Pubblications Falzanaro
Selvatici R, Falzarano S, Traniello S, Pagani Zecchini G, Spisani S.
Formylpeptides trigger selective molecular pathways that are required in the
physiological functions of human neutrophils. Cell Signal. 2003
Apr;15(4):377-83. doi: 10.1016/s0898-6568(02)00123-7. PMID: 12618212.
Spisani S, Turchetti M, Varani K, Falzarano S, Cavicchioni G. Hydrophilic
residues at position 3 highlight unforeseen features of the fMLP receptor
pocket. Eur J Pharmacol. 2003 May 23;469(1-3):13-9. doi:
10.1016/s0014-2999(03)01672-8. PMID: 12782180.
Cavicchioni G, Turchetti M, Varani K, Falzarano S, Spisani S. Properties of a
novel chemotactic esapeptide, an analogue of the prototypical N-formylmethionyl
peptide. Bioorg Chem. 2003 Aug;31(4):322-30. doi: 10.1016/s0045-2068(03)00070-1.
PMID: 12877881.
Spisani S, Falzarano S, Traniello S, Nalli M, Selvatici R. A 'pure'
chemoattractant formylpeptide analogue triggers a specific signalling pathway in
human neutrophil chemotaxis. FEBS J. 2005 Feb;272(4):883-91. doi:
10.1111/j.1742-4658.2004.04497.x. PMID: 15691323.
Manzati E, Aguiari G, Banzi M, Manzati M, Selvatici R, Falzarano S, Maestri
I, Pinton P, Rizzuto R, del Senno L. The cytoplasmic C-terminus of polycystin-1
increases cell proliferation in kidney epithelial cells through serum-activated
and Ca(2+)-dependent pathway(s). Exp Cell Res. 2005 Apr 1;304(2):391-406. doi:
10.1016/j.yexcr.2004.10.023. Epub 2004 Dec 15. PMID: 15748886.
Cavicchioni G, Fraulini A, Turchetti M, Varani K, Falzarano S, Pavan B,
Spisani S. Biological activity of for-Met-Leu-Phe-OMe analogs: relevant
substitutions specifically trigger killing mechanisms in human neutrophils. Eur
J Pharmacol. 2005 Apr 4;512(1):1-8. doi: 10.1016/j.ejphar.2005.02.013. PMID:
15814083.
Trombella S, Vergura R, Falzarano S, Guerrini R, Calo G, Spisani S.
Nociceptin/orphanin FQ stimulates human monocyte chemotaxis via NOP receptor
activation. Peptides. 2005 Aug;26(8):1497-502. doi:
10.1016/j.peptides.2005.03.015. PMID: 15922491.
Selvatici R, Falzarano S, Mollica A, Spisani S. Signal transduction pathways
triggered by selective formylpeptide analogues in human neutrophils. Eur J
Pharmacol. 2006 Mar 18;534(1-3):1-11. doi: 10.1016/j.ejphar.2006.01.034. Epub
2006 Mar 3. PMID: 16516193.
Cavicchioni G, Fraulini A, Falzarano S, Spisani S. Structure-activity
relationship of for-L-Met L-Leu-L-Phe-OMe analogues in human neutrophils. Bioorg
Chem. 2006 Oct;34(5):298-318. doi: 10.1016/j.bioorg.2006.07.001. Epub 2006 Aug
17. PMID: 16919307.
Selvatici R, Falzarano S, Franceschetti L, Cavallini S, Marino S,
Siniscalchi A. Differential activation of protein kinase C isoforms following
chemical ischemia in rat cerebral cortex slices. Neurochem Int. 2006
Dec;49(8):729-36. doi: 10.1016/j.neuint.2006.06.003. Epub 2006 Sep 11. PMID:
16963162.
Siniscalchi A, Cavallini S, Marino S, Falzarano S, Franceschetti L,
Selvatici R. Effects of chemical ischemia on cerebral cortex slices: focus on
mitogen-activated protein kinase cascade. Ann N Y Acad Sci. 2006
Dec;1090:445-54. doi: 10.1196/annals.1378.047. PMID: 17384288.
Selvatici R, Falzarano S, Franceschetti L, Spisani S, Siniscalchi A. Effects
of PKI55 protein, an endogenous protein kinase C modulator, on specific PKC
isoforms activity and on human T cells proliferation. Arch Biochem Biophys. 2007
Jun 1;462(1):74-82. doi: 10.1016/j.abb.2007.03.018. Epub 2007 Apr 4. PMID:
17467651.
Spisani S, Fraulini A, Varani K, Falzarano S, Cavicchioni G. New chemotactic
dimeric peptides show high affinity and potency at the human formylpeptide
receptor. Eur J Pharmacol. 2007 Jul 12;567(1-2):171-6. doi:
10.1016/j.ejphar.2007.04.006. Epub 2007 Apr 14. PMID: 17481605.
Selvatici R, Falzarano S, Franceschetti L, Mollica A, Guerrini R,
Siniscalchi A, Spisani S. Study of synthetic peptides derived from the PKI55
protein, a protein kinase C modulator, in human neutrophils stimulated by the
methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-
OH. FEBS J. 2008 Feb;275(3):449-57. doi: 10.1111/j.1742-4658.2007.06212.x. Epub
2007 Dec 21. PMID: 18167144.
Borgatti M, Finotti A, Falzarano S, Selvatici R. Structural characterization
of promoter sequences of the gene coding human PKI55 protein, a protein kinase C
inhibitor. Biochimie. 2009 Apr;91(4):466-74. doi: 10.1016/j.biochi.2008.11.007.
Epub 2008 Dec 7. PMID: 19095038.
Selvatici R, Previati M, Marino S, Marani L, Falzarano S, Lanzoni I,
Siniscalchi A. Sodium azide induced neuronal damage in vitro: evidence for non-
apoptotic cell death. Neurochem Res. 2009 May;34(5):909-16. doi:
10.1007/s11064-008-9852-0. Epub 2008 Oct 8. PMID: 18841470.
Spitali P, Rimessi P, Fabris M, Perrone D, Falzarano S, Bovolenta M,
Trabanelli C, Mari L, Bassi E, Tuffery S, Gualandi F, Maraldi NM, Sabatelli-
Giraud P, Medici A, Merlini L, Ferlini A. Exon skipping-mediated dystrophin
reading frame restoration for small mutations. Hum Mutat. 2009
Nov;30(11):1527-34. doi: 10.1002/humu.21092. PMID: 19760747.
Cavicchioni G, Fraulini A, Falzarano S, Spisani S. Oligomeric formylpeptide
activity on human neutrophils. Eur J Med Chem. 2009 Dec;44(12):4926-30. doi:
10.1016/j.ejmech.2009.08.010. Epub 2009 Aug 31. PMID: 19748709.
Ferlini A, Sabatelli P, Fabris M, Bassi E, Falzarano S, Vattemi G, Perrone
D, Gualandi F, Maraldi NM, Merlini L, Sparnacci K, Laus M, Caputo A, Bonaldo P,
Braghetta P, Rimessi P. Dystrophin restoration in skeletal, heart and skin
arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes. Gene Ther. 2010
Mar;17(3):432-8. doi: 10.1038/gt.2009.145. Epub 2009 Nov 12. PMID: 19907501.
Rimessi P, Fabris M, Bovolenta M, Bassi E, Falzarano S, Gualandi F, Rapezzi
C, Coccolo F, Perrone D, Medici A, Ferlini A. Antisense modulation of both
exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon
responsible for x-linked dilated cardiomyopathy. Hum Gene Ther. 2010
Sep;21(9):1137-46. doi: 10.1089/hum.2010.010. PMID: 20486769.
Bassi E, Falzarano S, Fabris M, Gualandi F, Merlini L, Vattemi G, Perrone D,
Marchesi E, Sabatelli P, Sparnacci K, Laus M, Bonaldo P, Rimessi P, Braghetta P,
Ferlini A. Persistent dystrophin protein restoration 90 days after a course of
intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx
mice. J Biomed Biotechnol. 2012;2012:897076. doi: 10.1155/2012/897076. Epub 2012
Oct 2. PMID: 23091362; PMCID: PMC3471065.
Martoni E, Petrini S, Trabanelli C, Sabatelli P, Urciuolo A, Selvatici R,
D'Amico A, Falzarano S, Bertini E, Bonaldo P, Ferlini A, Gualandi F.
Characterization of a rare case of Ullrich congenital muscular dystrophy due to
truncating mutations within the COL6A1 gene C-terminal domain: a case report.
BMC Med Genet. 2013 Jun 5;14:59. doi: 10.1186/1471-2350-14-59. PMID: 23738969;
PMCID: PMC3681647.
Witkowska R, Zabrocki J, Spisani S, Falzarano MS, Toniolo C, Formaggio F.
Synthetic formyl tripeptide chemoattractants: a C(alpha,alpha)-dialkylated,
amphiphilic glycyl residue at position 1. J Pept Sci. 2003 Jun;9(6):354-60. doi:
10.1002/psc.461. PMID: 12846481.
Bruno O, Brullo C, Bondavalli F, Ranise A, Schenone S, Falzarano MS, Varani
K, Spisani S. 2-Phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole derivatives: new
potent inhibitors of fMLP-induced neutrophil chemotaxis. Bioorg Med Chem Lett.
2007 Jul 1;17(13):3696-701. doi: 10.1016/j.bmcl.2007.04.036. Epub 2007 Apr 19.
PMID: 17475488.
Bovolenta M, Neri M, Fini S, Fabris M, Trabanelli C, Venturoli A, Martoni E,
Bassi E, Spitali P, Brioschi S, Falzarano MS, Rimessi P, Ciccone R, Ashton E,
McCauley J, Yau S, Abbs S, Muntoni F, Merlini L, Gualandi F, Ferlini A. A novel
custom high density-comparative genomic hybridization array detects common
rearrangements as well as deep intronic mutations in dystrophinopathies. BMC
Genomics. 2008 Nov 28;9:572. doi: 10.1186/1471-2164-9-572. PMID: 19040728;
PMCID: PMC2612025.
Bruno O, Brullo C, Bondavalli F, Schenone S, Spisani S, Falzarano MS, Varani
K, Barocelli E, Ballabeni V, Giorgio C, Tognolini M. 1-Methyl and 1-(2-hydroxyal
kyl)-5-(3-alkyl/cycloalkyl/phenyl/naphthylureido)-1H-pyrazole-4-carboxylic acid
ethyl esters as potent human neutrophil chemotaxis inhibitors. Bioorg Med Chem.
2009 May 1;17(9):3379-87. doi: 10.1016/j.bmc.2009.03.035. Epub 2009 Mar 25.
PMID: 19362486.
Bovolenta M, Erriquez D, Valli E, Brioschi S, Scotton C, Neri M, Falzarano
MS, Gherardi S, Fabris M, Rimessi P, Gualandi F, Perini G, Ferlini A. The DMD
locus harbours multiple long non-coding RNAs which orchestrate and control
transcription of muscle dystrophin mRNA isoforms. PLoS One. 2012;7(9):e45328.
doi: 10.1371/journal.pone.0045328. Epub 2012 Sep 21. PMID: 23028937; PMCID:
PMC3448672.
Bovolenta M, Scotton C, Falzarano MS, Gualandi F, Ferlini A. Rapid,
comprehensive analysis of the dystrophin transcript by a custom micro-fluidic
exome array. Hum Mutat. 2012 Mar;33(3):572-81. doi: 10.1002/humu.22017. Epub
2012 Jan 25. PMID: 22223181.
Brioschi S, Gualandi F, Scotton C, Armaroli A, Bovolenta M, Falzarano MS,
Sabatelli P, Selvatici R, D'Amico A, Pane M, Ricci G, Siciliano G, Tedeschi S,
Pini A, Vercelli L, De Grandis D, Mercuri E, Bertini E, Merlini L, Mongini T,
Ferlini A. Genetic characterization in symptomatic female DMD carriers: lack of
relationship between X-inactivation, transcriptional DMD allele balancing and
phenotype. BMC Med Genet. 2012 Aug 16;13:73. doi: 10.1186/1471-2350-13-73. PMID:
22894145; PMCID: PMC3459813.
Falzarano MS, Passarelli C, Bassi E, Fabris M, Perrone D, Sabatelli P,
Maraldi NM, Donà S, Selvatici R, Bonaldo P, Sparnacci K, Laus M, Braghetta P,
Rimessi P, Ferlini A. Biodistribution and molecular studies on orally
administered nanoparticle-AON complexes encapsulated with alginate aiming at
inducing dystrophin rescue in mdx mice. Biomed Res Int. 2013;2013:527418. doi:
10.1155/2013/527418. Epub 2013 Dec 12. PMID: 24392452; PMCID: PMC3874323.
Falzarano MS, Passarelli C, Ferlini A. Nanoparticle delivery of antisense
oligonucleotides and their application in the exon skipping strategy for
Duchenne muscular dystrophy. Nucleic Acid Ther. 2014 Feb;24(1):87-100. doi:
10.1089/nat.2013.0450. PMID: 24506782; PMCID: PMC3922138.
Falzarano MS, Bassi E, Passarelli C, Braghetta P, Ferlini A. Biodistribution
studies of polymeric nanoparticles for drug delivery in mice. Hum Gene Ther.
2014 Nov;25(11):927-8. doi: 10.1089/hum.2014.073. Epub 2014 Sep 22. PMID:
25244215; PMCID: PMC4236061.
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN,
Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Brioschi S, Bovolenta
M, Neri M, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg
DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Corrigendum: Translation from a
DMD exon 5 IRES results in a functional dystrophin isoform that attenuates
dystrophinopathy in humans and mice. Nat Med. 2015 May;21(5):537. doi:
10.1038/nm0515-537c. Erratum for: Nat Med. 2014 Sep;20(9):992-1000. PMID:
25951531.
Falzarano MS, Scotton C, Passarelli C, Ferlini A. Duchenne Muscular
Dystrophy: From Diagnosis to Therapy. Molecules. 2015 Oct 7;20(10):18168-84.
doi: 10.3390/molecules201018168. PMID: 26457695; PMCID: PMC6332113.
Scotton C, Bovolenta M, Schwartz E, Falzarano MS, Martoni E, Passarelli C,
Armaroli A, Osman H, Rodolico C, Messina S, Pegoraro E, D'Amico A, Bertini E,
Gualandi F, Neri M, Selvatici R, Boffi P, Maioli MA, Lochmüller H, Straub V,
Bushby K, Castrignanò T, Pesole G, Sabatelli P, Merlini L, Braghetta P, Bonaldo
P, Bernardi P, Foley R, Cirak S, Zaharieva I, Muntoni F, Capitanio D, Gelfi C,
Kotelnikova E, Yuryev A, Lebowitz M, Zhang X, Hodge BA, Esser KA, Ferlini A.
Deep RNA profiling identified CLOCK and molecular clock genes as
pathophysiological signatures in collagen VI myopathy. J Cell Sci. 2016 Apr
15;129(8):1671-84. doi: 10.1242/jcs.175927. Epub 2016 Mar 4. PMID: 26945058;
PMCID: PMC4852766.
Falzarano MS, D'Amario D, Siracusano A, Massetti M, Amodeo A, La Neve F,
Maroni CR, Mercuri E, Osman H, Scotton C, Armaroli A, Rossi R, Selvatici R, Crea
F, Ferlini A. Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem
Cells Recapitulate the Dystrophin Genotype and Phenotype. Hum Gene Ther. 2016
Oct;27(10):772-783. doi: 10.1089/hum.2016.079. PMID: 27530229.
Sardone V, Zhou H, Muntoni F, Ferlini A, Falzarano MS. Antisense
Oligonucleotide-Based Therapy for Neuromuscular Disease. Molecules. 2017 Apr
5;22(4):563. doi: 10.3390/molecules22040563. PMID: 28379182; PMCID: PMC6154734.
Gherardi S, Bovolenta M, Passarelli C, Falzarano MS, Pigini P, Scotton C,
Neri M, Armaroli A, Osman H, Selvatici R, Gualandi F, Recchia A, Mora M,
Bernasconi P, Maggi L, Morandi L, Ferlini A, Perini G. Transcriptional and
epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that
govern muscle dystrophin expression. Biochim Biophys Acta Gene Regul Mech. 2017
Nov;1860(11):1138-1147. doi: 10.1016/j.bbagrm.2017.08.010. Epub 2017 Sep 1.
Erratum in: Biochim Biophys Acta Gene Regul Mech. 2020 Nov;1863(11):194646.
PMID: 28867298.
Falzarano MS, Flesia C, Cavalli R, Guiot C, Ferlini A. Nanodiagnostics and
Nanodelivery Applications in Genetic Alterations. Curr Pharm Des.
2018;24(15):1717-1726. doi: 10.2174/1381612824666180110151318. PMID: 29318963.
Hiller M, Falzarano MS, Garcia-Jimenez I, Sardone V, Verheul RC, Popplewell
L, Anthony K, Ruiz-Del-Yerro E, Osman H, Goeman JJ, Mamchaoui K, Dickson G,
Ferlini A, Muntoni F, Aartsma-Rus A, Arechavala-Gomeza V, Datson NA, Spitali P.
A multicenter comparison of quantification methods for antisense
oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell
cultures. PLoS One. 2018 Oct 2;13(10):e0204485. doi:
10.1371/journal.pone.0204485. PMID: 30278058; PMCID: PMC6168132.
Bigoni S, Neri M, Scotton C, Farina R, Sabatelli P, Jiang C, Zhang J,
Falzarano MS, Rossi R, Ognibene D, Selvatici R, Gualandi F, Bosshardt D, Perri
P, Campa C, Brancati F, Salvatore M, De Stefano MC, Taruscio D, Trombelli L,
Fang M, Ferlini A. Homozygous Recessive Versican Missense Variation Is
Associated With Early Teeth Loss in a Pakistani Family. Front Genet. 2019 Jan
21;9:723. doi: 10.3389/fgene.2018.00723. PMID: 30740127; PMCID: PMC6357929.
Falzarano MS, Ferlini A. Urinary Stem Cells as Tools to Study Genetic
Disease: Overview of the Literature. J Clin Med. 2019 May 8;8(5):627. doi:
10.3390/jcm8050627. PMID: 31071994; PMCID: PMC6572423.
Neri M, Rossi R, Trabanelli C, Mauro A, Selvatici R, Falzarano MS, Spedicato
N, Margutti A, Rimessi P, Fortunato F, Fabris M, Gualandi F, Comi G, Tedeschi S,
Seia M, Fiorillo C, Traverso M, Bruno C, Giardina E, Piemontese MR, Merla G, Cau
M, Marica M, Scuderi C, Borgione E, Tessa A, Astrea G, Santorelli FM, Merlini L,
Mora M, Bernasconi P, Gibertini S, Sansone V, Mongini T, Berardinelli A, Pini A,
Liguori R, Filosto M, Messina S, Vita G, Toscano A, Vita G, Pane M, Servidei S,
Pegoraro E, Bello L, Travaglini L, Bertini E, D'Amico A, Ergoli M, Politano L,
Torella A, Nigro V, Mercuri E, Ferlini A. The Genetic Landscape of Dystrophin
Mutations in Italy: A Nationwide Study. Front Genet. 2020 Mar 3;11:131. doi:
10.3389/fgene.2020.00131. PMID: 32194622; PMCID: PMC7063120.
Passarelli C, Selvatici R, Carrieri A, Di Raimo FR, Falzarano MS, Fortunato
F, Rossi R, Straub V, Bushby K, Reza M, Zharaieva I, D'Amico A, Bertini E,
Merlini L, Sabatelli P, Borgiani P, Novelli G, Messina S, Pane M, Mercuri E,
Claustres M, Tuffery-Giraud S, Aartsma-Rus A, Spitali P, T'Hoen PAC, Lochmüller
H, Strandberg K, Al-Khalili C, Kotelnikova E, Lebowitz M, Schwartz E, Muntoni F,
Scapoli C, Ferlini A. Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs
Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy. Front
Genet. 2020 Jul 3;11:605. doi: 10.3389/fgene.2020.00605. PMID: 32719714; PMCID:
PMC7350910.
Fortunato F, Rossi R, Falzarano MS, Ferlini A. Innovative Therapeutic
Approaches for Duchenne Muscular Dystrophy. J Clin Med. 2021 Feb 17;10(4):820.
doi: 10.3390/jcm10040820. PMID: 33671409; PMCID: PMC7922390.
Falzarano MS, Argenziano M, Marsollier AC, Mariot V, Rossi D, Selvatici R,
Dumonceaux J, Cavalli R, Ferlini A. Chitosan-Shelled Nanobubbles Irreversibly
Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective
for Phosphorodiamidate Morpholino-Mediated Gene Silencing of <i>DUX4</i>.
Nucleic Acid Ther. 2021 Jun;31(3):201-207. doi: 10.1089/nat.2020.0862. Epub 2020
Jul 13. PMID: 32679000.
Rossi R, Falzarano MS, Osman H, Armaroli A, Scotton C, Mantuano P,
Boccanegra B, Cappellari O, Schwartz E, Yuryev A, Mercuri E, Bertini E, D'Amico
A, Mora M, Johansson C, Al-Khalili Szigyarto C, De Luca A, Ferlini A. Circadian
Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse
Model and Patients. Front Physiol. 2021 Jul 8;12:678974. doi:
10.3389/fphys.2021.678974. PMID: 34305639; PMCID: PMC8300012.
Betts CA, Jagannath A, van Westering TL, Bowerman M, Banerjee S, Meng J,
Falzarano MS, Cravo L, McClorey G, Meijboom KE, Bhomra A, Lim WF, Rinaldi C,
Counsell JR, Chwalenia K, O'Donovan E, Saleh AF, Gait MJ, Morgan JE, Ferlini A,
Foster RG, Wood MJ. Dystrophin involvement in peripheral circadian SRF
signalling. Life Sci Alliance. 2021 Aug 13;4(10):e202101014. doi:
10.26508/lsa.202101014. PMID: 34389686; PMCID: PMC8363758.
Falzarano MS, Rossi R, Grilli A, Fang M, Osman H, Sabatelli P, Antoniel M,
Lu Z, Li W, Selvatici R, Al-Khalili C, Gualandi F, Bicciato S, Torelli S,
Ferlini A. Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing
Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic Diseases.
Front Physiol. 2021 Oct 20;12:716471. doi: 10.3389/fphys.2021.716471. PMID:
34744760; PMCID: PMC8565768.
Falzarano MS, Grilli A, Zia S, Fang M, Rossi R, Gualandi F, Rimessi P, El
Dani R, Fabris M, Lu Z, Li W, Mongini T, Ricci F, Pegoraro E, Bello L, Barp A,
Sansone VA, Hegde M, Roda B, Reschiglian P, Bicciato S, Selvatici R, Ferlini A.
RNA-seq in DMD urinary stem cells recognized muscle-related transcription
signatures and addressed the identification of atypical mutations by whole-
genome sequencing. HGG Adv. 2021 Aug 24;3(1):100054. doi:
10.1016/j.xhg
Selvatici R, Falzarano S, Traniello S, Pagani Zecchini G, Spisani S.
Formylpeptides trigger selective molecular pathways that are required in the
physiological functions of human neutrophils. Cell Signal. 2003
Apr;15(4):377-83. doi: 10.1016/s0898-6568(02)00123-7. PMID: 12618212.
Spisani S, Turchetti M, Varani K, Falzarano S, Cavicchioni G. Hydrophilic
residues at position 3 highlight unforeseen features of the fMLP receptor
pocket. Eur J Pharmacol. 2003 May 23;469(1-3):13-9. doi:
10.1016/s0014-2999(03)01672-8. PMID: 12782180.
Cavicchioni G, Turchetti M, Varani K, Falzarano S, Spisani S. Properties of a
novel chemotactic esapeptide, an analogue of the prototypical N-formylmethionyl
peptide. Bioorg Chem. 2003 Aug;31(4):322-30. doi: 10.1016/s0045-2068(03)00070-1.
PMID: 12877881.
Spisani S, Falzarano S, Traniello S, Nalli M, Selvatici R. A 'pure'
chemoattractant formylpeptide analogue triggers a specific signalling pathway in
human neutrophil chemotaxis. FEBS J. 2005 Feb;272(4):883-91. doi:
10.1111/j.1742-4658.2004.04497.x. PMID: 15691323.
Manzati E, Aguiari G, Banzi M, Manzati M, Selvatici R, Falzarano S, Maestri
I, Pinton P, Rizzuto R, del Senno L. The cytoplasmic C-terminus of polycystin-1
increases cell proliferation in kidney epithelial cells through serum-activated
and Ca(2+)-dependent pathway(s). Exp Cell Res. 2005 Apr 1;304(2):391-406. doi:
10.1016/j.yexcr.2004.10.023. Epub 2004 Dec 15. PMID: 15748886.
Cavicchioni G, Fraulini A, Turchetti M, Varani K, Falzarano S, Pavan B,
Spisani S. Biological activity of for-Met-Leu-Phe-OMe analogs: relevant
substitutions specifically trigger killing mechanisms in human neutrophils. Eur
J Pharmacol. 2005 Apr 4;512(1):1-8. doi: 10.1016/j.ejphar.2005.02.013. PMID:
15814083.
Trombella S, Vergura R, Falzarano S, Guerrini R, Calo G, Spisani S.
Nociceptin/orphanin FQ stimulates human monocyte chemotaxis via NOP receptor
activation. Peptides. 2005 Aug;26(8):1497-502. doi:
10.1016/j.peptides.2005.03.015. PMID: 15922491.
Selvatici R, Falzarano S, Mollica A, Spisani S. Signal transduction pathways
triggered by selective formylpeptide analogues in human neutrophils. Eur J
Pharmacol. 2006 Mar 18;534(1-3):1-11. doi: 10.1016/j.ejphar.2006.01.034. Epub
2006 Mar 3. PMID: 16516193.
Cavicchioni G, Fraulini A, Falzarano S, Spisani S. Structure-activity
relationship of for-L-Met L-Leu-L-Phe-OMe analogues in human neutrophils. Bioorg
Chem. 2006 Oct;34(5):298-318. doi: 10.1016/j.bioorg.2006.07.001. Epub 2006 Aug
17. PMID: 16919307.
Selvatici R, Falzarano S, Franceschetti L, Cavallini S, Marino S,
Siniscalchi A. Differential activation of protein kinase C isoforms following
chemical ischemia in rat cerebral cortex slices. Neurochem Int. 2006
Dec;49(8):729-36. doi: 10.1016/j.neuint.2006.06.003. Epub 2006 Sep 11. PMID:
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Siniscalchi A, Cavallini S, Marino S, Falzarano S, Franceschetti L,
Selvatici R. Effects of chemical ischemia on cerebral cortex slices: focus on
mitogen-activated protein kinase cascade. Ann N Y Acad Sci. 2006
Dec;1090:445-54. doi: 10.1196/annals.1378.047. PMID: 17384288.
Selvatici R, Falzarano S, Franceschetti L, Spisani S, Siniscalchi A. Effects
of PKI55 protein, an endogenous protein kinase C modulator, on specific PKC
isoforms activity and on human T cells proliferation. Arch Biochem Biophys. 2007
Jun 1;462(1):74-82. doi: 10.1016/j.abb.2007.03.018. Epub 2007 Apr 4. PMID:
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Spisani S, Fraulini A, Varani K, Falzarano S, Cavicchioni G. New chemotactic
dimeric peptides show high affinity and potency at the human formylpeptide
receptor. Eur J Pharmacol. 2007 Jul 12;567(1-2):171-6. doi:
10.1016/j.ejphar.2007.04.006. Epub 2007 Apr 14. PMID: 17481605.
Selvatici R, Falzarano S, Franceschetti L, Mollica A, Guerrini R,
Siniscalchi A, Spisani S. Study of synthetic peptides derived from the PKI55
protein, a protein kinase C modulator, in human neutrophils stimulated by the
methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-
OH. FEBS J. 2008 Feb;275(3):449-57. doi: 10.1111/j.1742-4658.2007.06212.x. Epub
2007 Dec 21. PMID: 18167144.
Borgatti M, Finotti A, Falzarano S, Selvatici R. Structural characterization
of promoter sequences of the gene coding human PKI55 protein, a protein kinase C
inhibitor. Biochimie. 2009 Apr;91(4):466-74. doi: 10.1016/j.biochi.2008.11.007.
Epub 2008 Dec 7. PMID: 19095038.
Selvatici R, Previati M, Marino S, Marani L, Falzarano S, Lanzoni I,
Siniscalchi A. Sodium azide induced neuronal damage in vitro: evidence for non-
apoptotic cell death. Neurochem Res. 2009 May;34(5):909-16. doi:
10.1007/s11064-008-9852-0. Epub 2008 Oct 8. PMID: 18841470.
Spitali P, Rimessi P, Fabris M, Perrone D, Falzarano S, Bovolenta M,
Trabanelli C, Mari L, Bassi E, Tuffery S, Gualandi F, Maraldi NM, Sabatelli-
Giraud P, Medici A, Merlini L, Ferlini A. Exon skipping-mediated dystrophin
reading frame restoration for small mutations. Hum Mutat. 2009
Nov;30(11):1527-34. doi: 10.1002/humu.21092. PMID: 19760747.
Cavicchioni G, Fraulini A, Falzarano S, Spisani S. Oligomeric formylpeptide
activity on human neutrophils. Eur J Med Chem. 2009 Dec;44(12):4926-30. doi:
10.1016/j.ejmech.2009.08.010. Epub 2009 Aug 31. PMID: 19748709.
Ferlini A, Sabatelli P, Fabris M, Bassi E, Falzarano S, Vattemi G, Perrone
D, Gualandi F, Maraldi NM, Merlini L, Sparnacci K, Laus M, Caputo A, Bonaldo P,
Braghetta P, Rimessi P. Dystrophin restoration in skeletal, heart and skin
arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes. Gene Ther. 2010
Mar;17(3):432-8. doi: 10.1038/gt.2009.145. Epub 2009 Nov 12. PMID: 19907501.
Rimessi P, Fabris M, Bovolenta M, Bassi E, Falzarano S, Gualandi F, Rapezzi
C, Coccolo F, Perrone D, Medici A, Ferlini A. Antisense modulation of both
exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon
responsible for x-linked dilated cardiomyopathy. Hum Gene Ther. 2010
Sep;21(9):1137-46. doi: 10.1089/hum.2010.010. PMID: 20486769.
Bassi E, Falzarano S, Fabris M, Gualandi F, Merlini L, Vattemi G, Perrone D,
Marchesi E, Sabatelli P, Sparnacci K, Laus M, Bonaldo P, Rimessi P, Braghetta P,
Ferlini A. Persistent dystrophin protein restoration 90 days after a course of
intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx
mice. J Biomed Biotechnol. 2012;2012:897076. doi: 10.1155/2012/897076. Epub 2012
Oct 2. PMID: 23091362; PMCID: PMC3471065.
Martoni E, Petrini S, Trabanelli C, Sabatelli P, Urciuolo A, Selvatici R,
D'Amico A, Falzarano S, Bertini E, Bonaldo P, Ferlini A, Gualandi F.
Characterization of a rare case of Ullrich congenital muscular dystrophy due to
truncating mutations within the COL6A1 gene C-terminal domain: a case report.
BMC Med Genet. 2013 Jun 5;14:59. doi: 10.1186/1471-2350-14-59. PMID: 23738969;
PMCID: PMC3681647.
Witkowska R, Zabrocki J, Spisani S, Falzarano MS, Toniolo C, Formaggio F.
Synthetic formyl tripeptide chemoattractants: a C(alpha,alpha)-dialkylated,
amphiphilic glycyl residue at position 1. J Pept Sci. 2003 Jun;9(6):354-60. doi:
10.1002/psc.461. PMID: 12846481.
Bruno O, Brullo C, Bondavalli F, Ranise A, Schenone S, Falzarano MS, Varani
K, Spisani S. 2-Phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole derivatives: new
potent inhibitors of fMLP-induced neutrophil chemotaxis. Bioorg Med Chem Lett.
2007 Jul 1;17(13):3696-701. doi: 10.1016/j.bmcl.2007.04.036. Epub 2007 Apr 19.
PMID: 17475488.
Bovolenta M, Neri M, Fini S, Fabris M, Trabanelli C, Venturoli A, Martoni E,
Bassi E, Spitali P, Brioschi S, Falzarano MS, Rimessi P, Ciccone R, Ashton E,
McCauley J, Yau S, Abbs S, Muntoni F, Merlini L, Gualandi F, Ferlini A. A novel
custom high density-comparative genomic hybridization array detects common
rearrangements as well as deep intronic mutations in dystrophinopathies. BMC
Genomics. 2008 Nov 28;9:572. doi: 10.1186/1471-2164-9-572. PMID: 19040728;
PMCID: PMC2612025.
Bruno O, Brullo C, Bondavalli F, Schenone S, Spisani S, Falzarano MS, Varani
K, Barocelli E, Ballabeni V, Giorgio C, Tognolini M. 1-Methyl and 1-(2-hydroxyal
kyl)-5-(3-alkyl/cycloalkyl/phenyl/naphthylureido)-1H-pyrazole-4-carboxylic acid
ethyl esters as potent human neutrophil chemotaxis inhibitors. Bioorg Med Chem.
2009 May 1;17(9):3379-87. doi: 10.1016/j.bmc.2009.03.035. Epub 2009 Mar 25.
PMID: 19362486.
Bovolenta M, Erriquez D, Valli E, Brioschi S, Scotton C, Neri M, Falzarano
MS, Gherardi S, Fabris M, Rimessi P, Gualandi F, Perini G, Ferlini A. The DMD
locus harbours multiple long non-coding RNAs which orchestrate and control
transcription of muscle dystrophin mRNA isoforms. PLoS One. 2012;7(9):e45328.
doi: 10.1371/journal.pone.0045328. Epub 2012 Sep 21. PMID: 23028937; PMCID:
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Bovolenta M, Scotton C, Falzarano MS, Gualandi F, Ferlini A. Rapid,
comprehensive analysis of the dystrophin transcript by a custom micro-fluidic
exome array. Hum Mutat. 2012 Mar;33(3):572-81. doi: 10.1002/humu.22017. Epub
2012 Jan 25. PMID: 22223181.
Brioschi S, Gualandi F, Scotton C, Armaroli A, Bovolenta M, Falzarano MS,
Sabatelli P, Selvatici R, D'Amico A, Pane M, Ricci G, Siciliano G, Tedeschi S,
Pini A, Vercelli L, De Grandis D, Mercuri E, Bertini E, Merlini L, Mongini T,
Ferlini A. Genetic characterization in symptomatic female DMD carriers: lack of
relationship between X-inactivation, transcriptional DMD allele balancing and
phenotype. BMC Med Genet. 2012 Aug 16;13:73. doi: 10.1186/1471-2350-13-73. PMID:
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Falzarano MS, Passarelli C, Bassi E, Fabris M, Perrone D, Sabatelli P,
Maraldi NM, Donà S, Selvatici R, Bonaldo P, Sparnacci K, Laus M, Braghetta P,
Rimessi P, Ferlini A. Biodistribution and molecular studies on orally
administered nanoparticle-AON complexes encapsulated with alginate aiming at
inducing dystrophin rescue in mdx mice. Biomed Res Int. 2013;2013:527418. doi:
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Falzarano MS, Passarelli C, Ferlini A. Nanoparticle delivery of antisense
oligonucleotides and their application in the exon skipping strategy for
Duchenne muscular dystrophy. Nucleic Acid Ther. 2014 Feb;24(1):87-100. doi:
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Falzarano MS, Bassi E, Passarelli C, Braghetta P, Ferlini A. Biodistribution
studies of polymeric nanoparticles for drug delivery in mice. Hum Gene Ther.
2014 Nov;25(11):927-8. doi: 10.1089/hum.2014.073. Epub 2014 Sep 22. PMID:
25244215; PMCID: PMC4236061.
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN,
Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Brioschi S, Bovolenta
M, Neri M, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg
DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Corrigendum: Translation from a
DMD exon 5 IRES results in a functional dystrophin isoform that attenuates
dystrophinopathy in humans and mice. Nat Med. 2015 May;21(5):537. doi:
10.1038/nm0515-537c. Erratum for: Nat Med. 2014 Sep;20(9):992-1000. PMID:
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Falzarano MS, Scotton C, Passarelli C, Ferlini A. Duchenne Muscular
Dystrophy: From Diagnosis to Therapy. Molecules. 2015 Oct 7;20(10):18168-84.
doi: 10.3390/molecules201018168. PMID: 26457695; PMCID: PMC6332113.
Scotton C, Bovolenta M, Schwartz E, Falzarano MS, Martoni E, Passarelli C,
Armaroli A, Osman H, Rodolico C, Messina S, Pegoraro E, D'Amico A, Bertini E,
Gualandi F, Neri M, Selvatici R, Boffi P, Maioli MA, Lochmüller H, Straub V,
Bushby K, Castrignanò T, Pesole G, Sabatelli P, Merlini L, Braghetta P, Bonaldo
P, Bernardi P, Foley R, Cirak S, Zaharieva I, Muntoni F, Capitanio D, Gelfi C,
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Deep RNA profiling identified CLOCK and molecular clock genes as
pathophysiological signatures in collagen VI myopathy. J Cell Sci. 2016 Apr
15;129(8):1671-84. doi: 10.1242/jcs.175927. Epub 2016 Mar 4. PMID: 26945058;
PMCID: PMC4852766.
Falzarano MS, D'Amario D, Siracusano A, Massetti M, Amodeo A, La Neve F,
Maroni CR, Mercuri E, Osman H, Scotton C, Armaroli A, Rossi R, Selvatici R, Crea
F, Ferlini A. Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem
Cells Recapitulate the Dystrophin Genotype and Phenotype. Hum Gene Ther. 2016
Oct;27(10):772-783. doi: 10.1089/hum.2016.079. PMID: 27530229.
Sardone V, Zhou H, Muntoni F, Ferlini A, Falzarano MS. Antisense
Oligonucleotide-Based Therapy for Neuromuscular Disease. Molecules. 2017 Apr
5;22(4):563. doi: 10.3390/molecules22040563. PMID: 28379182; PMCID: PMC6154734.
Gherardi S, Bovolenta M, Passarelli C, Falzarano MS, Pigini P, Scotton C,
Neri M, Armaroli A, Osman H, Selvatici R, Gualandi F, Recchia A, Mora M,
Bernasconi P, Maggi L, Morandi L, Ferlini A, Perini G. Transcriptional and
epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that
govern muscle dystrophin expression. Biochim Biophys Acta Gene Regul Mech. 2017
Nov;1860(11):1138-1147. doi: 10.1016/j.bbagrm.2017.08.010. Epub 2017 Sep 1.
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Falzarano MS, Flesia C, Cavalli R, Guiot C, Ferlini A. Nanodiagnostics and
Nanodelivery Applications in Genetic Alterations. Curr Pharm Des.
2018;24(15):1717-1726. doi: 10.2174/1381612824666180110151318. PMID: 29318963.
Hiller M, Falzarano MS, Garcia-Jimenez I, Sardone V, Verheul RC, Popplewell
L, Anthony K, Ruiz-Del-Yerro E, Osman H, Goeman JJ, Mamchaoui K, Dickson G,
Ferlini A, Muntoni F, Aartsma-Rus A, Arechavala-Gomeza V, Datson NA, Spitali P.
A multicenter comparison of quantification methods for antisense
oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell
cultures. PLoS One. 2018 Oct 2;13(10):e0204485. doi:
10.1371/journal.pone.0204485. PMID: 30278058; PMCID: PMC6168132.
Bigoni S, Neri M, Scotton C, Farina R, Sabatelli P, Jiang C, Zhang J,
Falzarano MS, Rossi R, Ognibene D, Selvatici R, Gualandi F, Bosshardt D, Perri
P, Campa C, Brancati F, Salvatore M, De Stefano MC, Taruscio D, Trombelli L,
Fang M, Ferlini A. Homozygous Recessive Versican Missense Variation Is
Associated With Early Teeth Loss in a Pakistani Family. Front Genet. 2019 Jan
21;9:723. doi: 10.3389/fgene.2018.00723. PMID: 30740127; PMCID: PMC6357929.
Falzarano MS, Ferlini A. Urinary Stem Cells as Tools to Study Genetic
Disease: Overview of the Literature. J Clin Med. 2019 May 8;8(5):627. doi:
10.3390/jcm8050627. PMID: 31071994; PMCID: PMC6572423.
Neri M, Rossi R, Trabanelli C, Mauro A, Selvatici R, Falzarano MS, Spedicato
N, Margutti A, Rimessi P, Fortunato F, Fabris M, Gualandi F, Comi G, Tedeschi S,
Seia M, Fiorillo C, Traverso M, Bruno C, Giardina E, Piemontese MR, Merla G, Cau
M, Marica M, Scuderi C, Borgione E, Tessa A, Astrea G, Santorelli FM, Merlini L,
Mora M, Bernasconi P, Gibertini S, Sansone V, Mongini T, Berardinelli A, Pini A,
Liguori R, Filosto M, Messina S, Vita G, Toscano A, Vita G, Pane M, Servidei S,
Pegoraro E, Bello L, Travaglini L, Bertini E, D'Amico A, Ergoli M, Politano L,
Torella A, Nigro V, Mercuri E, Ferlini A. The Genetic Landscape of Dystrophin
Mutations in Italy: A Nationwide Study. Front Genet. 2020 Mar 3;11:131. doi:
10.3389/fgene.2020.00131. PMID: 32194622; PMCID: PMC7063120.
Passarelli C, Selvatici R, Carrieri A, Di Raimo FR, Falzarano MS, Fortunato
F, Rossi R, Straub V, Bushby K, Reza M, Zharaieva I, D'Amico A, Bertini E,
Merlini L, Sabatelli P, Borgiani P, Novelli G, Messina S, Pane M, Mercuri E,
Claustres M, Tuffery-Giraud S, Aartsma-Rus A, Spitali P, T'Hoen PAC, Lochmüller
H, Strandberg K, Al-Khalili C, Kotelnikova E, Lebowitz M, Schwartz E, Muntoni F,
Scapoli C, Ferlini A. Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs
Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy. Front
Genet. 2020 Jul 3;11:605. doi: 10.3389/fgene.2020.00605. PMID: 32719714; PMCID:
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Fortunato F, Rossi R, Falzarano MS, Ferlini A. Innovative Therapeutic
Approaches for Duchenne Muscular Dystrophy. J Clin Med. 2021 Feb 17;10(4):820.
doi: 10.3390/jcm10040820. PMID: 33671409; PMCID: PMC7922390.
Falzarano MS, Argenziano M, Marsollier AC, Mariot V, Rossi D, Selvatici R,
Dumonceaux J, Cavalli R, Ferlini A. Chitosan-Shelled Nanobubbles Irreversibly
Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective
for Phosphorodiamidate Morpholino-Mediated Gene Silencing of <i>DUX4</i>.
Nucleic Acid Ther. 2021 Jun;31(3):201-207. doi: 10.1089/nat.2020.0862. Epub 2020
Jul 13. PMID: 32679000.
Rossi R, Falzarano MS, Osman H, Armaroli A, Scotton C, Mantuano P,
Boccanegra B, Cappellari O, Schwartz E, Yuryev A, Mercuri E, Bertini E, D'Amico
A, Mora M, Johansson C, Al-Khalili Szigyarto C, De Luca A, Ferlini A. Circadian
Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse
Model and Patients. Front Physiol. 2021 Jul 8;12:678974. doi:
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Betts CA, Jagannath A, van Westering TL, Bowerman M, Banerjee S, Meng J,
Falzarano MS, Cravo L, McClorey G, Meijboom KE, Bhomra A, Lim WF, Rinaldi C,
Counsell JR, Chwalenia K, O'Donovan E, Saleh AF, Gait MJ, Morgan JE, Ferlini A,
Foster RG, Wood MJ. Dystrophin involvement in peripheral circadian SRF
signalling. Life Sci Alliance. 2021 Aug 13;4(10):e202101014. doi:
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Falzarano MS, Rossi R, Grilli A, Fang M, Osman H, Sabatelli P, Antoniel M,
Lu Z, Li W, Selvatici R, Al-Khalili C, Gualandi F, Bicciato S, Torelli S,
Ferlini A. Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing
Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic Diseases.
Front Physiol. 2021 Oct 20;12:716471. doi: 10.3389/fphys.2021.716471. PMID:
34744760; PMCID: PMC8565768.
Falzarano MS, Grilli A, Zia S, Fang M, Rossi R, Gualandi F, Rimessi P, El
Dani R, Fabris M, Lu Z, Li W, Mongini T, Ricci F, Pegoraro E, Bello L, Barp A,
Sansone VA, Hegde M, Roda B, Reschiglian P, Bicciato S, Selvatici R, Ferlini A.
RNA-seq in DMD urinary stem cells recognized muscle-related transcription
signatures and addressed the identification of atypical mutations by whole-
genome sequencing. HGG Adv. 2021 Aug 24;3(1):100054. doi:
10.1016/j.xhgg.2021.100054. PMID: 35047845; PMCID: PMC8756543.
Falzarano MS, Mietto M, Fortunato F, Farnè M, Martini F, Ala P, Selvatici R,
Muntoni F, Ferlini A. mRNA in situ hybridization exhibits unbalanced
nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells
and skeletal muscle biopsies. Sci Rep. 2023 Sep 24;13(1):15942. doi:
10.1038/s41598-023-43134-6. PMID: 37743371; PMCID: PMC10518324.
Caputo L, Stamenkovic C, Tierney MT, Falzarano MS, Bassel-Duby R, Ferlini A, Olson EN, Puri PL, Sacco A. Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSCs-derived myogenic progenitor cells. bioRxiv [Preprint]. 2024 Dec 10:2024.12.09.624203. doi: 10.1101/2024.12.09.624203. PMID: 39713478; PMCID: PMC11661153.
g.2021.100054. PMID: 35047845; PMCID: PMC8756543.
Falzarano MS, Mietto M, Fortunato F, Farnè M, Martini F, Ala P, Selvatici R,
Muntoni F, Ferlini A. mRNA in situ hybridization exhibits unbalanced
nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells
and skeletal muscle biopsies. Sci Rep. 2023 Sep 24;13(1):15942. doi:
10.1038/s41598-023-43134-6. PMID: 37743371; PMCID: PMC10518324.
Caputo L, Stamenkovic C, Tierney MT, Falzarano MS, Bassel-Duby R, Ferlini A, Olson EN, Puri PL, Sacco A. Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSCs-derived myogenic progenitor cells. bioRxiv [Preprint]. 2024 Dec 10:2024.12.09.624203. doi: 10.1101/2024.12.09.624203. PMID: 39713478; PMCID: PMC11661153.