IRIS
VISONE, Rosa
 Distribuzione geografica
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Continente #
NA - Nord America 3.380
EU - Europa 2.600
AS - Asia 2.042
SA - Sud America 240
AF - Africa 31
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.298
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Nazione #
US - Stati Uniti d'America 3.323
SG - Singapore 809
IT - Italia 654
CN - Cina 525
DE - Germania 336
IE - Irlanda 273
UA - Ucraina 260
VN - Vietnam 228
TR - Turchia 215
GB - Regno Unito 212
RU - Federazione Russa 207
BR - Brasile 191
SE - Svezia 177
FI - Finlandia 173
FR - Francia 156
IN - India 106
HK - Hong Kong 37
CA - Canada 30
BE - Belgio 26
NL - Olanda 25
BD - Bangladesh 22
AT - Austria 21
AR - Argentina 20
KR - Corea 19
MX - Messico 19
PL - Polonia 17
JP - Giappone 16
ES - Italia 14
IQ - Iraq 12
CZ - Repubblica Ceca 11
EC - Ecuador 11
ZA - Sudafrica 11
UZ - Uzbekistan 9
CH - Svizzera 8
GR - Grecia 7
LT - Lituania 7
RO - Romania 6
SA - Arabia Saudita 5
AZ - Azerbaigian 4
IR - Iran 4
KE - Kenya 4
MA - Marocco 4
PY - Paraguay 4
AU - Australia 3
CL - Cile 3
CO - Colombia 3
DZ - Algeria 3
ID - Indonesia 3
IL - Israele 3
PH - Filippine 3
PK - Pakistan 3
TH - Thailandia 3
UY - Uruguay 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
CR - Costa Rica 2
CU - Cuba 2
HU - Ungheria 2
JO - Giordania 2
KZ - Kazakistan 2
MM - Myanmar 2
MY - Malesia 2
NG - Nigeria 2
PA - Panama 2
PE - Perù 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BW - Botswana 1
EG - Egitto 1
ET - Etiopia 1
EU - Europa 1
IM - Isola di Man 1
LB - Libano 1
LI - Liechtenstein 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
VC - Saint Vincent e Grenadine 1
ZW - Zimbabwe 1
Totale 8.298
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Città #
Singapore 582
San Jose 378
Chandler 349
Dallas 311
Jacksonville 304
Dublin 271
Chieti 217
Ashburn 215
Munich 202
Beijing 143
Princeton 124
Southend 124
Dearborn 122
Izmir 111
Ann Arbor 108
Helsinki 101
Council Bluffs 87
Los Angeles 87
The Dalles 79
Ho Chi Minh City 70
Nanjing 67
Hanoi 62
Santa Clara 61
Wilmington 58
Cambridge 45
Pescara 45
New York 44
Tongling 42
Boardman 36
Hong Kong 30
Altamura 26
Redondo Beach 26
Rome 26
Buffalo 25
Woodbridge 23
Brussels 22
Nanchang 21
Washington 20
Montesilvano Marina 19
Orem 19
Dong Ket 18
São Paulo 18
Brooklyn 16
Jiaxing 16
Seoul 16
Hefei 15
London 15
Moscow 15
Tokyo 15
Vienna 15
Hebei 14
Shenyang 14
Amsterdam 12
Carini 12
Chicago 12
Denver 11
Houston 11
Kunming 11
Tianjin 11
Toronto 11
Da Nang 10
Jinan 10
Jyväskylä 10
Mexico City 10
Warsaw 10
Frankfurt am Main 9
Guangzhou 9
Nuremberg 9
Ancona 8
Ankara 8
Changsha 8
Collecorvino 8
L'aquila 8
Leawood 8
Manchester 8
Montreal 8
Mumbai 8
Orsogna 8
Stockholm 8
Atlanta 7
Brno 7
Charlotte 7
Haiphong 7
Johannesburg 7
Milan 7
Poplar 7
Seattle 7
Tashkent 7
Belo Horizonte 6
Columbus 6
Lappeenranta 6
Shanghai 6
Teramo 6
Turku 6
Ascoli Piceno 5
Grevenbroich 5
Hangzhou 5
Hải Dương 5
Ningbo 5
Quito 5
Totale 5.274
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Nome #
DNA methylation of shelf, shore and open sea CpG positions distinguish high microsatellite instability from low or stable microsatellite status colon cancer stem cells 260
Genetic dynamics in untreated CLL patients with either stable or progressive disease: A longitudinal study 257
Paragangliomas arise through an autonomous vasculo-angio-neurogenic program inhibited by imatinib 253
Allele-specific loss and transcription of the miR-15a/16-1 cluster in chronic lymphocytic leukemia. 240
A POSSIBLE ROLE OF A CMV-LIKE VIRUS IN HEAD AND NECK PARAGANGLIOMA PATHOGENESIS 219
Possible role of a CMV-like virus in paragangliomas 211
A developmental perspective on paragangliar tumorigenesis 202
A developmental model of paragangliar tumorigenesis highlights therapeutic targets 192
Hsa-miR-200 and hsa-miR34 miRNA family members target cellular and viral genes regulating HCMV infection in head and neck paraganglioma 187
CAR-T-Derived Extracellular Vesicles: A Promising Development of CAR-T Anti-Tumor Therapy 172
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 171
MiR-181b in Chronic Lymphocytic Leukemia B Cells Is Regulated By Cellular Interaction with CD4+ T Cells and Increases the CTL Toxicity Versus the Leukemic Clone 170
Enhanced expression of mir-181b in b cells of cll improves the anti-tumor cytotoxic t cell response 158
Regulation of miR-483-3p by the O-linked N-acetylglucosamine transferase links chemosensitivity to glucose metabolism in liver cancer cells 154
Impact of BCR Stimulation on Mir-181b in Chronic Lymphocityc Leukemia 154
Epigenetics and microRNAs in cancer 143
MicroRNAs in autoimmunity and hematological malignancies 141
Over-expression of the miR-483-3p overcomes the miR-145/TP53 pro-apoptotic loop in hepatocellular carcinoma 140
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 140
B-RAF mutations are a rare event in pituitary adenomas. 137
Reprogramming of miRNA networks in cancer and leukemia. 136
A perspective analysis: microRNAs, glucose metabolism, and drug resistance in colon cancer stem cells 136
A novel miR-371a-5p-mediated pathway, leading to BAG3 upregulation in cardiomyocytes in response to epinephrine, is lost in Takotsubo cardiomyopathy 135
E2F1 activation is responsible for pituitary adenomas induced byHMGA2 gene overexpression 134
PDGFRA is controlled by miRNAs in head and neck paraganglioma cells: in vitro and in vivo treatment with imatinib mesylate. 134
Deregulation of microRNA expression infollicular cell-derived human thyroidcarcinomas 131
Wnt signalling modulates transcribed-ultraconserved regions in hepatobiliary cancers 131
Oncogenic role of miR-483-3p at the IGF2/483 locus. 124
Differential Regulation of Wingless-Wnt/c-Jun N-Terminal Kinase Crosstalk via Oxidative Eustress in Primary and Metastatic Colorectal Cancer Cells 123
Karyotype-specific microRNA signature in chronic lymphocytic leukemia. 123
The glucose-regulated MiR-483-3p influences key signaling pathways in cancer 123
UCbase & miRfunc: a database of ultraconservedsequences and microRNA function 122
Tagging enhances histochemical and biochemical detection of Ran Binding Protein 9 in vivo and reveals its interaction with Nucleolin 122
A microRNA expression signature of humansolid tumors defines cancer gene targets 119
Overexpression of the HMGA2 gene in transgenic mice leads to the onset of pituitary adenomas 119
Genechip Microarray analysis of pituitary adenomas developed by HMGA transgenic mice 117
Critical Role of the HMGA2 Gene in Pituitary Adenomas 115
MiR-130a targets MET and induces TRAIL-sensitivity in NSCLC by downregulating miR-221 and 222 115
A truncated HMGA1 gene induces proliferation of the 3T3-L1 pre-adipocytic cells: a model of human lipomas 114
Critical role of the RB-E2F pathway in the generation of pituitary adenomas in transgenic mice overexpressing the HMGA2 gene 113
Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling 113
Therapeutic effect of microRNA-15/16 cluster in a mouse model of chronic lymphocytic leukemia 107
Expression of a truncated Hmga1b gene induces gigantism, lipomatosis and B-cell lymphomas in mice 106
Transgenic mice overexpressing the wild-type form of the HMGA1 gene develop mixed growth hormone/prolactin cell pituitary adenomas and natural killer cell lymphomas 102
Mutated β-catenin evades a microRNA-dependentregulatory loop 101
miR-181b is a biomarker of disease progression in chronic lymphocytic leukemia 101
Genechip microarray analysis of pituitary adenomas developed by HMG transgenic mice. 100
Haploinsufficiency of the Hmga1 Gene Causes Cardiac Hypertrophyand Myelo-Lymphoproliferative Disorders in Mice 98
Targeted Disruption of the Murine Homeodomain-InteractingProtein Kinase-2 Causes Growth Deficiency In Vivoand Cell Cycle Arrest In Vitro 98
Ucbase and miRfunc: A database which links ultraconserved sequences and microRNA with cancer and mendelian inheritance human disorders 98
Overexpression of the HMGA2 gene induces mixed growth hormone cell/prolactin cell pituitary adenomas by impairment of the RB/E2F pathway 96
HMGA Proteins Up-regulate CCNB2 Gene in Mouse and HumanPituitary Adenomas 95
Regulation of microRNA expression by HMGA1 proteins 95
Targeted disruption of the murine PATZ gene induces growth retardation 92
MiR-181b: New perspective to evaluate disease progression in chronic lymphocytic leukemia 92
Overexpression of the HMGA2 gene induces mixed growth hormon cell/prolactin cell pituitary adenomas by impairment of the Rb/E2F pathway 91
Identification of microRNA activity by Targets’ ReverseEXpression 90
The Mia/Cd-rap gene expression isdownregulated by the high-mobility group Aproteins in mouse pituitary adenomas 88
miR-483-3p is an oncogene involved in nephroblastoma and in adult tumors with activated ß-catenin 88
Generation of vectors that coexpress intronic microRNAs and exonic reporters 88
Role of microRNAs in Chronic Lymphocytic Leukemia 86
RANBP9 as potential therapeutic target in non-small cell lung cancer 85
SOM230, a new somatostatin analogue, is highly effective in the therapy of growth hormone/prolactin-secreting pituitary adenomas. 84
High-mobility-group A1 (HMGA1) proteins down-regulate the expression of the recombination activating gene 2 (RAG2) 83
MiR-181b expression levels decrease during the progression of Chronic Lymphocytic Leukemia: a new potential prognostic tool 79
Ibrutinib increases miR-181a/b in leukemic cells from patients with chronic lymphocytic leukemia 25
RANBP9 and RANBP10 cooperate in regulating non-small cell lung cancer proliferation 3
Totale 8.571
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Categoria #
all - tutte 30.628
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 30.628
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202135 0 0 0 0 0 0 0 0 0 0 0 35
2021/2022365 4 11 5 44 25 5 29 45 51 14 32 100
2022/2023905 89 106 56 105 95 171 51 73 104 14 29 12
2023/2024454 20 17 48 14 29 134 102 8 2 15 25 40
2024/20251.518 60 185 151 27 29 137 169 125 188 82 158 207
2025/20262.784 193 115 412 326 244 145 538 173 274 181 155 28
Totale 8.571