IRIS PubliCatt

Tartaglia, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 1.730
EU - Europa 1.461
AS - Asia 506
AF - Africa 9
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 3.708
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Nazione #
US - Stati Uniti d'America 1.721
PL - Polonia 425
DE - Germania 328
CN - Cina 271
SE - Svezia 209
UA - Ucraina 152
SG - Singapore 112
IT - Italia 89
IE - Irlanda 64
GB - Regno Unito 40
ID - Indonesia 39
FI - Finlandia 36
AT - Austria 29
FR - Francia 28
IN - India 24
RU - Federazione Russa 24
VN - Vietnam 16
TR - Turchia 15
NL - Olanda 12
HK - Hong Kong 8
CI - Costa d'Avorio 7
IR - Iran 7
JP - Giappone 7
BE - Belgio 6
ES - Italia 6
CA - Canada 5
MX - Messico 4
KR - Corea 3
LT - Lituania 3
CH - Svizzera 2
KZ - Kazakistan 2
RO - Romania 2
A1 - Anonimo 1
BR - Brasile 1
DZ - Algeria 1
EE - Estonia 1
GR - Grecia 1
HR - Croazia 1
LU - Lussemburgo 1
MN - Mongolia 1
NO - Norvegia 1
PT - Portogallo 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 3.708
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Città #
Warsaw 422
Chandler 237
Fairfield 149
Ashburn 139
Woodbridge 135
Seattle 106
Jacksonville 100
Nanjing 83
Wilmington 83
San Mateo 71
Singapore 68
Houston 67
Dublin 64
Cambridge 63
Ann Arbor 53
Dearborn 50
Jakarta 39
Redmond 32
Boston 30
Nanchang 30
Vienna 28
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
Milan 11
Kunming 10
Changsha 9
Shenyang 9
Hong Kong 8
London 8
University Park 8
Abidjan 7
Los Angeles 7
Marseille 7
Phoenix 7
Shanghai 7
Brussels 6
Guangzhou 6
Norwalk 6
Tianjin 6
Boardman 5
Hefei 5
Helsinki 5
Lancaster 5
Mountain View 5
San Diego 5
Shahid 5
Andover 4
Auburn Hills 4
Chicago 4
Falls Church 4
Acton 3
Amsterdam 3
Changchun 3
Chongqing 3
Jinan 3
Nuremberg 3
Ottawa 3
Sannicola 3
Augusta 2
Aversa 2
Cagliari 2
Cuauhtémoc 2
Edinburgh 2
Falkenstein 2
Fiorano Modenese 2
Fort Worth 2
Fremont 2
Groningen 2
Kraków 2
Lanzhou 2
Madrid 2
Orange 2
Philadelphia 2
Samarate 2
Seoul 2
Taramani 2
Zurich 2
Algiers 1
Almaty 1
Astana 1
Athens 1
Atlanta 1
Berlin 1
Bilbao 1
Bucharest 1
Busto Arsizio 1
Totale 2.537
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Nome #
CHK1-targeted therapy to deplete DNA replication- stressed, p53-deficient, hyperdiploid colorectal cancer stem cells 361
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 257
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 256
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 247
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 235
Enhanced human brain associative plasticity in Costello syndrome 194
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 136
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 121
Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. 103
Dystonia in Costello syndrome 98
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 90
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome 88
Diversity parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome 83
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy 83
A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME 76
Noonan syndrome: clinical aspects and molecular pathogenesis. 71
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 68
CRANIOSYNOSTOSIS IN PATIENTS WITH NOONAN SYNDROME CAUSED BY GERMLINE KRAS MUTATIONS 67
Novel SEC61G-EGFR fusion gene in pediatric ependymomas discovered by clonal expansion of stem cells in absence of exogenous mitogens 66
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome 64
GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. 62
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair 62
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype -phenotype correlations. 61
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 61
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. 58
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. 56
Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation 55
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer. 55
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 54
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 54
NF1 gene mutations represent the major molecular event underlying Neurofibromatosis-Noonan syndrome 52
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype 51
GERMLINE BRAF MUTATIONS IN NOONAN, LEOPARD, AND CARDIOFACIOCUTANEOUS SYNDROMES: MOLECULAR DIVERSITY AND ASSOCIATED PHENOTYPIC SPECTRUM 50
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors 44
Proceeding from the 2009 genetic syndromes of the Ras/MAPK pathway: from bedside to bench and back 42
absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. 42
DIVERSITY AND FUNCTIONAL CONSEQUENCES OF GERMLINE AND SOMATIC PTPN11 MUTATIONS IN HUMAN DISEASE 42
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome 41
Exclusion of PTPN1 mutations in Costello syndrome: further evidence for distinct genic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes 35
Totale 3.741
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Categoria #
all - tutte 14.024
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 14.024
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020398 0 0 0 0 0 96 69 40 53 24 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
2024/2025169 16 18 49 23 46 17 0 0 0 0 0 0
Totale 3.741