IRIS
BRANCOLINI, Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 10.023
AS - Asia 3.406
EU - Europa 2.282
SA - Sud America 457
Continente sconosciuto - Info sul continente non disponibili 229
AF - Africa 57
OC - Oceania 1
Totale 16.455
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Nazione #
US - Stati Uniti d'America 9.857
SG - Singapore 1.628
CN - Cina 677
IT - Italia 476
UA - Ucraina 466
BR - Brasile 355
HK - Hong Kong 324
DE - Germania 299
VN - Vietnam 228
FI - Finlandia 187
RU - Federazione Russa 165
SE - Svezia 157
FR - Francia 129
GB - Regno Unito 117
TR - Turchia 110
IE - Irlanda 99
CA - Canada 95
BD - Bangladesh 76
IN - India 74
JP - Giappone 57
KR - Corea 51
MX - Messico 32
AR - Argentina 28
BE - Belgio 26
NL - Olanda 26
PL - Polonia 25
AT - Austria 23
EC - Ecuador 18
ES - Italia 18
IQ - Iraq 18
PK - Pakistan 18
ID - Indonesia 15
CO - Colombia 14
PH - Filippine 14
VE - Venezuela 14
CZ - Repubblica Ceca 13
IR - Iran 13
ZA - Sudafrica 13
SA - Arabia Saudita 12
AE - Emirati Arabi Uniti 11
CL - Cile 11
UZ - Uzbekistan 11
CH - Svizzera 10
JM - Giamaica 10
EG - Egitto 9
MY - Malesia 8
EU - Europa 7
PT - Portogallo 7
PY - Paraguay 7
AD - Andorra 6
NP - Nepal 6
CR - Costa Rica 5
JO - Giordania 5
KG - Kirghizistan 5
KZ - Kazakistan 5
LT - Lituania 5
MA - Marocco 5
TN - Tunisia 5
AZ - Azerbaigian 4
DZ - Algeria 4
HN - Honduras 4
IL - Israele 4
OM - Oman 4
PA - Panama 4
PE - Perù 4
PR - Porto Rico 4
PS - Palestinian Territory 4
TH - Thailandia 4
AM - Armenia 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
GE - Georgia 3
GR - Grecia 3
HR - Croazia 3
KE - Kenya 3
LV - Lettonia 3
TG - Togo 3
TW - Taiwan 3
UY - Uruguay 3
AL - Albania 2
BO - Bolivia 2
EE - Estonia 2
ET - Etiopia 2
HU - Ungheria 2
KW - Kuwait 2
ML - Mali 2
QA - Qatar 2
RO - Romania 2
RS - Serbia 2
SN - Senegal 2
TT - Trinidad e Tobago 2
AG - Antigua e Barbuda 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
BZ - Belize 1
DM - Dominica 1
Totale 16.211
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Città #
Woodbridge 1.142
Singapore 889
Fairfield 836
Ashburn 773
Houston 688
Ann Arbor 642
Chandler 520
San Jose 339
Wilmington 331
Hong Kong 319
Seattle 317
Jacksonville 312
Beijing 311
Cambridge 291
Dallas 231
Dearborn 219
Council Bluffs 213
Los Angeles 178
Chicago 169
Boardman 146
Udine 145
Lauterbourg 104
Princeton 95
Dublin 90
Izmir 70
Buffalo 69
Salt Lake City 62
Ho Chi Minh City 59
New York 59
Santa Clara 58
San Diego 55
Hefei 47
Dong Ket 45
Phoenix 45
Seoul 44
Des Moines 40
Munich 40
Hanoi 39
Tampa 38
Helsinki 33
Ottawa 32
Elk Grove Village 31
Frankfurt am Main 31
São Paulo 31
The Dalles 29
Milan 27
Brussels 25
Redondo Beach 25
Tokyo 25
Falls Church 22
Nuremberg 22
Dulles 21
Nanjing 21
Warsaw 21
Orem 20
Sterling 20
Brooklyn 19
Codroipo 17
Denver 17
Kocaeli 17
Miami 17
Rome 17
London 16
Poplar 16
Toronto 16
Washington 16
Chennai 15
Lancaster 15
Montreal 15
Norwalk 15
Ogden 15
Philadelphia 14
Vienna 14
Baltimore 13
Mumbai 13
Remanzacco 13
Amsterdam 12
Atlanta 12
Manchester 12
Mexico City 12
Redmond 12
San Francisco 12
Wuhan 12
Brasília 11
Düsseldorf 11
Tashkent 11
Boston 10
Haiphong 10
Kunming 10
Lappeenranta 10
Pittsburgh 10
Shanghai 10
Stockholm 10
Belo Horizonte 9
Birmingham 9
Bologna 9
Charlotte 9
Guangzhou 9
Trieste 9
Ankara 8
Totale 11.065
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Nome #
Epigenetic mechanisms beyond tumour–stroma crosstalk 714
Super-enhancer landscape rewiring in cancer: The epigenetic control at distal sites 290
The co-existence of transcriptional activator and transcriptional repressor MEF2 complexes influences tumor aggressiveness 254
The control operated by the cell cycle machinery on mef2 stability contributes to the downregulation of cdkn1a and entry into s phase 233
Type I IFNs signaling and apoptosis resistance in glioblastoma cells 229
The isopeptidase inhibitor 2cPE triggers proteotoxic stress and ATM activation in chronic lymphocytic leukemia cells 218
Twist is substrate for caspase cleavage and proteasome-mediated degradation 215
IFNs, ISGylation and cancer: Cui prodest? 211
Altering protein turnover in tumor cells: New opportunities for anti-cancer therapies 211
Caspase-dependent regulation of histone deacetylase 4 nuclear-cytoplasmic shuttling promotes apoptosis 207
Regulation of class IIa HDAC activities: It is not only matter of subcellular localization 207
Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A 204
Identification and characterization of a new member of the gas3/PMP22 gene family in C. elegans 198
Ubiquitin-dependent degradation of HDAC4, a new regulator of random cell motility 198
Caspase-2 can trigger cytochrome C release and apoptosis from the nucleus 194
Apoptotic pathways activated by histone deacetylase inhibitors: implications for the drug-resistant phenotype 191
Characterization of caspase-dependent and caspase-independent deaths in glioblastoma cells treated with inhibitors of the ubiquitin-proteasome system. 190
Transformation by different oncogenes relies on specific metabolic adaptations 187
Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA 185
MEF2 and the tumorigenic process, hic sunt leones 185
PP2A regulates HDAC4 nuclear import 182
Change in the expression of a nuclear matrix associated protein is correlated with cellular transformation 181
Caspase-2-induced apoptosis is dependent on caspase-9, but its processing during UV- or tumor necrosis factor-dependent cell death requires caspase-3 181
Beside the MEF2 axis: Unconventional functions of HDAC4. 180
CAPNS1 regulates USP1 stability and maintenance of genome integrity. 180
Measurement of Caspase Activity: From Cell Populations to Individual Cells 180
Calpain is required for macroautophagy in mammalian cells 177
The binding landscape of a partially-selective isopeptidase inhibitor with potent pro-death activity, based on the bis(arylidene)cyclohexanone scaffold 176
Potent and Selective Non-hydroxamate Histone Deacetylase 8 Inhibitors 174
Caspase activation and apoptosis in response to proteasome inhibitors 172
Class IIa HDACs repressive activities on MEF2-depedent transcription are associated with poor prognosis of ER+ breast tumors. 168
Gas2 is a multifunctional gene involved in the regulation of apoptosis and chondrogenesis in the developing mouse limb 167
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 167
Tau cleavage and dephosphorylation in cerebellar granule neurons undergoing apoptosis 165
Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22 165
Susceptibility to p53 dependent apoptosis correlates with increased levels of Gas2 and Gas3 proteins 164
Functions of the growth arrest specific 1 gene in the development of the mouse embryo 164
Guidelines for the use and interpretation of assays for monitoring autophagy 164
Dephosphorylation and caspase processing generate distinct nuclear pools of histone deacetylase 4 163
Synthesis, characterization, and optimization for in vivo delivery of a nonselective isopeptidase inhibitor as new antineoplastic agent 161
The neuronal microtubule-associated protein tau is a substrate for caspase-3 and an effector of apoptosis 160
Inhibitors of the ubiquitin-proteasome system are not all alike: Identification of a new necrotic pathway 158
Different class IIa HDACs repressive complexes regulate specific epigenetic responses related to cell survival in leiomyosarcoma cells 158
Microfilament reorganization during apoptosis: the role of Gas2, a possible substrate for ICE-like proteases 157
A receptor-interacting protein 1 (RIP1)-independent necrotic death under the control of protein phosphatase PP2A that involves the reorganization of actin cytoskeleton and the action of cofilin-1. 156
Expression of growth arrest specific (gas) genes in murine keratinocytes: gas2 is specifically regulated 153
METABOLIC ALTERATION AND MITOCHONDRIAL BIOENERGETIC PROFILE IN HDAC4-DRIVEN TUMORIGENESIS 153
Alteration in the Arf6-regulated plasma membrane endosomal recycling pathway in cells overexpressing the tetraspan protein Gas3/PMP22 153
The MEF2-HDAC axis controls proliferation of mammary epithelial cells and acini formation in vitro 150
The death substrate Gas2 binds m-calpain and increases susceptibility to p53-dependent apoptosis 149
The transcriptional repressor hDaxx potentiates p53-dependent apoptosis 149
Gas2 a growth arrest specific protein is a component of microfilament network system 147
Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants 147
A Biological Circuit Involving Mef2c, Mef2d, and Hdac9 Controls the Immunosuppressive Functions of CD4+Foxp3+ T-Regulatory Cells 146
Transcriptomic analysis unveils correlations between regulative apoptotic caspases and genes of cholesterol homeostasis in human brain 145
The Protein Encoded by a Growth Arrest-Specific Gene (gas6) Is a New Member of the Vitamin K-Dependent Proteins Related to Protein S, a Negative Coregulator in the Blood Coagulation Cascade 144
Identification of new compounds that trigger apoptosome-independent caspase activation and apoptosis 142
MEF2 is a converging hub for HDAC4 and PI3K/Akt-induced transformation. 142
HDAC7-mediated control of tumour microenvironment maintains proliferative and stemness competence of human mammary epithelial cells 142
Identification of USP18 as an important regulator of the susceptibility to IFN-alpha and drug-induced apoptosis 141
Tissue transglutaminase is a caspase substrate during apoptosis. Cleavage causes loss of transamidating function and is a biochemical marker of caspase-3 activation 141
Sensitivity of human multiple myelomas and myeloid leukemias to the proteasome inhibitor I. 140
Selective class IIa HDAC inhibitors: myth or reality. 140
GSK3β is a key regulator of the ROS-dependent necrotic death induced by the quinone DMNQ 140
Quis custodiet ipsos custodes (Who controls the controllers)? two decades of studies on HDAC9 138
Caspase-3 and caspase-7 but not caspase-6 cleave Gas2 in vitro: implications for microfilament reorganization during apoptosis 137
Dissection of c-myc domains involved in S phase induction of NIH 3T3 fibroblasts 130
Genetic programs driving oncogenic transformation: Lessons from in vitro models 130
Unscheduled HDAC4 repressive activity in human fibroblasts triggers TP53-dependent senescence and favors cell transformation 129
HDAC4 degradation during senescence unleashes an epigenetic program driven by AP-1/p300 at selected enhancers and super-enhancers 126
Enhancing proteotoxic stress in leiomyosarcoma cells triggers mitochondrial dysfunctions, cell death, and antitumor activity in vivo 125
Phosphorylation of the growth arrest specific protein Gas2 is coupled to actin rearrangements during G0->G1 transition in NIH 3T3 cells 122
Proteolytic processing of the adherens junctions components beta-catenin and gamma-catenin/plakoglobin during apoptosis 122
cDNA characterization and chromosome mapping of the human Gas2 gene 120
CLASS IIA HDACs: FROM IMPORTANT ROLES IN DIFFERENTIATION TO POSSIBLE IMPLICATIONS IN TUMORIGENESIS 114
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A diseas 113
Proteotoxic stress-induced apoptosis in cancer cells: understanding the susceptibility and enhancing the potency 112
Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 110
Changes in chromatin accessibility and transcriptional landscape induced by HDAC inhibitors in TP53 mutated patient-derived colon cancer organoids 110
The Histone Code of Senescence 109
Acetylation and Phosphorylation in the Regulation of Hypoxia-Inducible Factor Activities: Additional Options to Modulate Adaptations to Changes in Oxygen Levels 107
Transcription of endogenous retroviruses in senescent cells contributes to the accumulation of double-stranded RNAs that trigger an anti-viral response that reinforces senescence 107
USP18 is a key regulator of the nterferon-driven gene network modulating pancreatic beta cell inflammation and apoptosis. 107
Exposure at the cell surface is required for gas3/PMP22 To regulate both cell death and cell spreading: implication for the Charcot-Marie-Tooth type 1A and Dejerine-Sottas diseases 107
A regulative epigenetic circuit supervised by HDAC7 represses IGFBP6 and IGFBP7 expression to sustain mammary stemness 107
Inhibitors of the Ubiquitin-proteasome system (UPS) and the cell death machinery: How many pathways are activated? 106
Cytoplasmic HDAC4 regulates the membrane repair mechanism in Duchenne muscular dystrophy 105
The isopeptidase inhibitor G5 triggers a caspase-independent necrotic death in cells resistant to apoptosis: A comparative study with the proteasome inhibitor bortezomib 104
The DeISGylase USP18 limits TRAIL-induced apoptosis through the regulation of TRAIL levels: Cellular levels of TRAIL influences responsiveness to TRAIL-induced apoptosis 104
Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription 104
HDACs and the epigenetic plasticity of cancer cells: Target the complexity 103
Identification of a gene signature for the prediction of recurrence and progression in non-muscle-invasive bladder cancer 102
Dismantling cell-cell contacts during apoptosis is copuled to a caspase dependent proteolyitic cleavage of beta-catenin 101
Cut and die: proteolytic cascade regulating apoptosis 96
Proteotoxic stress and cell death in cancer cells 92
In Vitro and In Vivo Evaluation of the Effects of Drug 2c and Derivatives on Ovarian Cancer Cells 87
Isopeptidases in anticancer therapy: looking for inhibitors 86
Gas6 anti-apoptotic signaling requires NF-kappa B activation 85
The Calpain System Is Involved in the Constitutive Regulation of beta-Catenin Signaling Function. 84
Folding of Class IIa HDAC Derived Peptides into α-helices Upon Binding to Myocyte Enhancer Factor-2 in Complex with DNA 82
Totale 15.628
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Categoria #
all - tutte 57.897
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 57.897
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022752 0 0 37 77 28 44 52 30 31 138 169 146
2022/20231.142 111 100 12 167 118 268 7 81 132 14 48 84
2023/2024554 71 40 52 20 68 58 30 77 36 28 13 61
2024/20252.069 51 127 93 81 194 110 119 143 206 145 389 411
2025/20264.833 386 796 669 319 623 376 562 118 288 300 259 137
2026/2027476 107 234 135 0 0 0 0 0 0 0 0 0
Totale 16.455