CIR-Myo
News
Institution of the Padua University Interdepartmental
Research Center of “Myology: Biology,
Physiopathology, Clinics and Biotechnologies of
Skeletal Muscle Tissue (CIR-Myo)
The July 30, 2013 the Rector of the University of
Padova signed the Decreto
Rettoriale Rep n. 2047, Prot. N. 66226, Anno 2008,
Tit. Vi, Cl. 8, Fasc 8 that approved and activates the
Institution of the Interdepartmental Research Center of
Myology of the Padua University.
The “Decreto Rettorale” and
the Statute
of CIR-Myo could be downloaded from the BAM On-Line
website at the link: http://www.bio.unipd.it/bam/
The CIR-Myo Organs are: 1. the Director Prof. Marco
Sandri, and 2. The Council that is composed by the acting
Directors of the five ”Founder University Departments” of
the CIR-Myo, i. e., the Department of Biology, the
Department of Biomedical Sciences, the Department of
Neurosciences, the Department of Comparative Biomedicine and
Nutrition, and the Department of Surgery, Oncology and
Gastroenterology Sciences, and by three elected members,
Prof. Carlo Reggiani, Prof. Stefano Masiero and Prof. Marco
Sandri. After resignation of Marco Sandri, elected by the
Council CIR-Myo Director, a third representative of the
afferent university personnel is expected to be soon
elected.
The CIR-Myo scientists will operate along the
following researcher lines:
A)
Biologia
del muscolo denervato,
Biology of the
denervated muscle;
B) Miopatie
e organizzazione spaziale dei mionuclei,
Myopathies and
spatial redistribution of muscle nuclei;
C) Applicazioni
in Riabilitazione dell’Elettro-Stimolazione Funzionale del
muscolo denervato,
Functional
Electrical Stimulation of denervated muscle in
Rehabilitation;
D) Marcatori
tessutali e sierologici di miopatia associata a neoplasia
del colon retto,
Serum and tissue
markers of myopathies associated to the colorectal cancer;
E) Imaging
muscolare funzionale, Functional
Muscle Imaging;
F)
Meccanismi patogenetici della Sclerosi Laterale
Amiotrofica (SLA),
Pathogenesis of
Amyotrophic lateral
sclerosis (ALS);
G) La
proteina chinasi della Distrofia miotonica: funzione
mitocondriale e morte cellulare,
Protein-kinase of
Myotonic Dystrophy: Mitocondrial function and cell death;
H) Impianto
di cellule staminali miogeniche tramite matrici
tridimensionali biocompatibili;
un nuovo approccio per il trattamento di patologie
muscolari ereditarie ed acquisite,
Myogenic cell stem
implants using tridimensional biocompatible matrices:
a new approach for genetic and acquired muscle
pathologies;
I)
Strategie
di accelerazione della rigenerazione assonale in Chirurgia
Plastica,
Strategies to
accelerate axonal regeneration in Plastic Surgery;
J)
Ruolo
di segnali Ca2+ mitocondriali nel controllo
dell’omeostasi muscolare,
Mitochondrial Ca2+
signalling in muscle homeostasis;
K)
Atrofia
ed autofagia nelle miopatie umane,
Atrophy and
Autophagy in human myopathies;
L)
Regolazione
dell'atrofia/ipertrofia del muscolo scheletrico: meccanismi
energetici,
Regulation of muscle
Atrophy/Hypertrophy: energetic mechanismsm;
M)
Specializzazione
e plasticità delle fibre muscolari scheletriche,
Specialization and plasticity of skeletal muscle
fibers.