S. Fernandes

发表

Oligonucleotide-Based Therapy for FTD/ALS Caused by the C9orf72 Repeat Expansion: A Perspective

Yoshitsugu Aoki, Matthew J. A. Wood, M. Wood, 2013, Journal of nucleic acids.

The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors

C. Almeida, M. Vainzof, D. Ayub-Guerrieri, 2016, PloS one.

Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy

A. Bigot, V. Mouly, C. Almeida, 2019, Disease Models & Mechanisms.

Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies

C. Almeida, M. Vainzof, P. Onofre-Oliveira, 2019, Scientific Reports.

Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse

C. Almeida, M. Vainzof, D. Ayub-Guerrieri, 2019, Journal of Molecular Histology.

The Multifaceted Role of Nutrient Sensing and mTORC1 Signaling in Physiology and Aging

S. Fernandes, C. Demetriades, 2021, Frontiers in Aging.

Muscle Satellite Cells: Exploring the Basic Biology to Rule Them

C. Almeida, M. Vainzof, S. Fernandes, 2016, Stem cells international.

Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse

C. Almeida, M. Vainzof, D. Ayub-Guerrieri, 2019, Journal of Molecular Histology.

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

M. Zatz, M. Vainzof, G. Yamamoto, 2014, BMC Research Notes.