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Mostrati risultati da 2.492 a 2.511 di 4.008
Data di pubblicazione Titolo Autore(i) File
1-gen-1999 Multiple paraneoplastic diseases associated with thymoma. Evoli, Amelia; Marra, Roberto; Batocchi, Anna Paola; Tonali, Pietro Attilio; Lo Monaco, Mauro; Lino, Maddalena
1-gen-2010 Multiple tumor marker elevation in androgen ablation-refractory prostate cancer with long-term response to metronomic chemotherapy: a case report Massaccesi, Mariangela; Forni, Franca; Spagnuolo, Rocco; Macchia, Gabriella; Mignogna, Samantha; De Ninno, Maria; Cellini, Numa; Giardina, Bruno; Carbone, Arnaldo; Morganti, Alessio Giuseppe
1-gen-2009 Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. Concolino, Paola; Mello, Enrica; Toscano, V; Ameglio, F; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2011 Multiplex Ligation-Dependent Probe Amplification Analysis Is Useful for Diagnosing Congenital Adrenal Hyperplasia but Requires a Deep Knowledge of CYP21A2 Genetics Concolino, Paola; Mello, E; Minucci, Angelo; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2015 Multipotent mesenchymal stromal cell-based therapies: Regeneration versus Repair. Caruso, Maddalena; Parolini, Ornella
1-gen-2019 Murine platelet production is suppressed by S1P release in the hematopoietic niche, not facilitated by blood S1P sensing. Niazi, H; Zoghdani, N; Couty, L; Leuci, A; Nitzsche, A; Allende, Ml; Mariko, B; Ishaq, R; Aslan, Y; Becker, Ph; Gazit, Sl; Poirault-Chassac, S; Decouture, B; Baudrie, V; De Candia, E; Kono, M; Benarab, A; Gaussem, P; Tharaux, Pl; Chun, J; Provot, S; Debili, N; Therond, P; Proia, Rl; Bachelot-Loza, C; Camerer, E
1-gen-2009 Muscle bioenergetics and metabolic control at altitude Cerretelli, P; Marzorati, Mauro; Marconi, C.
1-gen-2018 Muscle Expression of SOD1G93A Triggers the Dismantlement of Neuromuscular Junction via PKC-Theta. Dobrowolny, G; Martini, M; Scicchitano, Bm; Romanello, V; Boncompagni, S; Nicoletti, C; Pietrangelo, L; De Panfilis, S; Catizone, A; Bouchè, M; Sandri, M; Rudolf, R; Protasi, F; Musarò, A
1-gen-2015 Muscle expression of SOD1G93Amodulates microRNA and mRNA transcription pattern associated with the myelination process in the spinal cord of transgenic mice Dobrowolny, Gabriella; Bernardini, Camilla; Martini, Martina; Baranzini, Mirko; Barba, Marta; Musarò, Antonio
1-gen-2009 Mutagenesis at the alpha-beta interface impairs the cleavage of the dystroglycan precursor Sciandra, Francesca; Bozzi, Manuela; Morlacchi, Simona; Galtieri, Antonio; Giardina, Bruno; Brancaccio, Andrea
1-gen-1999 Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists Michieli, Paolo; Basilico, Cristina; Pennacchietti, Selma; Maffè, Antonella; Tamagnone, Luca; Giordano, Silvia; Bardelli, Alberto; Comoglio, Paolo M.
1-gen-1998 Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1) Wengler, G. S; Giliani, S; Fiorini, M; Mella, P; Mantuano, E; Zanola, Annalisa; Pollonini, G; Eibl, M. M; Ugazio, A. G; Notarangelo, L. D; Parolini, Ornella
1-gen-1995 Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNA Wengler, G. S; Notarangelo, L. D; Giliani, S; Pirastru, M. G; Ugazio, A. G; Parolini, Ornella
1-gen-2008 Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients Gurrieri, Fiorella; Franco, Brunella
1-gen-2016 Mutations in rpoB sequences of Actinobacteria: a confounding factor in conjugal transfer experiments Puglisi, Edoardo; Guerrieri, Maria Chiara; Morelli, Lorenzo
1-gen-2013 Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis Sabatelli, Mario; Moncada, Alice; Conte, Amelia; Lattante, Serena; Marangi, Giuseppe; Luigetti, Marco; Lucchini, Matteo; Mirabella, Massimiliano; Romano, Angela; Del Grande, Alessandra; Bisogni, Giulia; Doronzio, Pn; Rossini, Paolo Maria; Zollino, Marcella
1-gen-2014 Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis Johnson, Jo; Pioro, Ep; Boehringer, A; Chia, R; Feit, H; Renton, Ae; Pliner, Ha; Abramzon, Y; Marangi, Giuseppe; Winborn, Bj; Gibbs, Jr; Nalls, Ma; Morgan, S; Shoai, M; Hardy, J; Pittman, A; Orrell, Rw; Malaspina, A; Sidle, Kc; Fratta, P; Harms, Mb; Baloh, Rh; Pestronk, A; Weihl, Cc; Rogaeva, E; Zinman, L; Drory, Ve; Borghero, G; Mora, G; Calvo, A; Rothstein, Jd; Drepper, C; Sendtner, M; Singleton, Ab; Taylor, Jp; Cookson, Mr; Restagno, G; Sabatelli, Mario; Bowser, R; Chiò, A; Traynor, Bj; Conte, Amelia; Luigetti, Marco; Zollino, Marcella; Lattante, Serena
1-gen-2013 Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France Lattante, Serena; Le Ber, I; Camuzat, A; Brice, A; Kabashi, E.
1-gen-2015 Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review Evoli, Amelia; Alboini, Paolo Emilio; Damato, Valentina; Iorio, Raffaele; Luigetti, Marco
1-gen-2020 MYC up-regulation confers resistance to everolimus and establishes vulnerability to cyclin dependent kinase inhibitors in pancreatic neuroendocrine neoplasms cells Terracciano, Francesca; Capone, Alessia; Montori, Andrea; Rinzivillo, Maria; Partelli, Stefano; Panzuto, Francesco; Pilozzi, Emanuela; Arcidiacono, Paolo Giorgio; Sette, Claudio; Capurso, Gabriele
Mostrati risultati da 2.492 a 2.511 di 4.008
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