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Mostrati risultati da 151 a 170 di 357
Data di pubblicazione Titolo Autore(i) File
1-gen-2020 Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis Cuellar, Araceli; Bala, Krithi; Di Pietro, Lorena; Barba, Marta; Yagnik, Garima; Liu, Jia Lie; Stevens, Christina; Hur, David J; Ingersoll, Roxann G; Justice, Cristina M; Drissi, Hicham; Kim, Jinoh; Lattanzi, Wanda; Boyadjiev, Simeon A
1-gen-2017 Genetic advances in craniosynostosis Lattanzi, Wanda; Barba, Marta; Di Pietro, Lorena; Boyadjiev, Simeon A.
1-gen-2018 Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophy Iannotti, F. A.; Pagano, E.; Guardiola, O.; Adinolfi, S.; Saccone, V.; Consalvi, S.; Piscitelli, F.; Gazzerro, E.; Busetto, G.; Carrella, D.; Capasso, R.; Puri, P. L.; Minchiotti, G.; Di Marzo, V.
1-gen-2006 Genistein affects adipose tissue deposition in a dose-dependent and gender-specific manner Penza, M; Montani, C; Romani, A; Vignolini, P; Pampaloni, B; Tanini, A; Brandi, M. L; Alonso Magdalena, P; Nadal, A; Ottobrini, L; Parolini, Ornella; Bignotti, E; Calza, S; Maggi, Aldo Marco; Grigolato, P. G; Di Lorenzo, Andrea Alessandro Daniele
1-gen-2020 A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis Justice, Cm; Cuellar, A; Bala, K; Sabourin, Ja; Cunningham, Ml; Crawford, K; Phipps, Jm; Zhou, Y; Cilliers, D; Byren, Jc; Johnson, D; Wall, Sa; Morton, Jev; Noons, P; Sweeney, E; Weber, Bertram; Rees, Kem; Wilson, Lc; Simeonov, E; Kaneva, R; Yaneva, N; Georgiev, K; Bussarsky, A; Senders, C; Zwienenberg, M; Boggan, J; Roscioli, T; Tamburrini, Gianpiero; Barba, Marta; Conway, K; Sheffield, Vc; Brody, L; Mills, Jl; Kay, D; Sicko, Rj; Langlois, Ph; Tittle, Rk; Botto, Ld; Jenkins, Mm; Lasalle, Jm; Lattanzi, Wanda; Wilkie, Aom; Wilson, Af; Romitti, Pa; Boyadjiev, Sa
1-gen-1994 The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia Rohrer, J; Parolini, Ornella; Belmont, J. W; Conley, M. E; Parolino O. [corrected to Parolini, O.
1-gen-2014 Gestational stage affects amniotic epithelial cells phenotype, methylation status, immunomodulatory and stemness properties Barboni, Barbara; Russo, Valentina; Curini, Valentina; Martelli, Alessandra; Berardinelli, Paolo; Mauro, Annunziata; Mattioli, Mauro; Marchisio, Marco; Bonassi Signoroni, Patrizia; Parolini, Ornella; Colosimo, Alessia
1-gen-2020 Gli1 and axin2 are distinctive markers of human calvarial mesenchymal stromal cells in nonsyndromic craniosynostosis Di Pietro, Lorena; Barba, Marta; Prampolini, Chiara; Ceccariglia, Sabrina; Frassanito, Paolo; Vita, A.; Guadagni, E.; Bonvissuto, Davide; Massimi, Luca; Tamburrini, Gianpiero; Parolini, Ornella; Lattanzi, Wanda
1-gen-2018 Graphene Oxide Induced Osteogenesis Quantification by In-Situ 2D-Fluorescence Spectroscopy Palmieri, Valentina; Barba, Marta; Di Pietro, Lorena; Conti, C.; De Spirito, Marco; Lattanzi, Wanda; Papi, Massimiliano
1-gen-2020 Graphene Oxide Nano-concentrators Selectively Modulate RNA Trapping According to Metal Cations in Solution Palmieri, Valentina; Di Pietro, Lorena; Perini, Giordano; Barba, Marta; Parolini, Ornella; De Spirito, Marco; Lattanzi, Wanda; Papi, Massimiliano
1-gen-1999 The growth of malignant and nonmalignant human cells is modulated by a human placental extract Angelucci, C; Lama, G; Sica, G
1-gen-2016 HDAC inhibitors for muscular dystrophies: Progress and prospects Sandona, M.; Consalvi, S.; Tucciarone, L.; Puri, P. L.; Saccone, Valentina
1-gen-2020 HDAC inhibitors tune miRNAs in extracellular vesicles of dystrophic muscle-resident mesenchymal cells Sandona, M.; Consalvi, S.; Tucciarone, L.; De Bardi, M.; Scimeca, M.; Angelini, D. F.; Buffa, V.; D'Amico, A.; Bertini, E. S.; Cazzaniga, S.; Bettica, P.; Bouche, M.; Bongiovanni, A.; Puri, P. L.; Saccone, Valentina
1-gen-2018 HDAC4 regulates satellite cell proliferation and differentiation by targeting P21 and Sharp1 genes Marroncelli, N.; Bianchi, M.; Bertin, M.; Consalvi, Sara; Saccone, Valentina; De Bardi, M.; Puri, P. L.; Palacios, Daniela; Adamo, S.; Moresi, V.
1-gen-1995 High prevalence of nonsense, frame shift, and splice-site mutations in 16 patients with full-blown Wiskott-Aldrich syndrome Wengler, G. S; Notarangelo, L. D; Berardelli, S; Pollonni, G; Mella, P; Fasth, A; Ugazio, A. G; Parolini, Ornella
1-gen-1998 High-porosity and normal-porosity prostheses. Differences in growth factor release Sapienza, P; Di Marzo, L; Cucina, A; Burchi, C; Corvino, Valentina; Mingoli, A; Cavallaro, A.
1-gen-2022 HIPGEN: a randomized, multicentre phase III study using intramuscular PLacenta-eXpanded stromal cells therapy for recovery following hip fracture arthroplasty : a study design Winkler, Tobias; Costa, Matthew L; Ofir, Racheli; Parolini, Ornella; Geissler, Sven; Volk, Hans-Dieter; Eder, Christian
1-gen-1981 [Histochemical localization of acetylcholinesterase in the chick ciliary ganglion during development] Olivieri Sangiacomo, C; Del Fa' Gangitano, Aurora; Gangitano, Carlo
1-gen-2019 Histone deacetylase 4 protects from denervation and skeletal muscle atrophy in a murine model of amyotrophic lateral sclerosis Pigna, E.; Simonazzi, E.; Sanna, K.; Bernadzki, K. M.; Proszynski, T.; Heil, C.; Palacios, Daniela; Adamo, S.; Moresi, V.
1-gen-2023 Histone Deacetylases: Molecular Mechanisms and Therapeutic Implications for Muscular Dystrophies Sandonà, Martina; Cavioli, Giorgia; Renzini, Alessandra; Cedola, Alessia; Gigli, Giuseppe; Coletti, Dario; Mckinsey, Timothy A; Moresi, Viviana; Saccone, Valentina
Mostrati risultati da 151 a 170 di 357
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