BILIO, MARCHESA
BILIO, MARCHESA
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome
2022 Lania, Gabriella; Franzese, Monica; Adachi, Noritaka; Bilio, Marchesa; Flore, Gemma; Russo, Annalaura; D'Agostino, Erika; Angelini, Claudia; Kelly Robert, G; Baldini, Antonio
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome
2022 Cioffi, Sara; Flore, Gemma; Martucciello, Stefania; Bilio, Marchesa; Giuseppina Turturo, Maria; Illingworth, Elizabeth
EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm
2021 Caprio, Cinzia; Lania, Gabriella; Bilio, Marchesa; Ferrentino, Rosa; Chen, Li; Baldini, Antonio
Tbx1 regulates cardiac lymphangiogenesis through genetic interaction with Vegfr3
2021 Martucciello, S.; Turturo, M. G.; Bilio, M.; Cioffi, S.; Chen, L.; Baldini, A.; Illingworth, E. A.
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3
2020 Martucciello, S; Turturo, Mg; Bilio, M; Cioffi, S; Chen, L; Baldini, A; Illingworth, E
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx
2020 Adachi, N; Bilio, M; Baldini, A; Kelly, Rg
Tbx1 and basal cell carcinoma: Expression and interactions with gli2 and dvl2 signaling
2020 Caprio, C; Varricchio, S; Bilio, M; Feo, F; Ferrentino, R; Russo, D; Staibano, S; Alfano, D; Missero, C; Ilardi, G; Baldini, A
The penetrance of aortic arch defects in 22q11DS can be modulated by dietary vitamin A levels and is dependent on the maternal genotype
2020 AmengualCladera, E.; Medina Chavez, D.; Lynton Pons, E.; Sureda Horrach, P.; Asensio Landa, V. J.; Rocha, J.; Ruiz Rodriguez, J.; Tubau, A.; Juan, M.; Lania, G.; Bilio, M.; Baldini, A.; Ruiz Guerra, L.; Vives Bauza, C.; Logotheti, M.; Pilalis, E.; Chatziioannou, A.; Heine Suner, D.
Tbx1 regulates extracellular matrix-cell interactions in the second heart field
2019 Alfano D.; Altomonte A.; Cortes C.; Bilio M.; Kelly R.G.; Baldini A.
Cortical Development Requires Mesodermal Expression of Tbx1 , a Gene Haploinsufficient in 22q11.2 Deletion Syndrome
2017 Flore, Gemma; Cioffi, Sara; Bilio, Marchesa; Illingworth, Elizabeth
Tbx1 regulates brain vascularization.
2013 Cioffi, S; Martucciello, S; Fulcoli, Fg; Bilio, M; Ferrentino, R; Nusco, E; Illingworth, E
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome | 1-gen-2022 | Lania, Gabriella; Franzese, Monica; Adachi, Noritaka; Bilio, Marchesa; Flore, Gemma; Russo, Annalaura; D'Agostino, Erika; Angelini, Claudia; Kelly Robert, G; Baldini, Antonio | |
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome | 1-gen-2022 | Cioffi, Sara; Flore, Gemma; Martucciello, Stefania; Bilio, Marchesa; Giuseppina Turturo, Maria; Illingworth, Elizabeth | |
EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm | 1-gen-2021 | Caprio, Cinzia; Lania, Gabriella; Bilio, Marchesa; Ferrentino, Rosa; Chen, Li; Baldini, Antonio | |
Tbx1 regulates cardiac lymphangiogenesis through genetic interaction with Vegfr3 | 1-gen-2021 | Martucciello, S.; Turturo, M. G.; Bilio, M.; Cioffi, S.; Chen, L.; Baldini, A.; Illingworth, E. A. | |
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 | 1-gen-2020 | Martucciello, S; Turturo, Mg; Bilio, M; Cioffi, S; Chen, L; Baldini, A; Illingworth, E | |
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx | 1-gen-2020 | Adachi, N; Bilio, M; Baldini, A; Kelly, Rg | |
Tbx1 and basal cell carcinoma: Expression and interactions with gli2 and dvl2 signaling | 1-gen-2020 | Caprio, C; Varricchio, S; Bilio, M; Feo, F; Ferrentino, R; Russo, D; Staibano, S; Alfano, D; Missero, C; Ilardi, G; Baldini, A | |
The penetrance of aortic arch defects in 22q11DS can be modulated by dietary vitamin A levels and is dependent on the maternal genotype | 1-gen-2020 | AmengualCladera, E.; Medina Chavez, D.; Lynton Pons, E.; Sureda Horrach, P.; Asensio Landa, V. J.; Rocha, J.; Ruiz Rodriguez, J.; Tubau, A.; Juan, M.; Lania, G.; Bilio, M.; Baldini, A.; Ruiz Guerra, L.; Vives Bauza, C.; Logotheti, M.; Pilalis, E.; Chatziioannou, A.; Heine Suner, D. | |
Tbx1 regulates extracellular matrix-cell interactions in the second heart field | 1-gen-2019 | Alfano D.; Altomonte A.; Cortes C.; Bilio M.; Kelly R.G.; Baldini A. | |
Cortical Development Requires Mesodermal Expression of Tbx1 , a Gene Haploinsufficient in 22q11.2 Deletion Syndrome | 1-gen-2017 | Flore, Gemma; Cioffi, Sara; Bilio, Marchesa; Illingworth, Elizabeth | |
Tbx1 regulates brain vascularization. | 1-gen-2013 | Cioffi, S; Martucciello, S; Fulcoli, Fg; Bilio, M; Ferrentino, R; Nusco, E; Illingworth, E |