UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2.959
AS - Asia 2.735
EU - Europa 893
SA - Sud America 181
AF - Africa 19
OC - Oceania 2
Totale 6.789
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Nazione #
US - Stati Uniti d'America 2.937
HK - Hong Kong 1.773
SG - Singapore 427
CN - Cina 312
RU - Federazione Russa 222
IT - Italia 212
UA - Ucraina 194
BR - Brasile 139
VN - Vietnam 86
DE - Germania 62
IE - Irlanda 60
FI - Finlandia 53
TR - Turchia 33
KR - Corea 28
SE - Svezia 23
AR - Argentina 19
IN - India 18
PH - Filippine 15
GB - Regno Unito 13
MX - Messico 11
ES - Italia 9
BD - Bangladesh 8
FR - Francia 8
NL - Olanda 8
CA - Canada 7
EC - Ecuador 6
ID - Indonesia 6
IL - Israele 6
ZA - Sudafrica 6
AT - Austria 5
CO - Colombia 5
PY - Paraguay 5
JP - Giappone 4
PK - Pakistan 4
CL - Cile 3
IQ - Iraq 3
IR - Iran 3
LT - Lituania 3
PL - Polonia 3
AL - Albania 2
BE - Belgio 2
CZ - Repubblica Ceca 2
EG - Egitto 2
GE - Georgia 2
JO - Giordania 2
KE - Kenya 2
MD - Moldavia 2
NZ - Nuova Zelanda 2
VE - Venezuela 2
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
CV - Capo Verde 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GA - Gabon 1
HR - Croazia 1
HU - Ungheria 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MA - Marocco 1
ME - Montenegro 1
NE - Niger 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SO - Somalia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UZ - Uzbekistan 1
YT - Mayotte 1
Totale 6.789
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Città #
Hong Kong 1.773
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Singapore 223
Houston 199
Princeton 186
Dallas 160
Ashburn 109
Wilmington 83
San Jose 70
Dublin 60
Beijing 50
Nanjing 49
Andover 46
Boardman 42
Moscow 42
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Hanoi 22
Ho Chi Minh City 22
Norwalk 21
Fairfield 19
Nanchang 19
Hebei 15
Jiaxing 15
Changsha 14
The Dalles 14
Dong Ket 13
Los Angeles 12
Shenyang 12
Sarno 11
Milan 10
Naples 10
Dearborn 9
Nuremberg 9
Pune 9
Tianjin 9
Amsterdam 8
New York 8
São Paulo 8
Brasília 7
Fisciano 7
Munich 7
Washington 7
Bracigliano 6
Lappeenranta 6
Avellino 5
Council Bluffs 5
Atlanta 4
Boston 4
Brooklyn 4
Buenos Aires 4
Chennai 4
Denver 4
Falls Church 4
Haiphong 4
London 4
Mexico City 4
Rio de Janeiro 4
Santa Clara 4
Seattle 4
Stockholm 4
Tokyo 4
Aracaju 3
Asunción 3
Cambridge 3
Columbus 3
Edinburgh 3
Fuzhou 3
Guarulhos 3
Helsinki 3
Jinan 3
Joinville 3
Kunming 3
Lahore 3
Montreal 3
Pars 3
Phoenix 3
Porto Alegre 3
Quận Bình Thạnh 3
Rome 3
San Diego 3
San Francisco 3
Seoul 3
Tel Aviv 3
Vienna 3
Warsaw 3
Amman 2
Barquisimeto 2
Belo Horizonte 2
Biên Hòa 2
Brussels 2
Buffalo 2
Cairo 2
Charlotte 2
Curitiba 2
Totale 5.291
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Nome #
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 495
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 351
Congenital heart disease in mice deficient for the DiGeorge syndrome region 273
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 266
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 261
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 221
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 189
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 185
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 178
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 149
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 131
Chromosomal microdeletions: dissecting del22q11 syndrome. 131
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 127
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 124
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 118
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 117
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 116
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 105
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 102
A genetic link between Tbx1 and fibroblast growth factor signaling. 99
Tbx1: Transcriptional and Developmental Functions 99
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 98
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 98
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 96
Mesodermal expression of Tbx1 is required for cortical development in mice 95
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 95
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 95
Tbx1 regulates brain vascularization 95
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 95
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 94
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 93
Tbx1 is required in brain endothelial cells to establish vascular patterning 93
Congenital heart defects and 22q11 deletions: Which genes count? 92
Tbx1 regulates brain vascularization 91
Mouse models of 22q11 deletion syndrome. 88
Modello murino della sindrome da delezione 22q11.2 88
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 87
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 86
The role of the DiGeorge gene TBX1 in heart development 85
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 84
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 84
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 83
TBX1 is required for inner ear morphogenesis. 82
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 80
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 79
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 78
Tbx1 is required in brain endothelial cells to establish vascular patterning 77
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 75
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 72
Tbx1 interacts with the BAF chromatin remodeling complex 70
Tbx1 functions and chromatin 70
Tbx1 is required in brain vascularization 65
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 62
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 59
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 49
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 48
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 35
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome 33
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 28
A genetic etiology for interruption of the aortic arch type B 28
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 23
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 19
Schizophrenia and Chromosomal Deletions within 22q11.2 18
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 16
Totale 6.918
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Categoria #
all - tutte 20.850
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 20.850
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021162 0 0 0 0 0 0 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
2025/20262.867 266 932 1.050 104 260 151 104 0 0 0 0 0
Totale 6.918