Rezultati pretrage - Ciolfi, Andrea
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Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity od Carabelli, Monica, Possenti, Marco, Sessa, Giovanna, Ciolfi, Andrea, Sassi, Massimiliano, Morelli, Giorgio, Ruberti, Ida
Izdano 2007Tekst -
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A dynamic balance between gene activation and repression regulates the shade avoidance response in Arabidopsis od Sessa, Giovanna, Carabelli, Monica, Sassi, Massimiliano, Ciolfi, Andrea, Possenti, Marco, Mittempergher, Francesca, Becker, Jorg, Morelli, Giorgio, Ruberti, Ida
Izdano 2005Tekst -
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Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome od Flex, Elisabetta, Ciolfi, Andrea, Caputo, Viviana, Fodale, Valentina, Leoni, Chiara, Melis, Daniela, Bedeschi, Maria Francesca, Mazzanti, Laura, Pizzuti, Antonio, Tartaglia, Marco, Zampino, Giuseppe
Izdano 2013Tekst -
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Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review od Petruzzellis, Giuseppe, Alessi, Iside, Colafati, Giovanna Stefania, Diomedi-Camassei, Francesca, Ciolfi, Andrea, Pedace, Lucia, Cacchione, Antonella, Carai, Andrea, Tartaglia, Marco, Mastronuzzi, Angela, Miele, Evelina
Izdano 2019Tekst -
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Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review od Niceta, Marcello, Dentici, Maria Lisa, Ciolfi, Andrea, Marini, Romana, Barresi, Sabina, Lepri, Francesca Romana, Novelli, Antonio, Bertini, Enrico, Cappa, Marco, Digilio, Maria Cristina, Dallapiccola, Bruno, Tartaglia, Marco
Izdano 2020Tekst -
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DNA Methylation Profiling for Diagnosing Undifferentiated Sarcoma with Capicua Transcriptional Receptor (CIC) Alterations od Miele, Evelina, De Vito, Rita, Ciolfi, Andrea, Pedace, Lucia, Russo, Ida, De Pasquale, Maria Debora, Di Giannatale, Angela, Crocoli, Alessandro, Angelis, Biagio De, Tartaglia, Marco, Alaggio, Rita, Milano, Giuseppe Maria
Izdano 2020Tekst -
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Melanotic Neuroectodermal Tumor of Infancy (MNTI) and Pineal Anlage Tumor (PAT) Harbor A Medulloblastoma Signature by DNA Methylation Profiling od Lopez-Nunez, Oscar, Alaggio, Rita, John, Ivy, Ciolfi, Andrea, Pedace, Lucia, Mastronuzzi, Angela, Gianno, Francesca, Giangaspero, Felice, Rossi, Sabrina, Donofrio, Vittoria, Cinalli, Giuseppe, Surrey, Lea F., Tartaglia, Marco, Locatelli, Franco, Miele, Evelina
Izdano 2021Tekst -
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A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3 od Flex, Elisabetta, Imperatore, Valentina, Carpentieri, Giovanna, Bruselles, Alessandro, Ciolfi, Andrea, Pizzi, Simone, Tedesco, Maria Giovanna, Rogaia, Daniela, Mencarelli, Amedea, Di Cara, Giuseppe, Verrotti, Alberto, Troiani, Stefania, Merla, Giuseppe, Tartaglia, Marco, Prontera, Paolo
Izdano 2021Tekst -
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Expanding the spectrum of EWSR1‐PATZ1 rearranged CNS tumors: An infantile case with leptomeningeal dissemination od Rossi, Sabrina, Barresi, Sabina, Giovannoni, Isabella, Alesi, Viola, Ciolfi, Andrea, Colafati, Giovanna Stefania, Diomedi‐Camassei, Francesca, Miele, Evelina, Cacchione, Antonella, Quacquarini, Denise, Carai, Andrea, Tartaglia, Marco, Giannini, Caterina, Giangaspero, Felice, Mastronuzzi, Angela, Alaggio, Rita
Izdano 2021Tekst -
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Modeling medulloblastoma in vivo and with human cerebellar organoids od Ballabio, Claudio, Anderle, Marica, Gianesello, Matteo, Lago, Chiara, Miele, Evelina, Cardano, Marina, Aiello, Giuseppe, Piazza, Silvano, Caron, Davide, Gianno, Francesca, Ciolfi, Andrea, Pedace, Lucia, Mastronuzzi, Angela, Tartaglia, Marco, Locatelli, Franco, Ferretti, Elisabetta, Giangaspero, Felice, Tiberi, Luca
Izdano 2020Tekst -
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MODL-23. DNA METHYLATION AND COPY NUMBER VARIATION PROFILE FOR CHARACTERIZATION OF PEDIATRIC BRAIN TUMOR PRIMARY CELL LINES od Pedace, Lucia, Vinci, Maria, Pizzi, Simone, Pericoli, Giulia, Catanzaro, Giuseppina, Abballe, Luana, Del Bufalo, Francesca, Caruana, Ignazio, Camassei, Francesca Diomedi, Rossi, Sabrina, Giangaspero, Felice, Ferretti, Elisabetta, Ciolfi, Andrea, Tartaglia, Marco, Locatelli, Franco, Mastronuzzi, Angela, Miele, Evelina
Izdano 2020Tekst -
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TMOD-05. GENOME-WIDE DNA METHYLATION PROFILE: A POWERFUL STRATEGY TO RECAPITULATE HETEROGENEITY OF PEDIATRIC BRAIN TUMORS IN PRIMARY CELL LINES od Pedace, Lucia, Pizzi, Simone, Vinci, Maria, Pericoli, Giulia, Catanzaro, Giuseppina, Abballe, Luana, Po, Agnese, Del Bufalo, Francesca, Rossi, Sabrina, Camassei, Francesca Diomedi, Giangaspero, Felice, Tiberi, Luca, Mastronuzzi, Angela, Ferretti, Elisabetta, Tartaglia, Marco, Locatelli, Franco, Ciolfi, Andrea, Miele, Evelina
Izdano 2021Tekst -
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A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome od Caputo, Viviana, Cianetti, Luciano, Niceta, Marcello, Carta, Claudio, Ciolfi, Andrea, Bocchinfuso, Gianfranco, Carrani, Eugenio, Dentici, Maria Lisa, Biamino, Elisa, Belligni, Elga, Garavelli, Livia, Boccone, Loredana, Melis, Daniela, Andria, Generoso, Gelb, Bruce D., Stella, Lorenzo, Silengo, Margherita, Dallapiccola, Bruno, Tartaglia, Marco
Izdano 2012Tekst -
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Establishment and Characterization of a Cell Line (S-RMS1) Derived from an Infantile Spindle Cell Rhabdomyosarcoma with SRF-NCOA2 Fusion Transcript od Colletti, Marta, Galardi, Angela, Miele, Evelina, Di Paolo, Virginia, Russo, Ida, De Stefanis, Cristiano, De Vito, Rita, Rinelli, Martina, Ciolfi, Andrea, De Angelis, Biagio, Zin, Angelica, Guffanti, Alessandro, Digilio, Maria Cristina, Novelli, Antonio, Alaggio, Rita, Milano, Giuseppe Maria, Di Giannatale, Angela
Izdano 2021Tekst -
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A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl(−)/H(+)-Exchanger, Causes Early-Onset Neurodegeneration od Polovitskaya, Maya M., Barbini, Carlo, Martinelli, Diego, Harms, Frederike L., Cole, F. Sessions, Calligari, Paolo, Bocchinfuso, Gianfranco, Stella, Lorenzo, Ciolfi, Andrea, Niceta, Marcello, Rizza, Teresa, Shinawi, Marwan, Sisco, Kathleen, Johannsen, Jessika, Denecke, Jonas, Carrozzo, Rosalba, Wegner, Daniel J., Kutsche, Kerstin, Tartaglia, Marco, Jentsch, Thomas J.
Izdano 2020Tekst -
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Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations od Nasca, Alessia, Rizza, Teresa, Doimo, Mara, Legati, Andrea, Ciolfi, Andrea, Diodato, Daria, Calderan, Cristina, Carrara, Gianfranco, Lamantea, Eleonora, Aiello, Chiara, Di Nottia, Michela, Niceta, Marcello, Lamperti, Costanza, Ardissone, Anna, Bianchi-Marzoli, Stefania, Iarossi, Giancarlo, Bertini, Enrico, Moroni, Isabella, Tartaglia, Marco, Salviati, Leonardo, Carrozzo, Rosalba, Ghezzi, Daniele
Izdano 2017Tekst -
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Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature od Ciolfi, Andrea, Aref-Eshghi, Erfan, Pizzi, Simone, Pedace, Lucia, Miele, Evelina, Kerkhof, Jennifer, Flex, Elisabetta, Martinelli, Simone, Radio, Francesca Clementina, Ruivenkamp, Claudia A. L., Santen, Gijs W. E., Bijlsma, Emilia, Barge-Schaapveld, Daniela, Ounap, Katrin, Siu, Victoria Mok, Kooy, R. Frank, Dallapiccola, Bruno, Sadikovic, Bekim, Tartaglia, Marco
Izdano 2020Tekst