MUSIO, ANTONIO
MUSIO, ANTONIO
Istituto di Tecnologie Biomediche - ITB
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature
2024 Frattini, A.; Micheloni, G.; Musio, A.; Antunes, M.; Barbot, J.; Costa, E.; Seabra, P.; Righi, R.; Orsini, F.; Montalbano, G.; Acquati, F.; Porta, G.; Pasquali, F.; Valli, R.
Synthetic Lethality between Cohesin and WNT Signaling Pathways in Diverse Cancer Contexts
2024 Pallotta, M. M.; Di Nardo, M.; Musio, A.
The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer
2024 Di Nardo, Maddalena; Astigiano, Simonetta; Baldari, Silvia; Pallotta, Maria Michela; Porta, Giovanni; Pigozzi, Simona; Antonini, Annalisa; Emionite, Laura; Frattini, Annalisa; Valli, Roberto; Toietta, Gabriele; Soddu, Silvia; Musio, Antonio
Donor cell Acute Myeloid Leukemia after hematopoietic stem cell transplantation for Chronic Granulomatous Disease: a case report and literature review
2023 Micheloni, Giovanni; Frattini, Annalisa; Donini, Marta; Dusi, Stefano; Leszl, Anna; Di Meglio, Annamaria; Pigazzi, Martina; Musio, Antonio; Zecca, Marco; Mina, Tommaso; Rabusin, Marco; Roccia, Pamela; Bernasconi, Paolo; Dambruoso, Irene; Minelli, Antonella; Montalbano, Giuseppe; Acquati, Francesco; Porta, Giovanni; Valli, Roberto; Pasquali, Francesco
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms
2023 Kaur, Maninder; Blair, Justin; Devkota, Batsal; Fortunato, Sierra; Clark, Dinah; Lawrence, Audrey; Kim, Jiwoo; Do, Wonwook; Semeo, Benjamin; Katz, Olivia; Mehta, Devanshi; Yamamoto, Nobuko; Schindler, Emma; Al Rawi, Zayd; Wallace, Nina; Wilde, Jonathan J; Mccallum, Jennifer; Liu, Jinglan; Xu, Dongbin; Jackson, Marie; Rentas, Stefan; Tayoun, Ahmad Abou; Zhe, Zhang; Abdul-Rahman, Omar; Allen, Bill; Angula, Moris A; Anyane-Yeboa, Kwame; Argente, Jesús; Arn, Pamela H; Armstrong, Linlea; Basel-Salmon, Lina; Baynam, Gareth; Bird, Lynne M; Bruegger, Daniel; Ch'Ng, Gaik-Siew; Chitayat, David; Clark, Robin; Cox, Gerald F; Dave, Usha; Debaere, Elfrede; Field, Michael; Graham, John M; Gripp, Karen W; Greenstein, Robert; Gupta, Neerja; Heidenreich, Randy; Hoffman, Jodi; Hopkin, Robert J; Jones, Kenneth L; Jones, Marilyn C; Kariminejad, Ariana; Kogan, Jillene; Lace, Baiba; Leroy, Julian; Lynch, Sally Ann; Mcdonald, Marie; Meagher, Kirsten; Mendelsohn, Nancy; Micule, Ieva; Moeschler, John; Nampoothiri, Sheela; Ohashi, Kaoru; Powell, Cynthia M; Ramanathan, Subhadra; Raskin, Salmo; Roeder, Elizabeth; Rio, Marlene; Rope, Alan F; Sangha, Karan; Scheuerle, Angela E; Schneider, Adele; Shalev, Stavit; Siu, Victoria; Smith, Rosemarie; Stevens, Cathy; Tkemaladze, Tinatin; Toimie, John; Toriello, Helga; Turner, Anne; Wheeler, Patricia G; White, Susan M; Young, Terri; Loomes, Kathleen M; Pipan, Mary; Harrington, Ann Tokay; Zackai, Elaine; Rajagopalan, Ramakrishnan; Conlin, Laura; Deardorff, Matthew A; Mceldrew, Deborah; Pie, Juan; Ramos, Feliciano; Musio, Antonio; Kline, Antonie D; Izumi, Kosuke; Raible, Sarah E; Krantz, Ian D
Case report: A novel case of parental mosaicism in SMC1A gene causes inherited Cornelia de Lange syndrome
2022 GilSalvador, Marta; LatorrePellicer, Ana; LuciaCampos, Cristina; Arnedo, María; Darnaude, María Teresa; Díaz de Bustamante, Aránzazu; Villares, Rebeca; Palma Milla, Carmen; Puisac, Beatriz; Musio, Antonio; Ramos, Feliciano J.; Pié, Juan
Cornelia de Lange syndrome and cancer: An open question
2022 Pallotta Maria, M; DI NARDO, Maddalena; Hennekam Raoul, C M; Kaiser Frank, J; Parenti, Ilaria; Pie, Juan; Ramos Feliciano, J; Kline Antonie, D; Musio, Antonio
Disease-associated c-MYC downregulation in human disorders of transcriptional regulation
2022 Pallotta M.M.; Di Nardo M.; Sarogni P.; Krantz I.D.; Musio A.
The multifaceted roles of cohesin in cancer
2022 Di Nardo, Maddalena; Pallotta, Maria M.; Musio, Antonio
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile
2020 Barone, Stefano; Sarogni, Patrizia; Valli, Roberto; Pallotta Maria, Michela; Silvia, Gazzi; Frattini, Annalisa; Khan Abdul, Waheed; Rapalini, Erika; Parri, Cristiana; Musio, Antonio
Cohesin mutations are synthetic lethal with stimulation of WNT signaling
2020 Chin Chue, Vin; Antony, Jisha; Ketharnathan, Sarada; Labudina, Anastasia; Gimenez, Gregory; Parsons Kate, M; He, Jinshu; George Amee, J; Pallotta Maria, Michela; Musio, Antonio; Braithwaite, Antony; Guilford, Parry; Hannan Ross, D; Horsfield Julia, A
Cohesin mutations are synthetic lethal with stimulation of WNT signaling
2020 Chin, Chue Vin; Antony, Jisha; Ketharnathan, Sarada; Labudina, Anastasia; Gimenez, Gregory; Parsons, Kate M.; He, Jinshu; George, Amee J.; Pallotta, Maria Michela; Musio, Antonio; Braithwaite, Antony; Guilford, Parry; Hannan, Ross D.; Horsfield, Julia A.
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
2020 Sarogni, Patrizia; Pallotta, Maria M.; Musio, Antonio
Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes
2020 LatorrePellicer, Ana; Ascaso, Angela; Trujillano, Laura; GilSalvador, Marta; Arnedo, Maria; LuciaCampos, Cristina; AntonanzasPerez, Rebeca; MarcosAlcalde, Inigo; Parenti, Ilaria; BuenoLozano, Gloria; Musio, Antonio; Puisac, Beatriz; Kaiser, Frank J.; Ramos, Feliciano J.; GomezPuertas, Paulino; Pie, Juan
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome
2020 Cucco, Francesco; Sarogni, Patrizia; Rossato, Sara; Alpa, Mirella; Patimo, Alessandra; Latorre, Ana; Magnani, Cinzia; Puisac, Beatriz; Ramos Feliciano, J; Pie, Juan; Musio, Antonio
The multiple facets of the SMC1A gene
2020 Musio, Antonio; Musio, Antonio
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018
2019 Kline, Antonie D.; Krantz, Ian D.; Bando, Masashige; Shirahige, Katsuhiko; Chea, Stephenson; Sakata, Toyonori; Rao, Suhas; Dorsett, Dale; Singh, Vijay Pratap; Gerton, Jennifer L.; Horsfield, Julia A.; Calof, Anne L.; Katz, Olivia; Grados, Marco; Raible, Sarah; Baranano, Kristin; Lyon, Gholson; Musio, Antonio; Carrico, Cheri S.; Clemens, Douglas K.; Caudill, Patti; Massa, Valentina; McGill, Bryan E.; Dommestrup, Aila; O'Connor, Julia; Haaland, Richard E.
Overexpression of the cohesin-core subunit SMC1A contributes to colorectal cancer development
2019 Sarogni, Patrizia; Palumbo, Orazio; Servadio, Adele; Astigiano, Simonetta; D'Alessio, Barbara; Gatti, Veronica; Cukrov, Dubravka; Baldari, Silvia; Pallotta, MARIA MICHELA; Aretini, Paolo; Dell'Orletta, Felice; Soddu, Silvia; Carella, Massimo; Toietta, Gabriele; Barbieri, Ottavia; Fontanini, Gabriella; Musio, Antonio
p53 mitotic centrosome localization preserves centrosome integrity and works as sensor for the mitotic surveillance pathway
2019 Contadini, Claudia; Monteonofrio, Laura; Virdia, Ilaria; Prodosmo, Andrea; Valente, Davide; Chessa, Luciana; Musio, Antonio; Fava Luca, L; Rinaldo, Cinzia; Di Rocco, Giuliana; Soddu, Silvia
Antioxidant treatment ameliorates phenotypic features of SMC1A-mutated Cornelia de Lange syndrome in vitro and in vivo
2018 Cukrov, Dubravka; Newman Trent, A C; Leask, Megan; Leeke, Bryony; Sarogni, Patrizia; Patimo, Alessandra; Kline Antonie, D; Krantz Ian, D; Horsfield Julia, A; Musio, Antonio
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature | 1-gen-2024 | Frattini, A.; Micheloni, G.; Musio, A.; Antunes, M.; Barbot, J.; Costa, E.; Seabra, P.; Righi, R.; Orsini, F.; Montalbano, G.; Acquati, F.; Porta, G.; Pasquali, F.; Valli, R. | |
Synthetic Lethality between Cohesin and WNT Signaling Pathways in Diverse Cancer Contexts | 1-gen-2024 | Pallotta, M. M.; Di Nardo, M.; Musio, A. | |
The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer | 1-gen-2024 | Di Nardo, Maddalena; Astigiano, Simonetta; Baldari, Silvia; Pallotta, Maria Michela; Porta, Giovanni; Pigozzi, Simona; Antonini, Annalisa; Emionite, Laura; Frattini, Annalisa; Valli, Roberto; Toietta, Gabriele; Soddu, Silvia; Musio, Antonio | |
Donor cell Acute Myeloid Leukemia after hematopoietic stem cell transplantation for Chronic Granulomatous Disease: a case report and literature review | 1-gen-2023 | Micheloni, Giovanni; Frattini, Annalisa; Donini, Marta; Dusi, Stefano; Leszl, Anna; Di Meglio, Annamaria; Pigazzi, Martina; Musio, Antonio; Zecca, Marco; Mina, Tommaso; Rabusin, Marco; Roccia, Pamela; Bernasconi, Paolo; Dambruoso, Irene; Minelli, Antonella; Montalbano, Giuseppe; Acquati, Francesco; Porta, Giovanni; Valli, Roberto; Pasquali, Francesco | |
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms | 1-gen-2023 | Kaur, Maninder; Blair, Justin; Devkota, Batsal; Fortunato, Sierra; Clark, Dinah; Lawrence, Audrey; Kim, Jiwoo; Do, Wonwook; Semeo, Benjamin; Katz, Olivia; Mehta, Devanshi; Yamamoto, Nobuko; Schindler, Emma; Al Rawi, Zayd; Wallace, Nina; Wilde, Jonathan J; Mccallum, Jennifer; Liu, Jinglan; Xu, Dongbin; Jackson, Marie; Rentas, Stefan; Tayoun, Ahmad Abou; Zhe, Zhang; Abdul-Rahman, Omar; Allen, Bill; Angula, Moris A; Anyane-Yeboa, Kwame; Argente, Jesús; Arn, Pamela H; Armstrong, Linlea; Basel-Salmon, Lina; Baynam, Gareth; Bird, Lynne M; Bruegger, Daniel; Ch'Ng, Gaik-Siew; Chitayat, David; Clark, Robin; Cox, Gerald F; Dave, Usha; Debaere, Elfrede; Field, Michael; Graham, John M; Gripp, Karen W; Greenstein, Robert; Gupta, Neerja; Heidenreich, Randy; Hoffman, Jodi; Hopkin, Robert J; Jones, Kenneth L; Jones, Marilyn C; Kariminejad, Ariana; Kogan, Jillene; Lace, Baiba; Leroy, Julian; Lynch, Sally Ann; Mcdonald, Marie; Meagher, Kirsten; Mendelsohn, Nancy; Micule, Ieva; Moeschler, John; Nampoothiri, Sheela; Ohashi, Kaoru; Powell, Cynthia M; Ramanathan, Subhadra; Raskin, Salmo; Roeder, Elizabeth; Rio, Marlene; Rope, Alan F; Sangha, Karan; Scheuerle, Angela E; Schneider, Adele; Shalev, Stavit; Siu, Victoria; Smith, Rosemarie; Stevens, Cathy; Tkemaladze, Tinatin; Toimie, John; Toriello, Helga; Turner, Anne; Wheeler, Patricia G; White, Susan M; Young, Terri; Loomes, Kathleen M; Pipan, Mary; Harrington, Ann Tokay; Zackai, Elaine; Rajagopalan, Ramakrishnan; Conlin, Laura; Deardorff, Matthew A; Mceldrew, Deborah; Pie, Juan; Ramos, Feliciano; Musio, Antonio; Kline, Antonie D; Izumi, Kosuke; Raible, Sarah E; Krantz, Ian D | |
Case report: A novel case of parental mosaicism in SMC1A gene causes inherited Cornelia de Lange syndrome | 1-gen-2022 | GilSalvador, Marta; LatorrePellicer, Ana; LuciaCampos, Cristina; Arnedo, María; Darnaude, María Teresa; Díaz de Bustamante, Aránzazu; Villares, Rebeca; Palma Milla, Carmen; Puisac, Beatriz; Musio, Antonio; Ramos, Feliciano J.; Pié, Juan | |
Cornelia de Lange syndrome and cancer: An open question | 1-gen-2022 | Pallotta Maria, M; DI NARDO, Maddalena; Hennekam Raoul, C M; Kaiser Frank, J; Parenti, Ilaria; Pie, Juan; Ramos Feliciano, J; Kline Antonie, D; Musio, Antonio | |
Disease-associated c-MYC downregulation in human disorders of transcriptional regulation | 1-gen-2022 | Pallotta M.M.; Di Nardo M.; Sarogni P.; Krantz I.D.; Musio A. | |
The multifaceted roles of cohesin in cancer | 1-gen-2022 | Di Nardo, Maddalena; Pallotta, Maria M.; Musio, Antonio | |
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile | 1-gen-2020 | Barone, Stefano; Sarogni, Patrizia; Valli, Roberto; Pallotta Maria, Michela; Silvia, Gazzi; Frattini, Annalisa; Khan Abdul, Waheed; Rapalini, Erika; Parri, Cristiana; Musio, Antonio | |
Cohesin mutations are synthetic lethal with stimulation of WNT signaling | 1-gen-2020 | Chin Chue, Vin; Antony, Jisha; Ketharnathan, Sarada; Labudina, Anastasia; Gimenez, Gregory; Parsons Kate, M; He, Jinshu; George Amee, J; Pallotta Maria, Michela; Musio, Antonio; Braithwaite, Antony; Guilford, Parry; Hannan Ross, D; Horsfield Julia, A | |
Cohesin mutations are synthetic lethal with stimulation of WNT signaling | 1-gen-2020 | Chin, Chue Vin; Antony, Jisha; Ketharnathan, Sarada; Labudina, Anastasia; Gimenez, Gregory; Parsons, Kate M.; He, Jinshu; George, Amee J.; Pallotta, Maria Michela; Musio, Antonio; Braithwaite, Antony; Guilford, Parry; Hannan, Ross D.; Horsfield, Julia A. | |
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach | 1-gen-2020 | Sarogni, Patrizia; Pallotta, Maria M.; Musio, Antonio | |
Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes | 1-gen-2020 | LatorrePellicer, Ana; Ascaso, Angela; Trujillano, Laura; GilSalvador, Marta; Arnedo, Maria; LuciaCampos, Cristina; AntonanzasPerez, Rebeca; MarcosAlcalde, Inigo; Parenti, Ilaria; BuenoLozano, Gloria; Musio, Antonio; Puisac, Beatriz; Kaiser, Frank J.; Ramos, Feliciano J.; GomezPuertas, Paulino; Pie, Juan | |
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome | 1-gen-2020 | Cucco, Francesco; Sarogni, Patrizia; Rossato, Sara; Alpa, Mirella; Patimo, Alessandra; Latorre, Ana; Magnani, Cinzia; Puisac, Beatriz; Ramos Feliciano, J; Pie, Juan; Musio, Antonio | |
The multiple facets of the SMC1A gene | 1-gen-2020 | Musio, Antonio; Musio, Antonio | |
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018 | 1-gen-2019 | Kline, Antonie D.; Krantz, Ian D.; Bando, Masashige; Shirahige, Katsuhiko; Chea, Stephenson; Sakata, Toyonori; Rao, Suhas; Dorsett, Dale; Singh, Vijay Pratap; Gerton, Jennifer L.; Horsfield, Julia A.; Calof, Anne L.; Katz, Olivia; Grados, Marco; Raible, Sarah; Baranano, Kristin; Lyon, Gholson; Musio, Antonio; Carrico, Cheri S.; Clemens, Douglas K.; Caudill, Patti; Massa, Valentina; McGill, Bryan E.; Dommestrup, Aila; O'Connor, Julia; Haaland, Richard E. | |
Overexpression of the cohesin-core subunit SMC1A contributes to colorectal cancer development | 1-gen-2019 | Sarogni, Patrizia; Palumbo, Orazio; Servadio, Adele; Astigiano, Simonetta; D'Alessio, Barbara; Gatti, Veronica; Cukrov, Dubravka; Baldari, Silvia; Pallotta, MARIA MICHELA; Aretini, Paolo; Dell'Orletta, Felice; Soddu, Silvia; Carella, Massimo; Toietta, Gabriele; Barbieri, Ottavia; Fontanini, Gabriella; Musio, Antonio | |
p53 mitotic centrosome localization preserves centrosome integrity and works as sensor for the mitotic surveillance pathway | 1-gen-2019 | Contadini, Claudia; Monteonofrio, Laura; Virdia, Ilaria; Prodosmo, Andrea; Valente, Davide; Chessa, Luciana; Musio, Antonio; Fava Luca, L; Rinaldo, Cinzia; Di Rocco, Giuliana; Soddu, Silvia | |
Antioxidant treatment ameliorates phenotypic features of SMC1A-mutated Cornelia de Lange syndrome in vitro and in vivo | 1-gen-2018 | Cukrov, Dubravka; Newman Trent, A C; Leask, Megan; Leeke, Bryony; Sarogni, Patrizia; Patimo, Alessandra; Kline Antonie, D; Krantz Ian, D; Horsfield Julia, A; Musio, Antonio |