UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2372
EU - Europa 526
AS - Asia 254
SA - Sud America 1
Totale 3153
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Nazione #
US - Stati Uniti d'America 2370
UA - Ucraina 190
CN - Cina 188
IT - Italia 146
IE - Irlanda 61
FI - Finlandia 44
DE - Germania 39
TR - Turchia 31
SE - Svezia 20
PH - Filippine 15
VN - Vietnam 13
FR - Francia 7
RU - Federazione Russa 4
IR - Iran 3
BE - Belgio 2
CA - Canada 2
ES - Italia 2
GB - Regno Unito 2
NL - Olanda 2
BG - Bulgaria 1
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
HR - Croazia 1
IL - Israele 1
IN - India 1
LT - Lituania 1
LU - Lussemburgo 1
PK - Pakistan 1
SG - Singapore 1
Totale 3153
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Città #
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Houston 199
Princeton 186
Wilmington 83
Dublin 61
Nanjing 49
Andover 46
Boardman 37
Beijing 36
Pellezzano 33
Izmir 31
Napoli 28
Norwalk 21
Fairfield 19
Nanchang 19
Salerno 19
Hebei 15
Changsha 14
Ashburn 13
Dong Ket 13
Jiaxing 13
Shenyang 12
Dearborn 9
Tianjin 9
Bracigliano 6
Falls Church 4
Cambridge 3
Jinan 3
Kunming 3
Pars 3
San Diego 3
Amsterdam 2
Brussels 2
Fuzhou 2
London 2
Ningbo 2
Palermo 2
Rome 2
Seattle 2
Xian 2
Zhengzhou 2
Ariano Irpino 1
Bacoli 1
Charlotte 1
Copenhagen 1
Dalian 1
Delhi 1
Faisalabad 1
Hangzhou 1
Helsinki 1
Le Havre 1
Los Angeles 1
Luxembourg 1
Madrid 1
Milan 1
Naples 1
New Orleans 1
Oklahoma City 1
Orlando 1
Ottawa 1
Redwood City 1
Rehovot 1
Saint Paul 1
San Francisco 1
San Martino Valle Caudina 1
Shaoxing 1
Sofia 1
Stockholm 1
São Paulo 1
Taizhou 1
Toronto 1
Valencia 1
Vilnius 1
Zagreb 1
Zurich 1
Totale 2634
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Nome #
Congenital heart disease in mice deficient for the DiGeorge syndrome region 96
Chromosomal microdeletions: dissecting del22q11 syndrome. 96
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 96
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 92
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 92
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 85
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 84
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 82
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 82
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 80
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 78
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 78
Tbx1 regulates brain vascularization 78
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 76
Tbx1 is required in brain endothelial cells to establish vascular patterning 72
Tbx1 regulates brain vascularization 72
Tbx1: Transcriptional and Developmental Functions 71
Mouse models of 22q11 deletion syndrome. 70
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 69
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 69
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 69
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 69
The role of the DiGeorge gene TBX1 in heart development 68
TBX1 is required for inner ear morphogenesis. 66
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 66
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 66
A genetic link between Tbx1 and fibroblast growth factor signaling. 65
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 65
Modello murino della sindrome da delezione 22q11.2 65
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 64
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 64
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 64
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 61
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 61
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 61
Mesodermal expression of Tbx1 is required for cortical development in mice 60
Congenital heart defects and 22q11 deletions: Which genes count? 57
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 56
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 55
Tbx1 interacts with the BAF chromatin remodeling complex 55
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 51
Tbx1 is required in brain endothelial cells to establish vascular patterning 50
Tbx1 functions and chromatin 48
Tbx1 is required in brain vascularization 47
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 46
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 41
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 34
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 32
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 20
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 14
Totale 3258
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Categoria #
all - tutte 4860
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4860
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018101 0000 00 00 848639
2018/2019241 1217626 4353 336 63342
2019/2020455 1327453 689 477 4621628
2020/2021315 146514 447 431 4344823
2021/2022335 0010 63 612 544746160
2022/2023555 5453794 80119 180 67000
Totale 3258