LaghaM., BrunelliS., MessinaG., et al. (2009). Pax3:Foxc2 reciprocal repression in the somite modulates muscular versus vascular cell fate choice in multipotent progenitors. Dev. Cell, 17, 892–899.
2.
BonfantiP., ClaudinotS., AmiciA.W., et al. (2010). Microenvironmental reprogramming of thymic epithelial cells to skin multipotent stem cells. Nature, 466, 978–982.
3.
CoradaM., NyqvistD., OrsenigoF., et al. (2010). The Wnt/beta-catenin pathway modulates vascular remodeling and specification by upregulating Dll4/Notch signaling. Dev. Cell., 18, 938–949.
4.
EnglishK., FrenchA., and WoodK.J. (2010). Mesenchymal stromal cells: facilitators of successful transplantation?. Stem Cell. Dev., 7, 431–442.
5.
MessinaG., BiressiS., MonteverdeS., et al. (2010). Nfix regulates fetal-specific transcription in developing skeletal muscle. Cell, 140, 554–566.
6.
MitchellK.J., PannérecA., CadotB., et al. (2010). Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development. Cell Biol., 12, 257–266.
7.
RamaP., MatuskaS., PaganoniG., et al. (2010). Limbal stem-cell therapy and long-term corneal regeneration. N. Engl. J. Med., 363, 147–155.
8.
DellavalleA., MaroliG., CovarelloD., et al. (2011). Pericytes resident in postnatal skeletal muscle differentiate into muscle fibres and generate satellite cells. Nat. Commun., 2, 499.
9.
TedescoF.S., HoshiyaH., D'AntonaG., et al. (2011). Stem cell-mediated transfer of a human artificial chromosome ameliorates muscular dystrophy. Sci. Transl. Med., 3, 96ra78.
10.
ArditeE., PerdigueroE., VidalB., et al. (2012). PAI-1-regulated miR-21 defines a novel age-associated fibrogenic pathway in muscular dystrophy. J. Cell Biol., 196, 163–175.
11.
CristC.G., MontarrasD., and BuckinghamM. (2012). Muscle satellite cells are primed for myogenesis but maintain quiescence with sequestration of Myf5 mRNA targeted by microRNA-31 in mRNP granules. Cell Stem Cell, 11, 118–126.
12.
MourikisP., GopalakrishnanS., SambasivanR., et al. (2012). Cell-autonomous Notch activity maintains the temporal specification potential of skeletal muscle stem cells. Development, 139, 4536–4548.
13.
TajbakhshS. (2012). A subpopulation of adult skeletal muscle stem cells retains all template DNA strands after cell division. Cell, 148, 112–125.
14.
TedescoF.S., GerliM.F., PeraniL., et al. (2012). Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy. Sci. Transl. Med., 4, 140ra89.
15.
VidalB., ArditeE., SuelvesM., et al. (2012). Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor. Hum. Mol. Genet., 21, 1989–2004.
16.
CappellariO., BenedettiS., InnocenziA., et al. (2013). Dll4 and PDGF-BB convert committed skeletal myoblasts to pericytes without erasing their myogenic memory. Dev. Cell., 24, 586–599.
17.
DriskellR.R., LichtenbergerB.M., HosteE., et al. (2013). Distinct fibroblast lineages determine dermal architecture in skin development and repair. Nature, 504, 277–281.
18.
MaddalunoL., RudiniN., CuttanoR., et al. (2013). EndMT contributes to the onset and progression of cerebral cavernous malformations. Nature, 498, 492–496.
De RosaL., CarulliS., CocchiarellaF., et al. (2014). Long-term stability and safety of transgenic cultured epidermal stem cells in gene therapy of junctional epidermolysis bullosa. Stem Cell Rep., 2, 1–8.
21.
GiannottaM., BenedettiS., TedescoF.S., et al. (2014). Targeting endothelial junctional adhesion molecule-A/EPAC/Rap-1 axis as a novel strategy to increase stem cell engraftment in dystrophic muscles. EMBO Mol. Med., 6, 239–258.