News

Generation of allogenic and xenogeneic functional muscle stem cells for intramuscular transplantation.

Lenardič A, Domenig SA, Zvick J, Bundschuh N, Tarnowska-Sengül M, Furrer R, Noé FJ, Trautmann CLL, Ghosh A, Bacchin G, Gjonlleshaj P, Qabrati X, Masschelein E, De Bock...

27 Mai 2024

CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I.

Falcetta D, Quirim S, Cocchiararo I, Chabry F, Théodore M, Stiefvater A, Lin S, Tintignac L, Ivanek R, Kinter J, Rüegg MA, Sinnreich M, Castets P. Skelet Muscle. 2024...

21 Mai 2024

Cyclo His-Pro Attenuates Muscle Degeneration in Murine Myopathy Models.

De Masi A, Zanou N, Strotjohann K, Lee D, Lima TI, Li X, Jeon J, Place N, Jung HY, Auwerx J. Adv Sci (Weinh). 2024 May 10:e2305927.

10 Mai 2024

A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice.

Benucci S, Ruiz A, Franchini M, Ruggiero L, Zoppi D, Sitsapesan R, Lindsay C, Pelczar P, Pietrangelo L, Protasi F, Treves S, Zorzato F. J Gen Physiol. 2024 Apr...

01 April 2024

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD).

Van Damme P, Al-Chalabi A, Andersen PM, Chiò A, Couratier P, De Carvalho M, Hardiman O, Kuźma-Kozakiewicz M, Ludolph A, McDermott CJ, Mora JS, Petri S, Probyn K, Reviers...

30 März 2024

A solid beta-sheet structure is formed at the surface of FUS droplets during aging.

Emmanouilidis L, Bartalucci E, Kan Y, Ijavi M, Pérez ME, Afanasyev P, Boehringer D, Zehnder J, Parekh SH, Bonn M, Michaels TCT, Wiegand T, Allain FH. Nat Chem Biol....

12 März 2024

Cervical and thoracic spinal cord gray matter atrophy is associated with disability in patients with amyotrophic lateral sclerosis.

Wendebourg MJ, Weigel M, Weidensteiner C, Sander L, Kesenheimer E, Naumann N, Haas T, Madoerin P, Braun N, Neuwirth C, Weber M, Jahn K, Kappos L, Granziera C, Schweikert...

11 März 2024

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News

Generation of allogenic and xenogeneic functional muscle stem cells for intramuscular transplantation.

CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I.

Cyclo His-Pro Attenuates Muscle Degeneration in Murine Myopathy Models.

A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice.

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD).

A solid beta-sheet structure is formed at the surface of FUS droplets during aging.

Cervical and thoracic spinal cord gray matter atrophy is associated with disability in patients with amyotrophic lateral sclerosis.

SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

A model of human neural networks reveals NPTX2 pathology in ALS and FTLD.

Direct reprogramming of non-limb fibroblasts to cells with properties of limb progenitors.

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