Tabolacci, Elisabetta
 Distribuzione geografica
Continente #
NA - Nord America 3.041
AS - Asia 2.455
EU - Europa 2.212
SA - Sud America 471
AF - Africa 61
OC - Oceania 8
Totale 8.248
Nazione #
US - Stati Uniti d'America 2.932
SG - Singapore 1.015
CN - Cina 574
IT - Italia 394
SE - Svezia 385
BR - Brasile 374
DE - Germania 369
VN - Vietnam 313
PL - Polonia 260
FR - Francia 186
GB - Regno Unito 130
UA - Ucraina 116
HK - Hong Kong 97
FI - Finlandia 91
IN - India 90
IE - Irlanda 86
JP - Giappone 72
ID - Indonesia 61
CA - Canada 58
RU - Federazione Russa 44
NL - Olanda 42
TR - Turchia 39
MX - Messico 36
AR - Argentina 34
IQ - Iraq 30
BD - Bangladesh 29
AT - Austria 23
KR - Corea 23
PK - Pakistan 23
ES - Italia 19
CL - Cile 17
ZA - Sudafrica 14
AE - Emirati Arabi Uniti 13
CZ - Repubblica Ceca 13
VE - Venezuela 13
BE - Belgio 12
IR - Iran 12
CH - Svizzera 10
EC - Ecuador 10
LT - Lituania 10
EG - Egitto 9
CO - Colombia 8
MA - Marocco 8
SA - Arabia Saudita 8
UZ - Uzbekistan 8
AU - Australia 7
CI - Costa d'Avorio 7
MY - Malesia 7
PH - Filippine 7
AZ - Azerbaigian 6
PY - Paraguay 6
GA - Gabon 4
IL - Israele 4
JM - Giamaica 4
KE - Kenya 4
RO - Romania 4
TN - Tunisia 4
AL - Albania 3
AO - Angola 3
LB - Libano 3
LY - Libia 3
PE - Perù 3
TH - Thailandia 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GR - Grecia 2
GY - Guiana 2
JO - Giordania 2
KW - Kuwait 2
MD - Moldavia 2
NI - Nicaragua 2
NP - Nepal 2
RS - Serbia 2
UY - Uruguay 2
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CM - Camerun 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GE - Georgia 1
HN - Honduras 1
IS - Islanda 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LU - Lussemburgo 1
LV - Lettonia 1
MM - Myanmar 1
MN - Mongolia 1
NG - Nigeria 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 8.245
Città #
Singapore 581
Ashburn 388
San Jose 287
Chandler 282
Warsaw 244
Ho Chi Minh City 109
Beijing 106
New York 98
Rome 95
Los Angeles 87
Dublin 85
Hong Kong 85
Hanoi 83
The Dalles 80
Hefei 73
Jacksonville 70
Milan 68
Nanjing 67
Seattle 66
Fairfield 65
Wilmington 65
Tokyo 63
Woodbridge 63
Ann Arbor 61
Lauterbourg 55
Council Bluffs 53
San Mateo 53
Jakarta 51
São Paulo 48
Cattolica 47
Helsinki 44
Houston 44
Chicago 42
Munich 42
Frankfurt am Main 39
Boston 31
Santa Clara 30
Marseille 29
Cambridge 28
Buffalo 27
Nanchang 27
Kent 26
Moscow 24
Dallas 23
London 22
North Bergen 22
Nuremberg 22
St Louis 20
Seoul 19
Denver 18
Lawrence 18
Orem 18
Da Nang 17
Izmir 17
Montreal 17
Rio de Janeiro 17
Atlanta 16
Brooklyn 15
Redwood City 15
Tianjin 15
Verona 15
Baghdad 14
Brasília 14
Poplar 14
Salvador 14
Turku 14
Chennai 13
Dearborn 13
Mexico City 13
Paris 13
Philadelphia 13
Princeton 13
Bremen 12
Brussels 12
Guangzhou 12
Hangzhou 12
Kunming 12
Amsterdam 11
Ankara 11
Boardman 11
Brno 11
Lancaster 11
Nürnberg 11
Toronto 11
Washington 11
Falls Church 10
Lappeenranta 10
Manchester 10
Mumbai 10
Phoenix 10
Santiago 10
Shanghai 10
Bologna 9
Pune 9
Stockholm 9
Zhengzhou 9
Bexley 8
Busto Arsizio 8
Charlotte 8
Düsseldorf 8
Totale 4.771
Nome #
Transcriptional reactivation of the FMR1 Gene. A possible approach to the treatment of the fragile X syndrome 389
CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations 332
Effects of remifentanil on human C20 microglial pro-inflammatory activation 273
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene 251
DNA Methylation in the Diagnosis of Monogenic Diseases. 206
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys 200
Role of CTCF protein in regulating FMR1 locus transcription. 200
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization 197
A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy 192
The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cells 188
L-acetylcarnitine treatment on fragile X patients hyperactive behaviour 185
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 182
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis 180
Defining the role of the CGGBP1 protein in FMR1 gene expression 171
Remifentanil-induced hyperalgesia in healthy volunteers: a systematic review and meta-analysis of randomized controlled trials 170
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation 169
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype 166
Treatment with Valproic acid ameiorates ADHD symptoms in Fragile X syndrome boys. 164
Prevalence of spinocellulart ataxia type 2 mutation among ittalian Parkinsonian patients 157
Assisted reproductive technology and congenital overgrowth:some speculations on a case of Pallister-Killian syndrome 154
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue 152
Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family 148
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand? 141
Modest reactivation of the mutatnt FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylation. 140
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway. 139
The emerging role of the BDNF-TrkB signaling pathway in the modulation of pain perception 139
The polyphenolic compound punicalagin protects skin fibroblasts from UVA radiation oxidative damage 138
Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview 136
New Insight into the genotype-phenotype correlation of PTH1R variants and primary failure of tooth eruption on an Italian Cohort 136
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome 135
No Correlation between X Chromosome Inactivation Pattern and Autistic Spectrum Disorders in an Italian Cohort of Patients 130
Epigenetic modifications of the FMR1 gene 130
Epigenetics, fragile X syndrome and transcriptional therapy. 127
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families 126
REMIFENTANIL DOES NOT AFFECT HUMAN MICROGLIAL IMMUNE ACTIVATION IN RESPONSE TO PRO-INFLAMMATORY CYTOKINES 125
The FRAXopathies: Definition, overview, and update 125
The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro. 125
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders 120
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals 116
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort 116
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine 116
Tumorigenic potential of olfactory bulb-derived human adult neural stem cells associates with activation of TERT and NOTCH1. 116
Genetic Aspects of Tooth Agenesis 114
RADX Gene Variant May Predispose to Familial Asperger Syndrome 109
Permanent First Molar Eruption Failure in Children: clinical management of three clinical scenarios 107
Permanent first molar eruption failure in children: leading signs for early diagnosis 99
Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations. 99
The role of sevoflurane exposure on systemic inflammation and neuroinflammation: a systematic review and meta-analysis of in vivo and in vitro studies 94
Evidence for a Functional Link Between the Nrf2 Signalling Pathway and Cytoprotective Effect of S-Petasin in Human Retinal Pigment Epithelium Cells Exposed to Oxidative Stress 84
Enviromental maternal exposures and the risk of premature birth and intrauterine growth restriction: The Generation Gemelli study protocol of newborn exposome 79
X-linked mental retardation (XLMR): from clinical conditions to cloned genes 76
A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family 70
Telomeric associations and chromosome instability in ataxia telangiectasia T cells characterized by TCL1 expression 60
Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments 59
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identified 54
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome 53
Molecular dissection of the events leading to inactivation of the FMR1 gene 52
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability 51
GAPO syndrome: a comprehensive examination and review of 105 clinical cases 41
Genetic Determinants of Primary Failure of Eruption: A Comprehensive Review of PTH1R Variants 26
Role of Circulating X-Chromosome Inactivation and Xist as Biomarkers in Female Carriers of Fabry Disease 20
Totale 8.349
Categoria #
all - tutte 29.410
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 29.410


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202170 0 0 0 0 0 0 0 0 0 0 60 10
2021/2022432 33 78 5 33 27 13 17 43 16 18 88 61
2022/2023885 145 128 51 115 69 65 57 64 106 27 37 21
2023/2024649 30 116 36 78 29 104 61 12 8 29 76 70
2024/20251.346 22 40 75 74 80 65 36 68 240 96 315 235
2025/20263.542 413 131 220 475 589 232 743 163 306 257 13 0
Totale 8.349