News

The Solution Structure of FUS Bound to RNA Reveals a Bipartite Mode of RNA Recognition with Both Sequence and Shape Specificity.

Loughlin FE, Lukavsky PJ, Kazeeva T, Reber S, Hock EM, Colombo M, Von Schroetter C, Pauli P, Cléry A, Mühlemann O, Polymenidou M, Ruepp MD, Allain FH. Mol Cell. 2018...

11 Dezember 2018


STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility.

Zaharieva IT, Sarkozy A, Munot P, Manzur A, O'Grady G, Rendu J, Malfatti E, Amthor H, Servais L, Urtizberea JA, Neto OA, Zanoteli E, Donkervoort S, Taylor J, Dixon J,...

02 Dezember 2018


Distinct patterns of skeletal muscle mitochondria fusion, fission and mitophagy upon duration of exercise training.

Arribat Y, Broskey NT, Greggio C, Boutant M, Conde Alonso S, Kulkarni SS, Lagarrigue S, Carnero EA, Besson C, Cantó C, Amati F. Acta Physiol (Oxf). 2018 Aug 24:e13179.

02 September 2018


STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility.

Zaharieva I, Sarkozy A, Munot P, Manzur A, et al. Hum Mutat. 2018 Aug 31.

31 August 2018


Muscle Wasting Diseases: Novel Targets and Treatments.

Furrer R, Handschin C. Annu Rev Pharmacol Toxicol. 2018 Aug 27

27 August 2018


Residual force enhancement contributes to increased performance during stretch-shortening cycles of human plantar flexor muscles in vivo.

Hahn D, Riedel TN. J Biomech. 2018 Aug 22;77:190-193

22 August 2018


Estimation of voluntary elicited motor neuron discharge using a peripheral nerve collision technique at different contraction strengths.

Scheidegger O, Kamber N, Rösler KM. Clin Neurophysiol. 2018 Aug;129(8):1579-1587.

17 Juli 2018


Transcriptomic analyses reveal rhythmic and CLOCK-driven pathways in human skeletal muscle.

Perrin L, Loizides-Mangold U, Chanon S, Gobet C, Hulo N, Isenegger L, Weger BD, Migliavacca E, Charpagne A, Betts JA, Walhin JP, Templeman I, Stokes K, Thompson D,...

31 Mai 2018


Targeting RNA structure in SMN2 reverses spinal muscular atrophy molecular phenotypes.

Garcia-Lopez A, Tessaro F, Jonker HRA, Wacker A, Richter C, Comte A, Berntenis N, Schmucki R, Hatje K, Petermann O, Chiriano G, Perozzo R, Sciarra D, Konieczny P,...

23 Mai 2018