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Page 1
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.
Int J Mol Sci. 2019 Sep 13;20(18):4548. doi: 10.3390/ijms20184548.
Int J Mol Sci. 2019.
PMID: 31540302
Free PMC article.
Review.
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 Mutations.
Lasa-Elgarresta J, Mosqueira-Martín L, González-Imaz K, Marco-Moreno P, Gerenu G, Mamchaoui K, Mouly V, López de Munain A, Vallejo-Illarramendi A.
Lasa-Elgarresta J, et al.
Front Cell Dev Biol. 2022 Mar 2;10:822563. doi: 10.3389/fcell.2022.822563. eCollection 2022.
Front Cell Dev Biol. 2022.
PMID: 35309930
Free PMC article.
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A genotyping method combining primer competition PCR with HRM analysis to identify point mutations in Duchenne animal models.
Lasa-Fernandez H, Mosqueira-Martín L, Alzualde A, Lasa-Elgarresta J, Vallejo-Illarramendi A.
Lasa-Fernandez H, et al. Among authors: lasa elgarresta j.
Sci Rep. 2020 Oct 14;10(1):17224. doi: 10.1038/s41598-020-74173-y.
Sci Rep. 2020.
PMID: 33057138
Free PMC article.
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Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle.
Toral-Ojeda I, Aldanondo G, Lasa-Elgarresta J, Lasa-Fernández H, Fernández-Torrón R, López de Munain A, Vallejo-Illarramendi A.
Toral-Ojeda I, et al. Among authors: lasa elgarresta j.
Expert Rev Mol Med. 2016 Apr 8;18:e7. doi: 10.1017/erm.2016.9.
Expert Rev Mol Med. 2016.
PMID: 27055500
Free PMC article.
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