Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Klaudia González-Imaz"'
Autor:
Judit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, Eduard Juanola, Jovan Pesovic, Laura Mosqueira-Martín, Klaudia González-Imaz, Pau Maestre-Mora, Renato Odria, Dusanka Savic-Pavicevic, Ainara Vallejo-Illarramendi, Kamel Mamchaoui, Anne Bigot, Vincent Mouly, Mònica Suelves, Gisela Nogales-Gadea
Publikováno v:
iScience, Vol 27, Iss 6, Pp 109930- (2024)
Summary: Historically, cellular models have been used as a tool to study myotonic dystrophy type 1 (DM1) and the validation of therapies in said pathology. However, there is a need for in vitro models that represent the clinical heterogeneity observe
Externí odkaz:
https://doaj.org/article/e85112638359466e8d35d548c2c3be05
Autor:
Jaione Lasa-Elgarresta, Laura Mosqueira-Martín, Klaudia González-Imaz, Pablo Marco-Moreno, Gorka Gerenu, Kamel Mamchaoui, Vincent Mouly, Adolfo López de Munain, Ainara Vallejo-Illarramendi
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
LGMDR1 is caused by mutations in the CAPN3 gene that encodes calpain 3 (CAPN3), a non-lysosomal cysteine protease necessary for proper muscle function. Our previous findings show that CAPN3 deficiency leads to reduced SERCA levels through increased p
Externí odkaz:
https://doaj.org/article/781cec8fc0a748d9a7ce4095f342d7ed
Autor:
Jaione Lasa-Elgarresta, Laura Mosqueira-Martín, Klaudia González-Imaz, Pablo Marco-Moreno, Gorka Gerenu, Kamel Mamchaoui, Vincent Mouly, Adolfo López de Munain, Ainara Vallejo-Illarramendi
Publikováno v:
Addi. Archivo Digital para la Docencia y la Investigación
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[EN] LGMDR1 is caused by mutations in the CAPN3 gene that encodes calpain 3 (CAPN3), a non-lysosomal cysteine protease necessary for proper muscle function. Our previous findings show that CAPN3 deficiency leads to reduced SERCA levels through increa