Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity

Por Carabelli, Monica, Possenti, Marco, Sessa, Giovanna, Ciolfi, Andrea, Sassi, Massimiliano, Morelli, Giorgio, Ruberti, Ida
Publicado em 2007

A novel regulatory circuit underlying plant response to canopy shade

Por Carabelli, Monica, Possenti, Marco, Sessa, Giovanna, Ciolfi, Andrea, Sassi, Massimiliano, Morelli, Giorgio, Ruberti, Ida
Publicado em 2008

Dynamics of the Shade-Avoidance Response in Arabidopsis(1)([W])

Por Ciolfi, Andrea, Sessa, Giovanna, Sassi, Massimiliano, Possenti, Marco, Salvucci, Samanta, Carabelli, Monica, Morelli, Giorgio, Ruberti, Ida
Publicado em 2013

A dynamic balance between gene activation and repression regulates the shade avoidance response in Arabidopsis

Por Sessa, Giovanna, Carabelli, Monica, Sassi, Massimiliano, Ciolfi, Andrea, Possenti, Marco, Mittempergher, Francesca, Becker, Jorg, Morelli, Giorgio, Ruberti, Ida
Publicado em 2005

Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome

Por Flex, Elisabetta, Ciolfi, Andrea, Caputo, Viviana, Fodale, Valentina, Leoni, Chiara, Melis, Daniela, Bedeschi, Maria Francesca, Mazzanti, Laura, Pizzuti, Antonio, Tartaglia, Marco, Zampino, Giuseppe
Publicado em 2013

Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review

Por Petruzzellis, Giuseppe, Alessi, Iside, Colafati, Giovanna Stefania, Diomedi-Camassei, Francesca, Ciolfi, Andrea, Pedace, Lucia, Cacchione, Antonella, Carai, Andrea, Tartaglia, Marco, Mastronuzzi, Angela, Miele, Evelina
Publicado no Front Genet (2019)

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

Por 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
Publicado no BMC Pediatr (2020)

DNA Methylation Profiling for Diagnosing Undifferentiated Sarcoma with Capicua Transcriptional Receptor (CIC) Alterations

Por 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
Publicado no Int J Mol Sci (2020)

Melanotic Neuroectodermal Tumor of Infancy (MNTI) and Pineal Anlage Tumor (PAT) Harbor A Medulloblastoma Signature by DNA Methylation Profiling

Por 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
Publicado no Cancers (Basel) (2021)

Modeling medulloblastoma in vivo and with human cerebellar organoids

Por 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
Publicado no Nat Commun (2020)

MODL-23. DNA METHYLATION AND COPY NUMBER VARIATION PROFILE FOR CHARACTERIZATION OF PEDIATRIC BRAIN TUMOR PRIMARY CELL LINES

Por 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
Publicado no Neuro Oncol (2020)

A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome

Por 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
Publicado em 2012

A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl(−)/H(+)-Exchanger, Causes Early-Onset Neurodegeneration

Por 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.
Publicado no Am J Hum Genet (2020)

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

Por 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
Publicado no Orphanet J Rare Dis (2017)

Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature

Por 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
Publicado no Clin Epigenetics (2020)

Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases

Por Grassi, Ludovica, Alfonsi, Romina, Francescangeli, Federica, Signore, Michele, De Angelis, Maria Laura, Addario, Antonio, Costantini, Manuela, Flex, Elisabetta, Ciolfi, Andrea, Pizzi, Simone, Bruselles, Alessandro, Pallocca, Matteo, Simone, Giuseppe, Haoui, Mustapha, Falchi, Mario, Milella, Michele, Sentinelli, Steno, Di Matteo, Paola, Stellacci, Emilia, Gallucci, Michele, Muto, Giovanni, Tartaglia, Marco, De Maria, Ruggero, Bonci, Désirée
Publicado no Cell Death Dis (2019)

ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

Por Benetti, Elisa, Tita, Rossella, Spiga, Ottavia, Ciolfi, Andrea, Birolo, Giovanni, Bruselles, Alessandro, Doddato, Gabriella, Giliberti, Annarita, Marconi, Caterina, Musacchia, Francesco, Pippucci, Tommaso, Torella, Annalaura, Trezza, Alfonso, Valentino, Floriana, Baldassarri, Margherita, Brusco, Alfredo, Asselta, Rosanna, Bruttini, Mirella, Furini, Simone, Seri, Marco, Nigro, Vincenzo, Matullo, Giuseppe, Tartaglia, Marco, Mari, Francesca, Renieri, Alessandra, Pinto, Anna Maria
Publicado no Eur J Hum Genet (2020)

TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy

Por Sferra, Antonella, Baillat, Gilbert, Rizza, Teresa, Barresi, Sabina, Flex, Elisabetta, Tasca, Giorgio, D’Amico, Adele, Bellacchio, Emanuele, Ciolfi, Andrea, Caputo, Viviana, Cecchetti, Serena, Torella, Annalaura, Zanni, Ginevra, Diodato, Daria, Piermarini, Emanuela, Niceta, Marcello, Coppola, Antonietta, Tedeschi, Enrico, Martinelli, Diego, Dionisi-Vici, Carlo, Nigro, Vincenzo, Dallapiccola, Bruno, Compagnucci, Claudia, Tartaglia, Marco, Haase, Georg, Bertini, Enrico
Publicado no Am J Hum Genet (2016)

Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome

Por Bauer, Christiane K., Calligari, Paolo, Radio, Francesca Clementina, Caputo, Viviana, Dentici, Maria Lisa, Falah, Nadia, High, Frances, Pantaleoni, Francesca, Barresi, Sabina, Ciolfi, Andrea, Pizzi, Simone, Bruselles, Alessandro, Person, Richard, Richards, Sarah, Cho, Megan T., Claps Sepulveda, Daniela J., Pro, Stefano, Battini, Roberta, Zampino, Giuseppe, Digilio, Maria Cristina, Bocchinfuso, Gianfranco, Dallapiccola, Bruno, Stella, Lorenzo, Tartaglia, Marco
Publicado no Am J Hum Genet (2018)

De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment

Por Rodger, Catherine, Flex, Elisabetta, Allison, Rachel J., Sanchis-Juan, Alba, Hasenahuer, Marcia A., Cecchetti, Serena, French, Courtney E., Edgar, James R., Carpentieri, Giovanna, Ciolfi, Andrea, Pantaleoni, Francesca, Bruselles, Alessandro, Onesimo, Roberta, Zampino, Giuseppe, Marcon, Francesca, Siniscalchi, Ester, Lees, Melissa, Krishnakumar, Deepa, McCann, Emma, Yosifova, Dragana, Jarvis, Joanna, Kruer, Michael C., Marks, Warren, Campbell, Jonathan, Allen, Louise E., Gustincich, Stefano, Raymond, F. Lucy, Tartaglia, Marco, Reid, Evan
Publicado no Am J Hum Genet (2020)