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Ravi Singh Mandeep Randhawa sridhar bhavani UTTAM KUMAR JULIO HUERTA_ESPINO Evans Lagudah CAIXIA LAN (2022, [Artículo])
Co-Located Resistance Loci Puccinia triticina CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA RUSTS PUCCINIA STRIIFORMIS QUANTITATIVE TRAIT LOCI ADULT PLANT RESISTANCE WHEAT
Genomic regions associated with resistance to three rusts in CIMMYT wheat line “Mokue#1”
Naeela Qureshi Ravi Singh sridhar bhavani (2023, [Artículo])
Genetic Analysis Leaf Rust CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA GENETICS RUSTS QUANTITATIVE TRAIT LOCI MAPPING DISEASE RESISTANCE STRIPE RUST STEM RUST
David Berger Yoseph Beyene Collins Juma Suresh L.M. Manje Gowda (2023, [Artículo])
Gray Leaf Spot Northern Corn Leaf Blight CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA MAIZE LEAF SPOTS QUANTITATIVE TRAIT LOCI ASSOCIATION MAPPING GENOME-WIDE ASSOCIATION STUDIES
Editorial: Functional genomic approaches in molecular breeding for crop improvement
Philomin Juliana (2023, [Artículo])
CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA DNA MARKER-ASSISTED SELECTION QUANTITATIVE TRAIT LOCI CROP IMPROVEMENT
Adrián Andrés Morales Guadarrama (2024, [Tesis de maestría])
El ostión Magallana gigas es ampliamente cultivado a nivel mundial. En Baja California, México, los laboratorios de reproducción deben acondicionar ostiones para su maduración y producción de gametos, y abastecer de semilla a los productores. En nuestro laboratorio, Sistemas de Recirculación Acuícola (SRA), con control del sistema CO2-Carbonatos (SRA-R) o sin control (SRA-C), han permitido madurar ostiones M. gigas y M. sikamea. Recientemente, los ostiones M. gigas acondicionados en nuestros SRA no maduraron, y algunos presentaron prevalencia de polidóridos (PP), poliquetos parásitos excavadores de concha. Para comprender la condición de los ostiones, evaluamos el efecto del SRA y de la PP sobre la expresión relativa de ocho genes asociados a biomineralización (VpATP y Tyr), inmunidad innata (P38, PGRP-L y TLR2) y reproducción (GnRH-RI, Vasa-like y SP1b) de M. gigas en dos etapas del acondicionamiento, 18 °C y 24 °C. La PP se determinó por la presencia de ampollas en la concha. Mediante RT-qPCR se determinó la expresión de VpATP, Tyr, P38, PGRP-L y TLR2 en el manto, y de GnRH-RI, Vasa-like y SP1b en la gónada. La expresión relativa se evaluó con un enfoque estadístico basado en un análisis Bayesiano de dos vías y comparaciones múltiples, p-valor significativo < 0.05 y corrección de Bonferroni. En 18 °C, la expresión de VpATP, Tyr, TLR2 y P38 fue mayor en ostiones con PP (CPP) que sin PP (SPP). En contraste, la expresión de GnRH-RI, Vasa-like y SP1b fue menor CPP que SPP. Dentro del SRA-C, en los ostiones CPP hubo mayor expresión de Tyr y menor expresión de Vasa-like y SP1b, respecto a los ostiones SPP. Esto sugiere que la PP induce la reparación de la concha y las respuestas inmune e inflamatoria en el manto mientras que en la gónada reduce el desarrollo de las células germinales. En 24 °C, en el SRA-R hubo menor expresión de SP1b respecto del SRA-C y sugiere menor división celular en la gónada. En conclusión, el SRA-R y la PP afectaron el balance energético del ostión japonés, limitando la energía y reflejando menor esfuerzo reproductivo en los ostiones del SRA-R al final del acondicionamiento reproductivo.
The Japanese oyster (Magallana gigas) is highly cultured worldwide. In Baja California, Mexico, the reproduction laboratories must condition oysters to maturity and have gametes to supply oyster seeds to producers. In our laboratory, recirculating aquaculture systems (RAS), with control of the CO2-Carbonate system (RAS-R) and without this control (RAS-C), have allowed oysters M. gigas and M. sikamea to mature. Recently, the M. gigas oysters conditioned in our RAS did not mature, and some have the prevalence of Polidorids (PP), shell-boring polychaete parasites. To understand the oysters' condition, we evaluated the effect of RAS and the PP on the relative expression of eight genes associated with biomineralization (VpATP and Tyr), innate immunity (P38, PGRP-L, and TLR2), and reproduction (GnRH-RI, Vasa-like, and SP1b) of M. gigas at two phases of broodstock conditioning, 18 °C and 24 °C. The PP was determined by mud blisters at the inner oyster shell. RT-qPCR determined the expression of VpATP, Tyr, p38, PGRP-L, and TLR2 in the mantle tissue and GnRH-RI, Vasa-like, and SP1b in the gonad tissue. The relative gene expression was evaluated by a Bayesian statistics frame based on a two-way and multiple comparison analysis, with significant p-value < 0.05 and Bonferroni correction. At 18 °C, there was higher expression of VpATP, Tyr, TLR2, and P38 in oysters with PP (WPP) than without PP (WOPP). In contrast, the expression of GnRH-RI, Vasa-like, and SP1b was less WPP than WOPP. It suggests that the PP induces shell repair and immune and inflammatory responses in mantle tissue, while in gonad tissue, it reduces the development of germinal cells. At 24 °C, in RAS-R, there was less expression of SP1b respect RAS-C, and it suggests less cellular division in the gonad. In conclusion, the RAS-R and the PP affect the energetic balance of the Japanese oyster, limiting the energy and reflecting less reproduction effort in oysters from RAS-R at the end of broodstock conditioning.
SRA, biomineralización, Vasa-like, Tyr, ostión RAS, biomineralization, Vasa-like, Tyr, oyster BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA GENÉTICA CITOGENÉTICA ANIMAL CITOGENÉTICA ANIMAL
Molecular modeling simulation studies reveal new potential inhibitors against HPV E6 protein
Joel Ricci-Lopez (2019, [Artículo])
High-risk strains of human papillomavirus (HPV) have been identified as the etiologic agent of some anogenital tract, head, and neck cancers. Although prophylactic HPV vaccines have been approved; it is still necessary a drug-based treatment against the infection and its oncogenic effects. The E6 oncoprotein is one of the most studied therapeutic targets of HPV, it has been identified as a key factor in cell immortalization and tumor progression in HPV-positive cells. E6 can promote the degradation of p53, a tumor suppressor protein, through the interaction with the cellular ubiquitin ligase E6AP. Therefore, preventing the formation of the E6-E6AP complex is one of the main strategies to inhibit the viability and proliferation of infected cells. Herein, we propose an in silico pipeline to identify small-molecule inhibitors of the E6-E6AP interaction. Virtual screening was carried out by predicting the ADME properties of the molecules and performing ensemble-based docking simulations to E6 protein followed by binding free energy estimation through MM/PB(GB)SA methods. Finally, the top-three compounds were selected, and their stability in the E6 docked complex and their effect in the inhibition of the E6-E6AP interaction was corroborated by molecular dynamics simulation. Therefore, this pipeline and the identified molecules represent a new starting point in the development of anti-HPV drugs. © 2019 Ricci-López 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.
ligand, luteolin, protein E6, protein inhibitor, ubiquitin protein ligase, ubiquitin protein ligase E6AP, unclassified drug, antivirus agent, DNA binding protein, E6 protein, Human papillomavirus type 18, oncoprotein, protein binding, protein p53, TP CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA CIENCIAS AGROPECUARIAS Y BIOTECNOLOGÍA