UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2.833
AS - Asia 2.369
EU - Europa 877
SA - Sud America 124
AF - Africa 13
OC - Oceania 2
Totale 6.218
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Nazione #
US - Stati Uniti d'America 2.816
HK - Hong Kong 1.764
CN - Cina 242
RU - Federazione Russa 221
IT - Italia 209
UA - Ucraina 192
SG - Singapore 180
BR - Brasile 108
VN - Vietnam 64
DE - Germania 61
IE - Irlanda 60
FI - Finlandia 51
TR - Turchia 33
KR - Corea 28
SE - Svezia 22
PH - Filippine 15
IN - India 14
GB - Regno Unito 13
FR - Francia 8
NL - Olanda 8
CA - Canada 7
ES - Italia 7
BD - Bangladesh 6
MX - Messico 6
IL - Israele 5
ID - Indonesia 4
PY - Paraguay 4
ZA - Sudafrica 4
AR - Argentina 3
AT - Austria 3
EC - Ecuador 3
IR - Iran 3
JP - Giappone 3
LT - Lituania 3
PK - Pakistan 3
AL - Albania 2
BE - Belgio 2
CO - Colombia 2
CZ - Repubblica Ceca 2
EG - Egitto 2
IQ - Iraq 2
MD - Moldavia 2
NZ - Nuova Zelanda 2
PL - Polonia 2
VE - Venezuela 2
BG - Bulgaria 1
BO - Bolivia 1
CH - Svizzera 1
CV - Capo Verde 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
HR - Croazia 1
HU - Ungheria 1
KE - Kenya 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MA - Marocco 1
ME - Montenegro 1
NE - Niger 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
YT - Mayotte 1
Totale 6.218
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Città #
Hong Kong 1.764
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Houston 199
Princeton 186
Dallas 160
Singapore 92
Ashburn 87
Wilmington 83
Dublin 60
Nanjing 49
Andover 46
Boardman 42
Moscow 42
Beijing 37
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Norwalk 21
Fairfield 19
Nanchang 19
Hanoi 18
Hebei 15
Jiaxing 15
Changsha 14
Ho Chi Minh City 14
Dong Ket 13
Shenyang 12
Sarno 11
Los Angeles 10
Milan 10
Naples 10
Dearborn 9
Pune 9
Tianjin 9
Amsterdam 8
Nuremberg 8
Fisciano 7
Munich 7
New York 7
São Paulo 7
Washington 7
Bracigliano 6
Avellino 5
Council Bluffs 5
The Dalles 5
Boston 4
Brooklyn 4
Falls Church 4
Lappeenranta 4
London 4
Rio de Janeiro 4
Seattle 4
Aracaju 3
Asunción 3
Atlanta 3
Brasília 3
Cambridge 3
Columbus 3
Denver 3
Edinburgh 3
Helsinki 3
Jinan 3
Kunming 3
Montreal 3
Pars 3
Quận Bình Thạnh 3
Rome 3
San Diego 3
Seoul 3
Stockholm 3
Tokyo 3
Barquisimeto 2
Brussels 2
Buffalo 2
Cairo 2
Charlotte 2
Chennai 2
Curitiba 2
Feira de Santana 2
Fortaleza 2
Frankfurt am Main 2
Fuzhou 2
Guangzhou 2
Guarulhos 2
Haiphong 2
Hangzhou 2
Joinville 2
Lahore 2
Limatola 2
Madrid 2
Manaus 2
Manchester 2
Miami 2
Nha Trang 2
Ningbo 2
Palermo 2
Totale 4.992
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Nome #
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 490
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 345
Congenital heart disease in mice deficient for the DiGeorge syndrome region 262
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 258
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 254
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 213
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 182
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 172
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 170
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 137
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 120
Chromosomal microdeletions: dissecting del22q11 syndrome. 120
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 116
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 113
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 110
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 108
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 107
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 95
Tbx1: Transcriptional and Developmental Functions 94
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 91
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 91
A genetic link between Tbx1 and fibroblast growth factor signaling. 90
Mesodermal expression of Tbx1 is required for cortical development in mice 88
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 88
Tbx1 regulates brain vascularization 88
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 87
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 86
Congenital heart defects and 22q11 deletions: Which genes count? 85
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 84
Tbx1 regulates brain vascularization 84
Mouse models of 22q11 deletion syndrome. 83
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 83
Tbx1 is required in brain endothelial cells to establish vascular patterning 82
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 81
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 80
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 80
TBX1 is required for inner ear morphogenesis. 79
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 79
Modello murino della sindrome da delezione 22q11.2 78
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 78
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 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 72
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 72
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 71
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 70
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 67
Tbx1 is required in brain endothelial cells to establish vascular patterning 65
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 64
Tbx1 interacts with the BAF chromatin remodeling complex 63
Tbx1 functions and chromatin 62
Tbx1 is required in brain vascularization 58
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 43
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 43
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 40
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 39
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome 27
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 22
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 19
A genetic etiology for interruption of the aortic arch type B 18
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 16
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 12
Schizophrenia and Chromosomal Deletions within 22q11.2 11
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 10
Totale 6.347
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Categoria #
all - tutte 19.132
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 19.132
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021217 0 0 0 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
2025/20262.296 266 932 1.050 48 0 0 0 0 0 0 0 0
Totale 6.347