BALDINI, ANTONIO
BALDINI, ANTONIO
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
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
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome
2021 Favicchia, I; Flore, G; Cioffi, S; Lania, G; Baldini, A; Illingworth, E
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm.
2021 Nomaru, H; Liu, Y; De Bono, C; Righelli, D; Cirino, A; Wang, W; Song, H; Racedo, Se; Dantas, Ag; Zhang, L; Cai, Cl; Angelini, C; Christiaen, L; Kelly, Rg; Baldini, A; Zheng, D; Morrow, Be
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx
2020 Adachi, N; Bilio, M; Baldini, A; Kelly, Rg
Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly
2020 Wei, L; Wang, W; Yang, J; Huang, X; Baldini, A; Zhang, Z
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.
Defining Vegfr3-Tbx1 Interactions in Brain Vascular Development
2019 Cioffi, Sara; Turturo Maria, Giuseppina; Martucciello, Stefania; Flore, Gemma; Baldini, Antonio; Illingworth, Elizabeth
Gene-environment interaction impacts on heart development and embryo survival
2019 Moreau J.L.M.; Kesteven S.; Martin E.M.M.A.; Lau K.S.; Yam M.X.; O'reilly V.C.; Del MonteNieto G.; Baldini A.; Feneley M.P.; Moon A.M.; Harvey R.P.; Sparrow D.B.; Chapman G.; Dunwoodie S.L.
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice
2019 Mastromoro, G; Calcagni, G; Versacci, P; Putotto, C; Chinali, M; Lambiase, C; Unolt, M; Pelliccione, E; Anaclerio, S; Caprio, C; Cioffi, S; Bilio, M; Baban, A; Drago, F; Digilio, Mc; Marino, B; Baldini, A
Tbx1 regulates extracellular matrix-cell interactions in the second heart field
2019 Alfano, D; Altomonte, A; Cortes, C; Bilio, M; Kelly, Rg; Baldini, A
Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer
2018 Pane L.S.; Fulcoli F.G.; Cirino A.; Altomonte A.; Ferrentino R.; Bilio M.; Baldini A.
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
2017 Calcagni, Giulio; Unolt, Marta; Digilio, Maria Cristina; Baban, Anwar; Versacci, Paolo; Tartaglia, Marco; Baldini, Antonio; Marino, Bruno
Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome.
2017 Lania, G; Bresciani, A; Bisbocci, M; Francone, A; Colonna, V; Altamura, S; Baldini, A
Coronary stem development in wild-type and Tbx1 null mouse hearts
2016 Theveniauruissy, M; Perezpomares, Jm; Parisot, P; Baldini, A; Miquerol, L; Kelly, Rg
Rebalancing gene haploinsufficiency in vivo by targeting chromatin
2016 Fulcoli F.G.; Franzese M.; Liu X.; Zhang Z.; Angelini C.; Baldini A.
Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome.
2016 Lania, G; Bresciani, A; Bisbocci, M; Francone, A; Colonna, V; Altamura, S; Baldini, A
A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 deletion syndrome.
2015 Fuchs, Jc; Linden, Jf; Baldini, A; Tucker, As
TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
2015 Gao S; Moreno M; Eliason S; Cao H; Li X; Yu W; Bidlack FB; Margolis HC; Baldini A; Amendt BA.
TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+Cells
2015 Lania, Gabriella; Ferrentino, Rosa; Baldini, Antonio
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome
2014 Caprio, Cinzia; Baldini, Antonio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome | 1-gen-2021 | Favicchia, I; Flore, G; Cioffi, S; Lania, G; Baldini, A; Illingworth, E | |
| Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. | 1-gen-2021 | Nomaru, H; Liu, Y; De Bono, C; Righelli, D; Cirino, A; Wang, W; Song, H; Racedo, Se; Dantas, Ag; Zhang, L; Cai, Cl; Angelini, C; Christiaen, L; Kelly, Rg; Baldini, A; Zheng, D; Morrow, Be | |
| Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx | 1-gen-2020 | Adachi, N; Bilio, M; Baldini, A; Kelly, Rg | |
| Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly | 1-gen-2020 | Wei, L; Wang, W; Yang, J; Huang, X; Baldini, A; Zhang, Z | |
| 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. | |
| Defining Vegfr3-Tbx1 Interactions in Brain Vascular Development | 1-gen-2019 | Cioffi, Sara; Turturo Maria, Giuseppina; Martucciello, Stefania; Flore, Gemma; Baldini, Antonio; Illingworth, Elizabeth | |
| Gene-environment interaction impacts on heart development and embryo survival | 1-gen-2019 | Moreau J.L.M.; Kesteven S.; Martin E.M.M.A.; Lau K.S.; Yam M.X.; O'reilly V.C.; Del MonteNieto G.; Baldini A.; Feneley M.P.; Moon A.M.; Harvey R.P.; Sparrow D.B.; Chapman G.; Dunwoodie S.L. | |
| Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice | 1-gen-2019 | Mastromoro, G; Calcagni, G; Versacci, P; Putotto, C; Chinali, M; Lambiase, C; Unolt, M; Pelliccione, E; Anaclerio, S; Caprio, C; Cioffi, S; Bilio, M; Baban, A; Drago, F; Digilio, Mc; Marino, B; Baldini, A | |
| Tbx1 regulates extracellular matrix-cell interactions in the second heart field | 1-gen-2019 | Alfano, D; Altomonte, A; Cortes, C; Bilio, M; Kelly, Rg; Baldini, A | |
| Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer | 1-gen-2018 | Pane L.S.; Fulcoli F.G.; Cirino A.; Altomonte A.; Ferrentino R.; Bilio M.; Baldini A. | |
| Congenital heart disease and genetic syndromes: new insights into molecular mechanisms. | 1-gen-2017 | Calcagni, Giulio; Unolt, Marta; Digilio, Maria Cristina; Baban, Anwar; Versacci, Paolo; Tartaglia, Marco; Baldini, Antonio; Marino, Bruno | |
| Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome. | 1-gen-2017 | Lania, G; Bresciani, A; Bisbocci, M; Francone, A; Colonna, V; Altamura, S; Baldini, A | |
| Coronary stem development in wild-type and Tbx1 null mouse hearts | 1-gen-2016 | Theveniauruissy, M; Perezpomares, Jm; Parisot, P; Baldini, A; Miquerol, L; Kelly, Rg | |
| Rebalancing gene haploinsufficiency in vivo by targeting chromatin | 1-gen-2016 | Fulcoli F.G.; Franzese M.; Liu X.; Zhang Z.; Angelini C.; Baldini A. | |
| Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome. | 1-gen-2016 | Lania, G; Bresciani, A; Bisbocci, M; Francone, A; Colonna, V; Altamura, S; Baldini, A | |
| A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 deletion syndrome. | 1-gen-2015 | Fuchs, Jc; Linden, Jf; Baldini, A; Tucker, As | |
| TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome. | 1-gen-2015 | Gao S; Moreno M; Eliason S; Cao H; Li X; Yu W; Bidlack FB; Margolis HC; Baldini A; Amendt BA. | |
| TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+Cells | 1-gen-2015 | Lania, Gabriella; Ferrentino, Rosa; Baldini, Antonio | |
| p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome | 1-gen-2014 | Caprio, Cinzia; Baldini, Antonio |