UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2.581
EU - Europa 757
AS - Asia 468
SA - Sud America 33
AF - Africa 2
OC - Oceania 2
Totale 3.843
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Nazione #
US - Stati Uniti d'America 2.576
IT - Italia 208
CN - Cina 203
UA - Ucraina 190
SG - Singapore 158
RU - Federazione Russa 139
IE - Irlanda 60
DE - Germania 52
FI - Finlandia 48
TR - Turchia 32
BR - Brasile 31
KR - Corea 22
SE - Svezia 20
PH - Filippine 15
VN - Vietnam 15
IN - India 11
NL - Olanda 8
FR - Francia 7
GB - Regno Unito 7
CA - Canada 3
ES - Italia 3
IL - Israele 3
IR - Iran 3
BE - Belgio 2
IQ - Iraq 2
NZ - Nuova Zelanda 2
AL - Albania 1
AT - Austria 1
BG - Bulgaria 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EE - Estonia 1
EG - Egitto 1
HK - Hong Kong 1
HR - Croazia 1
HU - Ungheria 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LT - Lituania 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
ME - Montenegro 1
MX - Messico 1
PA - Panama 1
PE - Perù 1
PK - Pakistan 1
PY - Paraguay 1
Totale 3.843
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Città #
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Houston 199
Princeton 186
Wilmington 83
Ashburn 74
Singapore 70
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
Washington 7
Bracigliano 6
Nuremberg 6
Avellino 5
Falls Church 4
Los Angeles 4
Cambridge 3
Edinburgh 3
Helsinki 3
Jinan 3
Kunming 3
Pars 3
Rome 3
San Diego 3
Seattle 3
Brussels 2
Fortaleza 2
Frankfurt am Main 2
Fuzhou 2
Guangzhou 2
Hangzhou 2
Lappeenranta 2
Limatola 2
London 2
Madrid 2
Miami 2
Nha Trang 2
Ningbo 2
Palermo 2
São Paulo 2
Tel Aviv 2
The Dalles 2
Xian 2
Yubileyny 2
Zhengzhou 2
Amarah 1
Aracaju 1
Araranguá 1
Ariano Irpino 1
Asunción 1
Auckland 1
Bacoli 1
Bagé 1
Bishkek 1
Budapest 1
Buffalo 1
Bursa 1
Cairo 1
Carate Brianza 1
Carazinho 1
Caçapava 1
Charlotte 1
Chengdu 1
Chiclayo 1
Chisinau 1
Copenhagen 1
Council Bluffs 1
Dalian 1
Dallas 1
Delhi 1
Denver 1
Divinópolis 1
Faisalabad 1
Feira de Santana 1
Fort Worth 1
Totale 2.926
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Nome #
Congenital heart disease in mice deficient for the DiGeorge syndrome region 112
Chromosomal microdeletions: dissecting del22q11 syndrome. 111
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 109
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 106
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 105
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 102
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 98
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 96
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 92
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 92
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 91
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 88
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 88
Tbx1 regulates brain vascularization 86
Mesodermal expression of Tbx1 is required for cortical development in mice 83
Tbx1: Transcriptional and Developmental Functions 83
Tbx1 regulates brain vascularization 82
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 80
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 80
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
A genetic link between Tbx1 and fibroblast growth factor signaling. 78
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 78
Mouse models of 22q11 deletion syndrome. 77
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 76
The role of the DiGeorge gene TBX1 in heart development 76
TBX1 is required for inner ear morphogenesis. 75
Modello murino della sindrome da delezione 22q11.2 75
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 74
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 74
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 74
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 74
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 72
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 72
Congenital heart defects and 22q11 deletions: Which genes count? 71
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 71
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 69
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 69
Tbx1 interacts with the BAF chromatin remodeling complex 63
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 61
Tbx1 is required in brain endothelial cells to establish vascular patterning 61
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 60
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 59
Tbx1 functions and chromatin 59
Tbx1 is required in brain vascularization 56
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 56
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 54
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 48
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 35
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 24
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 23
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 22
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 12
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 10
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 9
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 8
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 7
A genetic etiology for interruption of the aortic arch type B 6
Schizophrenia and Chromosomal Deletions within 22q11.2 6
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 5
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 5
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 4
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 4
Totale 3.972
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Categoria #
all - tutte 13.167
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 13.167
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202070 0 0 0 0 0 0 0 0 0 0 62 8
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
2024/2025428 26 5 24 24 9 94 98 73 59 14 2 0
Totale 3.972