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Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis.
Cocchiararo I, Cattaneo O, Rajendran J, Chabry F, Cornut M, Soldati H, Bigot A, Mamchaoui K, Gibertini S, Bouche A, Ham DJ, Laumonier T, Prola A, Castets P. Cocchiararo I, et al. Among authors: prola a. Hum Mol Genet. 2023 Dec 1;32(24):3374-3389. doi: 10.1093/hmg/ddad164. Hum Mol Genet. 2023. PMID: 37756622 Free PMC article.
Hacd2 deficiency in mice leads to an early and lethal mitochondrial disease.
Khadhraoui N, Prola A, Vandestienne A, Blondelle J, Guillaud L, Courtin G, Bodak M, Prost B, Huet H, Wintrebert M, Péchoux C, Solgadi A, Relaix F, Tiret L, Pilot-Storck F. Khadhraoui N, et al. Among authors: prola a. Mol Metab. 2023 Mar;69:101677. doi: 10.1016/j.molmet.2023.101677. Epub 2023 Jan 21. Mol Metab. 2023. PMID: 36693621 Free PMC article.
Platelets facilitate the wound-healing capability of mesenchymal stem cells by mitochondrial transfer and metabolic reprogramming.
Levoux J, Prola A, Lafuste P, Gervais M, Chevallier N, Koumaiha Z, Kefi K, Braud L, Schmitt A, Yacia A, Schirmann A, Hersant B, Sid-Ahmed M, Ben Larbi S, Komrskova K, Rohlena J, Relaix F, Neuzil J, Rodriguez AM. Levoux J, et al. Among authors: prola a. Cell Metab. 2021 Mar 2;33(3):688-690. doi: 10.1016/j.cmet.2021.02.003. Cell Metab. 2021. PMID: 33657394 Free article. No abstract available.
Cardiolipin content controls mitochondrial coupling and energetic efficiency in muscle.
Prola A, Blondelle J, Vandestienne A, Piquereau J, Denis RGP, Guyot S, Chauvin H, Mourier A, Maurer M, Henry C, Khadhraoui N, Gallerne C, Molinié T, Courtin G, Guillaud L, Gressette M, Solgadi A, Dumont F, Castel J, Ternacle J, Demarquoy J, Malgoyre A, Koulmann N, Derumeaux G, Giraud MF, Joubert F, Veksler V, Luquet S, Relaix F, Tiret L, Pilot-Storck F. Prola A, et al. Sci Adv. 2021 Jan 1;7(1):eabd6322. doi: 10.1126/sciadv.abd6322. Print 2021 Jan. Sci Adv. 2021. PMID: 33523852 Free PMC article.
30 results