News

Creatine transporter-deficient rat model shows motor dysfunction, cerebellar alterations, and muscle creatine deficiency without muscle atrophy.

Duran-Trio L, Fernandes-Pires G, Grosse J, Soro-Arnaiz I, Roux-Petronelli C, Binz PA, De Bock K, Cudalbu C, Sandi C, Braissant O. J Inherit Metab Dis. 2021 Dec 22.

22 dicembre 2021


CRISPR/Cas9 editing of directly reprogrammed myogenic progenitors restores dystrophin expression in a mouse model of muscular dystrophy.

Domenig SA, Bundschuh N, Lenardič A, Ghosh A, Kim I, Qabrati X, D'Hulst G, Bar-Nur O. Stem Cell Reports. 2021 Dec 21:S2213-6711(21)00642-1.

21 dicembre 2021


Guillain-Barré syndrome after SARS-CoV-2 infection in an international prospective cohort study.

Luijten LWG, Leonhard SE, van der Eijk AA, Doets AY, Appeltshauser L, Arends S, Attarian S, Benedetti L, Briani C, Casasnovas C, Castellani F, Dardiotis E,...

16 dicembre 2021


Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity.

Zanou N, Dridi H, Reiken S, Imamura de Lima T, Donnelly C, De Marchi U, Ferrini M, Vidal J, Sittenfeld L, Feige JN, Garcia-Roves PM, Lopez-Mejia IC, Marks AR, Auwerx J,...

10 dicembre 2021


Rheological properties of skeletal muscles in a Duchenne muscular dystrophy murine model before and after autologous cell therapy.

Zemła J, Iyer PS, Pyka-Fościak G, Mermod N, Lekka M. J Biomech. 2021 Nov 9;128:110770.

09 dicembre 2021


Exon-independent recruitment of SRSF1 is mediated by U1 snRNP stem-loop 3.

Jobbins AM, Campagne S, Weinmeister R, Lucas CM, Gosliga AR, Clery A, Chen L, Eperon LP, Hodson MJ, Hudson AJ, Allain FH, Eperon IC. EMBO J. 2021 Nov 15:e107640.

02 dicembre 2021


Survival and Motor Phenotypes in FVB C9-500 ALS/FTD BAC Transgenic Mice Reproduced by Multiple Labs.

Nguyen L, Laboissonniere LA, Guo S, Pilotto F, Scheidegger O, Oestmann A, Hammond JW, Li H, Hyysalo A, Peltola R, Pattamatta A, Zu T, Voutilainen MH, Gelbard HA, Saxena...

30 novembre 2021


Biofabrication of 3D Human Muscle Model with Vascularization and Endomysium.

Bersini S, Francescato R, Moretti M. Methods Mol Biol. 2022;2373:213-230

26 novembre 2021


Longitudinal Quantitative MRI Evaluation of Muscle Involvement in Amyotrophic Lateral Sclerosis.

Paoletti M, Diamanti L, Muzic SI, Ballante E, Solazzo F, Foppoli L, Deligianni X, Santini F, Figini S, Bergsland N, Pichiecchio A. Front Neurol. 2021 Nov 24;12:749736.

24 novembre 2021


Molecular basis of impaired muscle function in a mouse model of congenital myopathy due to compound heterozygous RYR1 mutations.

Ruiz A, Eckhardt J, Treves S, Zorzato F. J Gen Physiol. 2022 Sep 5;154(9):e2021ecc26.

12 novembre 2021