News

Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction.

Jungbluth H, Treves S, Zorzato F, Sarkozy A, Ochala J, Sewry C, Phadke R, Gautel M, Muntoni F. Nat Rev Neurol. 2018 Mar;14(3):151-167.

01 März 2018


Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy.

Boido M, De Amicis E, Valsecchi V, Trevisan M, Ala U, Ruegg MA, Hettwer S, Vercelli A. Front Cell Neurosci. 2018 Jan 30;12:17.

31 Januar 2018


Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance.

Ruiz A, Dror E, Handschin C, Furrer R, Perez-Schindler J, Bachmann C, Treves S, Zorzato F. Sci Rep. 2018 Jan 12;8(1)

15 Januar 2018


Plasticity of the Muscle Stem Cell Microenvironment

Dinulovic I, Furrer R, Handschin C. Adv Exp Med Biol. 2017;1041:141-169

05 Januar 2018


Short vs. long pulses for testing knee extensor neuromuscular properties: does it matter?

Giroux C, Roduit B, Rodriguez-Falces J, Duchateau J, Maffiuletti NA, Place N. Eur J Appl Physiol. 2017 Dec 7

11 Dezember 2017


Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.

Yurchenco PD, McKee KK, Reinhard JR, Rüegg MA. Matrix Biol. 2017 Nov 27.

27 November 2017


An unbiased silencing screen in muscle cells identifies miR-320a, miR-150, miR-196b, and miR-34c as regulators of skeletal muscle mitochondrial metabolism.

Dahlmans D, Houzelle A, Andreux P, Jörgensen JA, Wang X, de Windt LJ, Schrauwen P, Auwerx J, Hoeks J. Mol Metab. 2017 Nov;6(11):1429-1442.

14 November 2017


Split GFP technologies to structurally characterize and quantify functional biomolecular interactions of FTD-related proteins.

Foglieni C, Papin S, Salvadè A, Afroz T, Pinton S, Pedrioli G, Ulrich G, Polymenidou M, Paganetti P. Sci Rep. 2017 Oct 25;7(1):14013.

07 November 2017