Actualités

Tandem hnRNP A1 RNA recognition motifs act in concert to repress the splicing of survival motor neuron exon 7.

Beusch I, Barraud P, Moursy A, Cléry A, Allain FH. Elife. 2017 Jun 26;6.

20 octobre 2017


Functional and dynamic polymerization of the ALS-linked protein TDP-43 antagonizes its pathologic aggregation.

Afroz T, Hock EM, Ernst P, Foglieni C, Jambeau M, Gilhespy LAB, Laferriere F, Maniecka Z, Plückthun A, Mittl P, Paganetti P, Allain FHT, Polymenidou M. Nat Commun. 2017...

06 octobre 2017


Distinct roles of NFATc1 and NFATc4 in human primary myoblast differentiation and in reserve cell maintenance.

Perroud J, Bernheim L, Frieden M, Koenig S. J Cell Sci. 2017 Jul 31. [Epub ahead of print]

31 juillet 2017


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