Actualités
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.
Schartner V, Romero NB, Donkervoort S, Treves S, Munot P, Pierson TM, Dabaj I, Malfatti E, Zaharieva IT, Zorzato F, et al. Acta Neuropathol. 2017 Apr;133(4):517-533.
04 avril 2017
A Cell Culture System to Investigate the Presynaptic Control of Subsynaptic Membrane Differentiation at the Neuromuscular Junction.
Schmidt N, Basu S, Kröger S, Brenner HR. Methods Mol Biol. 2017;1538:3-11.
27 mars 2017
Neuromuscular Fatigue After Repeated Jumping With Concomitant Electrical Stimulation.
Neyroud D, Samararatne J, Kayser B, Place N. Int J Sports Physiol Perform. 2017 Mar 24:1-24.
20 mars 2017
Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials.
Carlier PG, Marty B, Scheidegger O, Loureiro de Sousa P, Baudin PY, Snezhko E, Vlodavets D. J Neuromuscul Dis. 2016 Mar 3;3(1):1-28.
03 mars 2017
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.
McKee KK, Crosson SC, Meinen S, Reinhard JR, Rüegg MA, Yurchenco PD. J Clin Invest. 2017 Mar 1;127(3):1075-1089.
01 mars 2017
Automated microfluidic sorting of mammalian cells labeled with magnetic microparticles for those that efficiently express and secrete a protein of interest.
Droz X, Harraghy N, Lançon E, Le Fourn V, Calabrese D, Colombet T, Liechti P, Rida A, Girod PA, Mermod N. Biotechnol Bioeng. 2017 Feb 18. [Epub ahead of print]
18 février 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 Feb 6. [Epub ahead of print]
06 février 2017
Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I.
Brockhoff M, Rion N, Chojnowska K, Wiktorowicz T, Eickhorst C, Erne B, Frank S, Angelini C, Furling D, Rüegg MA, Sinnreich M, Castets P. J Clin Invest. 2017 Jan 9. pii:...
16 janvier 2017
Biological spectrum of Amyotrophic Lateral Sclerosis prions.
Polymenidou M, Cleveland DW. Cold Spring Harb Perspect Med. 2017 Jan 6. pii: a024133.
06 janvier 2017
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.
Schartner V, Romero NB, Donkervoort S, Treves S, Munot P, Pierson TM, Dabaj I, Malfatti E, Zaharieva IT, Zorzato F,.... Acta Neuropathol. 2016 Dec 23
23 décembre 2016
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