Search Results - "Raffa, Paolo"

Hydrogel-in-hydrogel live bioprinting for guidance and control of organoids and organotypic cultures by Urciuolo, Anna, Giobbe, Giovanni Giuseppe, Dong, Yixiao, Michielin, Federica, Brandolino, Luca, Magnussen, Michael, Gagliano, Onelia, Selmin, Giulia, Scattolini, Valentina, Raffa, Paolo, Caccin, Paola, Shibuya, Soichi, Scaglioni, Dominic, Wang, Xuechun, Qu, Ju, Nikolic, Marko, Montagner, Marco, Galea, Gabriel L., Clevers, Hans, Giomo, Monica, De Coppi, Paolo, Elvassore, Nicola

“…Three-dimensional hydrogel-based organ-like cultures can be applied to study development, regeneration, and disease in vitro. However, the control of…”
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Three-dimensional in vitro models of neuromuscular tissue by Raffa, Paolo, Easler, Maria, Urciuolo, Anna

“…Skeletal muscle is a dynamic tissue in which homeostasis and function are guaranteed by a very defined three-dimensional organization of myofibers in respect…”
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Decellularized skeletal muscles display neurotrophic effects in three‐dimensional organotypic cultures by Raffa, Paolo, Scattolini, Valentina, Gerli, Mattia Francesco Maria, Perin, Silvia, Cui, Meihua, De Coppi, Paolo, Elvassore, Nicola, Caccin, Paola, Luni, Camilla, Urciuolo, Anna

“…Skeletal muscle decellularization allows the generation of natural scaffolds that retain the extracellular matrix (ECM) mechanical integrity, biological…”
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Novel Technique of Transepithelial Corneal Cross-Linking Using Iontophoresis in Progressive Keratoconus by Rosati, Marianna, Raffa, Paolo, Serrao, Sebastiano, Lombardo, Marco, Lombardo, Giuseppe

“…In this work, the authors presented the techniques and the preliminary results at 6 months of a randomized controlled trial (NCT02117999) comparing a novel…”
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Decellularized Skeletal Muscles Support the Generation of In Vitro Neuromuscular Tissue Models by Raffa, Paolo, Easler, Maria, Cecchinato, Francesca, Auletta, Beatrice, Scattolini, Valentina, Perin, Silvia, Gerli, Mattia Francesco Maria, Caccin, Paola, Elvassore, Nicola, De Coppi, Paolo, Urciuolo, Anna

“…Decellularized skeletal muscle (dSkM) constructs have received much attention in recent years due to the versatility of their applications in vitro. In search…”
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Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome by Barbaro, Vanessa, Nasti, Annamaria Assunta, Raffa, Paolo, Migliorati, Angelo, Nespeca, Patrizia, Ferrari, Stefano, Palumbo, Elisa, Bertolin, Marina, Breda, Claudia, Miceli, Francesco, Russo, Antonella, Caenazzo, Luciana, Ponzin, Diego, Palù, Giorgio, Parolin, Cristina, Di Iorio, Enzo

“…: Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome is a rare autosomal dominant disease caused by mutations in the p63 gene. To date, approximately 40…”
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Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells by Artusi, Sara, Perrone, Rosalba, Lago, Sara, Raffa, Paolo, Di Iorio, Enzo, Palù, Giorgio, Richter, Sara N

“…We have previously shown that clusters of guanine quadruplex (G4) structures can form in the human herpes simplex-1 (HSV-1) genome. Here we used…”
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Intravital three-dimensional bioprinting by Urciuolo, Anna, Poli, Ilaria, Brandolino, Luca, Raffa, Paolo, Scattolini, Valentina, Laterza, Cecilia, Giobbe, Giovanni G., Zambaiti, Elisa, Selmin, Giulia, Magnussen, Michael, Brigo, Laura, De Coppi, Paolo, Salmaso, Stefano, Giomo, Monica, Elvassore, Nicola

“…Fabrication of three-dimensional (3D) structures and functional tissues directly in live animals would enable minimally invasive surgical techniques for organ…”
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Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele‐Specific Silencing Restores Defective Stem Cell Function by Barbaro, Vanessa, Nasti, Annamaria A., Vecchio, Claudia, Ferrari, Stefano, Migliorati, Angelo, Raffa, Paolo, Lariccia, Vincenzo, Nespeca, Patrizia, Biasolo, Mariangela, Willoughby, Colin E., Ponzin, Diego, Palù, Giorgio, Parolin, Cristina, Di Iorio, Enzo

“…Ectrodactyly‐Ectodermal dysplasia‐Clefting (EEC) syndrome is a rare autosomal dominant disease caused by heterozygous mutations in the p63 gene and…”
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Novel Variants of RPGR in X-Linked Retinitis Pigmentosa Families and Genotype-Phenotype Correlation by Parmeggiani, Francesco, Barbaro, Vanessa, Migliorati, Angelo, Raffa, Paolo, Nespeca, Patrizia, De Nadai, Katia, Del Vecchio, Claudia, Palù, Giorgio, Parolin, Cristina, Di Iorio, Enzo

“…Purpose To identify novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene and retinitis pigmentosa 2 (RP2) gene underlying X-linked…”
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