Actualités

Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells.

Azakir BA, Di Fulvio S, Kinter J, Sinnreich M. J Biol Chem. 2017 Jul 28;292(30):12542.

28 juillet 2017

Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules.

Azakir BA, Di Fulvio S, Salomon S, Brockhoff M, Therrien C, Sinnreich M. J Biol Chem. 2017 Jul 28;292(30):12543.

28 juillet 2017

Test-retest reliability of wide-pulse high-frequency neuromuscular electrical stimulation evoked force.

Neyroud D, Grosprêtre S, Gondin J, Kayser B, Place N. Muscle Nerve. 2017 Jul 19 [Epub ahead of print]

19 juillet 2017

Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice.

Reinhard JR, Lin S, McKee KK, Meinen S, Crosson SC, Sury M, Hobbs S, Maier G, Yurchenco PD, Rüegg MA. Sci Transl Med. 2017 Jun 28;9(396)

01 juillet 2017

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.

Willmann R, Gordish-Dressman H, Meinen S, Rüegg MA, Yu Q, Nagaraju K, Kumar A, Girgenrath M, Coffey CBM, Cruz V, Van Ry PM, Bogdanik L, Lutz C, Rutkowski A, Burkin...

23 juin 2017

Selective in vivo removal of pathogenic anti-MAG autoantibodies, an antigen-specific treatment option for anti-MAG neuropathy.

Herrendorff R, Hänggi P, Pfister H, Yang F, Demeestere D, Hunziker F, Frey S, Schaeren-Wiemers N, Steck AJ, Ernst B. Proc Natl Acad Sci U S A. 2017 May 2;114(18)

30 mai 2017

TRPC1 and TRPC4 channels functionally interact with STIM1L to promote myogenesis and maintain fast repetitive Ca2+ release in human myotubes.

Antigny F, Sabourin J, Saüc S, Bernheim L, Koenig S, Frieden M. Biochim Biophys Acta. 2017 May;1864(5):806-813.

19 mai 2017

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Actualités

Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells.

Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules.

Test-retest reliability of wide-pulse high-frequency neuromuscular electrical stimulation evoked force.

Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice.

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.

Selective in vivo removal of pathogenic anti-MAG autoantibodies, an antigen-specific treatment option for anti-MAG neuropathy.

TRPC1 and TRPC4 channels functionally interact with STIM1L to promote myogenesis and maintain fast repetitive Ca2+ release in human myotubes.

Role of Nuclear Receptors in Exercise-Induced Muscle Adaptations.

Molecular Basis for Exercise-Induced Fatigue: The Importance of Strictly Controlled Cellular Ca2+ Handling.

switchSENSE: A new technology to study protein-RNA interactions. Cléry A, Sohier TJM, Welte T, Langer A, Allain FHT.

La Fondation

FSRMM