IRIS PubliCatt

Tartaglia, Marco
 Distribuzione geografica
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Continente #
NA - Nord America 1.713
EU - Europa 1.405
AS - Asia 337
AF - Africa 9
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 3.466
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Nazione #
US - Stati Uniti d'America 1.708
PL - Polonia 424
DE - Germania 320
CN - Cina 237
SE - Svezia 208
UA - Ucraina 152
IT - Italia 79
IE - Irlanda 63
GB - Regno Unito 37
FI - Finlandia 32
AT - Austria 27
FR - Francia 27
IN - India 24
SG - Singapore 20
VN - Vietnam 16
TR - Turchia 15
NL - Olanda 11
HK - Hong Kong 8
CI - Costa d'Avorio 7
IR - Iran 7
JP - Giappone 7
BE - Belgio 6
ES - Italia 5
MX - Messico 4
RU - Federazione Russa 4
CH - Svizzera 2
RO - Romania 2
A1 - Anonimo 1
BR - Brasile 1
CA - Canada 1
DZ - Algeria 1
EE - Estonia 1
GR - Grecia 1
HR - Croazia 1
KR - Corea 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MN - Mongolia 1
NO - Norvegia 1
PT - Portogallo 1
ZA - Sudafrica 1
Totale 3.466
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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
Houston 67
Cambridge 63
Dublin 63
Ann Arbor 53
Dearborn 50
Redmond 32
Boston 30
Nanchang 30
Vienna 27
Lawrence 25
Beijing 21
Nürnberg 18
Cattolica 16
Dong Ket 15
Izmir 15
Redwood City 15
Princeton 14
Hangzhou 13
New York 13
Bremen 12
Munich 12
Rome 12
Hebei 11
Jiaxing 11
Milan 11
Kunming 10
Changsha 9
Shenyang 9
Hong Kong 8
University Park 8
Abidjan 7
Marseille 7
Phoenix 7
Brussels 6
Guangzhou 6
London 6
Norwalk 6
Tianjin 6
Boardman 5
Hefei 5
Lancaster 5
Los Angeles 5
Mountain View 5
San Diego 5
Shahid 5
Shanghai 5
Andover 4
Auburn Hills 4
Chicago 4
Falls Church 4
Acton 3
Amsterdam 3
Changchun 3
Chongqing 3
Jinan 3
Sannicola 3
Augusta 2
Cagliari 2
Cuauhtémoc 2
Edinburgh 2
Fremont 2
Groningen 2
Kraków 2
Lanzhou 2
Orange 2
Philadelphia 2
Samarate 2
Taramani 2
Zurich 2
Algiers 1
Astana 1
Athens 1
Atlanta 1
Berlin 1
Bilbao 1
Bucharest 1
Busto Arsizio 1
Capannelle 1
Cardiff 1
Charlotte 1
Chiswick 1
Costa Mesa 1
Den Haag 1
Forlì 1
Gaiarine 1
Group 1
Gunzenhausen 1
Hanoi 1
Helsinki 1
Huelva 1
Totale 2.390
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Nome #
CHK1-targeted therapy to deplete DNA replication- stressed, p53-deficient, hyperdiploid colorectal cancer stem cells 346
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 248
Tyr1068-phosphorylated epidermal growth factor receptor (EGFR) predicts cancer stem cell targeting by erlotinib in preclinical models of wild-type EGFR lung cancer 248
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 238
Noncanonical GLI1 signaling promotes stemness features and in vivo growth in lung adenocarcinoma 226
Enhanced human brain associative plasticity in Costello syndrome 189
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 129
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 110
Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. 96
Dystonia in Costello syndrome 91
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 83
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome 79
Diversity parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome 77
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy 76
A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME 70
Noonan syndrome: clinical aspects and molecular pathogenesis. 67
CRANIOSYNOSTOSIS IN PATIENTS WITH NOONAN SYNDROME CAUSED BY GERMLINE KRAS MUTATIONS 62
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 61
GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. 60
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome 59
Novel SEC61G-EGFR fusion gene in pediatric ependymomas discovered by clonal expansion of stem cells in absence of exogenous mitogens 58
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype -phenotype correlations. 57
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair 55
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. 53
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 53
MUTATION OF SHOC2 PROMOTES ABERRANT PROTEIN N-MYRISTOYLATION AND CAUSES NOONAN-LIKE SUNDROME WITH LOOSE ANAGEN HAIR. 51
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer. 50
Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation 49
GERMLINE BRAF MUTATIONS IN NOONAN, LEOPARD, AND CARDIOFACIOCUTANEOUS SYNDROMES: MOLECULAR DIVERSITY AND ASSOCIATED PHENOTYPIC SPECTRUM 48
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype 48
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 47
NF1 gene mutations represent the major molecular event underlying Neurofibromatosis-Noonan syndrome 47
Cancer stem cell-based models of colorectal cancer reveal molecular determinants of therapy resistance 42
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors 40
DIVERSITY AND FUNCTIONAL CONSEQUENCES OF GERMLINE AND SOMATIC PTPN11 MUTATIONS IN HUMAN DISEASE 39
Proceeding from the 2009 genetic syndromes of the Ras/MAPK pathway: from bedside to bench and back 38
absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. 38
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome 37
Exclusion of PTPN1 mutations in Costello syndrome: further evidence for distinct genic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes 34
Totale 3.499
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Categoria #
all - tutte 10.881
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 10.881
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201994 0 0 0 0 0 0 0 0 0 0 54 40
2019/2020871 124 40 92 159 58 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
2023/2024236 14 103 13 34 6 21 22 8 4 11 0 0
Totale 3.499