CNR Institutional Research Information System

D'ADDA DI FAGAGNA, FABRIZIO
 Distribuzione geografica
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Continente #
AS - Asia 1.146
NA - Nord America 1.047
EU - Europa 347
SA - Sud America 239
Continente sconosciuto - Info sul continente non disponibili 130
AF - Africa 26
OC - Oceania 2
Totale 2.937
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Nazione #
US - Stati Uniti d'America 1.001
SG - Singapore 465
CN - Cina 266
BR - Brasile 175
IT - Italia 143
VN - Vietnam 128
HK - Hong Kong 95
KR - Corea 52
FR - Francia 51
IN - India 34
FI - Finlandia 25
GB - Regno Unito 24
NL - Olanda 23
JP - Giappone 21
DE - Germania 20
CA - Canada 18
EC - Ecuador 17
BD - Bangladesh 16
ES - Italia 15
AR - Argentina 13
CO - Colombia 12
ID - Indonesia 12
MX - Messico 10
ZA - Sudafrica 10
SA - Arabia Saudita 9
IL - Israele 8
VE - Venezuela 7
AT - Austria 6
IE - Irlanda 6
PL - Polonia 6
UA - Ucraina 6
JM - Giamaica 5
RU - Federazione Russa 5
TR - Turchia 5
AE - Emirati Arabi Uniti 4
CL - Cile 4
HN - Honduras 4
KG - Kirghizistan 4
UY - Uruguay 4
EG - Egitto 3
LU - Lussemburgo 3
MA - Marocco 3
MY - Malesia 3
NP - Nepal 3
PE - Perù 3
PH - Filippine 3
BO - Bolivia 2
CR - Costa Rica 2
HU - Ungheria 2
IQ - Iraq 2
KE - Kenya 2
KZ - Kazakistan 2
LB - Libano 2
MT - Malta 2
MU - Mauritius 2
PK - Pakistan 2
PY - Paraguay 2
SV - El Salvador 2
TH - Thailandia 2
UZ - Uzbekistan 2
AO - Angola 1
AU - Australia 1
AZ - Azerbaigian 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
CG - Congo 1
CH - Svizzera 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DM - Dominica 1
DZ - Algeria 1
EE - Estonia 1
GR - Grecia 1
GT - Guatemala 1
JO - Giordania 1
LC - Santa Lucia 1
LT - Lituania 1
LY - Libia 1
MD - Moldavia 1
NI - Nicaragua 1
NO - Norvegia 1
PR - Porto Rico 1
PS - Palestinian Territory 1
QA - Qatar 1
RO - Romania 1
SE - Svezia 1
SN - Senegal 1
TN - Tunisia 1
WS - Samoa 1
Totale 2.808
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Città #
Santa Clara 315
Singapore 260
Hefei 124
San Jose 100
Hong Kong 93
Ashburn 88
Beijing 57
Ho Chi Minh City 49
Seoul 49
Lauterbourg 45
Pavia 29
Hanoi 28
Los Angeles 24
Milan 21
Dallas 20
Rome 17
Lappeenranta 15
New York 15
Tokyo 15
Frankfurt am Main 12
Orem 12
São Paulo 12
Chennai 10
Council Bluffs 10
Chicago 9
Houston 9
Atlanta 8
Bogotá 7
Boston 7
Buffalo 7
Helsinki 7
Phoenix 7
Johannesburg 6
Minamishinagawa 6
Mumbai 6
Vienna 6
Brasília 5
Brooklyn 5
Bắc Ninh 5
Guayaquil 5
Memphis 5
Montreal 5
Philadelphia 5
Poplar 5
Rio de Janeiro 5
Trieste 5
Amsterdam 4
Bengaluru 4
Bishkek 4
Bologna 4
Cambridge 4
Charlotte 4
City of London 4
Dublin 4
Haiphong 4
Las Vegas 4
Montevideo 4
Quito 4
Warsaw 4
Birmingham 3
Boardman 3
Carapicuíba 3
Da Nang 3
Dammam 3
Denver 3
Dubai 3
Gaithersburg 3
Guangzhou 3
Jeddah 3
Kingston 3
Lima 3
London 3
Manaus 3
Manchester 3
Mexico City 3
Nha Trang 3
Ninh Bình 3
San Francisco 3
Seattle 3
Turku 3
Washington 3
Alfenas 2
Asunción 2
Augusta 2
Baltimore 2
Belo Horizonte 2
Biên Hòa 2
Budapest 2
Bến Tre 2
Cairo 2
Cape Town 2
Caxias do Sul 2
Chattanooga 2
Cicero 2
Cincinnati 2
Cleveland 2
Duque de Caxias 2
Elk Grove Village 2
Falkenstein 2
Fargo 2
Totale 1.711
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Nome #
DNA damage response at telomeres boosts the transcription of SARS-CoV-2 receptor ACE2 during aging 98
Telomerase abrogates aneuploidy-induced telomere replication stress, senescence and cell depletion 97
Tissue fluidification promotes a cGAS-STING cytosolic DNA response in invasive breast cancer 96
Guidelines for minimal information on cellular senescence experimentation in vivo 91
NOTCH1 Inhibits Activation of ATM by Impairing the Formation of an ATM-FOXO3a-KAT5/Tip60 Complex 84
MRE11-RAD50-NBS1 Complex Is Sufficient to Promote Transcription by RNA Polymerase II at Double-Strand Breaks by Melting DNA Ends 83
Recent Advancements in DNA Damage-Transcription Crosstalk and High-Resolution Mapping of DNA Breaks 80
Cellular senescence in ageing: from mechanisms to therapeutic opportunities 73
DROSHA is recruited to DNA damage sites by the MRN complex to promote non-homologous end-joining 69
CRISPR/Cas9 screens identify LIG1 as a sensitizer of PARP inhibitors in castration-resistant prostate cancer 68
Alternative lengthening of telomeres (ALT) cells viability is dependent on C-rich telomeric RNAs 68
DNA Damage Triggers a New Phase in Neurodegeneration 68
SARS-CoV-2 infection induces DNA damage, through CHK1 degradation and impaired 53BP1 recruitment, and cellular senescence 66
Telomere dysfunction in ageing and age-related diseases 65
BRCA1 deficiency specific base substitution mutagenesis is dependent on translesion synthesis and regulated by 53BP1 63
A role for human dna polymerase λ in alternative lengthening of telomeres 62
Telomere damage promotes vascular smooth muscle cell senescence and immune cell recruitment after vessel injury 61
Site-specific DICER and DROSHA RNA products control the DNA-damage response. 59
Pharmacological boost of DNA damage response and repair by enhanced biogenesis of DNA damage response RNAs 59
The prolyl-isomerase PIN1 is essential for nuclear Lamin-B structure and function and protects heterochromatin under mechanical stress 57
RNase A treatment and reconstitution with DNA damage response RNA in living cells as a tool to study the role of non-coding RNA in the formation of DNA damage response foci 57
Detection of Telomeric DNA:RNA Hybrids Using TeloDRIP-qPCR. 57
A novel single-cell method provides direct evidence of persistent DNA damage in senescent cells and aged mammalian tissues 56
Colorectal cancer patient-derived organoids and cell lines harboring ATRX and/or DAXX mutations lack Alternative Lengthening of Telomeres (ALT) 56
Is cellular senescence an example of antagonistic pleiotropy? 53
DICER, DROSHA and DNA damage response RNAs are necessary for the secondary recruitment of DNA damage response factors 53
BRCA2 controls DNA:RNA hybrid level at DSBs by mediating RNase H2 recruitment 53
A direct role for small non-coding RNAs in DNA damage response 50
Express or repress? The transcriptional dilemma of damaged chromatin 50
Neural stem cells exposed to BrdU lose their global DNA methylation and undergo astrocytic differentiation. 47
A damaged genome's transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks 46
DNA Damage In Situ Ligation Followed by Proximity Ligation Assay (DI-PLA). 46
Inhibition of DNA damage response at telomeres improves the detrimental phenotypes of Hutchinson-Gilford Progeria Syndrome. 45
Transcription and DNA Damage: Holding Hands or Crossing Swords? 45
TGS1 mediates 2,2,7-trimethyl guanosine capping of the human telomerase RNA to direct telomerase dependent telomere maintenance 44
Functional transcription promoters at DNA double-strand breaks mediate RNA-driven phase separation of damage-response factors 43
Telomere transcription in ageing 43
Irreparable telomeric DNA damage and persistent DDR signalling as a shared causative mechanism of cellular senescence and ageing 42
Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation. 41
Differential regulation of DNA damage response activation between somatic and germline cells in Caenorhabditis elegans. 41
Transcriptional and post-transcriptional regulation of the ionizing radiation response by ATM and p53 41
DNA Damage in Mammalian Neural Stem Cells Leads to Astrocytic Differentiation Mediated by BMP2 Signaling through JAK-STAT 40
Notch is a direct negative regulator of the DNA-damage response 37
Resection is responsible for loss of transcription around a double-strand break in Saccharomyces cerevisiae 37
Stable Cellular Senescence Is Associated with Persistent DDR Activation. 37
Human nuclear ARGONAUTE 2 interacts in vivo only with small RNAs and not with DNA. 34
Target-enrichment sequencing for detailed characterization of small RNAs 33
Oncogene-induced telomere dysfunction enforces cellular senescence in human cancer precursor lesions. 32
The cohesin complex prevents Myc-induced replication stress 32
Crosstalk between chromatin state and DNA damage response in cellular senescence and cancer. 32
NOTCH1 modulates activity of DNA-PKcs 31
Polycomb proteins control proliferation and transformation independently of cell cycle checkpoints by regulating DNA replication 31
Oncogene-induced reactive oxygen species fuel hyperproliferation and DNA damage response activation 30
RNA-processing proteins regulate Mec1/ATR activation by promoting generation of RPA-coated ssDNA 26
DNA damage response defects induced by the formation of TDP-43 and mutant FUS cytoplasmic inclusions and their pharmacological rescue 21
null 8
Totale 2.937
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Categoria #
all - tutte 9.909
article - articoli 9.770
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 139
Totale 19.818
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 15 0 2 2
2024/20251.075 6 5 53 26 307 94 8 103 77 27 193 176
2025/20261.495 80 195 137 265 227 82 191 43 70 115 47 43
2026/2027348 109 74 165 0 0 0 0 0 0 0 0 0
Totale 2.937