Sfoglia per ???browse.type.metadata.typeResearch??? AREA05 - SCIENZE BIOLOGICHE
Murine platelet production is suppressed by S1P release in the hematopoietic niche, not facilitated by blood S1P sensing.
2019 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, Erica; Kono, M; Benarab, A; Gaussem, P; Tharaux, Pl; Chun, J; Provot, S; Debili, N; Therond, P; Proia, Rl; Bachelot-Loza, C; Camerer, E
Muscle bioenergetics and metabolic control at altitude
2009 Cerretelli, P; Marzorati, Mauro; Marconi, C.
Muscle Expression of SOD1G93A Triggers the Dismantlement of Neuromuscular Junction via PKC-Theta.
2018 Dobrowolny, G; Martini, M; Scicchitano, Bianca Maria; Romanello, V; Boncompagni, S; Nicoletti, C; Pietrangelo, L; De Panfilis, S; Catizone, A; Bouchè, M; Sandri, M; Rudolf, R; Protasi, F; Musarò, A
Muscle expression of SOD1G93Amodulates microRNA and mRNA transcription pattern associated with the myelination process in the spinal cord of transgenic mice
2015 Dobrowolny, Gabriella; Bernardini, Camilla; Martini, Martina; Baranzini, Mirko; Barba, Marta; Musarò, Antonio
Mutagenesis at the alpha-beta interface impairs the cleavage of the dystroglycan precursor
2009 Sciandra, Francesca; Bozzi, Manuela; Morlacchi, Simona; Galtieri, Antonio; Giardina, Bruno; Brancaccio, Andrea
Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists
1999 Michieli, Paolo; Basilico, Cristina; Pennacchietti, Selma; Maffè, Antonella; Tamagnone, Luca; Giordano, Silvia; Bardelli, Alberto; Comoglio, Paolo M.
Mutated axon guidance gene PLXNB2 sustains growth and invasiveness of stem cells isolated from cancers of unknown primary
2023 Brundu, Serena; Napolitano, Virginia; Franzolin, Giulia; Lo Cascio, Ettore; Mastrantonio, Roberta; Sardo, Gabriele; Cascardi, Eliano; Verginelli, Federica; Sarnataro, Sergio; Gambardella, Gennaro; Pisacane, Alberto; Arcovito, Alessandro; Boccaccio, Carla; M Comoglio, Paolo; Giraudo, Enrico; Tamagnone, Luca
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)
1998 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
Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNA
1995 Wengler, G. S; Notarangelo, L. D; Giliani, S; Pirastru, M. G; Ugazio, A. G; Parolini, Ornella
Mutational and Antigenic Landscape in Tumor Progression and Cancer Immunotherapy
2019 Vitale, Ilio; Sistigu, Antonella; Manic, Gwenola; Rudqvist, Nils-Petter; Trajanoski, Zlatko; Galluzzi, Lorenzo
Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients
2008 Gurrieri, Fiorella; Franco, Brunella
Mutations in rpoB sequences of Actinobacteria: a confounding factor in conjugal transfer experiments
2016 Puglisi, Edoardo; Guerrieri, Maria Chiara; Morelli, Lorenzo
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis
2013 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
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
2014 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
Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France
2013 Lattante, Serena; Le Ber, I; Camuzat, A; Brice, A; Kabashi, E.
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review
2015 Evoli Stampanoni-B, Amelia; Alboini, Paolo Emilio; Damato, Valentina; Iorio, Raffaele; Luigetti, Marco
MYC up-regulation confers resistance to everolimus and establishes vulnerability to cyclin dependent kinase inhibitors in pancreatic neuroendocrine neoplasms cells
2020 Terracciano, Francesca; Capone, Alessia; Montori, Andrea; Rinzivillo, Maria; Partelli, Stefano; Panzuto, Francesco; Pilozzi, Emanuela; Arcidiacono, Paolo Giorgio; Sette, Claudio; Capurso, Gabriele
MYC up-regulation confers vulnerability to dual inhibition of CDK12 and CDK13 in high-risk Group 3 medulloblastoma
2023 Pitolli, Consuelo; Marini, Alberto; Guerra, Marika; Pieraccioli, Marco; Marabitti, Veronica; Palluzzi, Fernando; Giacò, Luciano; Tamburrini, Gianpiero; Cecconi, Francesco; Nazio, Francesca; Sette, Claudio; Pagliarini, Vittoria
A Myc-SED mechanism?
2024 Pani, Giovambattista
The Mycobacterial HBHA Protein: a Promising Biomarker for Tuberculosis
2018 De Maio, Flavio; Squeglia, Flavia; Goletti, Delia; Delogu, Giovanni
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
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, Erica; 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, Bianca Maria; 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-2023 | Mutated axon guidance gene PLXNB2 sustains growth and invasiveness of stem cells isolated from cancers of unknown primary | Brundu, Serena; Napolitano, Virginia; Franzolin, Giulia; Lo Cascio, Ettore; Mastrantonio, Roberta; Sardo, Gabriele; Cascardi, Eliano; Verginelli, Federica; Sarnataro, Sergio; Gambardella, Gennaro; Pisacane, Alberto; Arcovito, Alessandro; Boccaccio, Carla; M Comoglio, Paolo; Giraudo, Enrico; Tamagnone, Luca | |
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-2019 | Mutational and Antigenic Landscape in Tumor Progression and Cancer Immunotherapy | Vitale, Ilio; Sistigu, Antonella; Manic, Gwenola; Rudqvist, Nils-Petter; Trajanoski, Zlatko; Galluzzi, Lorenzo | |
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 Stampanoni-B, 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 | |
1-gen-2023 | MYC up-regulation confers vulnerability to dual inhibition of CDK12 and CDK13 in high-risk Group 3 medulloblastoma | Pitolli, Consuelo; Marini, Alberto; Guerra, Marika; Pieraccioli, Marco; Marabitti, Veronica; Palluzzi, Fernando; Giacò, Luciano; Tamburrini, Gianpiero; Cecconi, Francesco; Nazio, Francesca; Sette, Claudio; Pagliarini, Vittoria | |
1-gen-2024 | A Myc-SED mechanism? | Pani, Giovambattista | |
1-gen-2018 | The Mycobacterial HBHA Protein: a Promising Biomarker for Tuberculosis | De Maio, Flavio; Squeglia, Flavia; Goletti, Delia; Delogu, Giovanni |
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