Actualités

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. Hum Mol...

11 octobre 2023

Fast, multiplexable and efficient somatic gene deletions in adult mouse skeletal muscle fibers using AAV-CRISPR/Cas9.

Thürkauf M, Lin S, Oliveri F, Grimm D, Platt RJ, Rüegg MA. Nat Commun. 2023 Sep 30;14(1):6116.

30 septembre 2023

Loss of TDP-43 oligomerization or RNA binding elicits distinct aggregation patterns.

Pérez-Berlanga M, Wiersma VI, Zbinden A, De Vos L, Wagner U, Foglieni C, Mallona I, Betz KM, Cléry A, Weber J, Guo Z, Rigort R, de Rossi P, Manglunia R, Tantardini E,...

04 septembre 2023

SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS.

Lone MA, Zeng S, Bourquin F, Wang M, Huang S, Lin Z, Tang B, Zhang R, Hornemann T. Biochim Biophys Acta Mol Cell Biol Lipids. 2023 Sep;1868(9):159359.

01 septembre 2023

Transgene-free direct conversion of murine fibroblasts into functional muscle stem cells.

Qabrati X, Kim I, Ghosh A, Bundschuh N, Noé F, Palmer AS, Bar-Nur O. NPJ Regen Med. 2023 Aug 8;8(1):43.

08 août 2023

Guideline "Motor neuron diseases" of the German Society of Neurology (Deutsche Gesellschaft für Neurologie).

Petri S, Grehl T, Grosskreutz J, Hecht M, Hermann A, Jesse S, Lingor P, Löscher W, Maier A, Schoser B, Weber M, Ludolph AC. Neurol Res Pract. 2023 Jun 15;5(1):25.

15 juin 2023

The mitochondrial calcium uniporter (MCU) activates mitochondrial respiration and enhances mobility by regulating mitochondrial redox state.

Weiser A, Hermant A, Bermont F, Sizzano F, Karaz S, Alvarez-Illera P, Santo-Domingo J, Sorrentino V, Feige JN, De Marchi U. Redox Biol. 2023 Jun 4;64:102759.

04 juin 2023

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Actualités

Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis.

Fast, multiplexable and efficient somatic gene deletions in adult mouse skeletal muscle fibers using AAV-CRISPR/Cas9.

Loss of TDP-43 oligomerization or RNA binding elicits distinct aggregation patterns.

SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS.

Transgene-free direct conversion of murine fibroblasts into functional muscle stem cells.

Guideline "Motor neuron diseases" of the German Society of Neurology (Deutsche Gesellschaft für Neurologie).

The mitochondrial calcium uniporter (MCU) activates mitochondrial respiration and enhances mobility by regulating mitochondrial redox state.

Inhibiting de novo ceramide synthesis restores mitochondrial and protein homeostasis in muscle aging.

ConFERMing the role of talin in integrin activation and mechanosignaling.

Nerve pathology is prevented by linker proteins in mouse models for LAMA2-related muscular dystrophy.

La Fondation

FSRMM