IRIS
IZZO, ANTONELLA
 Distribuzione geografica
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Continente #
NA - Nord America 510
EU - Europa 317
AS - Asia 97
OC - Oceania 1
Totale 925
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Nazione #
US - Stati Uniti d'America 506
IT - Italia 204
CN - Cina 66
NL - Olanda 50
IE - Irlanda 21
VN - Vietnam 20
FI - Finlandia 16
FR - Francia 11
IN - India 7
GB - Regno Unito 5
CA - Canada 4
UA - Ucraina 4
PL - Polonia 2
BE - Belgio 1
DE - Germania 1
ES - Italia 1
ID - Indonesia 1
IR - Iran 1
JP - Giappone 1
NZ - Nuova Zelanda 1
RO - Romania 1
SG - Singapore 1
Totale 925
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Città #
Chandler 129
Amsterdam 48
Ashburn 39
Millbury 32
Napoli 31
Beijing 27
Naples 27
Dong Ket 20
Des Moines 17
Princeton 16
Boston 14
Nanjing 14
Lawrence 12
Milan 8
Wilmington 8
Jacksonville 6
Jiaxing 6
Brest 5
Nanchang 5
Dearborn 4
Montesarchio 4
Ottawa 4
Salerno 4
Woodbridge 4
Hebei 3
Pozzuoli 3
Avellino 2
Boardman 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
San Giovanni Rotondo 2
Shanghai 2
Shenyang 2
Acerra 1
Augusta 1
Bacoli 1
Bolzano 1
Brussels 1
Cambridge 1
Campagna 1
Caserta 1
Changchun 1
Cormeilles-en-Parisis 1
Denver 1
Dublin 1
Dunedin 1
Ercolano 1
Formia 1
Giugliano In Campania 1
Godiasco 1
Guangzhou 1
Hangzhou 1
Harrisonburg 1
Houston 1
Jakarta 1
Kish 1
Kolkata 1
Kunming 1
Lappeenranta 1
Lequile 1
Misterbianco 1
New York 1
Nola 1
Palermo 1
Parma 1
Phoenix 1
Redwood City 1
San Mango 1
Sant'antimo 1
Tianjin 1
Tokyo 1
Valladolid 1
Warsaw 1
Totale 560
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Nome #
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells 74
Activation of Non-Canonical Autophagic Pathway through Inhibition of Non-Integrin Laminin Receptor in Neuronal Cells 54
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature 48
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets 45
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation 41
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features 39
Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: Genotype-phenotype correlation and literature review. 39
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency 39
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses 37
Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis and Thyroglobulin Internalization in a Thyroid Cell Line 36
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation 35
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 35
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 34
Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalities 34
Targeting mitochondrial network architecture in down syndrome and aging 34
Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects 32
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts 31
Pioglitazone improves mitochondrial organization and bioenergetics in down syndrome cells 30
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome 29
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 29
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report 29
Variegated silencing of a large Xq region causes hypomelanosis of Ito phenotype in a case of balanced X;2 translocation. 26
Variegated silencing throughepigenetic modifications of a large Xq region in a case of balanced X;2translocation with Incontinentia Pigmenti-like phenotype 26
Inhibition of 37/67kDa laminin-1 receptor restores APP maturation and reduces Amyloid- in human skin fibroblasts from familial Alzheimer’s disease 26
Human miRNAs on chromosome 21 are differentially expressed in Down syndrome fetal hearts. 25
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22 24
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications 18
PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3 18
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells 17
Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix Regulation 13
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression 11
Totale 1.008
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Categoria #
all - tutte 3.119
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 3.119
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201924 0 0 0 0 0 9 6 0 6 2 1 0
2019/2020110 31 2 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
2023/2024105 8 43 10 16 12 16 0 0 0 0 0 0
Totale 1.008