CLERICI, MICHELA
 Distribuzione geografica
Continente #
NA - Nord America 6.455
EU - Europa 3.863
AS - Asia 3.198
SA - Sud America 428
AF - Africa 62
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 14.016
Nazione #
US - Stati Uniti d'America 6.320
IT - Italia 991
SG - Singapore 985
CN - Cina 794
PL - Polonia 553
VN - Vietnam 542
DE - Germania 492
RU - Federazione Russa 379
HK - Hong Kong 364
SE - Svezia 325
BR - Brasile 302
FR - Francia 297
GB - Regno Unito 174
IE - Irlanda 165
UA - Ucraina 161
IN - India 133
CA - Canada 99
AT - Austria 74
FI - Finlandia 71
TR - Turchia 66
KR - Corea 55
DK - Danimarca 49
AR - Argentina 44
NL - Olanda 44
ID - Indonesia 40
BD - Bangladesh 39
IQ - Iraq 29
EC - Ecuador 28
PK - Pakistan 28
ES - Italia 27
ZA - Sudafrica 26
MX - Messico 23
PH - Filippine 19
SA - Arabia Saudita 18
BE - Belgio 16
CH - Svizzera 16
JP - Giappone 16
CO - Colombia 15
VE - Venezuela 15
UZ - Uzbekistan 12
AE - Emirati Arabi Uniti 10
KZ - Kazakistan 9
MA - Marocco 9
IR - Iran 8
PE - Perù 6
PY - Paraguay 6
TN - Tunisia 6
AU - Australia 5
RO - Romania 5
UY - Uruguay 5
AZ - Azerbaigian 4
CL - Cile 4
EG - Egitto 4
EU - Europa 4
KE - Kenya 4
MY - Malesia 4
NP - Nepal 4
PS - Palestinian Territory 4
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
JM - Giamaica 3
LT - Lituania 3
OM - Oman 3
TH - Thailandia 3
AL - Albania 2
BG - Bulgaria 2
BO - Bolivia 2
JO - Giordania 2
KW - Kuwait 2
MD - Moldavia 2
PT - Portogallo 2
SN - Senegal 2
TT - Trinidad e Tobago 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
CI - Costa d'Avorio 1
CM - Camerun 1
CR - Costa Rica 1
DM - Dominica 1
DZ - Algeria 1
ET - Etiopia 1
GA - Gabon 1
GD - Grenada 1
GH - Ghana 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
IL - Israele 1
IS - Islanda 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
MK - Macedonia 1
MU - Mauritius 1
MZ - Mozambico 1
NO - Norvegia 1
Totale 14.010
Città #
Ann Arbor 1.004
Ashburn 807
Singapore 596
Kraków 529
Woodbridge 448
Fairfield 440
Milan 380
Hong Kong 352
San Jose 323
Houston 308
Frankfurt am Main 307
Chandler 301
Wilmington 264
Seattle 175
Jacksonville 172
Ho Chi Minh City 162
Dublin 161
Dearborn 138
Los Angeles 135
New York 134
Cambridge 133
Beijing 120
Santa Clara 116
Hanoi 105
Hefei 96
Chicago 84
Princeton 74
Moscow 72
Vienna 70
The Dalles 69
Dallas 67
Nanjing 58
Dong Ket 55
Seoul 53
Shanghai 53
Buffalo 46
Lauterbourg 45
Council Bluffs 37
Lawrence 36
Altamura 32
San Diego 31
Nanchang 29
Helsinki 28
Lachine 27
São Paulo 26
Boardman 25
Da Nang 24
Fremont 24
Munich 24
Guangzhou 23
Jakarta 21
Orem 21
Rome 21
London 20
Toronto 20
Hebei 18
Haiphong 17
Montreal 17
New Delhi 17
Brussels 15
Zurich 15
Brooklyn 14
Ottawa 14
Tokyo 14
Changsha 13
Falls Church 13
Johannesburg 13
Poplar 13
Vedano al Lambro 13
Warsaw 13
Biên Hòa 12
Huizen 12
Sesto San Giovanni 12
Botticino 11
Chennai 11
Denver 11
Guayaquil 11
Ha Long 11
Novate Milanese 11
Tashkent 11
Hải Dương 10
Kunming 10
Nuremberg 10
Philadelphia 10
Seveso 10
Taizhou 10
Andover 9
Atlanta 9
Baghdad 9
City of London 9
Cuggiono 9
Desio 9
Edmonton 9
Istanbul 9
Jinan 9
Manchester 9
Mumbai 9
Tianjin 9
Turku 9
Zhengzhou 9
Totale 9.439
Nome #
Sae2 Function at DNA Double-Strand Breaks Is Bypassed by Dampening Tel1 or Rad53 Activity 552
Uncoupling Sae2 functions in downregulation of Tel1 and Rad53 signaling activities 528
Tel1/ATM Signaling to the Checkpoint Contributes to Replicative Senescence in the Absence of Telomerase 484
Alkaline denaturing southern blot analysis to monitor double-strand break processing 467
Exo1 cooperates with Tel1/ATM in promoting recombination events at DNA replication forks 450
Tel1 and Rif2 Regulate MRX Functions in End-Tethering and Repair of DNA Double-Strand Breaks 448
Tel1/ATM prevents degradation of replication forks that reverse after topoisomerase poisoning 428
Resection of a DNA Double-Strand Break by Alkaline Gel Electrophoresis and Southern Blotting 404
The regulation of the DNA damage response at telomeres: Focus on kinases 398
DNA double-strand breaks in meiosis: Checking their formation, processing and repair 384
Processing of DNA ends in the maintenance of genome stability 382
Distinct Cdk1 requirements during single-strand annealing, noncrossover and crossover recombination 352
Tbf1 and Vid22 promote resection and non-homologous end joining of DNA double-strand break ends 347
The MRX complex plays multiple functions in resection of Yku- and Rif2-protected DNA ends 345
Resection is responsible for loss of transcription around a double-strand break in Saccharomyces cerevisiae 343
The RNA binding protein Npl3 promotes resection of DNA double-strand breaks by regulating the levels of Exo1 339
A balance between Tel1 and Rif2 activities regulates nucleolytic processing and elongation at telomeres 334
Dpb4 promotes resection of DNA double-strand breaks and checkpoint activation by acting in two different protein complexes 333
A Tel1/MRX-dependent checkpoint inhibits the metaphase-to-anaphase transition after UV irradiation in the absence of Mec1 323
Mechanisms and regulation of DNA end resection 322
The Saccharomyces cerevisiae Sae2 protein promotes resection and bridging of double strand break ends 313
The S-phase checkpoint and its regulation in Saccharomyces cerevisiae 308
Hyperactivation of the yeast DNA damage checkpoint by TEL1 and DDC2 overexpression 304
Telomeres and DNA damage checkpoints 296
The cellular response to chromosome breakage 294
Multiple pathways regulate 3’ overhang generation at S. cerevisiae telomeres 293
Characterization of mec1 kinase-deficient mutants and of new hypomorphic mec1 alleles impairing subsets of the DNA damage response pathway 283
The Yku70-Yku80 complex contributes to regulate double-strand break processing and checkpoint activation during the cell cycle 278
Mec1/ATR regulates the generation of single-stranded DNA that attenuates Tel1/ATM signaling at DNA ends 277
The PP2A phosphatase counteracts the function of the 9-1-1 axis in checkpoint activation 276
Shelterin-like proteins and Yku inhibit nucleolytic processing of S. cerevisiae telomeres 276
Surveillance mechanisms monitoring chromosome breaks during mitosis and meiosis 272
Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation. 272
Interplay between Sae2 and Rif2 in the regulation of Mre11-Rad50 activities at DNA ends 270
The General Regulatory Factor Tbf1 and its interacting protein Vid22 promote repair of DNA double-strand breaks 266
The checkpoint protein Ddc2, functionally related to S. pombe Rad26, interacts with Mec1 and is regulated by Mec1-dependent phosphorylation in budding yeast. 263
Elevated levels of the polo kinase Cdc5 override the Mec1/ATR checkpoint in budding yeast by acting at different steps of the signaling pathway 259
The Saccharomyces cerevisiae Sae2 protein negatively regulates DNA damage checkpoint signalling 256
Dual role for Saccharomyces cerevisiae Tel1 in the checkpoint response to double-strand breaks. 255
The Chromatin Landscape around DNA Double-Strand Breaks in Yeast and Its Influence on DNA Repair Pathway Choice 236
Exploring the interconnections between DNA-RNA hybrids and the DNA damage response 187
Exploring the interconnections between DNA-RNA hybrids and the DNA damage response 186
Control of Replication Stress Response by Cytosolic Fe-S Cluster Assembly (CIA) Machinery 177
Development of Leather-like Materials from Enzymatically Treated Green Kiwi Peel and Valorization of By-Products for Microbial Bioprocesses 164
Understanding the interconnections between DNA-RNA hybrids and the DNA damage response 154
An MNase-ChIP-Seq Protocol to Profile Histone Modifications at a DNA Break in Yeast 23
Totale 14.401
Categoria #
all - tutte 38.980
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 38.980


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021371 0 0 0 0 0 0 0 0 0 139 75 157
2021/2022887 60 92 136 101 73 77 61 32 32 42 80 101
2022/20231.254 127 356 145 129 73 154 11 85 92 10 58 14
2023/2024829 31 30 25 47 102 183 134 116 50 12 24 75
2024/20251.747 113 162 125 73 119 66 108 49 113 392 172 255
2025/20264.498 537 373 335 585 574 280 682 241 398 493 0 0
Totale 14.401