Zobrazeno 1 - 10
of 26
pro vyhledávání: '"María T. Berciano"'
Autor:
Marián Mantecón-Oria, Olga Tapia, Miguel Lafarga, María T. Berciano, Jose M. Munuera, Silvia Villar-Rodil, Juan I. Paredes, María J. Rivero, Nazely Diban, Ane Urtiaga
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Composites of polymer and graphene-based nanomaterials (GBNs) combine easy processing onto porous 3D membrane geometries due to the polymer and cellular differentiation stimuli due to GBNs fillers. Aiming to step forward to the clinical appl
Externí odkaz:
https://doaj.org/article/fd2af4957ef64a2097c573b8b9ebf7c8
Autor:
Nazely Diban, Marián Mantecón-Oria, María T. Berciano, Alba Puente-Bedia, María J. Rivero, Ane Urtiaga, Miguel Lafarga, Olga Tapia
Publikováno v:
Cancer Nanotechnology, Vol 13, Iss 1, Pp 1-29 (2022)
Abstract Background Recent advances from studies of graphene and graphene-based derivatives have highlighted the great potential of these nanomaterials as migrastatic agents with the ability to modulate tumor microenvironments. Nevertheless, the admi
Externí odkaz:
https://doaj.org/article/3a5f3fc9f620408e84e688b76055fd1a
Publikováno v:
Antioxidants, Vol 11, Iss 12, p 2438 (2022)
Oxidative stress (OS) is one of the neuropathological mechanisms responsible for the deficits in cognition and neuronal function in Down syndrome (DS). The Ts65Dn (TS) mouse replicates multiple DS phenotypes including hippocampal-dependent learning a
Externí odkaz:
https://doaj.org/article/4b7788844856437dae89dfdd476ca29d
Autor:
Fernando C. Baltanás, María T. Berciano, Olga Tapia, Josep Oriol Narcis, Vanesa Lafarga, David Díaz, Eduardo Weruaga, Eugenio Santos, Miguel Lafarga
Publikováno v:
Neurobiology of Disease, Vol 127, Iss , Pp 312-322 (2019)
The Purkinje cell (PC) degeneration (pcd) mouse harbors a mutation in Agtpbp1 gene that encodes for the cytosolic carboxypeptidase, CCP1. The mutation causes degeneration and death of PCs during the postnatal life, resulting in clinical and pathologi
Externí odkaz:
https://doaj.org/article/3c29c9e9d4924c1983c4ed0e0463de9f
Autor:
Raquel de la Hoz, Nazely Diban, María T. Berciano, Carlos San Emeterio, Ane Urtiaga, Miguel Lafarga, José C. Rodríguez-Rey, Olga Tapia
Publikováno v:
Biomolecules, Vol 12, Iss 8, p 1012 (2022)
In this work, we performed a methodological comparative analysis to synthesize polyethyleneimine (PEI) nanoparticles using (i) conventional nanoprecipitation (NP), (ii) electrospraying (ES), and (iii) coaxial electrospraying (CA). The nanoparticles t
Externí odkaz:
https://doaj.org/article/5ecc6f46814142d3890d530444070f35
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Introduction: Amyotrophic lateral sclerosis (ALS) might not only be circumscribed to the motor system but also involves other neuronal systems including sensory abnormalities. In line with this notion, we aimed to assess the pathophysiology of sensor
Externí odkaz:
https://doaj.org/article/00871c42f6c64e93b0f10f25fbd536af
Publikováno v:
Biomedicines, Vol 9, Iss 9, p 1157 (2021)
Recent reports have identified rare, biallelic damaging variants of the AGTPBP1 gene that cause a novel and documented human disease known as childhood-onset neurodegeneration with cerebellar atrophy (CONDCA), linking loss of function of the AGTPBP1
Externí odkaz:
https://doaj.org/article/c38472fb8c8342c0ac398f5c7885c97d
Autor:
Alba Puente-Bedia, María T. Berciano, Olga Tapia, Carmen Martínez-Cué, Miguel Lafarga, Noemí Rueda
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 3, p 1259 (2021)
Down syndrome (DS) or trisomy of chromosome 21 (Hsa21) is characterized by impaired hippocampal-dependent learning and memory. These alterations are due to defective neurogenesis and to neuromorphological and functional anomalies of numerous neuronal
Externí odkaz:
https://doaj.org/article/99695426151f42e1bfa681b725ad60ac
Autor:
Rocío Bengoechea, Olga Tapia, Iñigo Casafont, José Berciano, Miguel Lafarga, María T. Berciano
Publikováno v:
Neurobiology of Disease, Vol 46, Iss 1, Pp 118-129 (2012)
Nuclear speckles are essential nuclear compartments involved in the assembly, delivery and recycling of pre-mRNA processing factors, and in the post-transcriptional processing of pre-mRNAs. Oculopharyngeal muscular dystrophy (OPMD) is caused by a sma
Externí odkaz:
https://doaj.org/article/baadb5819e514ebdb57ed557f8b1bed9
Autor:
José, Berciano, Elena, Gallardo, María J, Sedano, Pedro, Orizaola, Pascual, Sánchez-Juan, Andrea, González-Suárez, Antonio, García, Nuria, Terán-Villagrá, María, Ruiz-Soto, Rosa, Landeras-Álvaro, María T, Berciano, Miguel, Lafarga
Publikováno v:
Journal of the peripheral nervous system : JPNS. 19(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b5b65c8b00270f1b020555ff9538923
https://pubmed.ncbi.nlm.nih.gov/25418824
https://pubmed.ncbi.nlm.nih.gov/25418824