IRIS UniCatt

Tartaglia, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 1.766
EU - Europa 1.501
AS - Asia 570
SA - Sud America 41
AF - Africa 11
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 3.892
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Nazione #
US - Stati Uniti d'America 1.755
PL - Polonia 425
DE - Germania 338
CN - Cina 281
SE - Svezia 211
SG - Singapore 155
UA - Ucraina 154
IT - Italia 91
IE - Irlanda 66
GB - Regno Unito 43
ID - Indonesia 39
BR - Brasile 38
FI - Finlandia 38
FR - Francia 34
AT - Austria 32
RU - Federazione Russa 26
IN - India 24
VN - Vietnam 16
TR - Turchia 15
NL - Olanda 12
HK - Hong Kong 10
CI - Costa d'Avorio 7
IR - Iran 7
JP - Giappone 7
BE - Belgio 6
ES - Italia 6
CA - Canada 5
IQ - Iraq 4
MX - Messico 4
KR - Corea 3
LT - Lituania 3
PT - Portogallo 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
CH - Svizzera 2
HR - Croazia 2
KZ - Kazakistan 2
RO - Romania 2
TN - Tunisia 2
A1 - Anonimo 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BD - Bangladesh 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
GR - Grecia 1
KG - Kirghizistan 1
LU - Lussemburgo 1
LV - Lettonia 1
MN - Mongolia 1
NO - Norvegia 1
PA - Panama 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZA - Sudafrica 1
Totale 3.892
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Città #
Warsaw 422
Chandler 237
Fairfield 149
Ashburn 142
Woodbridge 135
Seattle 106
Jacksonville 100
Nanjing 83
Wilmington 83
Singapore 82
San Mateo 71
Houston 67
Dublin 66
Cambridge 63
Ann Arbor 53
Dearborn 50
Jakarta 39
Redmond 32
Vienna 31
Boston 30
Nanchang 30
Lawrence 25
Beijing 21
Nürnberg 18
Moscow 17
Cattolica 16
Dong Ket 15
Izmir 15
Redwood City 15
Munich 14
Princeton 14
Rome 14
Hangzhou 13
New York 13
Bremen 12
Hebei 11
Jiaxing 11
Los Angeles 11
Milan 11
Hong Kong 10
Kunming 10
Changsha 9
Guangzhou 9
Shenyang 9
London 8
Shanghai 8
University Park 8
Abidjan 7
Helsinki 7
Marseille 7
Phoenix 7
Brussels 6
Norwalk 6
Tianjin 6
Boardman 5
Düsseldorf 5
Frankfurt am Main 5
Hefei 5
Lancaster 5
Mountain View 5
San Diego 5
Shahid 5
Andover 4
Auburn Hills 4
Chicago 4
Falls Church 4
Nuremberg 4
Acton 3
Amsterdam 3
Changchun 3
Chongqing 3
Jinan 3
Lauterbourg 3
Manassas 3
Ottawa 3
Portsmouth 3
Sannicola 3
São Paulo 3
Augusta 2
Aversa 2
Baghdad 2
Bauru 2
Cagliari 2
Cuauhtémoc 2
Edinburgh 2
Erbil 2
Falkenstein 2
Fiorano Modenese 2
Fort Worth 2
Fremont 2
Groningen 2
Kraków 2
Lanzhou 2
Madrid 2
Orange 2
Perafita 2
Philadelphia 2
Samarate 2
Seoul 2
Taramani 2
Totale 2.591
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Nome #
CHK1-targeted therapy to deplete DNA replication- stressed, p53-deficient, hyperdiploid colorectal cancer stem cells 367
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 265
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 263
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 250
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 238
Enhanced human brain associative plasticity in Costello syndrome 198
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 140
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 128
Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. 107
Dystonia in Costello syndrome 104
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome 95
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 93
Diversity parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome 90
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy 87
A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME 80
Noonan syndrome: clinical aspects and molecular pathogenesis. 75
Novel SEC61G-EGFR fusion gene in pediatric ependymomas discovered by clonal expansion of stem cells in absence of exogenous mitogens 73
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 71
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome 69
GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. 68
CRANIOSYNOSTOSIS IN PATIENTS WITH NOONAN SYNDROME CAUSED BY GERMLINE KRAS MUTATIONS 68
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype -phenotype correlations. 66
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair 65
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 64
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 64
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. 63
Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation 61
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer. 61
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. 60
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype 59
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 58
NF1 gene mutations represent the major molecular event underlying Neurofibromatosis-Noonan syndrome 55
GERMLINE BRAF MUTATIONS IN NOONAN, LEOPARD, AND CARDIOFACIOCUTANEOUS SYNDROMES: MOLECULAR DIVERSITY AND ASSOCIATED PHENOTYPIC SPECTRUM 54
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors 48
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome 46
absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. 46
DIVERSITY AND FUNCTIONAL CONSEQUENCES OF GERMLINE AND SOMATIC PTPN11 MUTATIONS IN HUMAN DISEASE 44
Proceeding from the 2009 genetic syndromes of the Ras/MAPK pathway: from bedside to bench and back 43
Exclusion of PTPN1 mutations in Costello syndrome: further evidence for distinct genic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes 39
Totale 3.925
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Categoria #
all - tutte 15.441
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 15.441
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020116 0 0 0 0 0 0 0 0 0 0 76 40
2020/2021525 19 51 15 39 64 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
2024/2025353 16 18 49 23 46 19 25 30 74 48 5 0
Totale 3.925