Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Patricia Piñol‐Jurado"'
Autor:
Esther Fernández-Simón, Patricia Piñol-Jurado, Rasya Gokul-Nath, Adrienne Unsworth, Jorge Alonso-Pérez, Marianela Schiava, Andres Nascimento, Giorgio Tasca, Rachel Queen, Dan Cox, Xavier Suarez-Calvet, Jordi Díaz-Manera
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Background: Duchenne muscular dystrophy is a genetic disease produced by mutations in the dystrophin gene characterized by early onset muscle weakness leading to severe and irreversible disability. Muscle degeneration involves a complex interplay bet
Externí odkaz:
https://doaj.org/article/c79c38608dbf4e30a0c73d3b15edbb5a
Autor:
Patricia Piñol-Jurado, José Verdú-Díaz, Esther Fernández-Simón, Cristina Domínguez-González, Aurelio Hernández-Lain, Conor Lawless, Amy Vincent, Alejandro González-Chamorro, Elisa Villalobos, Alexandra Monceau, Zoe Laidler, Priyanka Mehra, James Clark, Andrew Filby, David McDonald, Paul Rushton, Andrew Bowey, Jorge Alonso Pérez, Giorgio Tasca, Chiara Marini-Bettolo, Michela Guglieri, Volker Straub, Xavier Suárez-Calvet, Jordi Díaz-Manera
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Becker muscular dystrophy (BMD) is characterised by fiber loss and expansion of fibrotic and adipose tissue. Several cells interact locally in what is known as the degenerative niche. We analysed muscle biopsies of controls and BMD patients
Externí odkaz:
https://doaj.org/article/61a0d77c3dfe43de98fb8cb832575a27
Autor:
Esther Fernández‐Simón, Xavier Suárez‐Calvet, Ana Carrasco‐Rozas, Patricia Piñol‐Jurado, Susana López‐Fernández, Gemma Pons, Joan Josep Bech Serra, Carolina de laTorre, Noemí deLuna, Eduard Gallardo, Jordi Díaz‐Manera
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 13, Iss 2, Pp 1373-1384 (2022)
Abstract Background The lack of dystrophin expression in Duchenne muscular dystrophy (DMD) induces muscle fibre and replacement by fibro‐adipose tissue. Although the role of some growth factors in the process of fibrogenesis has been studied, pathw
Externí odkaz:
https://doaj.org/article/8197b823bac74496a80deffb2f41763a
Autor:
Jorge Alonso-Pérez, Ana Carrasco-Rozas, Maria Borrell-Pages, Esther Fernández-Simón, Patricia Piñol-Jurado, Lina Badimon, Lutz Wollin, Cinta Lleixà, Eduard Gallardo, Montse Olivé, Jordi Díaz-Manera, Xavier Suárez-Calvet
Publikováno v:
Biomedicines, Vol 10, Iss 10, p 2629 (2022)
Sarcoglycanopathies are a group of recessive limb-girdle muscular dystrophies, characterized by progressive muscle weakness. Sarcoglycan deficiency produces instability of the sarcolemma during muscle contraction, leading to continuous muscle fiber i
Externí odkaz:
https://doaj.org/article/e87888f2dbfb4a99bacc0ccf348e687b
Autor:
Alicia Alonso-Jiménez, Esther Fernández-Simón, Daniel Natera-de Benito, Carlos Ortez, Carme García, Elena Montiel, Izaskun Belmonte, Irene Pedrosa, Sonia Segovia, Patricia Piñol-Jurado, Ana Carrasco-Rozas, Xavier Suárez-Calvet, Cecilia Jimenez-Mallebrera, Andrés Nascimento, Jaume Llauger, Claudia Nuñez-Peralta, Paula Montesinos, Jorge Alonso-Pérez, Eduard Gallardo, Isabel Illa, Jordi Díaz-Manera
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Duchenne (DMD) and Becker (BMD) muscular dystrophy are X-linked muscular disorders produced by mutations in the DMD gene which encodes the protein dystrophin. Both diseases are characterized by progressive involvement of skeletal, cardi
Externí odkaz:
https://doaj.org/article/71b9634a1f1544c0bdd507c958aefd2e
Autor:
Ana Carrasco-Rozas, Esther Fernández-Simón, Xavier Suárez-Calvet, Patricia Piñol-Jurado, Jorge Alonso-Pérez, Noemí de Luna, Benedikt Schoser, Peter Meinke, Cristina Domínguez-González, Aurelio Hernández-Laín, Carmen Paradas, Eloy Rivas, Isabel Illa, Montse Olivé, Eduard Gallardo, Jordi Díaz-Manera
Publikováno v:
The American Journal of Pathology. 192:1151-1166
Late-onset Pompe disease (LOPD) is a rare genetic disorder produced by mutations in the GAA gene and is characterized by progressive muscle weakness. LOPD muscle biopsies show accumulation of glycogen along with the autophagic vacuoles associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9863e23dad98ac435cb5d53e8332455a
https://doi.org/10.1016/j.ajpath.2022.05.003
https://doi.org/10.1016/j.ajpath.2022.05.003
Autor:
Jordi Diaz-Manera, Ana Carrasco, Esther Fernández-Simon, Xavier Suarez-Calvet, Patricia Piñol-Jurado, Jorge Alonso-Perez, Benedikt Schoser, Cristina Domínguez-González, Carmen Paradas, Eduard Gallardo
Publikováno v:
Molecular Genetics and Metabolism. 135:S37-S38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::381d36c335979429e1b16622aa9fe990
https://doi.org/10.1016/j.ymgme.2021.11.083
https://doi.org/10.1016/j.ymgme.2021.11.083
Autor:
Jordi-Díaz-Manera, Xavier Suárez-Calvet, Patricia Piñol-Jurado, Eduard Gallardo, Bech Serra Jj, E. Fernández-Simón, S. López-Fernández, Ana Carrasco-Rozas, de la Torre C, de Luna N
The lack of dystrophin expression in Duchenne muscular dystrophy (DMD) leads to muscle necrosis and replacement of muscle tissue by fibro-adipose tissue. Although the role of some growth factors in the process of fibrogenesis has been previously stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4a7b9ce17a683479c8fcb2ddb7246e7
https://doi.org/10.1101/2021.04.12.439417
https://doi.org/10.1101/2021.04.12.439417
Autor:
Jyoti K. Jaiswal, Anne Bigot, E. Fernández-Simón, Patricia Piñol-Jurado, G. Pons, Xavier Suárez-Calvet, L. Soria, Ana Carrasco-Rozas, J. Diaz-Manera, E. Gallardo, Cinta Lleixà, S. López-Fernández, Jorge Alonso-Pérez, Isabel Illa
Publikováno v:
Neuromuscular Disorders. 31:S143-S144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8f924de29970696e2d04b177628cab
https://doi.org/10.1016/j.nmd.2021.07.333
https://doi.org/10.1016/j.nmd.2021.07.333
Autor:
Vincent Mouly, Anne Bigot, Xavier Suárez-Calvet, Susana López-Fernández, Jorge Alonso-Pérez, Gemma Pons, Eduard Gallardo, Patricia Piñol-Jurado, Isabel Illa, Jyoti K. Jaiswal, E. Fernández-Simón, Jordi Diaz-Manera, Cinta Lleixà, Ana Carrasco-Rozas, Laura Soria
Publikováno v:
FASEB JOURNAL
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2021, 35 (9), ⟨10.1096/fj.202100588R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2021, 35 (9), ⟨10.1096/fj.202100588r⟩
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2021, 35 (9), ⟨10.1096/fj.202100588R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2021, 35 (9), ⟨10.1096/fj.202100588r⟩
Altres ajuts: Association Française contre les Myopathies (22525) Altres ajuts: Fundación Isabel Gemio Skeletal muscle contains multiple cell types that work together to maintain tissue homeostasis. Among these, satellite cells (SC) and fibroadipog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::205a795043620af71b716fd89e297f2c
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4387
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4387