Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Carla Sánchez-Castillo"'
Autor:
María José Ruiz-Pastor, Xavier Sánchez-Sáez, Oksana Kutsyr, Henar Albertos-Arranz, Carla Sánchez-Castillo, Isabel Ortuño-Lizarán, Natalia Martínez-Gil, Lorena Vidal-Gil, Lucía Méndez, Manuel Sánchez-Martín, Victoria Maneu, Pedro Lax, Nicolás Cuenca
Publikováno v:
Cell Death and Disease, Vol 14, Iss 11, Pp 1-17 (2023)
Abstract Central areolar choroidal dystrophy is an inherited disorder characterized by progressive choriocapillaris atrophy and retinal degeneration and is usually associated with mutations in the PRPH2 gene. We aimed to generate and characterize a m
Externí odkaz:
https://doaj.org/article/e0e59e4df12f4f508050012bf7b865b6
Autor:
Xavier Sánchez-Sáez, Isabel Ortuño-Lizarán, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca
Publikováno v:
Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-16 (2023)
Abstract Background The main clinical symptoms characteristic of Parkinson’s disease (PD) are bradykinesia, tremor, and other motor deficits. However, non-motor symptoms, such as visual disturbances, can be identified at early stages of the disease
Externí odkaz:
https://doaj.org/article/00736fbb7bb444c692ce47c80c3b6da4
Autor:
Natalia Martínez-Gil, Oksana Kutsyr, Laura Fernández-Sánchez, Xavier Sánchez-Sáez, Henar Albertos-Arranz, Carla Sánchez-Castillo, Lorena Vidal-Gil, Nicolás Cuenca, Pedro Lax, Victoria Maneu
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 22, p 16068 (2023)
Ischemia is the main cause of cell death in retinal diseases such as vascular occlusions, diabetic retinopathy, glaucoma, or retinopathy of prematurity. Although excitotoxicity is considered the primary mechanism of cell death during an ischemic even
Externí odkaz:
https://doaj.org/article/0e5b7b978401425ebc2e9aff31acb68d
Autor:
Natalia Martínez-Gil, Victoria Maneu, Oksana Kutsyr, Laura Fernández-Sánchez, Xavier Sánchez-Sáez, Carla Sánchez-Castillo, Laura Campello, Pedro Lax, Isabel Pinilla, Nicolás Cuenca
Publikováno v:
Frontiers in Neuroanatomy, Vol 16 (2022)
Multiple gene mutations have been associated with inherited retinal dystrophies (IRDs). Despite the spectrum of phenotypes caused by the distinct mutations, IRDs display common physiopathology features. Cell death is accompanied by inflammation and o
Externí odkaz:
https://doaj.org/article/e4a407effc654617ac0f4079c932c0a3
Autor:
Xavier Sánchez‑Sáez, Isabel Ortuño‑Lizarán, Carla Sánchez‑Castillo, Pedro Lax, Nicolás Cuenca
Publikováno v:
Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/89d1fa55fcc2406bb915a514d1ff20e2
Autor:
Natalia Martínez-Gil, Oksana Kutsyr, Agustina Noailles, Laura Fernández-Sánchez, Lorena Vidal, Xavier Sánchez-Sáez, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca, Antonio G. García, Victoria Maneu
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 23, p 14758 (2022)
The purinergic receptor P2X7 (P2X7R) is implicated in all neurodegenerative diseases of the central nervous system. It is also involved in the retinal degeneration associated with glaucoma, age-related macular degeneration, and diabetic retinopathy,
Externí odkaz:
https://doaj.org/article/b4a7ea34f6244840a289891e44d24a36
Autor:
Pau B Esparza-Moltó, Inés Romero-Carramiñana, Cristina Núñez de Arenas, Marta P Pereira, Noelia Blanco, Beatriz Pardo, Georgina R Bates, Carla Sánchez-Castillo, Rafael Artuch, Michael P Murphy, José A Esteban, José M Cuezva
Publikováno v:
PLoS Biology, Vol 19, Iss 5, p e3001252 (2021)
The mitochondrial ATP synthase emerges as key hub of cellular functions controlling the production of ATP, cellular signaling, and fate. It is regulated by the ATPase inhibitory factor 1 (IF1), which is highly abundant in neurons. Herein, we ablated
Externí odkaz:
https://doaj.org/article/3c469b3a87654a168245043c7e61234d
Autor:
Isabel Pinilla, Victoria Maneu, Laura Campello, Laura Fernández-Sánchez, Natalia Martínez-Gil, Oksana Kutsyr, Xavier Sánchez-Sáez, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca
Publikováno v:
Antioxidants, Vol 11, Iss 6, p 1086 (2022)
Inherited retinal dystrophies (IRDs) are a large group of genetically and clinically heterogeneous diseases characterized by the progressive degeneration of the retina, ultimately leading to loss of visual function. Oxidative stress and inflammation
Externí odkaz:
https://doaj.org/article/43c7198d3a4649b187f7588e2711ff7f
Autor:
Xavier Sanchez Saez, Isabel Ortuno‐Lizaran, Carla Sánchez Castillo, Lorena Vidal‐Gil, Victoria Maneu, Pedro Lax, Nicolas Cuenca
Publikováno v:
Acta Ophthalmologica. 100
Autor:
Carla Sánchez-Castillo, María I. Cuartero, Alba Fernández-Rodrigo, Víctor Briz, Sergio López-García, Raquel Jiménez-Sánchez, Juan A. López, Mariona Graupera, José A. Esteban
Neuronal connectivity and activity-dependent synaptic plasticity are fundamental properties that support brain function and cognitive performance. Phosphatidylinositol 3-kinase (PI3K) intracellular signaling controls multiple mechanisms mediating neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a28e65ca92fb379582336d7376f28d
https://hdl.handle.net/10045/129894
https://hdl.handle.net/10045/129894