IZZO, ANTONELLA
 Distribuzione geografica
Continente #
NA - Nord America 562
EU - Europa 370
AS - Asia 163
AF - Africa 8
OC - Oceania 1
Totale 1.104
Nazione #
US - Stati Uniti d'America 558
IT - Italia 254
CN - Cina 68
SG - Singapore 59
NL - Olanda 50
IE - Irlanda 21
VN - Vietnam 20
FI - Finlandia 16
FR - Francia 13
IN - India 12
CI - Costa d'Avorio 8
GB - Regno Unito 5
CA - Canada 4
UA - Ucraina 4
DE - Germania 2
PL - Polonia 2
BE - Belgio 1
ES - Italia 1
ID - Indonesia 1
IL - Israele 1
IR - Iran 1
JP - Giappone 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 1.104
Città #
Chandler 129
Amsterdam 48
Ashburn 44
Singapore 43
Naples 41
Millbury 32
Napoli 31
Beijing 27
Dong Ket 20
Des Moines 17
Princeton 16
Seattle 16
Boston 14
Nanjing 14
Lawrence 12
Formia 10
Santa Clara 9
Milan 8
Wilmington 8
Jacksonville 6
Jiaxing 6
Rome 6
Brest 5
Castellammare di Stabia 5
Nanchang 5
Pune 5
Caserta 4
Dearborn 4
Montesarchio 4
Ottawa 4
Salerno 4
Woodbridge 4
Boardman 3
Dallas 3
Hebei 3
Pozzuoli 3
Avellino 2
Caivano 2
Changsha 2
Eboli 2
Fairfield 2
Falls Church 2
Indiana 2
New Delhi 2
Pomigliano D'arco 2
Redmond 2
Roccarainola 2
Rosignano Marittimo 2
San Giovanni Rotondo 2
Shanghai 2
Shenyang 2
Strasbourg 2
Acerra 1
Augusta 1
Bacoli 1
Barco 1
Bolzano 1
Brussels 1
Cambridge 1
Campagna 1
Capaccio 1
Changchun 1
Cormeilles-en-Parisis 1
Denver 1
Dublin 1
Dunedin 1
Ercolano 1
Giugliano In Campania 1
Godiasco 1
Guangzhou 1
Hangzhou 1
Harrisonburg 1
Houston 1
Jakarta 1
Kish 1
Kolkata 1
Kronberg 1
Kunming 1
Lappeenranta 1
Lequile 1
Misterbianco 1
New York 1
Nola 1
Palermo 1
Parma 1
Phoenix 1
Quarto 1
Redwood City 1
San Mango 1
Sant'antimo 1
Shefa-'Amr 1
Springfield 1
Tianjin 1
Tokyo 1
Valladolid 1
Warsaw 1
Totale 689
Nome #
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells 77
Activation of Non-Canonical Autophagic Pathway through Inhibition of Non-Integrin Laminin Receptor in Neuronal Cells 63
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature 54
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets 53
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features 47
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses 46
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency 46
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation 46
Targeting mitochondrial network architecture in down syndrome and aging 45
Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: Genotype-phenotype correlation and literature review. 43
Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalities 42
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts 41
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation 39
Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects 38
Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis and Thyroglobulin Internalization in a Thyroid Cell Line 38
Pioglitazone improves mitochondrial organization and bioenergetics in down syndrome cells 38
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother 38
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 37
Variegated silencing of a large Xq region causes hypomelanosis of Ito phenotype in a case of balanced X;2 translocation. 34
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 33
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome 32
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report 32
Variegated silencing throughepigenetic modifications of a large Xq region in a case of balanced X;2translocation with Incontinentia Pigmenti-like phenotype 31
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts. 29
Inhibition of 37/67kDa laminin-1 receptor restores APP maturation and reduces Amyloid- in human skin fibroblasts from familial Alzheimer’s disease 29
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells 28
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22 27
Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix Regulation 25
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression 20
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications 20
PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3 20
Totale 1.191
Categoria #
all - tutte 4.910
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 4.910


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202077 0 0 2 14 13 3 1 1 5 21 15 2
2020/202197 1 0 6 2 19 9 3 1 18 12 6 20
2021/2022232 1 4 1 1 5 7 2 23 35 23 60 70
2022/2023342 33 16 19 26 38 32 10 34 60 50 17 7
2023/2024220 8 43 10 16 11 28 9 31 6 7 33 18
2024/202568 52 16 0 0 0 0 0 0 0 0 0 0
Totale 1.191