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ILLINGWORTH, Elizabeth Anne

ILLINGWORTH, Elizabeth Anne  

Dipartimento di Chimica e Biologia "Adolfo Zambelli"/DCB  

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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
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.
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
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 1-gen-2005 Ivins, S; LAMMERTS VAN BEUREN, K; Roberts, C; James, C; Illingworth, ELISABETH ANNE; Baldini, A; Ataliotis, P; Scambler, Pj
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 1-gen-2005 Prescott, K; Ivins, S; Hubank, M; Illingworth, ELISABETH ANNE; Baldini, A; Scambler, P.