Academic literature on the topic 'Proteina quinasa'

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Journal articles on the topic "Proteina quinasa"

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Pérez, Katherine, Carlos Elías, and Víctor Delgado. "High-protein snack: an extruded from quinoa (Chenopodium quinoa Willd.), tarwi (Lupinus mutabilis Sweet), and sweet potato (Ipomoea batatas L.)." Scientia Agropecuaria 8, no. 4 (2017): 377–88. http://dx.doi.org/10.17268/sci.agropecu.2017.04.09.

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Boonjakuakul, Jenni K., Helen L. Gerns, Yu-Ting Chen, et al. "Proteomic and Immunoblot Analyses of Bartonella quintana Total Membrane Proteins Identify Antigens Recognized by Sera from Infected Patients." Infection and Immunity 75, no. 5 (2007): 2548–61. http://dx.doi.org/10.1128/iai.01974-06.

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ABSTRACT Bartonella quintana is a fastidious, gram-negative, rod-shaped bacterium that causes prolonged bacteremia in immunocompetent humans and severe infections in immunocompromised individuals. We sought to define the outer membrane subproteome of B. quintana in order to obtain insight into the biology and pathogenesis of this emerging pathogen and to identify the predominant B. quintana antigens targeted by the human immune system during infection. We isolated the total membrane proteins of B. quintana and identified 60 proteins by two-dimensional sodium dodecyl sulfate-polyacrylamide gel
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Schulte, Berit, Dirk Linke, Sandra Klumpp, et al. "Bartonella quintana Variably Expressed Outer Membrane Proteins Mediate Vascular Endothelial Growth Factor Secretion but Not Host Cell Adherence." Infection and Immunity 74, no. 9 (2006): 5003–13. http://dx.doi.org/10.1128/iai.00663-06.

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ABSTRACT Bartonella quintana causes trench fever, endocarditis, and the vasculoproliferative disorders bacillary angiomatosis and peliosis hepatis in humans. Little is known about the interaction of this pathogen with host cells. We attempted to elucidate the interaction of B. quintana with human macrophages (THP-1) and epithelial cells (HeLa 229). Remarkably, only B. quintana strain JK-31 induced secretion of vascular endothelial growth factor (VEGF) from THP-1 and HeLa 229 cells upon infection similar to the secretion induced by B. henselae Marseille, whereas other strains (B. quintana 2-D70
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Kalač, P., and J. Moudrý. "Composition and nutritinal value of quinoa (Chenopodium quinoa) – a review." Czech Journal of Food Sciences 18, No. 3 (2000): 115–19. http://dx.doi.org/10.17221/8322-cjfs.

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Literature data on proteins, lipids, starch, minerals, vitamins and saponins contents and composition and their distribution within whole quinoa seeds, hulls, bran and flour are reviewed. An information on effects of quinoa processing on nutritional value and food applications is also given.
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Monteith, William B., Rachel D. Cohen, Austin E. Smith, Emilio Guzman-Cisneros, and Gary J. Pielak. "Quinary structure modulates protein stability in cells." Proceedings of the National Academy of Sciences 112, no. 6 (2015): 1739–42. http://dx.doi.org/10.1073/pnas.1417415112.

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Protein quinary interactions organize the cellular interior and its metabolism. Although the interactions stabilizing secondary, tertiary, and quaternary protein structure are well defined, details about the protein–matrix contacts that comprise quinary structure remain elusive. This gap exists because proteins function in the crowded cellular environment, but are traditionally studied in simple buffered solutions. We use NMR-detected H/D exchange to quantify quinary interactions between the B1 domain of protein G and the cytosol of Escherichia coli. We demonstrate that a surface mutation in t
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Mu, Xin, Seongil Choi, Lisa Lang, et al. "Physicochemical code for quinary protein interactions inEscherichia coli." Proceedings of the National Academy of Sciences 114, no. 23 (2017): E4556—E4563. http://dx.doi.org/10.1073/pnas.1621227114.

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How proteins sense and navigate the cellular interior to find their functional partners remains poorly understood. An intriguing aspect of this search is that it relies on diffusive encounters with the crowded cellular background, made up of protein surfaces that are largely nonconserved. The question is then if/how this protein search is amenable to selection and biological control. To shed light on this issue, we examined the motions of three evolutionary divergent proteins in theEscherichia colicytoplasm by in-cell NMR. The results show that the diffusive in-cell motions, after all, follow
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MacKichan, Joanna K., Helen L. Gerns, Yu-Ting Chen, Peng Zhang, and Jane E. Koehler. "A SacB Mutagenesis Strategy Reveals that the Bartonella quintana Variably Expressed Outer Membrane Proteins Are Required for Bloodstream Infection of the Host." Infection and Immunity 76, no. 2 (2007): 788–95. http://dx.doi.org/10.1128/iai.01174-07.

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ABSTRACT Bartonella bacteria adhere to erythrocytes and persistently infect the mammalian bloodstream. We previously identified four highly conserved Bartonella quintana adhesin genes that undergo phase variation during prolonged bloodstream infection. The variably expressed outer membrane proteins (Vomp) encoded by these genes are members of the trimeric autotransporter adhesin family. Each B. quintana Vomp appears to contribute a different adhesion phenotype, likely mediated by the major variable region at the adhesive tip of each Vomp. Although studies document that the Vomp adhesins confer
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Lee, Dahae, Jin Su Lee, Jurdas Sezirahiga, Hak Cheol Kwon, Dae Sik Jang, and Ki Sung Kang. "Bioactive Phytochemicals Isolated from Akebia quinata Enhances Glucose-Stimulated Insulin Secretion by Inducing PDX-1." Plants 9, no. 9 (2020): 1087. http://dx.doi.org/10.3390/plants9091087.

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Chocolate vine (Akebia quinata) is consumed as a fruit and is also used in traditional medicine. In order to identify the bioactive components of A. quinata, a phytosterol glucoside stigmasterol-3-O-β-d-glucoside (1), three triterpenoids maslinic acid (2), scutellaric acid (3), and hederagenin (4), and three triterpenoidal saponins akebia saponin PA (5), hederacoside C (6), and hederacolchiside F (7) were isolated from a 70% EtOH extract of the fruits of A. quinata (AKQU). The chemical structures of isolates 1–7 were determined by analyzing the 1D and 2D nuclear magnetic resonance (NMR) spectr
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Burz, David, Leonard Breindel, and Alexander Shekhtman. "The Inescapable Effects of Ribosomes on In-Cell NMR Spectroscopy and the Implications for Regulation of Biological Activity." International Journal of Molecular Sciences 20, no. 6 (2019): 1297. http://dx.doi.org/10.3390/ijms20061297.

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The effects of RNA on in-cell NMR spectroscopy and ribosomes on the kinetic activity of several metabolic enzymes are reviewed. Quinary interactions between labelled target proteins and RNA broaden in-cell NMR spectra yielding apparent megadalton molecular weights in-cell. The in-cell spectra can be resolved by using cross relaxation-induced polarization transfer (CRINEPT), heteronuclear multiple quantum coherence (HMQC), transverse relaxation-optimized, NMR spectroscopy (TROSY). The effect is reproduced in vitro by using reconstituted total cellular RNA and purified ribosome preparations. Fur
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Carroll, James A., Sherry A. Coleman, Laura S. Smitherman, and Michael F. Minnick. "Hemin-Binding Surface Protein fromBartonella quintana." Infection and Immunity 68, no. 12 (2000): 6750–57. http://dx.doi.org/10.1128/iai.68.12.6750-6757.2000.

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ABSTRACT Bartonella quintana, the agent of trench fever and a cause of endocarditis and bacillary angiomatosis in humans, has the highest reported in vitro hemin requirement for any bacterium. We determined that eight membrane-associated proteins from B. quintana bind hemin and that a ∼25-kDa protein (HbpA) was the dominant hemin-binding protein. Like many outer membrane proteins, HbpA partitions to the detergent phase of a Triton X-114 extract of the cell and is heat modifiable, displaying an apparent molecular mass shift from approximately 25 to 30 kDa when solubilized at 100°C. Immunoblots
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Dissertations / Theses on the topic "Proteina quinasa"

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Martínez, Bono Bárbara. "La ruta de la proteina Quinasa C en Saccharomyces cerevisiae. Conexiones con el control del ciclo celular." Doctoral thesis, Universitat de València, 2005. http://hdl.handle.net/10803/9531.

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La ruta de la Proteína quinasa C en Saccharomyces cerevisiae desempeña funciones esenciales en el control de la integridad celular y además se ha sugerido que participa en la coordinación entre el crecimiento y la división celular. En este trabajo se ha estudiado el mecanismo molecular de regulación de la expresión génica mediada por la ruta PKC, tomando como modelo en gen FKS1 que codifica para la subunidad catalítica de la glucano sintasa. Se ha caracterizado que la secuencia mínima responsable de la regulación mediada por la ruta PKC en el gen FKS1 corresponde con una secuencia de unión del
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González, García Carmen M. "El sistema par-1-proteina quinasa C en el procés d'eliminació sinàptica durant el desenvolupament postnatal de la unió neuromuscular." Doctoral thesis, Universitat Rovira i Virgili, 2004. http://hdl.handle.net/10803/8722.

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Aquesta tesi doctoral ha estat realitzada a la Unitat d'Histologia i Neurobiologia de la Facultat de Medicina i Ciències de la Salut i és fruit de 4 anys de treball dins el camp de la plasticitat sinàptica, concretament en la pèrdua de connexions nervioses.<br/><br/> La pèrdua de connexions nervioses és un procés que es dóna en diferents situacions de la vida dels organismes, com és per exemple l'envelliment o durant el decurs de determinades malalties neurodegeneratives. També, però, es dóna de manera fisiològica durant el desenvolupament postnatal. En aquest estudi s'intenta esclarir quin é
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López, Nicolás Rubén. "Estudio de la función de la familia de Proteínas Quinasas C en el cáncer de mama." Doctoral thesis, Universidad de Murcia, 2011. http://hdl.handle.net/10803/28234.

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En esta Tesis Doctoral se ha estudiado el efecto de una serie de ácidos grasos como el araquidónico, docosahexaenoico, eicosapentaenoico y oleico, así como un conjunto de derivados de DAG-lactonas en la activación de diferentes isoenzimas de PKC. El sistema modelo de estudio utilizado han sido diferentes líneas celulares de cáncer de mama (BT-474, MCF-7 y MDA-MB-231). Mediante técnicas de biología molecular y celular, microscopía confocal, ARN de interferencia y microarrays de expresión diferencial de genes se ha estudiado la función de la PKCalpha en la capacidad proliferativa, invasiva y de
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Koscky, Paier Carlos Roberto 1983. "Padronização da expressão heterologa e de modelo de ensaio de atividade para a proteina quinase humana S6K." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/314787.

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Orientador: Nilson Ivo Tonin Zanchin<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia<br>Made available in DSpace on 2018-08-14T12:40:52Z (GMT). No. of bitstreams: 1 KosckyPaier_CarlosRoberto_M.pdf: 3760581 bytes, checksum: 99331529324819b59a4360d60efd9b9a (MD5) Previous issue date: 2009<br>Resumo: A quinase de 70 kDa da proteína ribossomal S6, isoforma 1 (S6K1), é uma fosfoproteína implicada na regulação de genes relacionados ao controle da tradução em mamíferos e possui uma forma nuclear (a1) e uma citoplasmática (a2). A fosforilação do seu principal alv
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Di, Vona Chiara 1981. "Nuclear DYRK1A :new insights into its role within the nucleus." Doctoral thesis, Universitat Pompeu Fabra, 2013. http://hdl.handle.net/10803/283483.

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The view on how protein kinases regulate gene expression have recently expanded to include not only transcription factors but also histones, chromatin remodelers or components of the basal transcription machinery, which are directly modified on genomic loci. For the shuttling kinase DYRK1A (dual-specificity tyrosine-regulated kinase), most of its nuclear-associated functions can be explained by DYRK1A cytosolic activities, questioning a role for DYRK1A within the nuclear compartment. In the present study, through an unbiased proteomic approach the first “DYRK1A nuclear interactome” have been g
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Veloso, Roberto Vilela. "O efeito da farinha de soja na recuperação do estado nutricional e na secreção de insulina de ratos submetidos a restrição protéica durante a vida intra-uterina e na lactação." [s.n.], 2007. http://repositorio.unicamp.br/jspui/handle/REPOSIP/314750.

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Orientadores: Everardo Magalhães Carneiro, Marcia Queiroz Latorraca<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia<br>Made available in DSpace on 2018-08-10T10:35:57Z (GMT). No. of bitstreams: 1 Veloso_RobertoVilela_D.pdf: 1133010 bytes, checksum: ae2bb8d027240ebc20854087fa364a1b (MD5) Previous issue date: 2007<br>Resumo: A restrição protéica materna reduz o crescimento e promove alterações permanentes na estrutura e função de órgãos da prole, contribuindo para o desenvolvimento de doenças cardiovasculares, obesidade e diabetes. O consumo de alimentos à base d
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Diéguez, Martínez Nora. "MAP quinasa ERK5: una nueva diana antitumoral en cáncer endometrioide y neuroblastoma." Doctoral thesis, Universitat Autònoma de Barcelona, 2021. http://hdl.handle.net/10803/673853.

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La via de senyalització de la MAP quinasa ERK5 s'activa en resposta a factors de creixement i diferents formes d'estrès. Durant els últims anys, diversos treballs han mostrat que ERK5 juga un paper important en la proliferació i supervivència en diferents paradigmes del càncer. No obstant això, aquestes evidències experimentals s'han aconseguit utilitzant inhibidors d'ERK5 que posteriorment han demostrat no ser específics. Entre altres, aquests inhibidors d'ERK5 també afecten l'activitat del regulador transcripcional BRD4 (una coneguda diana antitumoral), per la qual cosa recentment s'ha posat
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Malnic, Bettina. "Clonagem e caracterização da proteína 80K-H, possível substrato de proteína quinase C." Universidade de São Paulo, 1991. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-03042012-120043/.

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Plaquetas apresentam um papel importante no desenvolvimento de metastases tumorais. Os eventos que levam à ativação plaquetária, como agragação e secreção de proteínas, podem significar etapas importantes neste papel. O agonista plaquetário trombospondina está envolvido no processo de agragação plaquetária. Com o intuito de clonar o receptor de trombospondina GpIIIb, produziu-se um soro policlonal contra uma banda eluída de SDS PAGE de extrato proteico de plaquetas, que apresentava peso molecular igual ao de GpIIIb (denominada banda 80kD). Uma biblioteca de cDNA de endotélio de cordão umbilica
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Nogueira, Maria Luiza Caldas 1984. "Expressão e caracterização de proteínas envolvidas na via da quinase mTOR e na divisão celular bacteriana." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313896.

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Orientador: Ana Carolina de Mattos Zeri<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia<br>Made available in DSpace on 2018-08-21T00:57:37Z (GMT). No. of bitstreams: 1 Nogueira_MariaLuizaCaldas_M.pdf: 8261820 bytes, checksum: 7c9ed2193fd77623b3a8beea794eb743 (MD5) Previous issue date: 2012<br>Resumo: A mTOR é uma via de sinalização muito conservada que controla o crescimento celular em resposta à presença de nutrientes e fatores de crescimento. A desregulação dessa via em humanos está relacionada a doenças como câncer e diabetes. A quinase TOR é ativada n
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Besalduch, Canes Núria Montserrat. "Serina/treonina quinases a la sinapsi neuromuscular: especialització de les isoformes de la proteïna quinasa c." Doctoral thesis, Universitat Rovira i Virgili, 2009. http://hdl.handle.net/10803/8741.

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Serina/Treonina quinases a la sinapsi neuromuscular: Especialització de les isoformes de la proteïna quinasa C<br/>Les serina/treonina quinases són una família d'enzims abundants en molts tipus cel·lulars i essencials per a la transducció de senyals intracel·lulars. A la sinapsi neuromuscular, les serina/treonina quinases PKC i PKA estan implicades en mecanismes de modulació de la neurotransmissió tant en l'adult com en el desenvolupament postnatal contribuint als mecanismes de consolidació de connexions sinàptiques i també d'eliminació d'altres per a configurar els circuits neurals madurs. Co
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Books on the topic "Proteina quinasa"

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Philippe, Barret, Charton Delphine, and Guerrero Pilar, eds. Quinoa: El tesoro de los Incas : una de las mejores proteínas vegetables del planeta. Editorial Hispano Europea, 2010.

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Jerry, Rafats. Quinoa (Chenopodium quinoa), high fiber, high protein grain, 1970-86: 43 citations. U.S. Dept. of Agriculture, National Agricultural Library, 1986.

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Gómez, Albino Feijóo. Quintas y protesta social en el Siglo 19. Ministerio de Defensa, 1996.

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author, Stepaniak Joanne 1954, ed. Quinoa: High protein, gluten free. Books Alive, 2013.

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Scanlin, Laurie Ann. Production and functionality of quinoa (Chenopodium quinoa) protein concentrate. 2006.

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Gomez, Albino Feijoo. Quintas y protesta social en el siglo XIX. Ministerio de Defensa, 1996.

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The Art of Cooking With Quinoa: A Complete Vegetable Protein. Pm Pub, 1991.

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Grey, Alissa Noel. Power Vegetarian Cooking : Healthy High Protein Recipes with Quinoa, Buckwheat, Beans and Legumes: Health and Fitness Books. Independently Published, 2017.

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Book chapters on the topic "Proteina quinasa"

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Segura-Nieto, Magdalena, Peter R. Shewry, and Octavio Paredes-López. "Globulins of the Pseudocereals: Amaranth, Quinoa, and Buckwheat." In Seed Proteins. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4431-5_19.

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Brinegar, Chris. "The Seed Storage Proteins of Quinoa." In Advances in Experimental Medicine and Biology. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-1792-8_8.

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Can Karaca, Asli. "Proteins from Pseudocereal Grains." In Pseudocereals [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.102504.

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Seeds such as quinoa, amaranth, chia, and teff are considered as potential sources of plant-based proteins for human consumption. Proteins isolated from pseudocereal grains have the potential to serve as nutritious alternatives to animal-based proteins for various food applications. Quinoa, amaranth, and chia proteins are among the most extensively studied pseudocereal proteins for the characterization of structural, physicochemical, and functional properties. This chapter will review the recent studies on composition, structural characteristics, physicochemical and functional properties of proteins isolated from pseudocereal grains, will discuss several modifications applied for improvement of functional properties and some potential end-product applications.
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Olivera, Luis, Ivan Best, Perla Paredes, Neyma Perez, Luis Chong, and Alejandro Marzano. "Nutritional Value, Methods for extraction and Bioactive Compounds of Quinoa." In Pseudocereals [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101891.

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Quinoa (Chenopodium quinoa Willd.) is a crop belonging to the Chenopodiaceae family that originated in the high Andean region of South America. Currently, the main producers of quinoa are Bolivia and Peru; this crop groups around 250 species and 3000 varieties. It has a high adaptability, which allows it to be cultivated in cold climates in the high Andean regions, as well as in subtropical conditions, and grows from sea level to more than 4000 meters above sea level. Due to its high nutritional value and nutritional properties, quinoa is considered “one of the grains of the 21st century.” It is high in protein without gluten, polyunsaturated fatty acids, carbohydrates, vitamins, minerals, and fiber, as well as high levels of bioactive compounds such as flavonoids, phenolic acids, bioactive peptides, phytosteroid betalains, phytosterols, and saponins. From quinoa, a protein concentrate of high biological value can be extracted due to its content of the nine essential amino acids, as well as an oil with high antioxidant activity due to its high levels of tocopherols. These by-products have a high economic and commercial value and can be produced on an industrial scale for use in the food, cosmetic, and pharmaceutical industries.
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Scanlin, L., and K. A. Lewis. "Quinoa as a Sustainable Protein Source." In Sustainable Protein Sources. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-802778-3.00014-7.

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Comai, Stefano, Antonella Bertazzo, Carlo V. L. Costa, and Graziella Allegri. "Quinoa: Protein and Nonprotein Tryptophan in Comparison with Other Cereal and Legume Flours and Bread." In Flour and Breads and their Fortification in Health and Disease Prevention. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-12-380886-8.10011-x.

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Conference papers on the topic "Proteina quinasa"

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Pereira, Érica Romão, Amanda Letícia Francelino, Laís Capelasso Lucas Pinheiro, Ilce Mara De Syllos Cólus, and Roberta Losi Guembarovski. "ANÁLISE DA IMUNOMARCAÇÃO DE PROTEÍNAS DA VIA PI3K/AKT/MTOR DE SOBREVIVÊNCIA CELULAR EM AMOSTRAS TUMORAIS DE PRÓSTATA METASTÁTICAS E NÃO METASTÁTICAS." In I Congresso Nacional On-line de Biologia Celular e Estrutural. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1948.

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Introdução: O câncer de próstata (CaP) é o segundo tipo de câncer mais comum em homens e a quinta causa de morte no mundo. A triagem para o rastreamento do CaP consiste no toque digital retal e na quantificação do PSA (antígeno prostático específico). Porém, esses métodos são incapazes de diferenciar tumores indolentes e doenças prostáticas benignas do adenocarcinoma maligno. Portanto, buscam-se maneiras alternativas de fazer um diagnóstico mais preciso e menos invasivo. Objetivos: Dentro deste contexto, este trabalho avaliou a imunomarcação tecidual do Homólogo de Fosfatase e Tensina (PTEN) e
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Moreira Simabuco, Fernando, and Alice Missagia De Mattos Springer. "CARACTERIZAÇÃO DAS PROTEÍNAS DE INTERAÇÃO DO DOMÍNIO DE QUINASE DE S6K1 EM CÉLULAS HUMAMAS." In XXIII Congresso de Iniciação Científica da Unicamp. Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-38261.

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Olivera-Montenegro, Luis, Ivan Best, Alejandra Bugarin, et al. "Techno-Economic Evaluation of the Production of Protein Hydrolysed from Quinoa (Chenopodium quinoa Willd.) Using Supercritical Fluids and Conventional Solvent Extraction." In Foods 2021. MDPI, 2021. http://dx.doi.org/10.3390/foods2021-11002.

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Lacerda, Anna Carolina de Castro, Estéfany Lauriano da Silva, Adonay Felipe Pereira Santos, and Ana Flávia Santos Almeida. "AMPK: PRINCIPAL MEDIDADOR NO EFEITO ANTINEOPLÁSICO DA METFORMINA." In I Congresso Brasileiro de Bioquímica Humana On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/663.

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Introdução: A proteína quinase ativada por AMP (AMPK) coordena uma gama de eventos celulares, como a síntese proteica, o metabolismo de carboidratos, lipídeos e a autofagia. Adicionalmente, ressalta-se que alterações na expressão gênica provocadas pela atuação da AMPK conferem a esta importante papel na tumorigênese. Dessa forma, a ativação da AMPK produzida por medicamentos como a metformina representa um potencial alvo a ser investigado para o tratamento de diversos tipos de câncer. Objetivo: Identificar os mecanismos pelos quais a interação AMPK-metformina promove efeito antineoplásico. Mat
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Zamprogno, Nathália Perini, and Maria Angélica Santos Novaes. "REVISÃO: DOENÇA DE PARKINSON E SUAS ETIOLOGIAS MITOCONDRIAIS." In I Congresso Nacional On-line de Biologia Celular e Estrutural. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1956.

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Introdução: A doença de Parkinson (DP) apresenta etiologia multifatorial, que inclui disfunções genéticas e ambientais. Resulta da perda progressiva de células produtoras de dopamina na substância negra e do acúmulo de proteínas, principalmente a alfa-sinucleína (SNCA), nos corpos de Lewy. Esses aspectos levam a sintomatologia de bradicinesia, tremor de repouso e rigidez. Neurônios dopaminérgicos necessitam de demanda energética, assim, distúrbios mitocondriais, como bioenergéticos, mutações no DNA nuclear ou mitocondrial, alterações no transporte, movimento e morfologia dessa organela, estão
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Jesus, Anderson Avelino de, Samuel Santana Moura, Rebeca Santos Da Silva, Raqueline Pastor De Santana E. Santana, and Irlandia Oliveira Almeida. "LEUCEMIA MIELÓIDE CRÔNICA: O CROMOSSOMO PHILADELPHIA E O GENE BCR-ABL." In I Congresso Nacional Multidisciplinar de Oncologia On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1529.

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Introdução: A Leucemia Mieloide Crônica (LMC) foi a primeira neoplasia humana relacionada a uma alteração cromossômica. Primeiros casos foram descritos em 1845. Porém, somente em 1960 quando Peter C. Nowell, estudando células de medula óssea de pacientes com LMC observou a presença de um pequeno cromossomo denominado Philadelphia (Ph) nestas células, sendo considerado um marco para a citogenética. Objetivo: Levantar relações da Leucemia Mieloide Crônica com o gene BCR-ABL e o cromossomo Philadelphia. Material e métodos: Trata-se de um estudo bibliográfico com abordagem descritiva e qualitativa
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Rosetto MuÑoz, Vitor, Jose Rodrigo Pauli, LEANDRO PEREIRA DE MOURA, et al. "O EXERCÍCIO FÍSICO AGUDO REDUZ A RESISTÊNCIA À INSULINA NO MÚSCULO EQUELÉTICO DE ANIMAIS IDOSOS ATRAVÉS DA PROTEÍNA RHO-QUINASE." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-50704.

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RUZAIĶE, Aija, Sandra MUIŽNIECE-BRASAVA, Zanda KRŪMA, and Kaspars KOVAĻENKO. "NUTRITIONAL VALUE DETERMINATION OF THERMALLY PROCESSED POTATO MAIN COURSE IN RETORT PACKAGING." In RURAL DEVELOPMENT. Aleksandras Stulginskis University, 2018. http://dx.doi.org/10.15544/rd.2017.078.

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Consumers are increasingly demanding choices of ready-made foods with excellent organoleptic and health-related properties. There are two main trends in Europe; firstly, consumers are increasingly choosing foods that are comfortable for use, secondly, the number of people who are overweight is increasing, with more consumers paying close attention to the ingredients and nutritional value of products in order to balance the amount of the food they consume per day. The aim of the research was to develop new potato main courses and to determine their nutritional value. The research was carried ou
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Wu, Xiaoyong, Yanxia Sun, Yujie Shi, Yuan Tang, Jijun Tian, and Gang Zhao. "Study on Kinetics of Protein Forward Extraction from Quinoa by AOT/ Isooctane Reverse Micelles System." In 2018 3rd International Conference on Modelling, Simulation and Applied Mathematics (MSAM 2018). Atlantis Press, 2018. http://dx.doi.org/10.2991/msam-18.2018.70.

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Silva, Jiviane Beatriz Cunha Barretto, and Ana Paula Dias Demasi. "EXPRESSÃO DE PROTEÍNAS DO METABOLISMO DA GLICOSE NA ERITROPOESE." In I Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/629.

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Introdução: Evidências indicam que o metabolismo orienta o destino das células-tronco hematopoéticas entre a auto renovação e a diferenciação. Particularmente para células eritróides, que perdem núcleo e organelas em estágios terminais, a via glicolítica deve ser crucial durante todo o processo de desenvolvimento. As principais proteínas envolvidas nessa via, como o transportador de glicose 1 (Glut1), a enzima glicolítica lactato desidrogenase (LDH) e a enzima reguladora metabólica piruvato desidrogenase quinase 1 (PDK1), podem ser úteis para a avaliação da eritropoese. Objetivos: Verificar a
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