IRIS UniCatt

Tartaglia, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 1.975
EU - Europa 1.577
AS - Asia 1.079
SA - Sud America 242
AF - Africa 34
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 4.910
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Nazione #
US - Stati Uniti d'America 1.945
SG - Singapore 441
PL - Polonia 433
CN - Cina 382
DE - Germania 353
SE - Svezia 216
BR - Brasile 209
UA - Ucraina 159
IT - Italia 94
VN - Vietnam 72
IE - Irlanda 67
GB - Regno Unito 55
FR - Francia 43
ID - Indonesia 43
FI - Finlandia 41
AT - Austria 35
IN - India 35
RU - Federazione Russa 31
TR - Turchia 20
AR - Argentina 14
NL - Olanda 14
IQ - Iraq 13
HK - Hong Kong 12
BD - Bangladesh 11
MX - Messico 11
CA - Canada 10
JP - Giappone 9
ES - Italia 8
CI - Costa d'Avorio 7
IR - Iran 7
BE - Belgio 6
ZA - Sudafrica 6
CL - Cile 5
MA - Marocco 5
VE - Venezuela 5
CO - Colombia 4
KE - Kenya 4
PK - Pakistan 4
SA - Arabia Saudita 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
BH - Bahrain 3
KR - Corea 3
LT - Lituania 3
PT - Portogallo 3
CH - Svizzera 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EC - Ecuador 2
EG - Egitto 2
HN - Honduras 2
HR - Croazia 2
KZ - Kazakistan 2
MY - Malesia 2
PA - Panama 2
PY - Paraguay 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
UZ - Uzbekistan 2
A1 - Anonimo 1
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BG - Bulgaria 1
CG - Congo 1
EE - Estonia 1
ET - Etiopia 1
GR - Grecia 1
GT - Guatemala 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KW - Kuwait 1
LB - Libano 1
LU - Lussemburgo 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NP - Nepal 1
PE - Perù 1
QA - Qatar 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZW - Zimbabwe 1
Totale 4.910
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Città #
Warsaw 429
Chandler 237
Ashburn 180
Singapore 160
Fairfield 149
Woodbridge 135
Seattle 107
Jacksonville 101
Nanjing 83
Wilmington 83
San Mateo 71
Houston 68
Dublin 67
Beijing 66
Cambridge 63
Ann Arbor 53
Dearborn 50
Jakarta 40
Vienna 33
Boston 32
Redmond 32
Nanchang 30
Lawrence 25
Los Angeles 25
Hefei 23
New York 20
São Paulo 20
Ho Chi Minh City 19
Nürnberg 18
Frankfurt am Main 17
Moscow 17
Cattolica 16
Rome 16
Buffalo 15
Dong Ket 15
Izmir 15
Munich 15
Redwood City 15
Hangzhou 14
Princeton 14
Bremen 12
Hong Kong 12
Hebei 11
Jiaxing 11
London 11
Milan 11
Brooklyn 10
Hanoi 10
Kunming 10
Changsha 9
Chicago 9
Guangzhou 9
Shenyang 9
Belo Horizonte 8
Phoenix 8
Shanghai 8
University Park 8
Abidjan 7
Helsinki 7
Marseille 7
Baghdad 6
Brussels 6
Kent 6
Norwalk 6
Nuremberg 6
Rio de Janeiro 6
Stockholm 6
Tianjin 6
Amsterdam 5
Boardman 5
Dallas 5
Düsseldorf 5
Lancaster 5
Mountain View 5
Porto Alegre 5
San Diego 5
Shahid 5
Andover 4
Auburn Hills 4
Caracas 4
Chongqing 4
Curitiba 4
Da Nang 4
Dammam 4
Falls Church 4
Johannesburg 4
Nairobi 4
San Francisco 4
Santa Clara 4
Acton 3
Changchun 3
Dhaka 3
Jinan 3
Lauterbourg 3
Manassas 3
Montreal 3
Newark 3
Ottawa 3
Portsmouth 3
Salvador 3
Totale 2.949
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Nome #
CHK1-targeted therapy to deplete DNA replication- stressed, p53-deficient, hyperdiploid colorectal cancer stem cells 415
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 302
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 292
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 273
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 265
Enhanced human brain associative plasticity in Costello syndrome 215
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 175
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 156
Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. 137
Dystonia in Costello syndrome 122
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome 122
Diversity parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome 117
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 113
A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME 108
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy 107
Novel SEC61G-EGFR fusion gene in pediatric ependymomas discovered by clonal expansion of stem cells in absence of exogenous mitogens 107
Noonan syndrome: clinical aspects and molecular pathogenesis. 106
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 101
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer. 100
GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. 97
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 91
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 90
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 89
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair 88
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome 88
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors 87
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. 86
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. 84
Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation 84
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype -phenotype correlations. 83
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype 82
CRANIOSYNOSTOSIS IN PATIENTS WITH NOONAN SYNDROME CAUSED BY GERMLINE KRAS MUTATIONS 81
NF1 gene mutations represent the major molecular event underlying Neurofibromatosis-Noonan syndrome 75
Exclusion of PTPN1 mutations in Costello syndrome: further evidence for distinct genic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes 74
GERMLINE BRAF MUTATIONS IN NOONAN, LEOPARD, AND CARDIOFACIOCUTANEOUS SYNDROMES: MOLECULAR DIVERSITY AND ASSOCIATED PHENOTYPIC SPECTRUM 70
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome 70
DIVERSITY AND FUNCTIONAL CONSEQUENCES OF GERMLINE AND SOMATIC PTPN11 MUTATIONS IN HUMAN DISEASE 67
absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. 63
Proceeding from the 2009 genetic syndromes of the Ras/MAPK pathway: from bedside to bench and back 61
Totale 4.943
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Categoria #
all - tutte 19.156
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 19.156
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021337 0 0 0 0 0 56 155 2 51 14 40 19
2021/2022319 31 25 5 15 14 17 2 61 13 29 47 60
2022/2023623 84 85 41 87 47 99 21 48 73 12 24 2
2023/2024309 14 103 13 34 6 21 22 8 4 11 31 42
2024/2025560 16 18 49 23 46 19 25 30 74 48 106 106
2025/2026811 247 45 85 188 237 9 0 0 0 0 0 0
Totale 4.943