IRIS UniCatt

Tabolacci, Elisabetta
 Distribuzione geografica
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Continente #
NA - Nord America 2.406
EU - Europa 2.036
AS - Asia 1.817
SA - Sud America 430
AF - Africa 49
OC - Oceania 8
Totale 6.746
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Nazione #
US - Stati Uniti d'America 2.317
SG - Singapore 813
CN - Cina 528
SE - Svezia 384
DE - Germania 353
BR - Brasile 348
IT - Italia 342
PL - Polonia 257
FR - Francia 124
GB - Regno Unito 119
UA - Ucraina 114
VN - Vietnam 108
IE - Irlanda 85
FI - Finlandia 82
IN - India 75
ID - Indonesia 60
CA - Canada 47
RU - Federazione Russa 43
HK - Hong Kong 40
NL - Olanda 36
TR - Turchia 34
MX - Messico 31
AR - Argentina 29
JP - Giappone 23
AT - Austria 22
KR - Corea 21
BD - Bangladesh 20
IQ - Iraq 19
ES - Italia 17
CL - Cile 15
AE - Emirati Arabi Uniti 13
BE - Belgio 12
CZ - Repubblica Ceca 12
PK - Pakistan 12
VE - Venezuela 11
ZA - Sudafrica 11
IR - Iran 10
LT - Lituania 10
CH - Svizzera 8
EC - Ecuador 8
AU - Australia 7
EG - Egitto 7
UZ - Uzbekistan 7
CI - Costa d'Avorio 6
CO - Colombia 6
MA - Marocco 6
PY - Paraguay 6
SA - Arabia Saudita 5
AZ - Azerbaigian 4
IL - Israele 4
TN - Tunisia 4
AO - Angola 3
GA - Gabon 3
LY - Libia 3
MY - Malesia 3
PE - Perù 3
RO - Romania 3
TW - Taiwan 3
AL - Albania 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GR - Grecia 2
JM - Giamaica 2
JO - Giordania 2
LB - Libano 2
NI - Nicaragua 2
NP - Nepal 2
TT - Trinidad e Tobago 2
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
BY - Bielorussia 1
CM - Camerun 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
HN - Honduras 1
IS - Islanda 1
KE - Kenya 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
OM - Oman 1
PH - Filippine 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
TH - Thailandia 1
TV - Tuvalu 1
UY - Uruguay 1
Totale 6.746
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Città #
Singapore 397
Ashburn 332
Chandler 282
Warsaw 241
Beijing 100
New York 95
Dublin 84
Rome 76
Hefei 73
Los Angeles 73
Jacksonville 70
Nanjing 67
Seattle 66
Fairfield 65
Wilmington 65
Woodbridge 63
Ann Arbor 60
Milan 60
San Mateo 53
Jakarta 51
Cattolica 47
The Dalles 46
Houston 44
São Paulo 43
Munich 42
Hong Kong 40
Chicago 39
Ho Chi Minh City 39
Helsinki 37
Boston 31
Marseille 29
Cambridge 28
Frankfurt am Main 28
Nanchang 27
Buffalo 26
Hanoi 26
Kent 26
Moscow 24
Dallas 23
North Bergen 21
Nuremberg 21
London 20
Seoul 19
Lawrence 18
Izmir 17
Santa Clara 17
Tokyo 17
Denver 16
Montreal 15
Redwood City 15
Verona 15
Brasília 14
Brooklyn 14
Poplar 14
Turku 14
Dearborn 13
Philadelphia 13
Princeton 13
Rio de Janeiro 13
Salvador 13
Tianjin 13
Atlanta 12
Bremen 12
Brussels 12
Chennai 12
Hangzhou 12
Kunming 12
Mexico City 12
Boardman 11
Brno 11
Lancaster 11
Nürnberg 11
Orem 11
Washington 11
Ankara 10
Falls Church 10
Manchester 10
Baghdad 9
Mumbai 9
Phoenix 9
Toronto 9
Zhengzhou 9
Amsterdam 8
Bexley 8
Busto Arsizio 8
Charlotte 8
Düsseldorf 8
Guangzhou 8
Jiaxing 8
Lappeenranta 8
Mountain View 8
Naaldwijk 8
New Delhi 8
Pune 8
San Francisco 8
Santiago 8
Stockholm 8
Vienna 8
Bologna 7
Dubai 7
Totale 3.730
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Nome #
Transcriptional reactivation of the FMR1 Gene. A possible approach to the treatment of the fragile X syndrome 355
CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations 315
Effects of remifentanil on human C20 microglial pro-inflammatory activation 230
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene 195
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys 176
A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy 172
DNA Methylation in the Diagnosis of Monogenic Diseases. 172
Role of CTCF protein in regulating FMR1 locus transcription. 168
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization 161
The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cells 159
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 158
L-acetylcarnitine treatment on fragile X patients hyperactive behaviour 156
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis 154
Treatment with Valproic acid ameiorates ADHD symptoms in Fragile X syndrome boys. 147
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation 143
Prevalence of spinocellulart ataxia type 2 mutation among ittalian Parkinsonian patients 142
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue 142
Defining the role of the CGGBP1 protein in FMR1 gene expression 141
Assisted reproductive technology and congenital overgrowth:some speculations on a case of Pallister-Killian syndrome 139
Modest reactivation of the mutatnt FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylation. 136
Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family 133
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype 126
Epigenetic modifications of the FMR1 gene 118
The emerging role of the BDNF-TrkB signaling pathway in the modulation of pain perception 118
No Correlation between X Chromosome Inactivation Pattern and Autistic Spectrum Disorders in an Italian Cohort of Patients 116
Remifentanil-induced hyperalgesia in healthy volunteers: a systematic review and meta-analysis of randomized controlled trials 114
Epigenetics, fragile X syndrome and transcriptional therapy. 114
The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro. 110
The FRAXopathies: Definition, overview, and update 109
The polyphenolic compound punicalagin protects skin fibroblasts from UVA radiation oxidative damage 107
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families 107
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine 103
New Insight into the genotype-phenotype correlation of PTH1R variants and primary failure of tooth eruption on an Italian Cohort 103
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand? 99
Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview 98
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway. 98
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome 97
REMIFENTANIL DOES NOT AFFECT HUMAN MICROGLIAL IMMUNE ACTIVATION IN RESPONSE TO PRO-INFLAMMATORY CYTOKINES 96
Tumorigenic potential of olfactory bulb-derived human adult neural stem cells associates with activation of TERT and NOTCH1. 94
Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations. 90
RADX Gene Variant May Predispose to Familial Asperger Syndrome 87
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals 86
Permanent First Molar Eruption Failure in Children: clinical management of three clinical scenarios 86
Genetic Aspects of Tooth Agenesis 85
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort 74
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders 74
Permanent first molar eruption failure in children: leading signs for early diagnosis 73
The role of sevoflurane exposure on systemic inflammation and neuroinflammation: a systematic review and meta-analysis of in vivo and in vitro studies 72
X-linked mental retardation (XLMR): from clinical conditions to cloned genes 66
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 58
Telomeric associations and chromosome instability in ataxia telangiectasia T cells characterized by TCL1 expression 47
Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments 44
A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family 44
Molecular dissection of the events leading to inactivation of the FMR1 gene 44
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome 42
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identified 42
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability 41
Enviromental maternal exposures and the risk of premature birth and intrauterine growth restriction: The Generation Gemelli study protocol of newborn exposome 34
GAPO syndrome: a comprehensive examination and review of 105 clinical cases 10
Totale 6.820
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Categoria #
all - tutte 26.297
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 26.297
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021189 0 0 0 0 0 20 35 7 36 21 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
2025/20262.013 413 131 220 475 589 185 0 0 0 0 0 0
Totale 6.820