UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2.624
EU - Europa 774
AS - Asia 487
SA - Sud America 53
AF - Africa 2
OC - Oceania 2
Totale 3.942
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Nazione #
US - Stati Uniti d'America 2.612
IT - Italia 208
CN - Cina 203
UA - Ucraina 190
SG - Singapore 164
RU - Federazione Russa 139
IE - Irlanda 60
DE - Germania 58
FI - Finlandia 49
BR - Brasile 47
TR - Turchia 33
KR - Corea 25
SE - Svezia 20
VN - Vietnam 16
PH - Filippine 15
IN - India 14
GB - Regno Unito 11
NL - Olanda 8
CA - Canada 7
FR - Francia 7
ES - Italia 5
IL - Israele 4
IR - Iran 3
LT - Lituania 3
AT - Austria 2
BE - Belgio 2
HK - Hong Kong 2
IQ - Iraq 2
MX - Messico 2
NZ - Nuova Zelanda 2
PK - Pakistan 2
AL - Albania 1
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
BO - Bolivia 1
CH - Svizzera 1
CO - Colombia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EC - Ecuador 1
EE - Estonia 1
EG - Egitto 1
HR - Croazia 1
HU - Ungheria 1
JP - Giappone 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
ME - Montenegro 1
NI - Nicaragua 1
PA - Panama 1
PE - Perù 1
PL - Polonia 1
PY - Paraguay 1
TT - Trinidad e Tobago 1
Totale 3.942
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Città #
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Houston 199
Princeton 186
Wilmington 83
Ashburn 77
Singapore 76
Dublin 60
Nanjing 49
Andover 46
Boardman 42
Moscow 42
Beijing 36
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Norwalk 21
Fairfield 19
Nanchang 19
Hebei 15
Jiaxing 15
Changsha 14
Dong Ket 13
Shenyang 12
Sarno 11
Naples 10
Dearborn 9
Milan 9
Pune 9
Tianjin 9
Amsterdam 8
Fisciano 7
Los Angeles 7
Washington 7
Bracigliano 6
Munich 6
Nuremberg 6
Avellino 5
The Dalles 5
Falls Church 4
London 4
New York 4
Brooklyn 3
Cambridge 3
Columbus 3
Edinburgh 3
Helsinki 3
Jinan 3
Kunming 3
Montreal 3
Pars 3
Rome 3
San Diego 3
Seattle 3
São Paulo 3
Boston 2
Brussels 2
Buffalo 2
Charlotte 2
Chennai 2
Dallas 2
Feira de Santana 2
Fortaleza 2
Frankfurt am Main 2
Fuzhou 2
Guangzhou 2
Hangzhou 2
Hong Kong 2
Lappeenranta 2
Limatola 2
Madrid 2
Miami 2
Nha Trang 2
Ningbo 2
Palermo 2
Tel Aviv 2
Toronto 2
Vienna 2
Xian 2
Yubileyny 2
Zhengzhou 2
Acreúna 1
Amarah 1
Aracaju 1
Araranguá 1
Ariano Irpino 1
Arima 1
Asunción 1
Atlanta 1
Auckland 1
Bacoli 1
Bagé 1
Bishkek 1
Brasília 1
Budapest 1
Bursa 1
Cairo 1
Totale 2.967
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Nome #
Congenital heart disease in mice deficient for the DiGeorge syndrome region 115
Chromosomal microdeletions: dissecting del22q11 syndrome. 113
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 112
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 108
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 107
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 104
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 101
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 97
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 93
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 93
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 93
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 89
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 88
Tbx1 regulates brain vascularization 87
Mesodermal expression of Tbx1 is required for cortical development in mice 86
Tbx1: Transcriptional and Developmental Functions 85
Tbx1 regulates brain vascularization 82
A genetic link between Tbx1 and fibroblast growth factor signaling. 81
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 81
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 81
Tbx1 is required in brain endothelial cells to establish vascular patterning 80
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 79
Mouse models of 22q11 deletion syndrome. 78
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 78
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 77
TBX1 is required for inner ear morphogenesis. 76
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 76
The role of the DiGeorge gene TBX1 in heart development 76
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 76
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 75
Congenital heart defects and 22q11 deletions: Which genes count? 75
Modello murino della sindrome da delezione 22q11.2 75
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 74
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 74
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 74
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 72
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 70
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 69
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 66
Tbx1 interacts with the BAF chromatin remodeling complex 63
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 62
Tbx1 is required in brain endothelial cells to establish vascular patterning 62
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 61
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 61
Tbx1 functions and chromatin 60
Tbx1 is required in brain vascularization 57
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 57
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 49
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 38
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 28
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 24
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 23
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome 17
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 14
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 12
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 12
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 10
A genetic etiology for interruption of the aortic arch type B 8
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 8
Schizophrenia and Chromosomal Deletions within 22q11.2 7
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 6
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 6
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 5
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 5
Totale 4.071
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Categoria #
all - tutte 14.086
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 14.086
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021315 1 46 51 4 44 7 43 1 43 4 48 23
2021/2022335 0 0 1 0 6 3 6 12 54 47 46 160
2022/2023620 54 53 7 94 80 119 1 80 73 0 42 17
2023/2024221 29 28 18 11 25 50 1 3 1 8 9 38
2024/2025507 26 5 24 24 9 94 98 73 59 14 54 27
2025/202620 20 0 0 0 0 0 0 0 0 0 0 0
Totale 4.071