ILLINGWORTH, Elizabeth Anne
 Distribuzione geografica
Continente #
NA - Nord America 3.495
AS - Asia 3.022
EU - Europa 1.329
SA - Sud America 224
Continente sconosciuto - Info sul continente non disponibili 133
AF - Africa 39
OC - Oceania 3
Totale 8.245
Nazione #
US - Stati Uniti d'America 3.452
HK - Hong Kong 1.788
IT - Italia 568
SG - Singapore 541
CN - Cina 328
RU - Federazione Russa 223
UA - Ucraina 196
BR - Brasile 163
VN - Vietnam 144
DE - Germania 68
FR - Francia 64
IE - Irlanda 60
FI - Finlandia 55
IN - India 36
TR - Turchia 36
KR - Corea 34
BD - Bangladesh 30
AR - Argentina 24
SE - Svezia 23
GB - Regno Unito 16
MX - Messico 16
PH - Filippine 16
CA - Canada 12
CO - Colombia 10
EC - Ecuador 10
ES - Italia 10
NL - Olanda 10
ZA - Sudafrica 10
IQ - Iraq 9
PK - Pakistan 9
ID - Indonesia 8
IL - Israele 7
JP - Giappone 7
VE - Venezuela 7
AT - Austria 5
PL - Polonia 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
SN - Senegal 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
CZ - Repubblica Ceca 2
EE - Estonia 2
ET - Etiopia 2
GT - Guatemala 2
JM - Giamaica 2
JO - Giordania 2
KG - Kirghizistan 2
KZ - Kazakistan 2
MD - Moldavia 2
ME - Montenegro 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
CR - Costa Rica 1
CV - Capo Verde 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GA - Gabon 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
KN - Saint Kitts e Nevis 1
LB - Libano 1
LU - Lussemburgo 1
LY - Libia 1
NE - Niger 1
NI - Nicaragua 1
OM - Oman 1
PE - Perù 1
PR - Porto Rico 1
PS - Palestinian Territory 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
YE - Yemen 1
YT - Mayotte 1
Totale 8.112
Città #
Hong Kong 1.787
Ann Arbor 771
Singapore 291
Chandler 287
San Jose 282
Woodbridge 277
Jacksonville 256
Milan 233
Houston 200
Princeton 186
Dallas 163
Ashburn 138
Wilmington 83
Council Bluffs 71
Beijing 60
Dublin 60
Rome 55
Lauterbourg 51
Nanjing 49
Andover 46
Ho Chi Minh City 46
Boardman 42
Moscow 42
The Dalles 36
Memphis 35
Hanoi 34
Pellezzano 33
Izmir 31
Napoli 28
Salerno 28
Figino 25
Los Angeles 21
Norwalk 21
Fairfield 19
Nanchang 19
Santa Clara 16
Hebei 15
Jiaxing 15
Naples 15
Changsha 14
Dong Ket 13
Shenyang 12
São Paulo 12
Turin 12
New York 11
Sarno 11
Nuremberg 10
Pune 10
Amsterdam 9
Dearborn 9
Tianjin 9
Brooklyn 8
Haiphong 8
Mexico City 8
Washington 8
Brasília 7
Fisciano 7
Munich 7
Tokyo 7
Boston 6
Bracigliano 6
Chennai 6
Frankfurt am Main 6
Lappeenranta 6
Avellino 5
Baghdad 5
Buenos Aires 5
Denver 5
Helsinki 5
London 5
Miami 5
Rio de Janeiro 5
Atlanta 4
Charlotte 4
Dhaka 4
Falls Church 4
Guarulhos 4
Lahore 4
Las Vegas 4
Montreal 4
Nha Trang 4
Orem 4
Phoenix 4
Quito 4
San Francisco 4
Seattle 4
Seoul 4
Stockholm 4
Tel Aviv 4
Warsaw 4
Aracaju 3
Asunción 3
Biên Hòa 3
Buffalo 3
Cambridge 3
Columbus 3
Dakar 3
Edinburgh 3
Florence 3
Fuzhou 3
Totale 6.231
Nome #
Low-copy number repeat sequences flank the DiGeorge/Velocardiofacial syndrome loci at 22q11 515
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 369
Congenital heart disease in mice deficient for the DiGeorge syndrome region 358
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 283
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 278
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 241
Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome 203
Transcriptional Control in Cardiac Progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a 202
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 201
Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome 167
Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment 158
Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11-deletion syndrome mouse model 150
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 146
Chromosomal microdeletions: dissecting del22q11 syndrome. 146
Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 145
A genetic link between Tbx1 and fibroblast growth factor signaling. 141
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation 140
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 132
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 131
Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis 126
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 124
Vegfr3 Overexpression Partially Rescues The Brain Vascular Defects of Tbx1 mutants 122
Tbx1: Transcriptional and Developmental Functions 118
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 118
Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia. 116
Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome 115
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. 114
Mesodermal expression of Tbx1 is required for cortical development in mice 112
Tbx1 is required in brain endothelial cells to establish vascular patterning 112
Tbx1 regulates brain vascularization 112
Tbx1 regulates brain vascularization 111
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 110
Congenital heart defects and 22q11 deletions: Which genes count? 110
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. 108
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 107
Wnt5a and Tbx1 in the SHF: Interacting pathways to congenital heart disease 106
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 105
TBX1 is required for inner ear morphogenesis. 105
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congential heart disease 105
Tbx1 Interacts Genetically with Vegfr3 to Regulate Lymphangiogenesis in mice 104
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 103
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 102
Tbx1 interacts with the BAF chromatin remodeling complex 102
Modello murino della sindrome da delezione 22q11.2 100
The role of the DiGeorge gene TBX1 in heart development 100
Mouse models of 22q11 deletion syndrome. 97
Tbx1 functions and chromatin 97
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 94
Tbx1 is required in brain endothelial cells to establish vascular patterning 91
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 90
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 87
Tbx1 is required in brain vascularization 84
Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway 82
A de novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic and molecular characterization 80
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 72
Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region 61
A mouse gene related to Drosphila gonadal is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome 49
Velocardiofacial syndrome: frequency and extent of 22q11 deletions 44
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 41
A genetic etiology for interruption of the aortic arch type B 41
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus 38
Schizophrenia and Chromosomal Deletions within 22q11.2 34
The microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic and molecular characterization 31
Tbx1 stabilizes differentiation of the cardiopharyngeal mesoderm and drives morphogenesis in the pharyngeal apparatus 13
Tbx1-Vegfr3 interaction is required in cardiac morphogenesis 2
Vegfr3 is required in the Tbx1 expression domain for cardiac outflow tract development. 1
Totale 8.245
Categoria #
all - tutte 23.976
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 23.976


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20264.053 266 932 1.050 104 260 151 366 77 160 228 82 377
2026/2027141 135 6 0 0 0 0 0 0 0 0 0 0
Totale 8.245