UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 3.384
AS - Asia 2.978
EU - Europa 977
SA - Sud America 220
AF - Africa 39
OC - Oceania 3
Totale 7.601
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Nazione #
US - Stati Uniti d'America 3.356
HK - Hong Kong 1.777
SG - Singapore 533
CN - Cina 319
IT - Italia 225
RU - Federazione Russa 223
UA - Ucraina 196
BR - Brasile 160
VN - Vietnam 143
DE - Germania 68
FR - Francia 63
IE - Irlanda 60
FI - Finlandia 55
IN - India 35
TR - Turchia 34
KR - Corea 33
AR - Argentina 24
SE - Svezia 23
BD - Bangladesh 19
PH - Filippine 16
GB - Regno Unito 15
MX - Messico 12
EC - Ecuador 10
ZA - Sudafrica 10
CA - Canada 9
CO - Colombia 9
ES - Italia 9
IQ - Iraq 9
NL - Olanda 9
PK - Pakistan 9
ID - Indonesia 8
IL - Israele 7
JP - Giappone 7
VE - Venezuela 7
AT - Austria 5
PY - Paraguay 5
MA - Marocco 4
SA - Arabia Saudita 4
TN - Tunisia 4
UZ - Uzbekistan 4
AL - Albania 3
CL - Cile 3
EG - Egitto 3
GE - Georgia 3
IR - Iran 3
KE - Kenya 3
LT - Lituania 3
MY - Malesia 3
PL - Polonia 3
SN - Senegal 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
CZ - Repubblica Ceca 2
ET - Etiopia 2
JO - Giordania 2
KG - Kirghizistan 2
KZ - Kazakistan 2
MD - Moldavia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PA - Panama 2
AG - Antigua e Barbuda 1
AO - Angola 1
AU - Australia 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
CV - Capo Verde 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
HR - Croazia 1
HU - Ungheria 1
KN - Saint Kitts e Nevis 1
LB - Libano 1
LU - Lussemburgo 1
LY - Libia 1
ME - Montenegro 1
NE - Niger 1
NI - Nicaragua 1
OM - Oman 1
PE - Perù 1
PS - Palestinian Territory 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
TT - Trinidad e Tobago 1
YE - Yemen 1
YT - Mayotte 1
Totale 7.601
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Città #
Hong Kong 1.776
Ann Arbor 771
Chandler 287
Singapore 283
San Jose 282
Woodbridge 277
Jacksonville 256
Houston 199
Princeton 186
Dallas 162
Ashburn 135
Wilmington 83
Council Bluffs 71
Dublin 60
Beijing 51
Lauterbourg 51
Nanjing 49
Andover 46
Ho Chi Minh City 45
Boardman 42
Moscow 42
The Dalles 36
Memphis 35
Hanoi 34
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Norwalk 21
Fairfield 19
Nanchang 19
Hebei 15
Jiaxing 15
Los Angeles 15
Changsha 14
Dong Ket 13
Naples 12
Shenyang 12
São Paulo 12
Sarno 11
Milan 10
Nuremberg 10
Pune 10
Amsterdam 9
Dearborn 9
New York 9
Tianjin 9
Haiphong 8
Brasília 7
Brooklyn 7
Fisciano 7
Munich 7
Tokyo 7
Washington 7
Bracigliano 6
Chennai 6
Frankfurt am Main 6
Lappeenranta 6
Avellino 5
Baghdad 5
Boston 5
Buenos Aires 5
Helsinki 5
Miami 5
Santa Clara 5
Atlanta 4
Denver 4
Dhaka 4
Falls Church 4
Guarulhos 4
Lahore 4
London 4
Mexico City 4
Nha Trang 4
Orem 4
Quito 4
Rio de Janeiro 4
Seattle 4
Stockholm 4
Tel Aviv 4
Warsaw 4
Aracaju 3
Asunción 3
Biên Hòa 3
Cambridge 3
Charlotte 3
Columbus 3
Dakar 3
Edinburgh 3
Fuzhou 3
Guayaquil 3
Jinan 3
Johannesburg 3
Joinville 3
Kunming 3
Montoro 3
Montreal 3
Nairobi 3
New Delhi 3
Pars 3
Totale 5.853
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Nome #
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 507
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 362
Congenital heart disease in mice deficient for the DiGeorge syndrome region 294
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 276
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 275
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 237
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 197
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 194
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 189
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 162
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 141
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 139
Chromosomal microdeletions: dissecting del22q11 syndrome. 139
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 138
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 130
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 128
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 127
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 127
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 120
A genetic link between Tbx1 and fibroblast growth factor signaling. 119
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 115
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 115
Tbx1: Transcriptional and Developmental Functions 111
Mesodermal expression of Tbx1 is required for cortical development in mice 110
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 110
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 110
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 109
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 108
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 107
Congenital heart defects and 22q11 deletions: Which genes count? 107
Tbx1 regulates brain vascularization 106
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 103
Tbx1 is required in brain endothelial cells to establish vascular patterning 101
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 100
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 99
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 99
Tbx1 regulates brain vascularization 99
Modello murino della sindrome da delezione 22q11.2 98
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 97
Mouse models of 22q11 deletion syndrome. 96
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 95
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 95
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 95
TBX1 is required for inner ear morphogenesis. 94
Tbx1 interacts with the BAF chromatin remodeling complex 92
The role of the DiGeorge gene TBX1 in heart development 91
Tbx1 functions and chromatin 90
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 89
Tbx1 is required in brain endothelial cells to establish vascular patterning 87
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 86
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 82
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 75
Tbx1 is required in brain vascularization 74
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 69
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 68
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 57
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 48
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome 43
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 40
A genetic etiology for interruption of the aortic arch type B 40
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 35
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 30
Schizophrenia and Chromosomal Deletions within 22q11.2 28
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 22
Tbx1 stabilizes differentiation of the cardiopharyngeal mesoderm and drives morphogenesis in the pharyngeal apparatus 5
Totale 7.731
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Categoria #
all - tutte 22.497
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 22.497
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202123 0 0 0 0 0 0 0 0 0 0 0 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
2025/20263.680 266 932 1.050 104 260 151 366 77 160 228 82 4
Totale 7.731