UniSa - IRIS Institutional Research Information System

ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
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Continente #
NA - Nord America 2.867
AS - Asia 2.626
EU - Europa 889
SA - Sud America 166
AF - Africa 15
OC - Oceania 2
Totale 6.565
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Nazione #
US - Stati Uniti d'America 2.846
HK - Hong Kong 1.766
SG - Singapore 359
CN - Cina 297
RU - Federazione Russa 222
IT - Italia 211
UA - Ucraina 194
BR - Brasile 133
VN - Vietnam 75
DE - Germania 62
IE - Irlanda 60
FI - Finlandia 53
TR - Turchia 33
KR - Corea 28
SE - Svezia 22
IN - India 16
PH - Filippine 15
AR - Argentina 13
GB - Regno Unito 13
MX - Messico 10
ES - Italia 9
BD - Bangladesh 8
FR - Francia 8
NL - Olanda 8
CA - Canada 7
EC - Ecuador 6
ID - Indonesia 6
IL - Israele 6
PY - Paraguay 5
ZA - Sudafrica 5
AT - Austria 4
JP - Giappone 4
PK - Pakistan 4
CO - Colombia 3
IQ - Iraq 3
IR - Iran 3
LT - Lituania 3
PL - Polonia 3
AL - Albania 2
BE - Belgio 2
CL - Cile 2
CZ - Repubblica Ceca 2
EG - Egitto 2
KE - Kenya 2
MD - Moldavia 2
NZ - Nuova Zelanda 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
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 6.565
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Città #
Hong Kong 1.766
Ann Arbor 771
Chandler 287
Woodbridge 277
Jacksonville 255
Houston 199
Princeton 186
Singapore 183
Dallas 160
Ashburn 102
Wilmington 83
Dublin 60
Beijing 50
Nanjing 49
Andover 46
Boardman 42
Moscow 42
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Norwalk 21
Ho Chi Minh City 20
Fairfield 19
Hanoi 19
Nanchang 19
Hebei 15
Jiaxing 15
Changsha 14
Dong Ket 13
Shenyang 12
Los Angeles 11
Sarno 11
Milan 10
Naples 10
Dearborn 9
Nuremberg 9
Pune 9
Tianjin 9
Amsterdam 8
New York 8
São Paulo 8
Fisciano 7
Munich 7
Washington 7
Bracigliano 6
Brasília 6
Lappeenranta 6
Avellino 5
Council Bluffs 5
The Dalles 5
Boston 4
Brooklyn 4
Chennai 4
Denver 4
Falls Church 4
London 4
Rio de Janeiro 4
Santa Clara 4
Seattle 4
Tokyo 4
Aracaju 3
Asunción 3
Atlanta 3
Cambridge 3
Columbus 3
Edinburgh 3
Fuzhou 3
Guarulhos 3
Helsinki 3
Jinan 3
Joinville 3
Kunming 3
Lahore 3
Mexico City 3
Montreal 3
Pars 3
Phoenix 3
Porto Alegre 3
Quận Bình Thạnh 3
Rome 3
San Diego 3
San Francisco 3
Seoul 3
Stockholm 3
Tel Aviv 3
Vienna 3
Warsaw 3
Barquisimeto 2
Belo Horizonte 2
Biên Hòa 2
Brussels 2
Buenos Aires 2
Buffalo 2
Cairo 2
Charlotte 2
Curitiba 2
Dhaka 2
Feira de Santana 2
Fortaleza 2
Totale 5.146
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Nome #
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 493
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 347
Congenital heart disease in mice deficient for the DiGeorge syndrome region 268
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 260
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 260
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 217
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 186
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 180
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 175
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 147
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 128
Chromosomal microdeletions: dissecting del22q11 syndrome. 125
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 123
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 121
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 115
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 114
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 114
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 104
Tbx1: Transcriptional and Developmental Functions 98
A genetic link between Tbx1 and fibroblast growth factor signaling. 95
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 94
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 93
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 93
Tbx1 regulates brain vascularization 93
Mesodermal expression of Tbx1 is required for cortical development in mice 92
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 91
Congenital heart defects and 22q11 deletions: Which genes count? 91
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 91
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 91
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 89
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 89
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 89
Tbx1 is required in brain endothelial cells to establish vascular patterning 88
Tbx1 regulates brain vascularization 88
Mouse models of 22q11 deletion syndrome. 86
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 84
Modello murino della sindrome da delezione 22q11.2 83
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 82
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 82
TBX1 is required for inner ear morphogenesis. 81
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 81
The role of the DiGeorge gene TBX1 in heart development 81
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 80
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 78
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 77
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 73
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 73
Tbx1 is required in brain endothelial cells to establish vascular patterning 72
Tbx1 functions and chromatin 70
Tbx1 interacts with the BAF chromatin remodeling complex 68
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 67
Tbx1 is required in brain vascularization 62
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 58
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 53
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 46
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 43
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 32
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome 31
A genetic etiology for interruption of the aortic arch type B 25
A transcription map in the CATCH-22 critical region: identification, mapping and ordering of 4 novel transcripts expressed in heart 24
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 18
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 16
Schizophrenia and Chromosomal Deletions within 22q11.2 14
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 12
Totale 6.694
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Categoria #
all - tutte 20.312
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 20.312
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021169 0 0 0 0 0 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
2025/20262.643 266 932 1.050 104 260 31 0 0 0 0 0 0
Totale 6.694