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Genética de la resistencia al complejo mancha de asfalto en 18 genotipos tropicales de maíz
George Mahuku Ignacio Benítez-Riquelme Serafin Cruz-Izquierdo (2015, [Artículo])
Horizontal Resistance Tar Spot Complex CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA FUNGI MONOGRAPHELLA PHYLLACHORALES ZEA MAYS DIALLEL ANALYSIS DISEASE RESISTANCE
LILIANA EUNICE SAUCEDO PICAZO Luis Guillermo Hernández Montiel NORMA FLORES ESTEVEZ PATRICIA GEREZ FERNANDEZ ANGEL FERNANDO ARGÜELLO ORTIZ JUAN CARLOS NOA CARRAZANA (2022, [Artículo])
"Dieback disease caused by fungal complexes is a severe problem in mango trees (Mangifera indica). Its main symptoms are branch rot, gummosis, and finally, the tree’s death. In this work, the species of the fungal complex causing mango dieback in the Manila variety in Veracruz, Mexico were identified. The in vitro interaction of two species belonging to the complex was evaluated and the severity of the co-infection in mango branches. Lasiodiplodia pseudotheobromae and Pestalotiopsis mangiferae were identified as causal agents of mango dieback in the producing area of Veracruz. In coinfected mango branches, greater severity of necrosis was observed than in individual infections. Liquid culture filtrates applied in co-cultures showed different results for each species of phytopathogen. The P. mangiferae filtrate had no significant antagonistic effects on the growth of L. pseudotheobromae (inhibition of 2.68%), while the L. pseudotheobromae filtrate inhibited 41.38% of P. mangiferae. The results show that multiple infections in mango trees increase the damage caused by dieback, which could directly impact the development of control strategies."
gummosis, virulence, interaction, fungal complex CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA CIENCIAS AGRARIAS FITOPATOLOGÍA FITOPATOLOGÍA FITOPATOLOGÍA
Itzel Mota Castañeda (2023, [Tesis de maestría])
La tesis se enfoca en abordar los desafíos en sistemas de comunicación inalámbrica, con el objetivo principal de diseñar redes de conformación de haz eficiente para un arreglo circular de antenas. Esta red debe reducir la dependencia de cambiadores de fase o dispositivos activos y cumplir con patrones de radiación específicos. Para lograr esto, se propone una solución que combina una red de excitación cofasal y una red CORPS cilíndrica. La red de alimentación cofasal, optimizada mediante algoritmos genéticos, demuestra la capacidad de generar un haz de radiación que puede ser escaneado en todo el plano azimutal. Esto se logra aprovechando las propiedades de rotación y simetría del arreglo circular. Además, se alcanza un rendimiento destacado en la supresión de lóbulos laterales, con una reducción significativa de -16 dB en comparación con el caso sin optimizar. Esta mejora en la calidad del haz de radiación es crucial para la transmisión confiable de señales en sistemas de comunicación. La red CORPS cilíndrica presentada en la investigación simplifica la red de alimentación en un 50%. Permite generar una cantidad distribuida de haces en todo el plano azimutal, y la dirección de escaneo de cada haz se ajusta según el número de puertos de entrada. Cada puerto de entrada controla un haz de radiación, lo que simplifica la complejidad del sistema y permite un mayor control sobre los lóbulos laterales. A medida que se aumenta el número de elementos y puertos de entrada en el arreglo, se mejora aún más el rendimiento en la supresión de lóbulos laterales. Esto ofrece la flexibilidad de ajustar el nivel de lóbulos laterales según los requisitos específicos de diseño. La investigación ha demostrado que la combinación de una red de alimentación cofasal optimizada y una red CORPS cilíndrica ofrecen una solución efectiva para la conformación de haz en arreglos circulares de antenas. Esta solución reduce significativamente la dependencia de dispositivos activos, mejora la calidad de la señal y simplifica la operación del sistema. Estos resultados abren oportunidades para futuras investigaciones y prometen mejoras en la industria de las comunicaciones inalámbricas.
This work is focused on the challenges in wireless communication systems, with the main objective of designing efficient beamforming networks for a circular antenna array. This network must reduce the reliance on phase shifters or active devices and meet specific radiation patterns. To achieve this, we propose two possible solutions: a cophasal excitation network and a cylindrical CORPS network. The cophasal feed network, optimized by genetic algorithms, generates a radiation beam that can be scanned in the whole azimuth plane. It is possible by taking advantage of the rotation and symmetry properties of the circular array. Furthermore, we achieve an outstanding performance in sidelobe suppression, with a significant reduction of -16 dB compared to the unoptimized case. This improvement in the quality of the radiation beam is crucial for the reliable transmission of signals in communication systems. The cylindrical CORPS network (presented in this research) simplifies the power network by 50%. It allows the entire azimuth plane to generate a distributed number of beams and adjust the scanning direction of each beam in according to the number of input ports. Each input port controls one radiation beam, simplifying the complexity of the system and allowing greater control over the side lobes. As the number of elements and input ports increases, sidelobe suppression performance is further improved. This proposal offers the flexibility to adjust the level of side lobes based on specific design requirements. Research has shown that the optimization of a cophasal feeder network and a cylindrical CORPS network offers an effective solution for beamforming in circular antenna arrays. This solution significantly reduces dependency on active devices, improves signal quality, and simplifies system operation. These results open up opportunities for future research and promise improvements in the wireless communications industry.
Arreglo circular de antenas, algoritmos genéticos, Red CORPS cilíndrica Circular array of antennas, Genetic algorithms, Cylindrical CORPS network INGENIERÍA Y TECNOLOGÍA CIENCIAS TECNOLÓGICAS TECNOLOGÍA DE LAS TELECOMUNICACIONES ANTENAS ANTENAS
RAMON OSVALDO ECHAURI ESPINOSA (2012, [Artículo])
Coronin plays a major role in the organization and dynamics of actin in yeast. To investigate the role of coronin in a filamentous fungus (Neurospora crassa), we examined its subcellular localization using fluorescent proteins and the phenotypic consequences of coronin gene (crn-1) deletion in hyphal morphogenesis, Spitzenkörper behavior and endocytosis. Coronin-GFP was localized in patches, forming a subapical collar near the hyphal apex; significantly, it was absent from the apex. The subapical patches of coronin colocalized with fimbrin, Arp2/3 complex, and actin, altogether comprising the endocytic collar. Deletion of crn-1 resulted in reduced hyphal growth rates, distorted hyphal morphology, uneven wall thickness, and delayed establishment of polarity during germination; it also affected growth directionality and increased branching. The Spitzenkörper of Δcrn-1 mutant was unstable; it appeared and disappeared intermittently giving rise to periods of hyphoid-like and isotropic growth respectively. Uptake of FM4-64 in Δcrn-1 mutant indicated a partial disruption in endocytosis. These observations underscore coronin as an important component of F-actin remodeling in N. crassa. Although coronin is not essential in this fungus, its deletion influenced negatively the operation of the actin cytoskeleton involved in the orderly deployment of the apical growth apparatus, thus preventing normal hyphal growth and morphogenesis. © 2012 Echauri-Espinosa et al.
actin related protein 2-3 complex, F actin, fimbrin protein, fluorescent dye, fungal protein, fungal protein coronin, green fluorescent protein, unclassified drug, actin binding protein, coronin proteins, fungal protein, article, cell polarity, contr BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA MICROBIOLOGÍA MICROBIOLOGÍA
CYNTHIA LIZZETH ARAUJO PALOMARES (2011, [Artículo])
Rho-type GTPases are key regulators that control eukaryotic cell polarity, but their role in fungal morphogenesis is only beginning to emerge. In this study, we investigate the role of the CDC-42 - RAC - CDC-24 module in Neurospora crassa. rac and cdc-42 deletion mutants are viable, but generate highly compact colonies with severe morphological defects. Double mutants carrying conditional and loss of function alleles of rac and cdc-42 are lethal, indicating that both GTPases share at least one common essential function. The defects of the GTPase mutants are phenocopied by deletion and conditional alleles of the guanine exchange factor (GEF) cdc-24, and in vitro GDP-GTP exchange assays identify CDC-24 as specific GEF for both CDC-42 and RAC. In vivo confocal microscopy shows that this module is organized as membrane-associated cap that covers the hyphal apex. However, the specific localization patterns of the three proteins are distinct, indicating different functions of RAC and CDC-42 within the hyphal tip. CDC-42 localized as confined apical membrane-associated crescent, while RAC labeled a membrane-associated ring excluding the region labeled by CDC42. The GEF CDC-24 occupied a strategic position, localizing as broad apical membrane-associated crescent and in the apical cytosol excluding the Spitzenkörper. RAC and CDC-42 also display distinct localization patterns during branch initiation and germ tube formation, with CDC-42 accumulating at the plasma membrane before RAC. Together with the distinct cellular defects of rac and cdc-42 mutants, these localizations suggest that CDC-42 is more important for polarity establishment, while the primary function of RAC may be maintaining polarity. In summary, this study identifies CDC-24 as essential regulator for RAC and CDC-42 that have common and distinct functions during polarity establishment and maintenance of cell polarity in N. crassa. © 2011 Araujo-Palomares et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
CDC24 protein, guanine nucleotide exchange factor, protein Cdc42, Rac protein, unclassified drug, cell cycle protein, fungal protein, membrane protein, multiprotein complex, protein Cdc42, Rac protein, allele, apical membrane, article, assay, cell me BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA MICROBIOLOGÍA MICROBIOLOGÍA