News
The F1 loop of the talin head domain acts as a gatekeeper in integrin activation and clustering.
Kukkurainen S, Azizi L, Zhang P, Jacquier MC, Baikoghli M, von Essen M, Tuukkanen A, Laitaoja M, Liu X, Rahikainen R, Orłowski A, Jänis J, Määttä JAE, Varjosalo M,...
12 Oktober 2020
On the optimal temporal resolution for phase contrast cardiovascular magnetic resonance imaging: establishment of baseline values.
Santini F, Pansini M, Hrabak-Paar M, Yates D, Langenickel TH, Bremerich J, Bieri O, Schubert T. J Cardiovasc Magn Reson. 2020 Oct 5;22(1):72.
05 Oktober 2020
Screening method to identify hydrogel formulations that facilitate myotube formation from encapsulated primary myoblasts.
Deshmukh DV, Pasquero N, Rathore G, Zvick J, Bar-Nur O, Dual J, Tibbitt MW. Bioeng Transl Med. 2020 Sep 3;5(3):e10181.
16 September 2020
The neuromuscular junction is a focal point of mTORC1 signaling in sarcopenia
Daniel J. Ham, Anastasiya Börsch, Shuo Lin, Marco Thürkauf, Martin Weihrauch, Judith R. Reinhard, Julien Delezie, et al. Nat Commun 11, 4510 (2020)
09 September 2020
Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow- twitch muscles in mice.
Elbaz M, Ruiz A, Nicolay S, Tupini C, Bachmann C, Eckhardt J, Benucci S, Pelczar P, Treves S, Zorzato F. J Biol Chem. 2020 Jun 4:jbc.RA120.013846.
24 Juli 2020
Exercise promotes satellite cell contribution to myofibers in a load-dependent manner.
Masschelein E, D'Hulst G, Zvick J, Hinte L, Soro-Arnaiz I, Gorski T, von Meyenn F, Bar-Nur O, De Bock K. Skelet Muscle. 2020 Jul 9;10(1):21.
09 Juli 2020
Hallmarks of frailty and osteosarcopenia in prematurely aged PolgA(D257A/D257A) mice.
Scheuren AC, D'Hulst G, Kuhn GA, Masschelein E, Wehrle E, De Bock K, Müller R. J Cachexia Sarcopenia Muscle. 2020 Jun 28.
28 Juni 2020
In vitro evaluation of human myoblast function after exposure to cobalt and chromium ions.
Laumonier T, Ruffieux E, Paccaud J, Kindler V, Hannouche D. J Orthop Res. 2020 Jun;38(6):1398-1406.
08 Juni 2020
Structural Transition, Function and Dysfunction of TDP-43 in Neurodegenerative Diseases.
Afroz T, Pérez-Berlanga M, Polymenidou M. Chimia (Aarau). 2019 May 29;73(6):380-390.
29 Mai 2020
Molecular basis of impaired extraocular muscle function in a mouse model of congenital myopathy due to compound heterozygous Ryr1 mutations.
Eckhardt J, Bachmann C, Benucci S, Elbaz M, Ruiz A, Zorzato F, Treves S. Hum Mol Genet. 2020 May 28;29(8):1330-1339.
28 Mai 2020
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