IRIS
DE ROSA, MARINA
 Distribuzione geografica
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Continente #
AS - Asia 3.642
EU - Europa 3.478
NA - Nord America 3.474
SA - Sud America 522
AF - Africa 88
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 11.211
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Nazione #
US - Stati Uniti d'America 3.324
SG - Singapore 2.180
RU - Federazione Russa 1.647
CN - Cina 741
IT - Italia 609
BR - Brasile 433
HK - Hong Kong 302
VN - Vietnam 213
FR - Francia 208
DE - Germania 207
FI - Finlandia 173
IE - Irlanda 137
UA - Ucraina 133
NL - Olanda 114
GB - Regno Unito 92
CA - Canada 88
IN - India 60
SE - Svezia 44
AR - Argentina 40
MX - Messico 39
ZA - Sudafrica 27
CI - Costa d'Avorio 26
PL - Polonia 25
TR - Turchia 24
BE - Belgio 23
BD - Bangladesh 18
ES - Italia 17
ID - Indonesia 17
EC - Ecuador 16
JP - Giappone 16
IQ - Iraq 13
LT - Lituania 12
AT - Austria 11
PY - Paraguay 11
PK - Pakistan 8
MA - Marocco 6
UZ - Uzbekistan 6
KR - Corea 5
SA - Arabia Saudita 5
TN - Tunisia 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
AO - Angola 4
CO - Colombia 4
JM - Giamaica 4
LB - Libano 4
PE - Perù 4
UY - Uruguay 4
CL - Cile 3
CZ - Repubblica Ceca 3
EG - Egitto 3
JO - Giordania 3
KE - Kenya 3
KZ - Kazakistan 3
LU - Lussemburgo 3
ME - Montenegro 3
PS - Palestinian Territory 3
TT - Trinidad e Tobago 3
BB - Barbados 2
BG - Bulgaria 2
BO - Bolivia 2
BS - Bahamas 2
BY - Bielorussia 2
CH - Svizzera 2
CV - Capo Verde 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EU - Europa 2
HU - Ungheria 2
IR - Iran 2
NI - Nicaragua 2
PA - Panama 2
TZ - Tanzania 2
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
BZ - Belize 1
CG - Congo 1
CU - Cuba 1
CY - Cipro 1
DK - Danimarca 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
HN - Honduras 1
HT - Haiti 1
IL - Israele 1
KW - Kuwait 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MR - Mauritania 1
MU - Mauritius 1
MY - Malesia 1
MZ - Mozambico 1
Totale 11.195
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Città #
Singapore 999
Chandler 423
Moscow 416
Hong Kong 301
Beijing 278
Ashburn 232
Santa Clara 169
Naples 159
Jacksonville 155
Dallas 135
Princeton 106
Los Angeles 104
Millbury 97
Amsterdam 95
Nanjing 83
Ho Chi Minh City 79
Munich 76
Napoli 66
Boston 58
Wilmington 58
Buffalo 50
New York 50
Hanoi 48
São Paulo 47
Redondo Beach 46
Helsinki 45
San Jose 40
Ottawa 38
Seattle 30
The Dalles 30
Nanchang 29
Atlanta 27
Des Moines 27
Norwalk 27
Hefei 26
Dublin 22
Johannesburg 22
Chicago 21
Orem 21
Woodbridge 21
Mexico City 20
Tianjin 20
Waanrode 20
Warsaw 20
Hebei 19
Milan 19
Nuremberg 19
Turku 19
Falkenstein 18
Pune 18
Rio de Janeiro 18
Shenyang 18
Brooklyn 17
Montreal 17
Falls Church 16
London 16
Redwood City 16
Denver 15
Chennai 14
Lawrence 14
Phoenix 14
Poplar 14
San Francisco 14
Tokyo 14
Ann Arbor 13
Kunming 13
Stockholm 13
Ankara 12
Boardman 12
Changsha 12
Rome 12
Toronto 12
Haiphong 11
Jiaxing 11
Houston 10
Brasília 9
Da Nang 9
Frankfurt am Main 9
Asunción 8
Dong Ket 8
São Gonçalo 8
Charlotte 7
Curitiba 7
Guangzhou 7
Kochi 7
Kronberg 7
Pompei 7
Porto Alegre 7
Quito 7
Salerno 7
Sarno 7
Shanghai 7
Belo Horizonte 6
Manchester 6
Salvador 6
Tashkent 6
Washington 6
Baghdad 5
Brescia 5
Calgary 5
Totale 5.469
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Nome #
Identificazione di tre nuove mutazioni del gene LKB1/STK11 associate all’insorgenza della syndrome di Peutz-Jeghers. 153
Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome. 141
Analisi quantitativa dell’espressione di un nuovo trascritto del gene APC nel corso del differenziamento e della tumorigenesi colorettale 139
Dyskerin Downregulation Can Induce ER Stress and Promote Autophagy via AKT-mTOR Signaling Deregulation 128
Identificazione di una delezione intragenica del gene LKB1/STK11 in un soggetto affetto da sindrome di Peutz-Jeghers mediata da sequenze Alu 127
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 122
Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana 120
Alteration of the tumor suppressor PTEN induce beta catenin accumulation and attivation of pro-inflammatory and cell survival signals in PTEN hamartoma tumor syndrome patients 119
Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript 118
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 118
Interleukin-10 receptor down-expression in early-onset inflammatory bowel disease: a case-report 118
Expression of truncated spliced variants of adenomatous polyposis coli gene is modulated by nonsense-mediated deay 118
Evidence for coupling of alternative splicing and nonsense-mediated mRNA decay in the regulation of a new APC transcript bearing nonsense codon 114
Identification of nine novel APC transcript: Enhanced Expression o the truncated APC Transcript Includine a Novel Exon during Colon Carcinogenesis 113
Lithium chloride increases sensitivity to photon irradiation treatment in primary mesenchymal colon cancer cells 112
“Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana” 110
The Benefits of Water from Nitrodi’s Spring: The In Vitro Studies Leading the Potential Clinical Applications 109
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 108
Identification of a novel exon in the APC gene and novel APC transcripts derived from alternative and aberrant splicing 106
“Analisi molecolare del gene STK11 in 10 so9getti affetti da Sindrome di Peutz-Jeghers”. 105
Mutazioni germinali nel gene APC in pazienti argentini affetti da FAP. 105
A novel Mbo II polymorphism in exon 15 of the human adenomatous polyposis coli gene 104
The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue 104
Mir-137 targets the 3′ untranslated region of msh2: Potential implications in lynch syndrome-related colorectal cancer 104
CHIRURGIA ONCOLOGICA COLO-RETTALE DNA GUIDATA 103
Identificazione di splicing alternativi e splicing aberranti nella regione 5' del gene APC. 103
Identification of seven novel mutations in HNPCC Patients 103
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 103
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 103
Genetics, diagnosis and management of colorectal cancer (Review) 103
The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care 103
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis. 102
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the “PTENhamartoma tumor syndrome” 102
Growth-arrested dependence of aldolase A L-type mRNA expression in rodent cell lines. 101
Molecular diagnosis of the APC gene in 42 Argentinean FAP patients. 101
Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment 101
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype 101
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression 101
Genetic and Clinical Characterisation of Familial Adenomatous Polyposis: Populations Based Studies. 100
Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature 99
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 98
Colo-rectal cancer: Importance of molecular diagnosis for clinical approach 98
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 98
Basi molecolari del cancro colorettale ereditario non poliposico. 97
Identification of molecular defects responsible for Familial Adenomatous Polyposis. 97
Interleukin-10 Receptor Down-Expression in Early-Onset Inflammatory Bowel Disease: A Case-Report 96
Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome. 96
"Turcot syndrome: evidence for autosomal recessive inheritance". 95
Role of Alu-sequences in susceptibility to large genomic rearrangements in Southern Italian families with Lynch Syndrome 95
Molecular analysis of APC mutations in familial adenomatous polyposis 95
Regulation of aldolase a L-type mRNA expression in rodent cell lines during differentiation 95
Familial Adenomatosus Polyposis Coli: five novel mutation in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients 94
Inhibition of interleukin-6-induced matrix metalloproteinase-2 expression and invasive ability of lemon peel polyphenol extract in human primary colon cancer cells 94
A potential role of il-6/il-6r in the development and management of colon cancer 94
The Epithelial to Mesenchymal Transition in Colorectal Cancer Progression: The Emerging Role of Succinate Dehydrogenase Alterations and Succinate Accumulation 93
Identification of novel mutations in HNPCC patients 93
The molecular basis of familial adenomatous polyposis in 20 families from campania: an update 92
Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion 92
“Minor” mismatch repair genes involvement in genetic predisposition to lynch syndrome. 90
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 90
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 90
‘‘Minor’’ mismatch repair genes involvement in geneticpredisposition to Lynch sindrome 89
Genetics, diagnosis and treatment of lynch syndrome: Old lessons and current challenges (Review) 87
Evidence for autosomal recessive inheritanceof Turcot Syndrome 86
Expression of truncated spliced variants of adenomatous poliposis coli gene is modulated by nonsense-mediated decay 86
Association of "minor" mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer:probability of synergistic effects 86
Molecular defects in a Turcot family with autosomal recessive inheritance 86
Molecular Genetic Analysis of the Adenomatous Polyposis Coli (APC) Gene in Familial Polyposis Colorectal Cancer 86
Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis 86
Synergistic Effects of Low-Risk Variant Alleles in Cancer Predisposition 86
“New mutations in HNPCC families and protein expression in patients with high-frequency microsatellite instability” 85
Microsatellite instability in patients with early onset of colorectal. 85
Detection of compound heterozygous PMS2 gene mutations in a Turcot family 85
Association of ‘minor’mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer: probability of synergistic effects 85
Caratterizzazione molecolare di pazienti FAP negativi per mutazioni troncanti del gene APC 83
The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations. 82
Microsatellite instability in patients with early onset of colorectal. 82
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 82
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 82
LiCI inhibits cell growth of spheroid colon cancer cell cultures expressing CD133 and CD44v6 markers at the membrane level 82
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds. 81
“Evidence for autosomal recessive inheritanceof Turcot Syndrome” 81
MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer 81
Isolation and molecular characterization of primary epithelial-mesenchymal colon cancer cell cultures 80
Promising colorectal cancer biomarkers for precision prevention and therapy 80
Analisi molecolare dei geni “minori” del MisMatch Repair mediante DHPLC: identificazione di 15 nuove mutazioni. 79
REAL-TIME PCR QUANTIFICATION OF HUMAN DKC1 EXPRESSION IN COLORECTAL CANCER 78
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 78
Microsatellite instability in patients with early onset of colorectal 77
Genetica e cancro in Trattato di Chirurgia Oncologica 76
Novel Implications in Molecular Diagnosis of Lynch Syndrome 76
Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion 75
Molecular Analysis of Genes Responsible for Familial Adenomatous Polyposis and Hereditary Non Polyposis Colorectal Cancer 74
The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience. 73
DNA methylation and lack of MSH2 and MLH1 expression in patients with high-frequency microsatellite instability. , Suppl. 1, Vol. 85, No 5, 1999, p 86-87. 72
Chirurgia oncologica colo-rettale <> 72
Three submicroscopic delections at the APC locus and their rapid detection by quantitative-PCR analysis 70
Sporadic pediatric severe familial adenomatous polyposis: A case report 70
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds 68
Genetica e Cancro 68
Totale 9.546
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Categoria #
all - tutte 37.909
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 37.909
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021185 0 0 0 0 0 0 32 14 53 8 64 14
2021/2022901 21 1 4 5 11 97 19 22 134 85 238 264
2022/2023963 129 101 21 51 117 125 15 106 157 88 39 14
2023/2024539 30 103 69 42 26 67 11 47 5 8 77 54
2024/20253.475 203 233 24 41 143 156 335 217 192 335 1.298 298
2025/20264.102 731 373 751 654 1.345 208 40 0 0 0 0 0
Totale 11.442