Relevant bibliographies by topics / PU61

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Academic literature on the topic 'PU61'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "PU61"

1

Mizan, Muhammad Rauful, Desta Wirnas, NFN Tasliah, Nurul Hidayatun, and Joko Prasetiyono, S.P., M.Si. "Molecular Analysis and Phenotypic Performances of BC3F2 Upland Rice Lines Containing Alt and Pup1 Loci." Jurnal AgroBiogen 15, no. 2 (December 31, 2019): 83. http://dx.doi.org/10.21082/jbio.v15n2.2019.p83-92.

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<p>The challenges in upland rice cultivation are phosphorous (P) deficiency and aluminum (Al) toxicity, each controlled by Pup1 and Alt loci, respectively. Pyramiding the two genes into Indonesian rice varieties were previously done through Marker-Assisted Backcrossing method to obtain BC3F2 populations. The aims of this study were to analyze the BC3F2 upland rice lines containing the Alt and Pup1 loci molecularly (foreground and background analyses) and to test their phenotypic performances. Genetic materials tested included Dupa variety (donor of Alt) and three improved Indonesian genotypes (Dodokan-Pup1, Situ Bagendit-Pup1, and Batur-Pup1) as recurrent parents, Kasalath (donor of Pup1), and 300 BC3F2 lines from Dodokan-Pup1+Alt, Situ Bagendit-Pup1+Alt, and Batur-Pup1+Alt, respectively. The rice genotypes were selected individually using modified Yoshida nutrient solution, followed by foreground and background analyses. 150 out of 300 seedlings were selected and maintained until harvest in the greenhouse. Foreground analysis using markers (RM1361, RM12031, and Kas46-2) and tiller number performances resulted in 18 plants from BC3F2 Dodokan-Pup1+Alt, 30 plants from BC3F2 Situ Bagendit-Pup1+Alt, and 25 plants from BC3F2 Batur-Pup1+Alt still carrying Alt and Pup1 loci. Background analysis using molecular markers showed that the best individual lines of BC3F2 were number 56 for BC3F2 Dodokan-Pup1+Alt, number 32 or 70 for BC3F2 Situ Bagendit-Pup1+Alt, and number 20 for BC3F2 Batur-Pup1+Alt. The selected lines having both both Alt and Pup1 loci in homozygote condition with highest number of tiller per plant which are useful genetic materials for developing upland rice variety tolerance to low P and Al toxicity.</p>
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Shin, Na-Hyun, O. New Lee, Jae-Hyuk Han, Kihwan Song, Hee-Jong Koh, Soo-Cheul Yoo, and Joong Hyoun Chin. "The Effect of Water Level in Rice Cropping System on Phosphorus Uptake Activity of Pup1 in a Pup1+Sub1 Breeding Line." Plants 10, no. 8 (July 26, 2021): 1523. http://dx.doi.org/10.3390/plants10081523.

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Pyramiding useful QTLs into an elite variety is a promising strategy to develop tolerant varieties against multiple abiotic stresses. However, some QTLs may not be functionally compatible when they are introgressed into the same variety. Here, we tested the functional compatibility of Pup1 and Sub1, major QTLs for tolerance to phosphorus (P)-deficiency and submergence conditions, respectively. Phenotypic analysis revealed that IR64-Pup1+Sub1 (IPS) plants harboring both Pup1 and Sub1 QTLs show significant tolerance to submerged conditions, similarly to IR64-Sub1, while IPS failed to tolerate P deficiency and mild drought conditions; only IR64-Pup1 showed P deficiency tolerance. In submerged conditions, Sub1A and OsPSTOL1, major genes for Sub1 and Pup1 QTLs, respectively, were expressed at the same levels as in IPS and IR64-Sub1 and in IPS and IR64-Pup1, respectively. On the other hand, in P-non-supplied condition, crown root number, root length, and OsPSTOL1 expression level were significantly lower in IPS compared to those of IR64-Pup1. However, there was no significant difference in P content between IPS and IR64-Pup1. These results imply that Pup1 does not compromise Sub1 function in submerged condition, while Sub1 suppresses Pup1 function in P-non-supplied condition, possibly by regulating the transcript level of Pup1. In conclusion, Pup1 and Sub1 are regarded as functionally compatible under submergence condition but not under P-non-supplied condition. Further study is needed to elucidate the functional incompatibility of Pup1 and Sub1 QTLs in IPS under P-non-supplied condition.
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Wang, S. S., and M. C. Brandriss. "Proline utilization in Saccharomyces cerevisiae: sequence, regulation, and mitochondrial localization of the PUT1 gene product." Molecular and Cellular Biology 7, no. 12 (December 1987): 4431–40. http://dx.doi.org/10.1128/mcb.7.12.4431.

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The PUT1 gene of Saccharomyces cerevisiae, believed to encode proline oxidase, has been completely sequenced and contains an open reading frame capable of encoding a polypeptide of 476 amino acids in length. The amino terminus of the protein deduced from the DNA sequence has a characteristic mitochondrial import signal; two PUT1-lacZ gene fusions were constructed that produced mitochondrially localized beta-galactosidase in vivo. The transcription initiation and termination sites of the PUT1 mRNA were determined. By using a PUT1-lacZ gene fusion that makes a cytoplasmic beta-galactosidase, the regulation of the PUT1 gene was studied. PUT1 is inducible by proline, responds only slightly to carbon catabolite repression, and is not regulated by the cytochrome activator proteins HAP1 and HAP2. The PUT1 gene is under oxygen regulation; expression in anaerobically grown cells is 10-fold lower than in aerobically grown cells. Oxygen regulation is abolished when cells are respiratory deficient. PUT1 expression in a [rho-] strain grown either aerobically or anaerobically is as high as that seen in a [rho+] strain grown aerobically. Studies on PUT1 promoter deletions define a region between positions -458 and -293 from the translation initiation site that is important for full expression of the PUT1 gene and required for oxygen regulation.
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Wang, S. S., and M. C. Brandriss. "Proline utilization in Saccharomyces cerevisiae: sequence, regulation, and mitochondrial localization of the PUT1 gene product." Molecular and Cellular Biology 7, no. 12 (December 1987): 4431–40. http://dx.doi.org/10.1128/mcb.7.12.4431-4440.1987.

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The PUT1 gene of Saccharomyces cerevisiae, believed to encode proline oxidase, has been completely sequenced and contains an open reading frame capable of encoding a polypeptide of 476 amino acids in length. The amino terminus of the protein deduced from the DNA sequence has a characteristic mitochondrial import signal; two PUT1-lacZ gene fusions were constructed that produced mitochondrially localized beta-galactosidase in vivo. The transcription initiation and termination sites of the PUT1 mRNA were determined. By using a PUT1-lacZ gene fusion that makes a cytoplasmic beta-galactosidase, the regulation of the PUT1 gene was studied. PUT1 is inducible by proline, responds only slightly to carbon catabolite repression, and is not regulated by the cytochrome activator proteins HAP1 and HAP2. The PUT1 gene is under oxygen regulation; expression in anaerobically grown cells is 10-fold lower than in aerobically grown cells. Oxygen regulation is abolished when cells are respiratory deficient. PUT1 expression in a [rho-] strain grown either aerobically or anaerobically is as high as that seen in a [rho+] strain grown aerobically. Studies on PUT1 promoter deletions define a region between positions -458 and -293 from the translation initiation site that is important for full expression of the PUT1 gene and required for oxygen regulation.
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Mizan, Muhammad Rauful, Desta Wirnas, and Dan Joko Prasetiyono. "Verifikasi Lokus Aluminum Tolerance (Alt) pada Tiga Populasi BC3F1 Padi." Jurnal Agronomi Indonesia (Indonesian Journal of Agronomy) 47, no. 1 (April 30, 2019): 9–17. http://dx.doi.org/10.24831/jai.v47i1.18664.

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Most of marginal lands in Indonesia are in the form of acid dry land with low available P and high Al concentrations. Development of tolerant rice varieties to P deficiency and Al toxicity is one way to increase rice production. This study aimed to select BC3F1-Pup1+Alt genotypes from three crosses based on foreground and background markers. This research was conducted at the Indonesian Center for Agricultural Biotechnology and Genetic Resources Research and Development, Bogor, from August to December 2015. The materials used were 300 genotypes of BC3F1 Dodokan-Pup1+Alt, BC3F1 Situ Bagendit-Pup1+Alt, BC3F1 Batur-Pup1+Alt, and the parents. The research included selection in modified Yoshida’s nutrient solutions (0.5 ppm P dan 60 ppm Al) followed by foreground selection and background selection. Selection using Yoshida’s nutrient solution resulted in 150 genotypes with longer root than the recipient parent in each of the BC3F1 populations. Selection with foreground markers using markers RM1361 and RM12031 produced 85 genotypes of BC3F1 Dodokan-Pup1+Alt (56.6%), 105 genotypes of BC3F1 Situ Bagendit-Pup1+Alt (70%), and 77 genotypes of BC3F1 Batur-Pup1+Alt (51.33%). Selection using background markers revealed that genotype number 116 (BC3F1 Dodokan-Pup1+Alt), number 2 (BC3F1 Situ Bagendit-Pup1+Alt), and number 129 (BC3F1 Batur-Pup1+Alt) were the best genotypes with percentage of parent recovery of 95%, 90%, and 90.5%, respectively. These three genotypes were verified to have Alt loci and had the largest genetic proportion of restoring parents. Keywords: Alt, background markers, foreground markers, Pup1, upland rice
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Saitoh, Atsushi, Yuki Takada, Mayu Horie, and Tomoya Kotani. "Pumilio1 phosphorylation precedes translational activation of its target mRNA in zebrafish oocytes." Zygote 26, no. 5 (October 2018): 372–80. http://dx.doi.org/10.1017/s0967199418000369.

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SummaryTranslational regulation of mRNAs is crucial for promoting various cellular and developmental processes. Pumilio1 (Pum1) has been shown to play key roles in translational regulation of target mRNAs in many systems of diverse organisms. In zebrafish immature oocytes, Pum1 was shown to bind to cyclin B1 mRNA and promote the formation of cyclin B1 RNA granules. This Pum1-mediated RNA granule formation seemed critical to determine the timing of translational activation of cyclin B1 mRNA during oocyte maturation, leading to activation of maturation/M-phase-promoting factor (MPF) at the appropriate timing. Despite its fundamental importance, the mechanisms of translational regulation by Pum1 remain elusive. In this study, we examined the phosphorylation of Pum1 as a first step to understand the mechanisms of Pum1-mediated translation. SDS-PAGE analyses and phosphatase treatments showed that Pum1 was phosphorylated at multiple sites during oocyte maturation. This phosphorylation began in an early period after induction of oocyte maturation, which preceded the polyadenylation of cyclin B1 mRNA. Interestingly, depolymerization of actin filaments in immature oocytes caused phosphorylation of Pum1, disassembly of cyclin B1 RNA granules, and polyadenylation of cyclin B1 mRNA but not translational activation of the mRNA. Overexpression of the Pum1 N-terminus prevented the phosphorylation of Pum1, disassembly of cyclin B1 RNA granules, and translational activation of the mRNA even after induction of oocyte maturation. These results suggest that Pum1 phosphorylation in the early period of oocyte maturation is one of the key processes for promoting the disassembly of cyclin B1 RNA granules and translational activation of target mRNA.
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Wang, S. S., and M. C. Brandriss. "Proline utilization in Saccharomyces cerevisiae: analysis of the cloned PUT1 gene." Molecular and Cellular Biology 6, no. 7 (July 1986): 2638–45. http://dx.doi.org/10.1128/mcb.6.7.2638.

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The PUT1 gene was isolated by functional complementation of a put1 (proline oxidase-deficient) mutation in Saccharomyces cerevisiae. Three independent clones with overlapping inserts of 6.8, 10.5, and 11 kilobases (kb) were isolated from S. cerevisiae genomic libraries in YEp24 (2 micron) and YCp50 (CEN) plasmids. The identity of the PUT1 gene was determined by a gene disruption technique, and Southern hybridization and genetic analyses confirmed that the bona fide gene had been cloned. Plasmids containing the PUT1 gene restored regulated levels of proline oxidase activity to put1 recipient strains. The PUT1 DNA was present in a single copy in the yeast genome and encoded a transcript of ca. 1.5 kb. S1 nuclease protection experiments were used to determine the direction of transcription of the PUT1 message and to localize its 5' and 3' termini within a subcloned 3-kb DNA fragment. Approximately 50-fold more PUT1-specific mRNA was detected in induced (proline-grown) cells than in uninduced (ammonia-grown) cells. A yeast strain carrying the previously identified put3 regulatory mutation that caused constitutive levels of proline oxidase activity was found to have sevenfold elevated PUT1 mRNA levels under noninducing conditions. The absence of a functional electron transport system in vegetative petite (rho-) strains interfered with their ability to use proline as a nitrogen source. Although these strains were Put- and made no detectable proline oxidase activity, PUT1 message was detected under inducing conditions. The PUT1 gene was mapped distal to the GAL2 gene on chromosome XII by tetrad analysis.
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Wang, S. S., and M. C. Brandriss. "Proline utilization in Saccharomyces cerevisiae: analysis of the cloned PUT1 gene." Molecular and Cellular Biology 6, no. 7 (July 1986): 2638–45. http://dx.doi.org/10.1128/mcb.6.7.2638-2645.1986.

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The PUT1 gene was isolated by functional complementation of a put1 (proline oxidase-deficient) mutation in Saccharomyces cerevisiae. Three independent clones with overlapping inserts of 6.8, 10.5, and 11 kilobases (kb) were isolated from S. cerevisiae genomic libraries in YEp24 (2 micron) and YCp50 (CEN) plasmids. The identity of the PUT1 gene was determined by a gene disruption technique, and Southern hybridization and genetic analyses confirmed that the bona fide gene had been cloned. Plasmids containing the PUT1 gene restored regulated levels of proline oxidase activity to put1 recipient strains. The PUT1 DNA was present in a single copy in the yeast genome and encoded a transcript of ca. 1.5 kb. S1 nuclease protection experiments were used to determine the direction of transcription of the PUT1 message and to localize its 5' and 3' termini within a subcloned 3-kb DNA fragment. Approximately 50-fold more PUT1-specific mRNA was detected in induced (proline-grown) cells than in uninduced (ammonia-grown) cells. A yeast strain carrying the previously identified put3 regulatory mutation that caused constitutive levels of proline oxidase activity was found to have sevenfold elevated PUT1 mRNA levels under noninducing conditions. The absence of a functional electron transport system in vegetative petite (rho-) strains interfered with their ability to use proline as a nitrogen source. Although these strains were Put- and made no detectable proline oxidase activity, PUT1 message was detected under inducing conditions. The PUT1 gene was mapped distal to the GAL2 gene on chromosome XII by tetrad analysis.
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Morris, Adam R., Neelanjan Mukherjee, and Jack D. Keene. "Ribonomic Analysis of Human Pum1 Reveals cis-trans Conservation across Species despite Evolution of Diverse mRNA Target Sets." Molecular and Cellular Biology 28, no. 12 (April 14, 2008): 4093–103. http://dx.doi.org/10.1128/mcb.00155-08.

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ABSTRACT PUF family proteins are among the best-characterized regulatory RNA-binding proteins in nonmammalian species, but relatively little is known about mRNA targets or functions of mammalian PUF proteins. In this study, we used ribonomic analysis to identify and analyze mRNAs associated with ribonucleoproteins containing an endogenous human PUF protein, Pum1. Pum1-associated mRNAs were highly enriched for genes encoding proteins that function in transcriptional regulation and cell cycle/proliferation, results consistent with the posttranscriptional RNA regulon model and the proposed ancestral functions of PUF proteins in stem cell biology. Analysis of 3′ untranslated region sequences of Pum1-associated mRNAs revealed a core Pum1 consensus sequence, UGUAHAUA. Pum1 knockdown demonstrated that Pum1 enhances decay of associated mRNAs, and relocalization of Pum1 to stress granules suggested that Pum1 functions in repression of translation. This study is the first in vivo genome-wide mRNA target identification of a mammalian PUF protein and provides direct evidence that human PUF proteins regulate stability of associated mRNAs. Comparison of Pum1-associated mRNAs to mRNA targets of PUF proteins from Saccharomyces cerevisiae and Drosophila melanogaster demonstrates how a well-conserved RNA-binding domain and cognate binding sequence have been evolutionarily rewired to regulate the collective expression of different sets of functionally related genes.
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Hidayatun, Nurul, and Joko Prasetiyono. "Effect of Introgression of Pup1 Locus on Rice Seedling under Phosphorus Deficiency." Jurnal AgroBiogen 14, no. 2 (March 15, 2019): 97. http://dx.doi.org/10.21082/jbio.v14n2.2018.p97-104.

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<p>The lack of soil-phosphorus (P) element will result in plant growth retardation. Plants could survive in P deficiency stress by increasing the ability of P uptake or by increasing the efficiency in the P utilization. The aims of this study were to understand genetic composition of rice genotypes possessing Pup1 locus and to know root and leaf growth responses at different P availability condition. The three rice genotypes (IR74, IR74-Pup1, and Kasalath) were analyzed for their genetic composition using SNP markers. The phenotypic experiment was arranged using a Completely Randomized Design with four replications and performed hydroponically in nutrient solution with different availability of P. The result showed that IR74-Pup1 had 84.4% similarities to its parent (IR74) with 13.6% of donor segments, where the Pup1 locus located. The influence of Pup1 locus<br />introgression on total length, surface area, diameter, and volume of the root varied at each growth stage. IR74 and IR74-Pup1 had root and leaf growth restriction on low P, but Pup1 locus introgression showed better growth performance, both in normal P and in low P conditions. The introgression of Pup1 locus increases plant ability to reduce the impact of growth inhibition<br />caused by P deficiency. </p>
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Dissertations / Theses on the topic "PU61"

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Cavassa, Castañeda De Wurst Claudia Isabel, Echegaray Peruska Chambi, Kifox Arce Ricardo Choy, Lazzari De Sousa Alfonzo Facundo De, Man Mariana Gabriela Montalvo, Alvino Keyko Paola Monteblanco, and Roach Joaquin Alejandro Rubio. "Fotografía Publicitaria - PU61 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623392.

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El curso de Fotografía Publicitaria va dirigido a dos carreras de la Facultad de Comunicaciones, la carrera de Comunicación y Publicidad y la carrera de Comunicación Audiovisual y Medios Interactivos. El curso es de carácter teórico-práctico y desarrolla en el alumno las competencias generales de Pensamiento Innovador y específicas de Análisis e Interpretación de la Realidad La fotografía publicitaria es un área de la fotografía destinada a exaltar las cualidades de un producto o servicio de modo que se incentive su consumo. En este curso los estudiantes aprenderán a convertir conceptos en imágenes y a dominar la técnica fotográfica en estudio.
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Montalvo, Man Mariana Gabriela. "Fotografía Publicitaria - PU61 201800." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623393.

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El curso de Fotografía Publicitaria va dirigido a dos carreras de la Facultad de Comunicaciones, la carrera de Comunicación y Publicidad y la carrera de Comunicación Audiovisual y Medios Interactivos. El curso es de carácter teórico-práctico y desarrolla en el alumno las competencias generales de Pensamiento Innovador y Análisis e Interpretación de la Realidad La fotografía publicitaria es un área de la fotografía destinada a exaltar las cualidades de un producto o servicio de modo que se incentive su consumo. En este curso los estudiantes aprenderán a convertir conceptos en imágenes y a dominar la técnica fotográfica en estudio.
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Felix, Limas Oscar Eduardo, Cubas Martha Irene Guerra, and Costa Rosario Marcela Vidurrizaga. "Casuística Publicitaria - PU65 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623391.

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Curso de especialidad en la carrera de Comunicación y Publicidad de carácter práctico-teórico dirigido a los estudiantes del noveno ciclo, que busca desarrollar las competencias generales de Pensamiento crítico y las competencias específicas de Análisis e interpretación de la realidad, Gestión de recursos y Creatividad. Actualmente la publicidad se está reinventando, dado que los medios de comunicación cada vez están más saturados de mensajes y en un mar de productos/servicios que se ofertan diariamente. Las marcas apuntan a llegar a los consumidores cuando lo necesitan a través de una comunicación bidireccional. Por ello enfocan sus estrategias en dos puntos clave: estableer una estrucutura fuerte de marca que las diferencie del resto (branding) y difundir el mensaje através de un mix de medios que amplifique el alcance, llegando en el momento preciso que el consumidor quiera recibir o necesite la información (content marketing).
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Barreto, Gonzales Diego Rodrigo, and Dongo Eduardo Enrique Yalán. "Semiótica Publicitaria - PU67 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623387.

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Curso de especialidad en la carrera de Comunicación y Publicidad, de carácter teórico-práctico, dirigido a los estudiantes de octavo ciclo. Busca desarrollar la competencia general de pensamiento crítico y las competencias específicas de creatividad y de análisis e interpretación de la realidad. En este caso, el alumno revisa con minuciosidad los conceptos semióticos expresados en texto o imágenes que lo llevan a comprender los recursos para la elaboración de mensajes poderosos. Este curso es una profundización de conceptos básicos estudiados en el curso de Semiótica y una aproximación sistemática a un análisis integral de la comunicación con fines publicitarios.
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Yalán, Dongo Eduardo Enrique. "Semiótica Publicitaria - PU67 201800." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623388.

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Curso de especialidad en la carrera de Comunicación y Publicidad, de carácter teórico-práctico, dirigido a los estudiantes de octavo ciclo. Busca desarrollar la competencia general de pensamiento crítico y la competencia específica de análisis e interpretación de la realidad. En este caso, el alumno revisa con minuciosidad los conceptos semióticos expresados en texto o imágenes que lo llevan a comprender los recursos para la elaboración de mensajes poderosos. Este curso es una profundización de conceptos básicos estudiados en el curso de Semiótica y una aproximación sistemática a un análisis integral de la comunicación con fines publicitarios.
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Carrillo, Portocarrero Vanessa Rosana, Belaunde Carolina Angelica Christen, Bravo Karina Janeth García, Basurto De Smolij Diana Fátima Nuñez, Ocampo Renzo Rojas, Díaz De Castro María Del Carmen Santillán, Canales Irene Villalaz, and Flores Jessica Esperanza Yamunaqué. "Fundamentos de Publicidad - PU01 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623385.

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Curso general de la Facultad de Comunicaciones, de carácter teórico, dirigido a los estudiantes de las carreras de Comunicación y Publicidad, Comunicación y Marketing (3er ciclo), Comunicación e Imagen Empresarial (4to ciclo) y Comunicación Audiovisual y Medios Interactivos (mención propia en Publicidad). Propósito: La vertiginosa evolución de las comunicaciones y el empoderamiento del consumidor conducen hoy a los fabricantes de productos y servicios a desarrollar modelos de publicidad cada vez más efectivos. Lograr que los compradores potenciales, encuentren, conozcan y se habitúen a sus productos y servicios es una de las principales tareas de la publicidad. Otro de los roles de la publicidad es generar soluciones creativas en función al conocimiento profundo de las personas, del perfil de la marca y de las características de los medios. "(...)La publicidad rodea nuestras vidas, nos persigue por todas partes, pero a pesar de estar presente y mostrarse tanto, oculta a los ojos del espectador cuáles son sus claves profesionales, cómo funciona, por qué funciona." Marçal Moliné. La Comunicación Activa (1997).
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Espinoza, Cabrera Marianela, Limas Oscar Eduardo Felix, Woolcott Fiorella Lama, and Ocampo Renzo Rojas. "Comportamiento del Consumidor - PU66 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623389.

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El curso Comportamiento del Consumidor realiza análisis constantes sobre las razones y situaciones que influyen en el consumo de un individuo o grupo. Por esta razón, a lo largo del curso, el estudiante identifica y comprende los principales procesos que se generan en la mente del consumidor con la finalidad de conocer la forma en la que evalúa productos y marcas. Este conocimiento es de total utilidad para todo comunicador, permitiéndole conocer a profundidad el comportamiento del consumidor. El curso de Comportamiento del Consumidor ha sido diseñado con el propósito de permitir al futuro comunicador desarrollar su capacidad de análisis, indispensable para que elabore futuras estrategias de comunicación. El curso contribuye directamente al desarrollo de la competencia de Pensamiento Crítico (general-UPC) a un nivel 2 y de la competencia específica (Facultad de Comunicaciones) de Estrategia Comunicacional a un nivel 1.
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Lama, Woolcott Fiorella. "Comportamiento del Consumidor - PU66 201800." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623390.

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Comportamiento del Consumidor es un curso general en la Facultad de Comunicaciones, de carácter teóricopráctico dirigido a los estudiantes del 3er ciclo, que busca desarrollar la competencia general Pensamiento crítico y la competencia específica de Estrategia comunicacional Desarrollar la capacidad de análisis es indispensable para que el estudiante elabore futuras estrategias de comunicación. Por esta razón, a lo largo del curso el estudiante comprende las necesidades y motivaciones de diferentes individuos o grupos, identifica los principales factores que influyen en su comportamiento y conoce la forma en la que se evalúan productos y se toman decisiones de consumo. Este conocimiento sirve como insumo primario que permite conocer a profundidad el comportamiento del consumidor.
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Bertini, Wiesse Luis Carlos, Marin Dario Enrique Flores, Hope Janeth Viviane Laos, and Miguel De Priego Domingo Luis Alberto Natteri. "Gerencia de Productos - PU51 201801." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623380.

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comunicador reconozca la perspectiva de la empresa desde un enfoque altamente analítico y competente, siendo importante que conozca todo el manejo en la creación y gestión de productos antes de preparar la campaña de comunicación. Debido a que las estrategias publicitarias deben estar alineadas a las estrategias de marketing, el publicista debe contar con un conocimiento sólido sobre las variables inmersas en este. Propósito: Curso de especialidad Gerencia de Producto en la carrera de Comunicación y Publicidad de carácter teóricopráctico, dirigido a los estudiantes del sexto ciclo, que busca desarrollar la Competencia General de Pensamiento Innovador y la Competencia de Facultad de Gestión de Recursos.
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Flores, Marin Dario Enrique, and Hope Janeth Viviane Laos. "Gerencia de Productos - PU51 201800." Universidad Peruana de Ciencias Aplicadas (UPC), 2018. http://hdl.handle.net/10757/623381.

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Curso de especialidad Gerencia de Producto en la carrera de Comunicación y Publicidad de carácter teóricopráctico, dirigido a los estudiantes del sexto ciclo, que busca desarrollar la competencia general de pensamiento innovador y la competencia específica de gestión de recursos. En un entorno de alto nivel de competitividad como el que rige en la actualidad es prioritario que el comunicador reconozca la perspectiva de la empresa desde un enfoque altamente analítico y competente, siendo importante que conozca todo el manejo en la creación y gestión de productos antes de preparar la campaña de comunicación. Debido a que las estrategias publicitarias deben estar alineadas a las estrategias de marketing, el publicista debe contar con un conocimiento sólido sobre las variables inmersas en este.
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Books on the topic "PU61"

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Zhang, Haoming. Chinese Picture Cookbook 1 ('Jia ting shi yong shi pu1', in traditional Chinese/English). Yao Sheng Wen Hua, 1995.

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Book chapters on the topic "PU61"

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Sarangi, Srikant. "Public discourse." In Handbook of Pragmatics, 1–21. Amsterdam: John Benjamins Publishing Company, 1997. http://dx.doi.org/10.1075/hop.2.pub1.

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Valdeón, Roberto A. "Publishing in Translation Studies." In Handbook of Translation Studies, 186–91. Amsterdam: John Benjamins Publishing Company, 2021. http://dx.doi.org/10.1075/hts.5.pub1.

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"PU.1 (PU1)." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics, 1599. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_13805.

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"Instructions for Puzzle Games with game boards (PuB1–PuB9)." In Paired Maths Handbook, 56–57. Routledge, 2013. http://dx.doi.org/10.4324/9781315068091-31.

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"13. Puzur-Šulgi to Šulgi 1 (PuŠ1, 3.1.7, RCU 11)." In The Correspondence of the Kings of Ur, 352–63. Penn State University Press, 2011. http://dx.doi.org/10.1515/9781575066509-026.

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"Instructions for Puzzle Games without game boards (Pu1–Pu10)." In Paired Maths Handbook, 68–71. Routledge, 2013. http://dx.doi.org/10.4324/9781315068091-35.

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Conference papers on the topic "PU61"

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Mantiuk, Rafal K., and Maryam Azimi. "PU21: A novel perceptually uniform encoding for adapting existing quality metrics for HDR." In 2021 Picture Coding Symposium (PCS). IEEE, 2021. http://dx.doi.org/10.1109/pcs50896.2021.9477471.

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Khasna, Elhah Nailul, Shelly Zairina, Ria Reinnata Juliandari, Bagus Paramajati, Mohammad Habibi, Andi Madihah, Septi Kurniama Sari, and Dwi Listyorini. "Polymorphism of Pun1 gene for pungency in Capsicum frutescens ‘Cakra Hijau’ Indonesian local pepper." In INVENTING PROSPEROUS FUTURE THROUGH BIOLOGICAL RESEARCH AND TROPICAL BIODIVERSITY MANAGEMENT: Proceedings of the 5th International Conference on Biological Science. Author(s), 2018. http://dx.doi.org/10.1063/1.5050115.

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Jung, Dawoon E., Kahee Kim, Chanyang Kim, Soo Been Park, Jung Hyun Jo, Hee Seung Lee, and Si Young Song. "Abstract 4337: Identification of novel fusion gene, PUM1-TRAF3, as potent biomarker in bile duct cancer." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-4337.

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