Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Xavier, Altafaj"'
Autor:
Xavier Altafaj, Ana Santos-Gómez, Adrián García-Recio, Federico Miguez-Cabello, David Soto, Mireia Olivella
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S71-S72 (2023)
Externí odkaz:
https://doaj.org/article/fe58e0b091804cebbe17cfb6824c56c7
Autor:
Mireia Olivella, Ana Santos-Gómez, Natalia Juliá-Palacios, Sílvia Locubiche Serra, David Soto, Àngels García-Cazorla, Xavier Altafaj
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S71- (2023)
Externí odkaz:
https://doaj.org/article/da16700c572d4667aeab98c75a1f6354
Autor:
Sílvia Locubiche Serra, Mireia Olivella, Flavia De Santis, Xavier Altafaj, Davide Rubbini, Javier Terriente
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S113- (2023)
Externí odkaz:
https://doaj.org/article/f46e99600ad14d478d203968f460d276
Autor:
Ana Santos-Gómez, Adrián García-Recio, Federico Miguez-Cabello, David Soto, Xavier Altafaj, Mireia Olivella
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
The clinical spectrum of GRIN-related neurodevelopmental disorders (GRD) results from gene- and variant-dependent primary alterations of the NMDA receptor, disturbing glutamatergic neurotransmission. Despite GRIN gene variants’ functional annotatio
Externí odkaz:
https://doaj.org/article/0648291dcb114d60a5ea10dded3f5c21
Autor:
Hannah Warming, Chrysia-Maria Pegasiou, Aleksandra P. Pitera, Hanna Kariis, Steven D. Houghton, Ksenia Kurbatskaya, Aminul Ahmed, Paul Grundy, Girish Vajramani, Diederik Bulters, Xavier Altafaj, Katrin Deinhardt, Mariana Vargas-Caballero
Publikováno v:
Molecular Brain, Vol 12, Iss 1, Pp 1-8 (2019)
Abstract Glutamate receptors of the N-methyl-D-aspartate (NMDA) family are coincident detectors of pre- and postsynaptic activity, allowing Ca2+ influx into neurons. These properties are central to neurological disease mechanisms and are proposed to
Externí odkaz:
https://doaj.org/article/a5400db007864598ab3bfb9dd2fff65d
Autor:
Nicolas Nalpas, Lesley Hoyles, Viktoria Anselm, Tariq Ganief, Laura Martinez-Gili, Cristina Grau, Irina Droste-Borel, Laetitia Davidovic, Xavier Altafaj, Marc-Emmanuel Dumas, Boris Macek
Publikováno v:
Gut Microbes, Vol 13, Iss 1 (2021)
Intestinal microbiota plays a key role in shaping host homeostasis by regulating metabolism, immune responses and behavior. Its dysregulation has been associated with metabolic, immune and neuropsychiatric disorders and is accompanied by changes in b
Externí odkaz:
https://doaj.org/article/d954ef4e0f404f5b8e59045d09517ca9
Autor:
Vincen Wu, Jocelyn Tillner, Emrys Jones, James S. McKenzie, Dipa Gurung, Anna Mroz, Liam Poynter, Daniel Simon, Cristina Grau, Xavier Altafaj, Marc-Emmanuel Dumas, Ian Gilmore, Josephine Bunch, Zoltan Takats
Publikováno v:
ANALYTICAL CHEMISTRY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
In this study, we examine the suitability of desorption electro-flow focusing ionization (DEFFI) for mass spectrometry imaging (MSI) of biological tissue. We also compare the performance of desorption electrospray ionization (DESI) with and without t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21d6ad0d564328d2ca31e5381995c88b
https://doi.org/10.1021/acs.analchem.2c00345
https://doi.org/10.1021/acs.analchem.2c00345
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Down syndrome (DS), the main genetic cause of intellectual disability, is associated with an imbalance of excitatory/inhibitory neurotransmitter systems. The phenotypic assessment and pharmacotherapy interventions in DS murine models strongly pointed
Externí odkaz:
https://doaj.org/article/fc349c8d96ce4465b22e68096f21c2c9
Autor:
Víctor Fernández-Dueñas, Andrea Pérez-Arévalo, Xavier Altafaj, Sergi Ferré, Francisco Ciruela
Publikováno v:
Frontiers in Neuroscience, Vol 11 (2017)
Externí odkaz:
https://doaj.org/article/1164b20cf5e5496f9072bafb6957e36e
Autor:
Xavier Altafaj, Eduardo D. Martín, Jon Ortiz-Abalia, Aitana Valderrama, Cristina Lao-Peregrín, Mara Dierssen, Cristina Fillat
Publikováno v:
Neurobiology of Disease, Vol 52, Iss , Pp 117-127 (2013)
The cognitive dysfunctions of Down Syndrome (DS) individuals are the most disabling alterations caused by the trisomy of human chromosome 21 (HSA21). In trisomic Ts65Dn mice, a genetic model for DS, the overexpression of HSA21 homologous genes has be
Externí odkaz:
https://doaj.org/article/708a6ae4ef8d4bb9b8c8cf2afa7fc8ac