News

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 April 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 März 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 März 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 März 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 März 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 Februar 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 Februar 2017

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News

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.

A Cell Culture System to Investigate the Presynaptic Control of Subsynaptic Membrane Differentiation at the Neuromuscular Junction.

Neuromuscular Fatigue After Repeated Jumping With Concomitant Electrical Stimulation.

Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials.

Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.

Automated microfluidic sorting of mammalian cells labeled with magnetic microparticles for those that efficiently express and secrete a protein of interest.

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

Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I.

Biological spectrum of Amyotrophic Lateral Sclerosis prions.

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.

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FSRMM