ubiquitin ligase, Gene expression, Messenger RNA and Ribosome. His Proteome study combines topics in areas such as Phenotype, Isobaric labeling, Tandem mass tag, In vivo and Islet.
Proteomics is a subfield of Biochemistry that he investigates. His work in Computational biology addresses subjects such as HEK 293 cells, which are connected to disciplines such as Human interactome, Interactome and Function. His studies deal with areas such as Data mining, Saccharomyces cerevisiae and Metabolic pathway as well as Quantitative proteomics.
Joao A. Paulo mainly focuses on Cell biology, Proteome, Gene expression, Chromatin and Data mining. He has researched Cell biology in several fields, including Translation, Ribosome and Cell growth. His Proteome study combines topics from a wide range of disciplines, such as Schizosaccharomyces pombe, Phenotype, Proteomics, Computational biology and In vivo.
His work deals with themes such as HEK 293 cells, Human interactome, Interactome and Islet, which intersect with Phenotype. Joao A. Paulo conducts interdisciplinary study in the fields of Proteomics and Redox through his research. Joao A. Paulo combines subjects such as Protein aggregation, Saccharomyces cerevisiae, Yeast, Period and Metabolic pathway with his study of Computational biology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The BioPlex Network: A Systematic Exploration of the Human Interactome
Edward L. Huttlin;Lily Ting;Raphael J. Bruckner;Fana Gebreab.
Cell (2015)
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin;Raphael J. Bruckner;Joao A. Paulo;Joe R. Cannon.
Nature (2017)
The PINK1-PARKIN Mitochondrial Ubiquitylation Pathway Drives a Program of OPTN/NDP52 Recruitment and TBK1 Activation to Promote Mitophagy.
Jin-Mi Heo;Alban Ordureau;Joao A. Paulo;Jesse Rinehart.
Molecular Cell (2015)
Detection and Quantitation of Circulating Human Irisin by Tandem Mass Spectrometry.
Mark P. Jedrychowski;Christiane D. Wrann;Joao A. Paulo;Kaitlyn K. Gerber.
Cell Metabolism (2015)
Defining roles of PARKIN and ubiquitin phosphorylation by PINK1 in mitochondrial quality control using a ubiquitin replacement strategy
Alban Ordureau;Jin-Mi Heo;David M. Duda;Joao A. Paulo.
Proceedings of the National Academy of Sciences of the United States of America (2015)
Autophagy promotes immune evasion of pancreatic cancer by degrading MHC-I
Keisuke Yamamoto;Anthony Venida;Julian Yano;Douglas E. Biancur.
Nature (2020)
Multidimensional Tracking of GPCR Signaling via Peroxidase-Catalyzed Proximity Labeling
Jaeho Paek;Marian Kalocsay;Dean P. Staus;Dean P. Staus;Laura Wingler;Laura Wingler.
Cell (2017)
Compensatory metabolic networks in pancreatic cancers upon perturbation of glutamine metabolism
Douglas E. Biancur;Joao A. Paulo;Beata Małachowska;Beata Małachowska;Maria Quiles Del Rey.
Nature Communications (2017)
A Triple Knockout (TKO) Proteomics Standard for Diagnosing Ion Interference in Isobaric Labeling Experiments.
Joao A. Paulo;Jeremy D. O’Connell;Steven P. Gygi.
Journal of the American Society for Mass Spectrometry (2016)
Excessive Cell Growth Causes Cytoplasm Dilution And Contributes to Senescence.
Gabriel E. Neurohr;Rachel L. Terry;Rachel L. Terry;Jette Lengefeld;Megan Bonney;Megan Bonney.
Cell (2019)
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