Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Jose M. Vidal-Taboada"'
Autor:
Carlos Cruchaga, Jose M. Vidal-Taboada, Mario Ezquerra, Elena Lorenzo, Pablo Martinez-Lage, Marta Blazquez, Eduardo Tolosa, Pau Pastor
Publikováno v:
Neurobiology of Disease, Vol 33, Iss 2, Pp 164-170 (2009)
Two different H1 sub-haplotypes at chromosome 17q21, H1C and H1E′A, have been associated with progressive supranuclear palsy (PSP) and cortical basal degeneration (CBD). We analyzed the SNPs included in the H1C and H1E′A haplotypes in a large Spa
Externí odkaz:
https://doaj.org/article/35e2ad79dee54b4daf6cfe112b1d5763
Autor:
Daniel Sanchez-Tejerina, Arnau Llaurado, Javier Sotoca, Veronica Lopez-Diego, Jose M. Vidal Taboada, Maria Salvado, Raul Juntas-Morales
Publikováno v:
Cells, Vol 12, Iss 8, p 1180 (2023)
Amyotrophic lateral sclerosis is a neurodegenerative disease characterized by the degeneration of motor neurons for which effective therapies are lacking. One of the most explored areas of research in ALS is the discovery and validation of biomarkers
Externí odkaz:
https://doaj.org/article/4f61f3b00db344e995bebe327e6837b7
Autor:
Alan Lopez-Lopez, Josep Gamez, Emilio Syriani, Miguel Morales, Maria Salvado, Manuel J Rodríguez, Nicole Mahy, Jose M Vidal-Taboada
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96528 (2014)
The objective of this study was to investigate the association of functional variants of the human CX3CR1 gene (Fractalkine receptor) with the risk of Amyotrophic Lateral Sclerosis (ALS), the survival and the progression rate of the disease symptoms
Externí odkaz:
https://doaj.org/article/05d08c4cbb274de394f76b842f83cd31
Autor:
Josep Gamez, Nicole Mahy, Maria Salvado, Manuel J. Rodriguez, Marco Pugliese, Jose M. Vidal-Taboada
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
The ATP-sensitive potassium (KATP) channel directly regulates the microglia-mediated inflammatory response following CNS injury. To determine the putative role of the KATP channel in amyotrophic lateral sclerosis (ALS) pathology, we investigated whet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1848e08ad8a1d53b3fa60336b1030501
http://hdl.handle.net/2445/126265
http://hdl.handle.net/2445/126265
Publikováno v:
Progress in Neurobiology. 132:1-33
CCAAT/enhancer binding protein (C/EBP) β and C/EBPδ are transcription factors of the basic-leucine zipper class which share phylogenetic, structural and functional features. In this review we first describe in depth their basic molecular biology wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b2b51424be1af6083d80334e4bedac
https://doi.org/10.1016/j.pneurobio.2015.06.003
https://doi.org/10.1016/j.pneurobio.2015.06.003
Publikováno v:
Molecular neurobiology. 55(3)
Neuroinflammation and microglial dysfunction have a prominent role in the pathogenesis of late-onset Alzheimer's disease (LOAD). CX3CR1 is a microglia-specific gene involved in microglia-neuron crosstalk and neuroinflammation. Numerous evidence show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edceba483fdde1a640360c01fcd83729
https://pubmed.ncbi.nlm.nih.gov/28343297
https://pubmed.ncbi.nlm.nih.gov/28343297
Publikováno v:
FEM: Revista de la Fundación Educación Médica v.22 n.1 2019
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
espanolIntroduccion. El proceso de adaptacion al Espacio Europeo de Educacion Superior ha comportado cambios en los sistemas de evaluacion de los aprendizajes en las facultades de medicina y ha introducido los conceptos de evaluacion de compe- tencia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba6865c27d1195726e66604ce1595fc9
https://doi.org/10.33588/fem.221.980
https://doi.org/10.33588/fem.221.980
Autor:
Judit Castillo, Meritxell Jodar, Jose M. Vidal-Taboada, Josep Oriola, Josep Lluís Ballescà, Rafael Oliva, G Mestre, Aleksander Giwercman
Publikováno v:
International Journal of Andrology. 34:470-485
Protamines are the most abundant nuclear proteins and alterations in their expression have been described in infertile patients. Also, protamine haplo-insufficient mice have been described as infertile. Therefore, the protamine 1 and 2 genes have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eca3464ddbf59fb41dbd862cc991a93
https://doi.org/10.1111/j.1365-2605.2010.01115.x
https://doi.org/10.1111/j.1365-2605.2010.01115.x
Autor:
Jose C. Masdeu, Jose M. Vidal-Taboada, Mario Riverol, Pau Pastor, Lluis Samaranch, Maria A. Pastor, Elena Lorenzo, Jaione Irigoyen, P. de Castro
Publikováno v:
Neurology. 71:332-336
Background: Autosomal recessive hereditary spastic paraparesis with thin corpus callosum (ARHSP-TCC) is being increasingly recognized as a variety of spastic paraplegia with mental retardation. SPG11 gene mutations have been reported to be associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::624e034d2f010c00c7ebc00c01e34c6f
https://doi.org/10.1212/01.wnl.0000319646.23052.d1
https://doi.org/10.1212/01.wnl.0000319646.23052.d1
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. 101:132-137
As pharmacogenetic studies frequently require establishment of DNA banks containing large cohorts with multi-centric designs, inexpensive methods for collecting and storing high-quality DNA are needed. The aims of this study were two-fold: to compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b34f8586fe75ec868751906bb21e67
https://doi.org/10.1111/j.1742-7843.2007.00089.x
https://doi.org/10.1111/j.1742-7843.2007.00089.x