ILLINGWORTH, Elizabeth Anne
ILLINGWORTH, Elizabeth Anne
Dipartimento di Chimica e Biologia "Adolfo Zambelli"/DCB
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3
2020-01-01 Martucciello, S.; Turturo, M. G.; Bilio, M.; Cioffi, S.; Chen, L.; Baldini, A.; Illingworth, E.
A genetic link between Tbx1 and fibroblast growth factor signaling.
2002-01-01 Vitelli, F; Taddei, I; Morishima, M; Meyers, En; Illingworth, ELISABETH ANNE; Baldini, A.
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome.
2006-01-01 Jurata, Lw; Gallagher, P; Lemire, Al; Charles, V; Brockman, Ja; Illingworth, ELISABETH ANNE; Altar, Ca
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment
2024-01-01 Aurigemma, I; Ferrentino, R; Poondi Krishnan, V; Lanzetta, O; Angelini, C; Illingworth, E; Baldini, A
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells
2020-01-01 Cirino, Andrea; Aurigemma, Ilaria; Franzese, Monica; Lania, Gabriella; Righelli, Dario; Ferrentino, Rosa; Illingworth, Elizabeth; Angelini, Claudia; Baldini, Antonio
Chromosomal microdeletions: dissecting del22q11 syndrome.
2001-01-01 Illingworth, ELISABETH ANNE
Congenital heart defects and 22q11 deletions: Which genes count?
1998-01-01 Illingworth, ELISABETH ANNE; Baldini, A.
Congenital heart disease in mice deficient for the DiGeorge syndrome region
1999-01-01 Illingworth, ELISABETH ANNE; Jurecic, V; CARATTINI RIVERA, S; Cheah, Y. C.; Rosenblatt, Hm; Bradley, A; Baldini,
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome
2017-01-01 Flore, Gemma; Cioffi, Sara; Bilio, Marchesa; Illingworth, ELISABETH ANNE
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model
2013-01-01 Toritsuka, M; Kimoto, S; Muraki, K; Landek Salgado, M; Yoshida, A; Yamamoto, N; Horiuchi, Y; Hiyama, H; Tajinda, K; Keni, N; Illingworth, ELISABETH ANNE; Iwamoto, T; Kishimoto, T; Sawa, A; Tanigaki, K.
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.
2007-01-01 Sivagnanasundaram, S; Fletcher, D; Hubank, M; Illingworth, ELISABETH ANNE; Skuse, D; Scambler, P.
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome
2010-01-01 Earls, L; Bayazitov, I; Fricke, R; Berry, R; Illingworth, ELISABETH ANNE; Mittleman, G; Zakharenko, S.
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation
2024-01-01 Aurigemma, I; Lanzetta, O; Cirino, A; Allegretti, S; Lania, G; Ferrentino, R; Poondi Krishnan, V; Angelini, C; Illingworth, E; Baldini, A
ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene
1998-01-01 Illingworth, ELISABETH ANNE; Harvey, El; Scambler, Pj; Baldini, A.
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes
1998-01-01 Wakamiya, M; Illingworth, ELISABETH ANNE; RIVERA PEREZ, Ja; Baldini, A; Behringer, R.
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome
2001-01-01 Taddei, I; Morishima, M; Huynh, T; Illingworth, ELISABETH ANNE
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis
2017-01-01 Flore, Gemma; di ruberto, Giuseppina; Parisot, Josephine; Sannino, Sara; Russo, Fabio; Illingworth, ELISABETH ANNE; Studer, Michèle; de leonibus, Elivira
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.
2009-01-01 Randall, V; Mccue, K; Roberts, C; Kyriakopoulou, V; Beddow, S; Barrett, An; Vitelli, F; Prescott, K; SHAW SMITH, C; Devriendt, K; Bosman, E; Steffes, G; Steel, Kp; Simrick, S; Basson, Ma; Illingworth, ELISABETH ANNE; Scambler, Pj
Mesodermal expression of Tbx1 is required for cortical development in mice
2014-01-01 G., Flore; S., Cioffi; M., Bilio; Illingworth, ELISABETH ANNE
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
2001-01-01 Paylor, R; Mcilwain, Kl; Mcaninch, R; Nellis, A; YUVA PAYLOR, La; Baldini, A; Illingworth, ELISABETH ANNE
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 | 1-gen-2020 | Martucciello, S.; Turturo, M. G.; Bilio, M.; Cioffi, S.; Chen, L.; Baldini, A.; Illingworth, E. | |
| A genetic link between Tbx1 and fibroblast growth factor signaling. | 1-gen-2002 | Vitelli, F; Taddei, I; Morishima, M; Meyers, En; Illingworth, ELISABETH ANNE; Baldini, A. | |
| Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. | 1-gen-2006 | Jurata, Lw; Gallagher, P; Lemire, Al; Charles, V; Brockman, Ja; Illingworth, ELISABETH ANNE; Altar, Ca | |
| Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment | 1-gen-2024 | Aurigemma, I; Ferrentino, R; Poondi Krishnan, V; Lanzetta, O; Angelini, C; Illingworth, E; Baldini, A | |
| Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells | 1-gen-2020 | Cirino, Andrea; Aurigemma, Ilaria; Franzese, Monica; Lania, Gabriella; Righelli, Dario; Ferrentino, Rosa; Illingworth, Elizabeth; Angelini, Claudia; Baldini, Antonio | |
| Chromosomal microdeletions: dissecting del22q11 syndrome. | 1-gen-2001 | Illingworth, ELISABETH ANNE | |
| Congenital heart defects and 22q11 deletions: Which genes count? | 1-gen-1998 | Illingworth, ELISABETH ANNE; Baldini, A. | |
| Congenital heart disease in mice deficient for the DiGeorge syndrome region | 1-gen-1999 | Illingworth, ELISABETH ANNE; Jurecic, V; CARATTINI RIVERA, S; Cheah, Y. C.; Rosenblatt, Hm; Bradley, A; Baldini, | |
| 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, ELISABETH ANNE | |
| Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model | 1-gen-2013 | Toritsuka, M; Kimoto, S; Muraki, K; Landek Salgado, M; Yoshida, A; Yamamoto, N; Horiuchi, Y; Hiyama, H; Tajinda, K; Keni, N; Illingworth, ELISABETH ANNE; Iwamoto, T; Kishimoto, T; Sawa, A; Tanigaki, K. | |
| Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. | 1-gen-2007 | Sivagnanasundaram, S; Fletcher, D; Hubank, M; Illingworth, ELISABETH ANNE; Skuse, D; Scambler, P. | |
| Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome | 1-gen-2010 | Earls, L; Bayazitov, I; Fricke, R; Berry, R; Illingworth, ELISABETH ANNE; Mittleman, G; Zakharenko, S. | |
| Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation | 1-gen-2024 | Aurigemma, I; Lanzetta, O; Cirino, A; Allegretti, S; Lania, G; Ferrentino, R; Poondi Krishnan, V; Angelini, C; Illingworth, E; Baldini, A | |
| ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene | 1-gen-1998 | Illingworth, ELISABETH ANNE; Harvey, El; Scambler, Pj; Baldini, A. | |
| Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes | 1-gen-1998 | Wakamiya, M; Illingworth, ELISABETH ANNE; RIVERA PEREZ, Ja; Baldini, A; Behringer, R. | |
| Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome | 1-gen-2001 | Taddei, I; Morishima, M; Huynh, T; Illingworth, ELISABETH ANNE | |
| Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis | 1-gen-2017 | Flore, Gemma; di ruberto, Giuseppina; Parisot, Josephine; Sannino, Sara; Russo, Fabio; Illingworth, ELISABETH ANNE; Studer, Michèle; de leonibus, Elivira | |
| Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. | 1-gen-2009 | Randall, V; Mccue, K; Roberts, C; Kyriakopoulou, V; Beddow, S; Barrett, An; Vitelli, F; Prescott, K; SHAW SMITH, C; Devriendt, K; Bosman, E; Steffes, G; Steel, Kp; Simrick, S; Basson, Ma; Illingworth, ELISABETH ANNE; Scambler, Pj | |
| Mesodermal expression of Tbx1 is required for cortical development in mice | 1-gen-2014 | G., Flore; S., Cioffi; M., Bilio; Illingworth, ELISABETH ANNE | |
| Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. | 1-gen-2001 | Paylor, R; Mcilwain, Kl; Mcaninch, R; Nellis, A; YUVA PAYLOR, La; Baldini, A; Illingworth, ELISABETH ANNE |