CICATIELLO, RITA
 Distribuzione geografica
Continente #
NA - Nord America 237
EU - Europa 155
AS - Asia 75
AF - Africa 3
Totale 470
Nazione #
US - Stati Uniti d'America 235
IT - Italia 124
CN - Cina 31
SG - Singapore 31
NL - Olanda 14
VN - Vietnam 8
FR - Francia 6
IE - Irlanda 5
IN - India 5
CI - Costa d'Avorio 3
FI - Finlandia 3
CA - Canada 2
PL - Polonia 2
DE - Germania 1
Totale 470
Città #
Chandler 57
Singapore 24
Napoli 19
Ashburn 18
Naples 17
Amsterdam 14
Beijing 11
Dong Ket 8
Boston 7
Des Moines 7
Millbury 7
Lawrence 6
Santa Clara 6
Formia 5
Milan 4
Princeton 4
Seattle 4
Brest 3
Dearborn 3
Nanjing 3
Wilmington 3
Castellammare di Stabia 2
Fairfield 2
Hebei 2
Jiaxing 2
New Delhi 2
New York 2
Ottawa 2
Redwood City 2
Shanghai 2
Strasbourg 2
Woodbridge 2
Wuhan 2
Acerra 1
Bolzano 1
Böblingen 1
Cambridge 1
Campagna 1
Caposele 1
Caserta 1
Changsha 1
Cormeilles-en-Parisis 1
Dublin 1
Godiasco 1
Guangzhou 1
Hangzhou 1
Harrisonburg 1
Misterbianco 1
Montesarchio 1
Nanchang 1
Nola 1
Palermo 1
Parma 1
Pozzuoli 1
Redmond 1
Rome 1
Salerno 1
San Mango 1
Sant'antimo 1
Shenzhen 1
Springfield 1
Warsaw 1
Totale 283
Nome #
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells 79
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features 49
Targeting mitochondrial network architecture in down syndrome and aging 49
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses 48
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency 48
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation 47
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs 44
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 39
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome 33
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report 33
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells 30
Totale 499
Categoria #
all - tutte 2.133
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 2.133


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202025 0 0 0 0 0 9 2 0 0 7 6 1
2020/202146 1 0 2 1 5 1 2 0 13 11 2 8
2021/202294 1 4 1 1 5 3 0 9 13 7 28 22
2022/2023140 13 9 10 11 13 14 4 18 27 14 4 3
2023/202472 1 16 2 4 2 12 2 8 0 3 15 7
2024/202553 27 5 5 4 12 0 0 0 0 0 0 0
Totale 499