Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Carolina Monzó"'
Autor:
Maarouf Baghdadi, Tobias Nespital, Carolina Monzó, Joris Deelen, Sebastian Grönke, Linda Partridge
Publikováno v:
Molecular Metabolism, Vol 81, Iss , Pp 101902- (2024)
Objective: Rapamycin, a powerful geroprotective drug, can have detrimental effects when administered chronically. We determined whether intermittent treatment of mice can reduce negative effects while maintaining benefits of chronic treatment. Method
Externí odkaz:
https://doaj.org/article/a82a0bef98704f7ea031b10a51fa7346
Autor:
Carolina Monzó, Lisonia Gkioni, Andreas Beyer, Dario Riccardo Valenzano, Sebastian Grönke, Linda Partridge
Publikováno v:
Cell Reports, Vol 42, Iss 7, Pp 112722- (2023)
Summary: Aging impairs the capacity to respond to novel antigens, reducing immune protection against pathogens and vaccine efficacy. Dietary restriction (DR) extends life- and health span in diverse animals. However, little is known about the capacit
Externí odkaz:
https://doaj.org/article/5ae3e8842d5b4add90a8f6f0dea4bb05
Autor:
Azahara Fuentes-Trillo, Carolina Monzó, Iris Manzano, Cristina Santiso-Bellón, Juliana da Silva Ribeiro de Andrade, Roberto Gozalbo-Rovira, Ana-Bárbara García-García, Jesús Rodríguez-Díaz, Felipe Javier Chaves
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background Genome assembly of viruses with high mutation rates, such as Norovirus and other RNA viruses, or from metagenome samples, poses a challenge for the scientific community due to the coexistence of several viral quasispecies and stra
Externí odkaz:
https://doaj.org/article/d27c4b42731d41e5a5c24552f2fedd12
Autor:
Raquel Rodríguez-López, Fátima Gimeno-Ferrer, Elena Montesinos, Irene Ferrer-Bolufer, Carola Guzmán Luján, David Albuquerque, Carolina Monzó Cataluña, Virginia Ballesteros, Monserrat Aleu Pérez-Gramunt
Publikováno v:
Genes, Vol 12, Iss 8, p 1197 (2021)
Jacobsen syndrome or JBS (OMIM #147791) is a contiguous gene syndrome caused by a deletion affecting the terminal q region of chromosome 11. The phenotype of patients with JBS is a specific syndromic phenotype predominately associated with hematologi
Externí odkaz:
https://doaj.org/article/edee6aca82864f28adb49732ced417c6
Autor:
Lorena Forqué, Mario Fernández-Ruiz, Eliseo Albert, Estela Giménez, Carolina Monzó, Javier Chaves, Natalia Redondo, Isabel Rodríguez-Goncer, Tamara Ruiz-Merlo, Patricia Parra, Amado Andrés, José María Aguado, David Navarro
Publikováno v:
Transplantation.
Torque teno virus, the major member of the genus Alphatorquevirus, is an emerging biomarker of the net state of immunosuppression after kidney transplantation. Genetic diversity constitutes a main feature of the Anelloviridae family, although its pos
Autor:
José Luis Piñana, Estela Giménez, Carlos Solano, Carolina Monzó, David Navarro, Azahara Fuentes-Trillo, Eliseo Albert, Enrique Seda, Javier F Chaves, Juan Carlos Hernández Boluda
Publikováno v:
Journal of medical virologyREFERENCES. 93(8)
Monitoring of alphatorquevirus (torque teno virus [TTV]) DNA in plasma may prove to be useful to assess the net state of immune competence following allogeneic hematopoietic stem cell transplantation (allo-HSCT). There are scarce data published on th
Autor:
Goitzane Marcaida, David Albuquerque, Alicia Amadoz, Francisco Barros Angueira, Fátima Gimeno Ferrer, Juan Carlos Ferrer García, Carolina Monzó, Raquel Rodríguez López
Publikováno v:
Indian Journal of Case Reports. 3:171-174
Reduced genetic variability in isolated populations promotes the prevalence of long contiguous stretches of homozygosity (LCSH) that may carry deleterious mutations, manifesting recessive syndromes such as Alstrom syndrome (OMIM # 203800), caused pri
Autor:
Concepción Tomás, María Miguel-Cabo, Carmen González-Muñoz, Carolina Monzó, Carlos Collado, Miguel de Lamo, Bárbara Ortiz, Raquel Rodríguez-López, Goitzane Marcaida, Victoria Valverde, Carola Guzmán, Guillermo Gervasini, Vicente Monzó
Publikováno v:
Revista del Laboratorio Clínico. 10:72-78
Introduction Hereditary hemochromatosis is a disease responsible for excess blood iron. The hemochromatosis gene has two predominant variants, H63D and C282Y single nucleotide polymorphisms. Our study aims to analyze the diagnostic utility of genotyp
Autor:
A.K. Torres, N. Escartín, C. Guzmán, Carolina Monzó, Iliana Ferrer, V. Monzó, C. González-Muñoz, R. Rodríguez-López, G. Marcaida, P. Peña
Publikováno v:
Revista Clínica Española. 217:1-6
Resumen Objetivo Describir la distribucion poblacional de la variante UGT1A1*28 (codigo de variante genetica rs8175347) localizada en el promotor del gen UGT1A1 y correlacionar sus genotipos con los resultados de la prueba de ayuno, asi como su relac
Autor:
Juliana da Silva Ribeiro de Andrade, Jesús Rodríguez-Díaz, Azahara Fuentes-Trillo, Cristina Santiso-Bellón, Javier Buesa, Susana Vila-Vicent, Carolina Monzó, Roberto Gozalbo-Rovira, Felipe J. Chaves
Publikováno v:
Santiso Bellón, Cristina Monzó, Carolina Fuentes-Trillo, Azahara Vila Vicent, Susana da Silva Ribeiro de Andrade, Juliana Gozalbo Rovira, Roberto Vicente Buesa Gómez, Javier Chaves Martínez, Felipe Javier Rodríguez Díaz, Jesús 2019 Nearly Complete Genome Sequences of Human Norovirus Belonging to Several Genotypes from Valencia, Spain Microbiology Resource Announcements 8 34 e00641-19
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC: Repositorio Institucional de la Universitat de Valéncia
Microbiology Resource Announcements
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC: Repositorio Institucional de la Universitat de Valéncia
Microbiology Resource Announcements
Human noroviruses are responsible for most nonbacterial acute gastroenteritis cases. The GII.2, GII.4, and GII.17 genotypes of human noroviruses have recently arisen as the most frequent genotypes found in humans worldwide. We report here seven nearl