Maria Sofia Falzarano
Overview
Explore the profile of Maria Sofia Falzarano including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
26
Citations
414
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Caputo L, Stamenkovic C, Tierney M, Falzarano M, Bassel-Duby R, Ferlini A, et al.
bioRxiv
. 2024 Dec;
PMID: 39713478
Generation of induced pluripotent cells (hiPSCs)-derived skeletal muscle progenitor cells (SMPCs) holds great promise for regenerative medicine for skeletal muscle wasting diseases, as for example Duchenne Muscular Dystrophy (DMD). Multiple...
2.
Falzarano M, Mietto M, Fortunato F, Farne M, Martini F, Ala P, et al.
Sci Rep
. 2023 Sep;
13(1):15942.
PMID: 37743371
To gain insight on dystrophin (DMD) gene transcription dynamics and spatial localization, we assayed the DMD mRNA amount and defined its compartmentalization in myoblasts, myotubes, and skeletal muscle biopsies of...
3.
Falzarano M, Rossi R, Grilli A, Fang M, Osman H, Sabatelli P, et al.
Front Physiol
. 2021 Nov;
12:716471.
PMID: 34744760
Neuromuscular disorders (NMDs) are a heterogeneous group of genetic diseases, caused by mutations in genes involved in spinal cord, peripheral nerve, neuromuscular junction, and muscle functions. To advance the knowledge...
4.
Betts C, Jagannath A, van Westering T, Bowerman M, Banerjee S, Meng J, et al.
Life Sci Alliance
. 2021 Aug;
4(10).
PMID: 34389686
Absence of dystrophin, an essential sarcolemmal protein required for muscle contraction, leads to the devastating muscle-wasting disease Duchenne muscular dystrophy. Dystrophin has an actin-binding domain, which binds and stabilises filamentous-(F)-actin,...
5.
Rossi R, Falzarano M, Osman H, Armaroli A, Scotton C, Mantuano P, et al.
Front Physiol
. 2021 Jul;
12:678974.
PMID: 34305639
Duchenne muscular dystrophy (DMD) is a rare genetic disease due to dystrophin gene mutations which cause progressive weakness and muscle wasting. Circadian rhythm coordinates biological processes with the 24-h cycle...
6.
Fortunato F, Rossi R, Falzarano M, Ferlini A
J Clin Med
. 2021 Mar;
10(4).
PMID: 33671409
Duchenne muscular dystrophy (DMD) is the most common childhood muscular dystrophy affecting ~1:5000 live male births. Following the identification of pathogenic variations in the dystrophin gene in 1986, the underlining...
7.
Passarelli C, Selvatici R, Carrieri A, Di Raimo F, Falzarano M, Fortunato F, et al.
Front Genet
. 2020 Jul;
11:605.
PMID: 32719714
Background: Duchenne muscular dystrophy (DMD) is a rare and severe X-linked muscular dystrophy in which the standard of care with variable outcome, also due to different drug response, is chronic...
8.
Falzarano M, Argenziano M, Marsollier A, Mariot V, Rossi D, Selvatici R, et al.
Nucleic Acid Ther
. 2020 Jul;
31(3):201-207.
PMID: 32679000
Orphan drugs, including antisense oligonucleotides (AONs), siRNAs/miRNAs, Cas9 nuclease, and recombinant genes, have recently been made available for rare diseases. However, the main bottleneck for these new therapies is delivery....
9.
Neri M, Rossi R, Trabanelli C, Mauro A, Selvatici R, Falzarano M, et al.
Front Genet
. 2020 Mar;
11:131.
PMID: 32194622
Dystrophinopathies are inherited diseases caused by mutations in the dystrophin () gene for which testing is mandatory for genetic diagnosis, reproductive choices and eligibility for personalized trials. We genotyped the...
10.
Falzarano M, Ferlini A
J Clin Med
. 2019 May;
8(5).
PMID: 31071994
Urine specimens represent a novel and non-invasive approach to isolate patient-specific stem cells by easy and low-cost procedures, replacing the traditional sources (muscle/skin biopsy/adipose tissue) obtained with invasive and time-consuming...