Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Carrasco-Rozas A"'
Autor:
Carrasco-Rozas, Ana, Fernández-Simón, Esther, Suárez-Calvet, Xavier, Piñol-Jurado, Patricia, Alonso-Pérez, Jorge, de Luna, Noemí, Schoser, Benedikt, Meinke, Peter, Domínguez-González, Cristina, Hernández-Laín, Aurelio, Paradas, Carmen, Rivas, Eloy, Illa, Isabel, Olivé, Montse, Gallardo, Eduard, Díaz-Manera, Jordi
Publikováno v:
In The American Journal of Pathology August 2022 192(8):1151-1166
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
Publikováno v:
Research Papers in Education; Aug2024, Vol. 39 Issue 4, p608-628, 21p
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:
Ana Carrasco‐Rozas, Esther Fernández‐Simón, Maria Cinta Lleixà, Izaskun Belmonte, Irene Pedrosa-Hernandez, Elena Montiel-Morillo, Claudia Nuñez‐Peralta, Jaume Llauger Rossello, Sonia Segovia, Noemí De Luna, Xavier Suarez‐Calvet, Isabel Illa, Pompe Spanish Study group, Jordi Díaz‐Manera, Eduard Gallardo
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1214-1224 (2019)
Abstract Objective To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). Methods We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expressio
Externí odkaz:
https://doaj.org/article/3d16d64d0a1c4c4685e9063dc785cefc
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
Publikováno v:
Research Papers in Education. :1-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2df4a48476a5506786064039b7a10fd3
https://doi.org/10.1080/02671522.2023.2188246
https://doi.org/10.1080/02671522.2023.2188246
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
Akademický článek
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Autor:
Fernández-Simón, Esther, Suarez-Calvet, Xavier, Carrasco-Rozas, Ana, Piñol-Jurado, Patricia, López-Fernández, Susana, Pons, Gemma, Bech Serra, Joan Josep, De La Torre Gómez, Gisela Carolina, de Luna Salva, Noemí, Gallardo, Eduard, Diaz-Manera, Jordi, Universitat Autònoma de Barcelona
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Universitat Autònoma de Barcelona
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, pathways activated by PDGF-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3447f13b5ec2c1e076469dec8ab58b68
https://doi.org/10.1002/jcsm.12923
https://doi.org/10.1002/jcsm.12923