Zobrazeno 1 - 10
of 102
pro vyhledávání: '"A Molares Vila"'
Autor:
Rodríguez-Fuentes, Manuel Eros, Pérez-Sayáns, Mario, Barbeito-Castiñeiras, Gema, Molares-Vila, Alberto, Prado-Pena, Irene B., Camolesi, Gisela C.V., López-López, Rafael
Publikováno v:
In Journal of Stomatology oral and Maxillofacial Surgery July 2024
Autor:
Camino, Tamara, Lago-Baameiro, Nerea, Bravo, Susana Belén, Molares-Vila, Alberto, Sueiro, Aurelio, Couto, Iván, Baltar, Javier, Casanueva, Eelipe F, Pardo, Maria
Publikováno v:
In Translational Research January 2022 239:85-102
Autor:
Carmen Rodríguez-Cerdeira, Alberto Molares-Vila, Carlos Daniel Sánchez-Cárdenas, Jimmy Steven Velásquez-Bámaca, Erick Martínez-Herrera
Publikováno v:
Antibiotics, Vol 12, Iss 3, p 566 (2023)
Antifungal peptides (AFPs) comprise a group of substances with a broad spectrum of activities and complex action mechanisms. They develop in nature via an evolutionary process resulting from the interactions between hosts and pathogens. The AFP datab
Externí odkaz:
https://doaj.org/article/beec9a3af8b148bc857cd45812b26bf7
Autor:
Rodríguez-Cerdeira, Carmen, Molares-Vila, Alberto, Carnero-Gregorio, Miguel, Corbalán-Rivas, Alberte
Publikováno v:
In Journal of Proteomics 30 September 2018 188:152-166
Autor:
Adrian Cordido, Marta Vizoso-Gonzalez, Laura Nuñez-Gonzalez, Alberto Molares-Vila, Maria del Pilar Chantada-Vazquez, Susana B. Bravo, Miguel A. Garcia-Gonzalez
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 290 (2022)
(1) Background: Polycystic liver disease (PLD) is a heterogeneous group of congenital disorders characterized by bile duct dilatation and cyst development derived from cholangiocytes. Nevertheless, the cystogenesis mechanism is currently unknown and
Externí odkaz:
https://doaj.org/article/3eedca8384ef4eb1a55ecc43aca17d37
Autor:
Alberto Molares-Vila, Alberte Corbalán-Rivas, Miguel Carnero-Gregorio, José Luís González-Cespón, Carmen Rodríguez-Cerdeira
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4381 (2021)
Glycogen storage diseases (GSDs) are a group of 19 hereditary diseases caused by a lack of one or more enzymes involved in the synthesis or degradation of glycogen and are characterized by deposits or abnormal types of glycogen in tissues. Their freq
Externí odkaz:
https://doaj.org/article/fc8075fc159d4b3d96d0b9e8dd1a3a16
Akademický článek
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Autor:
Molares-Vila, Alberto, Gregorio, Miguel Carnero, Rivas, Alberte Corbalán, Covarrubias, Mariana Sánchez
La Fundación Ediciones Clío constituye una institución sin fines de lucro que procura la promoción de la ciencia, la cultura y la formación integral dirigida a grupos y colectivos de investigación. Nuestro principal objetivo es el de difundir c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::230236dda83981861a2aae8979ee40f9
Autor:
Alberto Molares-Vila, Eelipe F Casanueva, Aurelio M. Sueiro, Tamara Camino, Nerea Lago-Baameiro, María Pardo, Javier Baltar, Iván Couto, Susana B. Bravo
Publikováno v:
Translational Research. 239:85-102
Extracellular vesicles (EVs) have been recently postulated as key players in metabolic disorders emerging as an alternative way of paracrine/endocrine communication. However, the nature of EVs shed by adipose tissue (AT) and their role in obesity is
Autor:
Miguel Carnero Gregorio, Paula Álvarez Freire, Alberto Molares Vila, Myrian Álvarez González, Oscar Carnero Gregorio, José Ramón Arias Álvarez, Miguel Ángel Blach Italiani, Carlos Villaverde Taboada, Luisa Fernanda Pérez Méndez
Publikováno v:
Nutrición Hospitalaria, Vol 29, Iss 2, Pp 300-304 (2014)
Objetivo: Evaluar la eficacia de un protocolo clínico para pacientes obesos utilizado en la consulta de obesidad del Complexo Hospitalario Universitario de Vigo (CHUVI). Pacientes y métodos: En el estudio participaron 47 pacientes procedentes de la
Externí odkaz:
https://doaj.org/article/6f0194ddfd4d44e8bce87b21c751e023