Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ana Pilar Gómez-Escribano"'
Autor:
Joan Carles Puchalt, Jose F. Gonzalez-Rojo, Ana Pilar Gómez-Escribano, Rafael P. Vázquez-Manrique, Antonio-José Sánchez-Salmerón
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Data from manual healthspan assays of the nematode Caenorhabditis elegans (C. elegans) can be complex to quantify. The first attempts to quantify motor performance were done manually, using the so-called thrashing or body bends assay. Some l
Externí odkaz:
https://doaj.org/article/a3444856d0d346b8a411a2f74aef0cbd
Autor:
Emma Koehorst, Judit Núñez-Manchón, Alfonsina Ballester-López, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Jakub Chojnacki, Rafael P. Vázquez-Manrique, Ana Pilar Gómez-Escribano, Guillem Pintos-Morell, Jaume Coll-Cantí, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Mònica Suelves, Gisela Nogales-Gadea
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 23, p 5520 (2021)
Myotonic Dystrophy type 1 (DM1) is a muscular dystrophy with a multi-systemic nature. It was one of the first diseases in which repeat associated non-ATG (RAN) translation was described in 2011, but has not been further explored since. In order to en
Externí odkaz:
https://doaj.org/article/b68277af270c4aeaafa08277017bb75c
Autor:
José Bono-Yagüe, Ana Pilar Gómez-Escribano, José María Millán, Rafael Pascual Vázquez-Manrique
Publikováno v:
Antioxidants, Vol 9, Iss 7, p 577 (2020)
Huntington disease (HD) is a neurodegenerative condition and one of the so-called rare or minority diseases, due to its low prevalence (affecting 1–10 of every 100,000 people in western countries). The causative gene, HTT, encodes huntingtin, a pro
Externí odkaz:
https://doaj.org/article/07ea54a2d80b42f4b6decf1bf9e1534a
Autor:
David Hervás, Victoria Fornés-Ferrer, Ana Pilar Gómez-Escribano, María Dolores Sequedo, Carmen Peiró, José María Millán, Rafael P Vázquez-Manrique
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179283 (2017)
Huntington's disease (HD) is an inherited, dominant neurodegenerative disorder caused by an abnormal expansion of CAG triplets in the huntingtin gene (htt). Despite extensive efforts to modify the progression of HD thus far only symptomatic treatment
Externí odkaz:
https://doaj.org/article/90fd00af281947b99272d6ae6b2f5139
Autor:
Cristina Trujillo-Del Río, Julia Tortajada-Pérez, Mar Collado-Pérez, Andrea Carranza, Ana Pilar Gómez-Escribano, José María Millán, Rafael Vázquez-Manrique
Publikováno v:
A: Pathogenic mechanisms.
Autor:
Julia Tortajada-Pérez, Cristina Trujillo-Del Río, Mar Collado-Pérez, Ana Pilar Gómez-Escribano, José María Millán, Rafael Vázquez-Manrique
Publikováno v:
A: Pathogenic mechanisms.
Autor:
David, Brinvillier, Melissa, Barrast, Petra, Couderc-Murillo, José, Bono-Yagüe, Alain, Rousteau, Ana Pilar, Gómez Escribano, Marcos V, Palmeira-Mello, Antonio, Doménech-Carbó, Nady, Passe-Coutrin, Muriel, Sylvestre, Rafael P, Vázquez-Manrique, Gerardo, Cebrián-Torrejón
Publikováno v:
ACS omega. 7(19)
Neurodegenerative disorders, caused by prone-to-aggregation proteins, such as Alzheimer disease or Huntington disease, share other traits such as disrupted homeostasis of essential metal ions, like copper. In this context, in an attempt to identify C
Autor:
S. C. Torres-Sánchez, José Bono-Yagüe, María Dolores Sequedo, V. Fornés-Ferrer, JM Millán, Pascual Sanz, Maria Adelaida Garcia-Gimeno, David Hervás, Ana Pilar Gómez-Escribano, Rafael P. Vázquez-Manrique
Publikováno v:
PHARMACOLOGICAL RESEARCH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Digital.CSIC. Repositorio Institucional del CSIC
Pharmacological research
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Digital.CSIC. Repositorio Institucional del CSIC
Pharmacological research
11 páginas, 4 figuras. Supplementary material related to this article can be found, in the online version, at doi: https://doi.org/10.1016/j.phrs.2020.105105.
Expression of abnormally long polyglutamine (polyQ) tracks is the source of a range o
Expression of abnormally long polyglutamine (polyQ) tracks is the source of a range o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc3673aa7815898f2203a6aa5b51d7b9
http://hdl.handle.net/10261/219295
http://hdl.handle.net/10261/219295
Publikováno v:
Antioxidants, Vol 9, Iss 577, p 577 (2020)
Antioxidants
Antioxidants
Huntington disease (HD) is a neurodegenerative condition and one of the so-called rare or minority diseases, due to its low prevalence (affecting 1–10 of every 100,000 people in western countries). The causative gene, HTT, encodes huntingtin, a pro
Autor:
María Yáñez-Mó, Francisco Domínguez, Roberto González-Martín, Silvia Pérez-Debén, Alicia Quiñonero, Soraya López-Martín, Stefania Salsano, Ana Pilar Gómez-Escribano
Publikováno v:
FERTILITY AND STERILITY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Objective: To investigate PGRMC1-precipitating proteins in human endometrial stromal cells (ESC) to understand its role during in vitro decidualization. Design: Prospective observational study. Setting: Academic fertility center. Patient(s): Fifteen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7527ece5fa0070f94e0c9134936ed547
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=12825
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=12825