Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jose Vicente Sanchez-Mut"'
Autor:
Raúl F. Pérez, Patricia Tezanos, Alfonso Peñarroya, Alejandro González-Ramón, Rocío G. Urdinguio, Javier Gancedo-Verdejo, Juan Ramón Tejedor, Pablo Santamarina-Ojeda, Juan José Alba-Linares, Lidia Sainz-Ledo, Annalisa Roberti, Virginia López, Cristina Mangas, María Moro, Elisa Cintado Reyes, Pablo Muela Martínez, Mar Rodríguez-Santamaría, Ignacio Ortea, Ramón Iglesias-Rey, Juan Castilla-Silgado, Cristina Tomás-Zapico, Eduardo Iglesias-Gutiérrez, Benjamín Fernández-García, Jose Vicente Sanchez-Mut, José Luis Trejo, Agustín F. Fernández, Mario F. Fraga
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-26 (2024)
Abstract Aging involves the deterioration of organismal function, leading to the emergence of multiple pathologies. Environmental stimuli, including lifestyle, can influence the trajectory of this process and may be used as tools in the pursuit of he
Externí odkaz:
https://doaj.org/article/4c4a8c6ac5de4ae1a06f001803b72c14
Autor:
Raúl Alelú-Paz, Francisco Carmona, Jose Vicente Sanchez-Mut, Ariel Cariaga-Martínez, Ana González-Corpas, Nadia Ashour, María Jesús Orea, Ana Escanilla, Alfonso Monje, Carmen Guerrero-Márquez, Jerónimo Saiz-Ruíz, Manel Esteller, Santiago Ropero
Publikováno v:
Frontiers in Psychology, Vol 7 (2016)
Attempts to discover genes that are involved in the pathogenesis of major psychiatric disorders have been frustrating and often fruitless. Concern is building about the need to understand the complex ways in which nature and nurture interact to produ
Externí odkaz:
https://doaj.org/article/3511756ebd1d452682c922171cf77a10
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 9 (2015)
Alzheimer’s disease (AD) is the major cause of dementia in Western societies. It progresses asymptomatically during decades before being belatedly diagnosed when therapeutic strategies have become unviable. Although several genetic alterations have
Externí odkaz:
https://doaj.org/article/805e1e4bff6048729cbfaf04d8b4082a
Autor:
Alexia Martínez de Paz, Jose Vicente Sanchez-Mut, Mireia Samitier-Martí, Paolo Petazzi, Mauricio Sáez, Karolina Szczesna, Dori Huertas, Manel Esteller, Juan Ausió
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0123693 (2015)
Methyl CpG binding protein 2 (MeCP2) is a chromosomal protein of the brain, very abundant especially in neurons, where it plays an important role in the regulation of gene expression. Hence it has the potential to be affected by the mammalian circadi
Externí odkaz:
https://doaj.org/article/c5d7ada75f8047a5a4adb019d982a626
Autor:
Jose Vicente, Sanchez-Mut, Holger, Heyn, Enrique, Vidal, Raúl, Delgado-Morales, Sebastian, Moran, Sergi, Sayols, Juan, Sandoval, Isidre, Ferrer, Manel, Esteller, Johannes, Gräff
Publikováno v:
Synapse (New York, N.Y.). 71(6)
The brain's neocortex is anatomically organized into grey and white matter, which are mainly composed by neuronal and glial cells, respectively. The neocortex can be further divided in different Brodmann areas according to their cytoarchitectural org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7340151e690bcfe335565d887ea13535
https://pubmed.ncbi.nlm.nih.gov/28105729
https://pubmed.ncbi.nlm.nih.gov/28105729
Autor:
Gorka Ruiz de Garibay, Carmen Herranz, Alicia Llorente, Jacopo Boni, Jordi Serra-Musach, Francesca Mateo, Helena Aguilar, Laia Gómez-Baldó, Anna Petit, August Vidal, Fina Climent, Javier Hernández-Losa, Álex Cordero, Eva González-Suárez, José Vicente Sánchez-Mut, Manel Esteller, Roger Llatjós, Mar Varela, José Ignacio López, Nadia García, Ana I Extremera, Anna Gumà, Raúl Ortega, María Jesús Plà, Adela Fernández, Sònia Pernas, Catalina Falo, Idoia Morilla, Miriam Campos, Miguel Gil, Antonio Román, María Molina-Molina, Piedad Ussetti, Rosalía Laporta, Claudia Valenzuela, Julio Ancochea, Antoni Xaubet, Álvaro Casanova, Miguel Angel Pujana
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0207586 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0132546.].
Externí odkaz:
https://doaj.org/article/dc0dbc0392fc45b2a2f5604af88deb2e
Autor:
Gorka Ruiz de Garibay, Carmen Herranz, Alicia Llorente, Jacopo Boni, Jordi Serra-Musach, Francesca Mateo, Helena Aguilar, Laia Gómez-Baldó, Anna Petit, August Vidal, Fina Climent, Javier Hernández-Losa, Álex Cordero, Eva González-Suárez, José Vicente Sánchez-Mut, Manel Esteller, Roger Llatjós, Mar Varela, José Ignacio López, Nadia García, Ana I Extremera, Anna Gumà, Raúl Ortega, María Jesús Plà, Adela Fernández, Sònia Pernas, Catalina Falo, Idoia Morilla, Miriam Campos, Miguel Gil, Antonio Román, María Molina-Molina, Piedad Ussetti, Rosalía Laporta, Claudia Valenzuela, Julio Ancochea, Antoni Xaubet, Álvaro Casanova, Miguel Angel Pujana
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132546 (2015)
Lymphangioleiomyomatosis (LAM) is a rare lung-metastasizing neoplasm caused by the proliferation of smooth muscle-like cells that commonly carry loss-of-function mutations in either the tuberous sclerosis complex 1 or 2 (TSC1 or TSC2) genes. While al
Externí odkaz:
https://doaj.org/article/b96bd48beb8a4064a7f089bf1ac9af08