Letteratura scientifica selezionata sul tema "Beta-Amyloid peptides"
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Articoli di riviste sul tema "Beta-Amyloid peptides"
Chiorcea-Paquim, Ana-Maria, Teodor Adrian Enache e Ana Maria Oliveira-Brett. "Electrochemistry of Alzheimer Disease Amyloid Beta Peptides". Current Medicinal Chemistry 25, n. 33 (24 ottobre 2018): 4066–83. http://dx.doi.org/10.2174/0929867325666180214112536.
Testo completoUéda, K., H. Fukushima, E. Masliah, Y. Xia, A. Iwai, M. Yoshimoto, D. A. Otero, J. Kondo, Y. Ihara e T. Saitoh. "Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease". Proceedings of the National Academy of Sciences 90, n. 23 (1 dicembre 1993): 11282–86. http://dx.doi.org/10.1073/pnas.90.23.11282.
Testo completoŞtefănescu, Raluca, Gabriela Dumitriṭa Stanciu, Andrei Luca, Ioana Cezara Caba, Bogdan Ionel Tamba e Cosmin Teodor Mihai. "Contributions of Mass Spectrometry to the Identification of Low Molecular Weight Molecules Able to Reduce the Toxicity of Amyloid-β Peptide to Cell Cultures and Transgenic Mouse Models of Alzheimer’s Disease". Molecules 24, n. 6 (24 marzo 2019): 1167. http://dx.doi.org/10.3390/molecules24061167.
Testo completoJiang, H., D. Burdick, C. G. Glabe, C. W. Cotman e A. J. Tenner. "beta-Amyloid activates complement by binding to a specific region of the collagen-like domain of the C1q A chain." Journal of Immunology 152, n. 10 (15 maggio 1994): 5050–59. http://dx.doi.org/10.4049/jimmunol.152.10.5050.
Testo completoBuneeva, O. A., O. V. Gnedenko, M. V. Medvedeva, A. S. Ivanov e A. E. Medvedev. "The effect of neuroprotector isatin on binding of some model proteins with beta-amyloid peptide: a biosensor study". Biomeditsinskaya Khimiya 62, n. 6 (2016): 720–24. http://dx.doi.org/10.18097/pbmc20166206720.
Testo completoFesta, Giulia, Francesco Mallamace, Giulia Maria Sancesario, Carmelo Corsaro, Domenico Mallamace, Enza Fazio, Laura Arcidiacono et al. "Aggregation States of Aβ1–40, Aβ1–42 and Aβp3–42 Amyloid Beta Peptides: A SANS Study". International Journal of Molecular Sciences 20, n. 17 (24 agosto 2019): 4126. http://dx.doi.org/10.3390/ijms20174126.
Testo completoMocanu, Cosmin Stefan, Marius Niculaua, Gheorghita Zbancioc, Violeta Mangalagiu e Gabi Drochioiu. "Novel Design of Neuropeptide-Based Drugs with β-Sheet Breaking Potential in Amyloid-Beta Cascade: Molecular and Structural Deciphers". International Journal of Molecular Sciences 23, n. 5 (5 marzo 2022): 2857. http://dx.doi.org/10.3390/ijms23052857.
Testo completoLee, Joo-Hee, Na-Hyun Ahn, Su-Bin Choi, Youngeun Kwon e Seung-Hoon Yang. "Natural Products Targeting Amyloid Beta in Alzheimer’s Disease". International Journal of Molecular Sciences 22, n. 5 (26 febbraio 2021): 2341. http://dx.doi.org/10.3390/ijms22052341.
Testo completoMiura, Yoshiko, Kiyofumi Yamamoto, Kikuko Yasuda, Yoshihiro Nishida e Kazukiyo Kobayashi. "Inhibition of Alzheimer Amyloid Aggregation with Sulfate Glycopolymers". Advances in Science and Technology 57 (settembre 2008): 166–69. http://dx.doi.org/10.4028/www.scientific.net/ast.57.166.
Testo completoUsui, Kenji, Shin-ichiro Yokota, Kazuya Iwata e Yoshio Hamada. "Novel Purification Process for Amyloid Beta Peptide(1-40)". Processes 8, n. 4 (15 aprile 2020): 464. http://dx.doi.org/10.3390/pr8040464.
Testo completoTesi sul tema "Beta-Amyloid peptides"
Kadlčík, Vojtěch. "Oxidation of beta-amyloid and model peptides". Paris 11, 2006. http://www.theses.fr/2006PA112008.
Testo completoThe goal of my thesis work was to characterize oxidation products of beta-amyloid peptide (Abeta), which is implied in the development of Alzheimer's disease. To study the effect of peptide structure on the redox processes, oxidation properties of Abeta(1-40) were compared to the peptide with reverse sequence, Abeta(40-1). Azide and hydroxyl radicals used for oxidation were produced by gamma radiolysis. Final products were characterized by a variety of analytical techniques (HPLC, GC, MALDI-TOF MS, fluorescence and raman spectrometry). To establish the role of peptide environment on its redox properties, oxidation was carried out in three different systems: homogeneous aqueous solution, micellar system (SDS) and in the presence of phospholipids vesicles (POPC). In homogeneous aqueous solution, oxidation products are different for both peptides. The main oxidation targets are Met35 for Abeta(1-40) and Tyr10 for Abeta(40-1). The presence of micelles and phospholipid vesicles has an important impact on the oxidation pathways. These changes could be related to changes in peptide conformations studied by circular dichroism. We have also shown that Abeta degradation products may catalytically induce alternation of phospholipids. This process is initiated by reaction of hydrogen radicals with the peptide. Our results are interesting in the context of the development of Alzheimer's disease as they may bring an insight into the role of Abeta(1-40) interaction with phospholipids membrane for the redox properties of the peptide
Tanase, Maria Elena. "Nanomaterials self-assembly driven by beta-amyloid peptides". ScholarWorks@UNO, 2005. http://louisdl.louislibraries.org/u?/NOD,223.
Testo completoTitle from electronic submission form. "A thesis ... in partial fulfillment of the requirements for the degree of Master of Science in the Department of Chemistry"--Thesis t.p. Vita. Includes bibliographical references.
Chen, Zhongjing. "NMR structural characterization of beta-amyloid peptides and their inhibitors". [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973392266.
Testo completoKittner, Madeleine. "Folding and aggregation of amyloid peptides". Phd thesis, Universität Potsdam, 2011. http://opus.kobv.de/ubp/volltexte/2011/5357/.
Testo completoDie Aggregation des Amyloid β (Aβ) Peptids zu Amyloidfibrillen wird mit dem Ausbruch der Alzheimer Krankheit in Verbindung gebracht. Die toxische Wirkung auf Zellen wird vor allem den zeitigen Intermediaten in Form von löslichen Oligomeren zugeschrieben. Aufgrund deren ungeordneter und flüchtiger Natur kann die molekulare Struktur solcher zeitigen Oligomere oft experimentell nicht aufgelöst werden. In der vorliegenden Arbeit wurden aufwendige atomistische Replica-Exchange-Molekulardynamik-Simulationen durchgeführt, um die molekulare Struktur von Monomeren und Oligomeren der Fragmente Aβ(25-35) und Aβ(10-35)-NH2 in Wasser zu untersuchen. Die Faltung und Aggregation von Aβ(25-35) wurde bei neutralem pH und 293 K untersucht. Monomere dieses Fragments bilden hauptsächlich β-Haarnadelkonformationen im Gleichgewicht mit Knäulstrukturen. Innerhalb der β-Haarnadelkonformationen bilden die Residuen G29 und A30 einen β-turn, während N27–K28 and I31–I32 ein β-Faltblatt bilden. Diese β-Haarnadelkonformationen bildeten den Ausgangspunkt zur Modellierung spontaner Aggregation. Wie zu erwarten, bilden sich eine Vielzahl verschiedener, gering besetzter Dimer- und Trimerkonformationen. Mit Hilfe einer gröberen Einteilung können diese in ungeordnete und fibrillähnliche Oligomere unterteilt werden. Ungeordnete Oligomere bilden kompakte Strukturen, die nur durch wenige intermolekulare Wasserstoffbrückenbindungen (HBB) stabilisiert sind. Typisch für fibrillähnliche Oligomere ist hingegen die Ausbildung großer intermolekularer β-Faltblätter. In vielen dieser Oligomere finden wir antiparallele, in- oder out-of-register β-Faltblätter gebildet durch vollständig ausgestreckte Peptide. Ein kleiner Teil der fibrillähnlichen Trimere bildet parallele, V-förmige β-Faltblätter. Die Ausdehnungen ausgestreckter und V-förmiger Oligomere entspricht in etwa den Durchmessern von zwei verschiedenen, experimentell gefundenen Fibrillmorphologien für Aβ(25-35). Die Umwandlung von ungeordneten zu fibrillähnlichen Aβ(25-35) Dimeren ist energetisch begünstigt, läuft aber nicht freiwillig ab. Fibrillähnliche Dimere haben eine geringere Energie aufgrund günstiger Peptidwechselwirkungen (HBB, Salzbrücken), welche durch den Verlust an Entropie kompensiert wird. Etwa 25 % entsprechen dem Verlust an Konfigurationsentropie. Der restliche Anteil wird einem Verlust an Lösungsmittelentropie aufgrund von hydrophoben und elektrostatischen Effekten zugesprochen. Im Gegensatz zur Umwandlung in fibrillähnliche Dimere, ist die Assoziation von Monomeren oder Oligomeren entropisch begünstigt. Beim Vergleich thermodynamischer Eigenschaften der Monomer-, Dimer- und Trimersysteme zeigt sich im Verlauf der Aggregation, wie erwartet, eine Abnahme der Konfigurationsentropie. Zusätzlich nimmt die dem Lösungsmittel zugängliche Oberfläche (SASA), insbesondere die hydrophobe SASA, ab. In Verbindung damit beobachten wir eine Abnahme der freien Solvatisierungsenergie, welche den Verlust an Konfigurationsentropie kompensiert. Mit anderen Worten, der hydrophobe Effekt in Kombination mit elektrostatischen Wechselwirkungen führt zu einem Ansteigen der Lösungsmittelentropie und begünstigt damit die Aggegation. Die spontane Faltung des Aβ(10-35)-NH2 Monomers wurde für zwei verschiedene Proteinkraftfelder, GROMOS96 43a1 und OPLS/AA, untersucht und mit primären NMR-Daten aus der Literatur, gemessen bei pH 5.6 und 283 K, verglichen. Beide Kraftfelder generieren unterschiedliche Hauptkonformationen. Der Vergleich zwischen experimentellen und berechneten Kern-Overhauser-Effekt (NOE) Abständen ist nicht ausreichend, um zwischen beiden Kraftfeldern zu unterscheiden. Der Vergleich mit Kopplungskonstanten aus Experiment und Simulation zeigt, dass beide Simulationen einem pH-Wert geringer als 5.6 ensprechen. Basierend auf den bisherigen Ergebnissen können wir nicht entscheiden, welches Kraftfeld eine bessere Beschreibung für dieses System liefert. Die Dimerisierung von Aβ(10-35)-NH2 wurde bei neutralem pH und 300 K untersucht. Wir finden eine Vielzahl verschiedener, gering besetzter Dimerstrukturen, welche eher durch Seitenkettenkontakte als durch spezifische HBB stabilisiert sind. Wie bei den Aβ(25-35) Dimeren, ist die Umwandlung zu β-Faltblattreichen, fibrillähnlichen Aβ(10-35) Dimeren energetisch begünstigt, konkurriert aber mit einem Entropieverlust. Die Umwandlung wird in diesem Fall durch elektrostatische Wechselwirkungen zwischen Peptid und Lösungsmittel und innerhalb des Lösungsmittels bestimmt.
Davison, Catherine J. "The interactions of the C-terminus of acetlycholinesterase with amyloid-beta peptides". Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496845.
Testo completoTang, Christian C. "Structure and Activity of Metallo-Peptides". Scholar Commons, 2017. http://scholarcommons.usf.edu/etd/6961.
Testo completoMishra, Pamela Haradhan. "Unbinding of abeta peptides from amyloid fibrils explicit solvent molecular dynamics study /". Fairfax, VA : George Mason University, 2008. http://hdl.handle.net/1920/3419.
Testo completoVita: p. 48. Thesis director: Dmitri Klimov. Submitted in partial fulfillment of the requirements for the degree of Master of Science in Bioinformatics and Computational Biology. Title from PDF t.p. (viewed Mar. 17, 2009). Includes bibliographical references (p. 45-47). Also issued in print.
Mikkonen, Saara. "Electrophoretic focusing in microchannels combined with mass spectrometry : Applications on amyloid beta peptides". Doctoral thesis, KTH, Tillämpad fysikalisk kemi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-193134.
Testo completoQC 20160930
Zhang, Qishan, e 张绮珊. "Investigating biological mechanisms for the induction of autophagy in neurons stressed by beta-amyloid peptides". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hdl.handle.net/10722/193067.
Testo completopublished_or_final_version
Anatomy
Doctoral
Doctor of Philosophy
Bautista, Mahealani Roberts. "Identification and design of small molecules that associate with aggregated Alzheimer's-related beta-amyloid peptides". Diss., [La Jolla, Calif.] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p3344755.
Testo completoTitle from first page of PDF file (viewed Apr. 3, 2009). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 178-202).
Libri sul tema "Beta-Amyloid peptides"
Indu, Kheterpal, e Wetzel Ronald, a cura di. Amyloid, prions, and other protein aggregates Part C. Amsterdam: Elsevier/Academic, 2006.
Cerca il testo completoIndu, Kheterpal, e Wetzel Ronald, a cura di. Amyloid, prions, and other protein aggregates Part B. Amsterdam: Elsevier/Academic, 2006.
Cerca il testo completoC, Dowler Brynn, a cura di. Endocytosis: Structural components, functions, and pathways. Hauppauge, N.Y: Nova Science Publishers, 2010.
Cerca il testo completoTanzi, Rudolph E. Decoding darkness: The search for the genetic causes of Alzheimer's disease. Cambridge, Mass: Perseus Pub., 2000.
Cerca il testo completoA, Nixon Ralph, Banner Carl D. B e New York Academy of Sciences., a cura di. Proteases and protease inhibitors in Alzheimer's disease pathogenesis. New York: NewYork Academy of Sciences, 1992.
Cerca il testo completoB, Banner Carl D., e Nixon Ralph A, a cura di. Proteases and protease inhibitors in Alzheimer's disease pathogenesis. New York, N.Y: New York Academy of Sciences, 1992.
Cerca il testo completoWetzel, Ronald, e Indu Kheterpal. Amyloid, Prions, and Other Protein Aggregates, Part C. Elsevier Science & Technology Books, 2006.
Cerca il testo completo(Editor), Ronald Wetzel, e Indu Kheterpal (Editor), a cura di. Amyloid, Prions, and Other Protein Aggregates, Part C, Volume 413 (Methods in Enzymology). Academic Press, 2006.
Cerca il testo completoAbelson, John N., Ronald Wetzel e Melvin I. Simon. Amyloid, Prions, and Other Protein Aggregates. Elsevier Science & Technology Books, 1999.
Cerca il testo completo(Editor), Ronald Wetzel, e Indu Kheterpal (Editor), a cura di. Amyloid, Prions, and Other Protein Aggregates, Part B, Volume 412 (Methods in Enzymology). Academic Press, 2006.
Cerca il testo completoCapitoli di libri sul tema "Beta-Amyloid peptides"
Durieux, J. P., F. Dick, M. Schwaller, G. Haas, U. Wixmerten, S. Mundwiler e R. Nyfeler. "Synthesis of beta amyloid protein [1-40] scope and limitations of convergent solid phase synthesis". In Peptides, 34–36. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_4.
Testo completoBenseny-Cases, Núria, Oksana Klementieva e Josep Cladera. "In vitroOligomerization and Fibrillogenesis of Amyloid-beta Peptides". In Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease, 53–74. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5416-4_3.
Testo completoTakahashi, Eddie, Anita Howe, Ole Vesterqvist e Zhaosheng Lin. "Quantitation of Amyloid Beta Peptides in CSF by Surface Enhanced MALDI-TOF". In Methods in Molecular Biology, 227–36. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-61779-418-6_16.
Testo completoLahiri, Debomoy K., e Martin R. Farlow. "Tacrine Reduces the Secretion of Soluble Amyloid Beta-Peptides in a Neuroblastoma Cell Line". In Advances in Behavioral Biology, 563–69. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5337-3_80.
Testo completoKondela, Tomáš, Pavol Hrubovčák, Dmitry Soloviov, Dina Badreeva, Tatiana Murugova, Vadim Skoi, Alexander Kuklin, Oleksandr Ivankov e Norbert Kučerka. "Approaches for a Closer Look at Problems of Liquid Membranes with Amyloid-Beta Peptides". In Springer Proceedings in Physics, 265–94. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-80924-9_10.
Testo completoBeffert, Uwe, Nicole Aumont, Doris Dea, Jean Davignon e Judes Poirier. "Apolipoprotein E Uptake is Increased by Beta-Amyloid Peptides and Reduced by Blockade of the LDL Receptor". In Neurodegenerative Diseases, 103–8. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-0209-2_15.
Testo completoOkochi, M., A. Fukumori, Y. Satoh, N. Aidaralieva, H. Tanii, K. Kamino, T. Tanaka, T. Kudo e M. Takeda. "Alzheimer�s γ-Secretase Mechanism Produces Amyloid-β-Protein Like Peptides Simultaneously with Release of Intracellular Signaling Fragments". In Molecular Neurobiology of Alzheimer Disease and Related Disorders, 31–41. Basel: KARGER, 2004. http://dx.doi.org/10.1159/000078524.
Testo completoKumar, Suresh, Edward J. Okello e J. Robin Harris. "Experimental Inhibition of Fibrillogenesis and Neurotoxicity by amyloid-beta (Aβ) and Other Disease-Related Peptides/Proteins by Plant Extracts and Herbal Compounds". In Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease, 295–326. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5416-4_13.
Testo completoAbraham, Carmela R. "Amyloid Beta Peptide and the Amyloid Cascade Hypothesis". In The Handbook of Alzheimer's Disease and Other Dementias, 262–76. Oxford, UK: Wiley-Blackwell, 2011. http://dx.doi.org/10.1002/9781444344110.ch8.
Testo completoKagan, Bruce L., e Jyothi Thundimadathil. "Amyloid Peptide Pores and the Beta Sheet Conformation". In Advances in Experimental Medicine and Biology, 150–67. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6327-7_13.
Testo completoAtti di convegni sul tema "Beta-Amyloid peptides"
Drochioiu, Gabi, Manuela Murariu, Laura Ion e Laura Habasescu. "Iron and aluminum interaction with amyloid-beta peptides associated with Alzheimer’s disease". In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2014 (ICCMSE 2014). AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4897686.
Testo completoIon, Laura, Monica Jureschi, Ancuta Lupaescu, Brindusa-Alina Petre e Gabi Drochioiu. "METAL IONS BINDING TO AMYLOID-BETA AND NEUROPROTECTIVE NAP-LIKE PEPTIDES: MS, FT-IR AND AFM INVESTIGATIONS". In 20th International Multidisciplinary Scientific GeoConference Proceedings SGEM 2020. STEF92 Technology, 2020. http://dx.doi.org/10.5593/sgem2020/6.1/s25.034.
Testo completoKi-Bong Song, Chang-Bum Kim e Yo-Han Choi. "Sensing and quantification of salivary beta-amyloid peptides and protein sequencing for the saliva of normal and AD patients". In 2015 IEEE Sensors. IEEE, 2015. http://dx.doi.org/10.1109/icsens.2015.7370592.
Testo completoMendonça, Pedro Henrique Carvalho Furtado de, Fernanda Rabello Detoni, Letícia Silva Brandão dos Santos, Talita Cardoso Gomes e Ivan Magalhães Viana. "Monoclonal antibodies in the treatment of Alzheimer’s disease: a literature review". In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.597.
Testo completoVolkova, Tatiana Danilovna, Armine Vrezovna Avetisyan, Dmitry Otarovich Koroev e Olga Volpina. "PROTECTIVE RAGE FRAGMENT INHIBITS AMYLOID BETA OLIGOMERIZATION". In NEW TECHNOLOGIES IN MEDICINE, BIOLOGY, PHARMACOLOGY AND ECOLOGY. Institute of information technology, 2021. http://dx.doi.org/10.47501/978-5-6044060-1-4.19.
Testo completoKissoon, Nicola N., Andre´s D. Gutierrez, Anant K. Paravastu e Ongi Englander. "Preparation and Integration of Beta Amyloid Protein Nanofibers With Microfabricated Electrodes". In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-38360.
Testo completoCarneiro, P., C. Delerue-Matos, S. Morais e Maria do Carmo Pereira. "Electrochemical immunosensor for amyloid beta-peptide detection: Preliminary study". In 2013 IEEE 3rd Portuguese Meeting in Bioengineering (ENBENG). IEEE, 2013. http://dx.doi.org/10.1109/enbeng.2013.6518403.
Testo completoAndrade, Stephanie, Joana A. Loureiro, Manuel A. N. Coelho e Maria do Carmo Pereira. "Interaction studies of amyloid beta-peptide with the natural compound resveratrol". In 2015 IEEE 4th Portuguese Meeting on Bioengineering (ENBENG). IEEE, 2015. http://dx.doi.org/10.1109/enbeng.2015.7088833.
Testo completo"The study of localization of beta-amyloid peptide monomers in cells by fluorescence microscopy". In Bioinformatics of Genome Regulation and Structure/Systems Biology (BGRS/SB-2022) :. Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences, 2022. http://dx.doi.org/10.18699/sbb-2022-188.
Testo completoGonçalves, Brenda, Isadora Ribeiro, Thamires Magalhães, Christian Gerbelli, Luciana Pimentel Silva, Helena Joaquim, Leda Talib, Orestes Forlenza e Marcio Balthazar. "NEUROPSYCHOLOGICAL TESTS AS PREDICTORS OF CONVERSION TO ALZHEIMER’S DISEASE IN BETA-AMYLOID POSITIVE INDIVIDUALS". In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda007.
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