Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jorge Espinós"'
Autor:
Albert Martin-Cardona, Josep Lloreta Trull, Raquel Albero-González, Marta Paraira Beser, Xavier Andújar, Pablo Ruiz-Ramirez, Jaume Tur-Martínez, Carme Ferrer, José Angel De Marcos Izquierdo, Anna Pérez-Madrigal, Laura Goiburú González, Jorge Espinós Perez, Maria Esteve
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background SARS-CoV-2 may produce intestinal symptoms that are generally mild, with a small percentage of patients developing more severe symptoms. The involvement of SARS-CoV-2 in the physiopathology of bowel damage is poorly known. Transmi
Externí odkaz:
https://doaj.org/article/014f1bba76fd4da68e6de6bea60ef328
Autor:
Arantzazu Rada-Palomino, Arantxa Muñoz-Duyos, Noelia Pérez-Romero, Harold Vargas-Pierola, Noelia Puértolas-Rico, Laura Ruiz-Campos, Jorge Espinós-Pérez, Enrique Veloso-Veloso
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 106, Iss 6, Pp 418-424 (2014)
Phlegmonous gastritis is a rare bacterial infection of the gastric wall, which progress rapidly. It is characterized by a purulent inflammation that can affect the entire gastrointestinal tract and presents a high mortality rate. We are reporting a c
Externí odkaz:
https://doaj.org/article/776135efea5a4944910fca35aabfbd16
Autor:
María Asunción García-González, David Nicolás-Pérez, Angel Lanas, Luis Bujanda, Patricia Carrera, Rafael Benito, Mark Strunk, Federico Sopeña, Santos Santolaria, Elena Piazuelo, Pilar Jiménez, Rafael Campo, Jesús Espinel, Marisa Manzano, Fernando Geijo, María Pellisé, Ferrán González-Huix, Jorge Espinós, Manuel Zaballa, Llúcia Titó, Luis Barranco, Roberto Pazo, Enrique Quintero
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e46179 (2012)
BACKGROUND: Genetic factors influencing the prognosis of gastric adenocarcinoma (GAC) are not well known. Given the relevance of cytokines and other pro-inflammatory mediators in cancer progression and invasiveness, we aimed to assess the prognostic
Externí odkaz:
https://doaj.org/article/b85da10020364c8e93bb697df70cd885
Autor:
Raquel Muñoz-González, Anna Calm, Noemí Caballero, Mercè Rosinach, Ingrid Marín, Juan Colán-Hernández, Ignacio Iborra, Edgar Castillo, Alfredo Mata, Román Turró, Jorge Espinós, Vicente Moreno, María Pellisé, Hugo Uchima
Publikováno v:
Gastroenterología y Hepatología. 46:S33
Publikováno v:
Tecnociencia, Vol 1, Iss 2 (2023)
Se presentan los resultados preliminares del monitoreo de la radiación UVB en la ciudad de Panamá, para el mes de julio de 1997. I\4ediante un radiómetro de banda ancha, modelo 501 UV-Biometer, está s¡endo medida, a partir del 1 de.julio, tanto
Externí odkaz:
https://doaj.org/article/cb115cffdcef44e7be3a707c0e020a27
Autor:
Irene González-Martínez, Estefanía Cerro-Herreros, Nerea Moreno, Andrea García-Rey, Jorge Espinosa-Espinosa, Marc Carrascosa-Sàez, Diego Piqueras-Losilla, Andrey Arzumanov, David Seoane-Miraz, Yahya Jad, Richard Raz, Matthew J. Wood, Miguel A. Varela, Beatriz Llamusí, Rubén Artero
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 34, Iss , Pp 102024- (2023)
Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disease caused by a CTG repeat expansion in the DMPK gene that generates toxic RNA with a myriad of downstream alterations in RNA metabolism. A key consequence is the sequestration of alternativ
Externí odkaz:
https://doaj.org/article/eab157fbac924adb8443e448d8ae4b14
Autor:
Javier Poyatos-García, Águeda Blázquez-Bernal, Marta Selva-Giménez, Ariadna Bargiela, Jorge Espinosa-Espinosa, Rafael P. Vázquez-Manrique, Anne Bigot, Ruben Artero, Juan Jesús Vilchez
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 31, Iss , Pp 324-338 (2023)
A single-nucleotide deletion in the stop codon of the nuclear import receptor transportin-3 (TNPO3), also involved in human immunodeficiency virus type 1 (HIV-1) infection, causes the ultrarare autosomal dominant disease limb-girdle muscular dystroph
Externí odkaz:
https://doaj.org/article/9a5a3e8ee08b4db28d543fbdc27b55f7
Autor:
María Asunción, García-González, Luis, Bujanda, Enrique, Quintero, Santos, Santolaria, Rafael, Benito, Mark, Strunk, Federico, Sopeña, Concha, Thomson, Angeles, Pérez-Aisa, David, Nicolás-Pérez, Elizabeth, Hijona, Patricia, Carrera-Lasfuentes, Elena, Piazuelo, Pilar, Jiménez, Jesús, Espinel, Rafael, Campo, Marisa, Manzano, Fernando, Geijo, María, Pellise, Manuel, Zaballa, Ferrán, González-Huix, Jorge, Espinós, Llúcia, Titó, Luis, Barranco, Roberto, Pazo-Cid, Angel, Lanas
Publikováno v:
International journal of cancer. 137(6)
Two recent genome-wide association studies in Asians have reported the association between the PSCA (prostate stem cell antigen) rs2294008CT gene polymorphism and two Helicobacter pylori infection-related diseases such as gastric cancer (GC) and duod
Autor:
Arantzazu, Rada-Palomino, Arantxa, Muñoz-Duyos, Noelia, Pérez-Romero, Harold, Vargas-Pierola, Noelia, Puértolas-Rico, Laura, Ruiz-Campos, Jorge, Espinós-Pérez, Enrique, Veloso-Veloso
Publikováno v:
Revista Española de Enfermedades Digestivas v.106 n.6 2014
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Revista Espanola de Enfermedades Digestivas, Vol 106, Iss 6, Pp 418-424 (2014)
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Revista Espanola de Enfermedades Digestivas, Vol 106, Iss 6, Pp 418-424 (2014)
Phlegmonous gastritis is a rare bacterial infection of the gastric wall, which progress rapidly. It is characterized by a purulent inflammation that can affect the entire gastrointestinal tract and presents a high mortality rate. We are reporting a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::97529df977a415465569ce74253dd073
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082014000600009
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082014000600009
Autor:
Estefanía Cerro-Herreros, Irene González-Martínez, Nerea Moreno, Jorge Espinosa-Espinosa, Juan M. Fernández-Costa, Anna Colom-Rodrigo, Sarah J. Overby, David Seoane-Miraz, Javier Poyatos-García, Juan J. Vilchez, Adolfo López de Munain, Miguel A. Varela, Matthew J. Wood, Manuel Pérez-Alonso, Beatriz Llamusí, Rubén Artero
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 26, Iss , Pp 174-191 (2021)
Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disease caused by expansion of unstable CTG repeats in a non-coding region of the DMPK gene. CUG expansions in mutant DMPK transcripts sequester MBNL1 proteins in ribonuclear foci. Depletion of
Externí odkaz:
https://doaj.org/article/fcb1590ef3cd430fb37c123264dbacdc