Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Luis M Valor"'
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0255168 (2021)
During surgical procedures for gliomas, tissue material obtained from cavitational ultrasonic surgical aspirators (CUSAs) is generally discarded but can actually exceed the amount and quality of certain tumour core resections (TCRs). Despite reports
Externí odkaz:
https://doaj.org/article/9f561cba2e9f428bbda85a8e9027ed6a
Autor:
Luis M Valor, Beatriz Rodríguez-Bayona, Ana B Ramos-Amaya, José A Brieva, Antonio Campos-Caro
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183264 (2017)
Plasma cells (PC) represent the heterogeneous final stage of the B cells (BC) differentiation process. To characterize the transition of BC into PC, transcriptomes from human naïve BC were compared to those of three functionally-different subsets of
Externí odkaz:
https://doaj.org/article/0f9e6106e60349a6a8c5f6c840d90c47
Autor:
Fátima Cano-Cano, Francisco Martín-Loro, Andrea Gallardo-Orihuela, María del Carmen González-Montelongo, Samanta Ortuño-Miquel, Irati Hervás-Corpión, Pedro de la Villa, Lucía Ramón-Marco, Jorge Navarro-Calvo, Laura Gómez-Jaramillo, Ana I. Arroba, Luis M. Valor
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Huntington’s disease (HD) is caused by an aberrant expansion of CAG repeats in the HTT gene that mainly affects basal ganglia. Although striatal dysfunction has been widely studied in HD mouse models, other brain areas can also be relevant
Externí odkaz:
https://doaj.org/article/a28da4c6e3eb41bb8444b446f86c65cb
Autor:
Luis M Valor, Seth G N Grant
Publikováno v:
PLoS ONE, Vol 2, Iss 12, p e1303 (2007)
Gene expression profiling using microarrays is a powerful technology widely used to study regulatory networks. Profiling of mRNA levels in mutant organisms has the potential to identify genes regulated by the mutated protein.Using tissues from multip
Externí odkaz:
https://doaj.org/article/a2892cb2fb234aecb20eba191cd10182
Autor:
Luis M. Valor
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4310 (2023)
Huntington’s disease (HD) is a devastating neurodegenerative disorder caused by an aberrant expansion of CAG triplets in the HTT (Huntingtin) gene [...]
Externí odkaz:
https://doaj.org/article/22dcca34733c40a9aafb7fe38de88384
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2992 (2023)
The retina is among the highest organized tissues of the central nervous system. To achieve such organization, a finely tuned regulation of developmental processes is required to form the retinal layers that contain the specialized neurons and suppor
Externí odkaz:
https://doaj.org/article/cb421e2f0f8447eea88fb560f8457990
Autor:
Irati Hervás-Corpión, Jorge Navarro-Calvo, Paula Martín-Climent, Marianela Iriarte-Gahete, Noelia Geribaldi-Doldán, Carmen Castro, Luis M. Valor
Publikováno v:
Cells, Vol 12, Iss 3, p 374 (2023)
Glioblastoma (GB) is the most prevalent primary brain cancer and the most aggressive form of glioma because of its poor prognosis and high recurrence. To confirm the importance of epigenetics in glioma, we explored The Cancer Gene Atlas (TCGA) databa
Externí odkaz:
https://doaj.org/article/f2ecfb0a40ea4fc6b803abb082b73ea5
Autor:
Silvia Martí-Martínez, Luis M. Valor
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 10, p 5411 (2022)
Huntington’s disease (HD) is a devastating neurodegenerative disorder that is caused by an abnormal expansion of CAG repeats in the Huntingtin (HTT) gene. Although the main symptomatology is explained by alterations at the level of the central nerv
Externí odkaz:
https://doaj.org/article/be3456a1a1554d2080b5b126ad127394
Retinal affectation in Huntington’s disease mouse models concurs with a local innate immune response
Autor:
Ana I. Arroba, Andrea Gallardo-Orihuela, Fátima Cano-Cano, Francisco Martín-Loro, María del Carmen González-Montelongo, Irati Hervás-Corpión, Pedro de la Villa, Lucía Ramón-Marco, Laura Gómez-Jaramillo, Luis M. Valor
Huntington’s disease (HD) is a devastating disorder caused by aberrant expansion of CAG repeats in theHTTgene. Striatal dysfunction has been widely studied in HD mouse models. However, cumulative evidence indicates that the retina can also be funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f832a173c0c10ba0931026ff773b6f11
https://doi.org/10.1101/2023.01.17.523578
https://doi.org/10.1101/2023.01.17.523578
Autor:
Luis M Valor, Fátima Cano-Cano, Andrea Gallardo-Orihuela, Francisco Martín-Loro, M Carmen González-Montelongo, Irati Hervás-Corpión, Pedro de la Villa, Ana I Arroba
Publikováno v:
B: Models for HD.