IRIS
DE ROSA, MARINA
 Distribuzione geografica
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Continente #
NA - Nord America 4.705
AS - Asia 4.647
EU - Europa 3.740
SA - Sud America 557
Continente sconosciuto - Info sul continente non disponibili 236
AF - Africa 105
OC - Oceania 4
Totale 13.994
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Nazione #
US - Stati Uniti d'America 4.512
SG - Singapore 2.239
RU - Federazione Russa 1.648
VN - Vietnam 825
CN - Cina 807
IT - Italia 647
BR - Brasile 451
FR - Francia 370
HK - Hong Kong 343
DE - Germania 232
FI - Finlandia 178
IE - Irlanda 139
UA - Ucraina 136
NL - Olanda 118
CA - Canada 114
GB - Regno Unito 100
IN - India 84
JP - Giappone 74
BD - Bangladesh 60
MX - Messico 45
SE - Svezia 44
AR - Argentina 43
ZA - Sudafrica 30
TR - Turchia 27
CI - Costa d'Avorio 26
PL - Polonia 26
BE - Belgio 24
PH - Filippine 21
ES - Italia 20
ID - Indonesia 20
KR - Corea 20
IQ - Iraq 19
EC - Ecuador 18
TH - Thailandia 18
TW - Taiwan 16
PK - Pakistan 15
LT - Lituania 12
PY - Paraguay 12
AT - Austria 11
MA - Marocco 10
CL - Cile 7
CO - Colombia 7
SA - Arabia Saudita 7
VE - Venezuela 7
EG - Egitto 6
TN - Tunisia 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
DZ - Algeria 5
HN - Honduras 5
PE - Perù 5
AO - Angola 4
BB - Barbados 4
BG - Bulgaria 4
JM - Giamaica 4
KE - Kenya 4
LB - Libano 4
PS - Palestinian Territory 4
UY - Uruguay 4
BO - Bolivia 3
BS - Bahamas 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
HU - Ungheria 3
JO - Giordania 3
KZ - Kazakistan 3
LU - Lussemburgo 3
ME - Montenegro 3
MY - Malesia 3
NP - Nepal 3
RO - Romania 3
TT - Trinidad e Tobago 3
AM - Armenia 2
BY - Bielorussia 2
CH - Svizzera 2
CR - Costa Rica 2
CV - Capo Verde 2
ET - Etiopia 2
EU - Europa 2
IR - Iran 2
KW - Kuwait 2
LV - Lettonia 2
MD - Moldavia 2
NI - Nicaragua 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
TZ - Tanzania 2
XK - ???statistics.table.value.countryCode.XK??? 2
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AU - Australia 1
AW - Aruba 1
AZ - Azerbaigian 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BZ - Belize 1
CG - Congo 1
CU - Cuba 1
CY - Cipro 1
Totale 13.736
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Città #
Singapore 1.044
San Jose 657
Chandler 423
Moscow 416
Ashburn 328
Hong Kong 322
Beijing 289
Ho Chi Minh City 240
Hanoi 203
The Dalles 184
Santa Clara 178
Naples 167
Jacksonville 155
Dallas 143
Los Angeles 116
Lauterbourg 114
Princeton 106
Millbury 97
Amsterdam 96
Nanjing 83
Munich 76
Napoli 66
Tokyo 62
New York 61
Boston 59
Wilmington 58
Buffalo 55
São Paulo 52
Helsinki 49
Redondo Beach 46
Ottawa 39
Orem 38
Haiphong 37
Frankfurt am Main 33
Seattle 32
Atlanta 31
Da Nang 31
Nanchang 29
Des Moines 28
Norwalk 27
Hefei 26
Milan 26
Johannesburg 25
Dublin 24
Chicago 22
Mexico City 22
Montreal 22
Woodbridge 22
Council Bluffs 21
Nuremberg 20
Tianjin 20
Waanrode 20
Warsaw 20
Brooklyn 19
Hebei 19
London 19
Pune 19
Turku 19
Falkenstein 18
Rio de Janeiro 18
Shenyang 18
Toronto 18
Chennai 17
San Francisco 17
Denver 16
Falls Church 16
Phoenix 16
Redwood City 16
Houston 15
Rome 15
Lawrence 14
Poplar 14
Ann Arbor 13
Kunming 13
Stockholm 13
Ankara 12
Boardman 12
Changsha 12
Jiaxing 11
Asunción 9
Brasília 9
Bắc Giang 9
Thái Nguyên 9
Bangkok 8
Charlotte 8
Curitiba 8
Dong Ket 8
Guangzhou 8
Porto Alegre 8
Quito 8
Shanghai 8
São Gonçalo 8
Washington 8
Belo Horizonte 7
Biên Hòa 7
Kochi 7
Kronberg 7
Manchester 7
Pompei 7
Salerno 7
Totale 7.134
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Nome #
Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome. 176
Identificazione di tre nuove mutazioni del gene LKB1/STK11 associate all’insorgenza della syndrome di Peutz-Jeghers. 170
Analisi quantitativa dell’espressione di un nuovo trascritto del gene APC nel corso del differenziamento e della tumorigenesi colorettale 167
Lithium chloride increases sensitivity to photon irradiation treatment in primary mesenchymal colon cancer cells 163
Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana 152
Dyskerin Downregulation Can Induce ER Stress and Promote Autophagy via AKT-mTOR Signaling Deregulation 152
The Benefits of Water from Nitrodi’s Spring: The In Vitro Studies Leading the Potential Clinical Applications 150
Identificazione di una delezione intragenica del gene LKB1/STK11 in un soggetto affetto da sindrome di Peutz-Jeghers mediata da sequenze Alu 149
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 149
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 147
Interleukin-10 receptor down-expression in early-onset inflammatory bowel disease: a case-report 144
Expression of truncated spliced variants of adenomatous polyposis coli gene is modulated by nonsense-mediated deay 144
Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript 139
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 138
Genetic and Clinical Characterisation of Familial Adenomatous Polyposis: Populations Based Studies. 134
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the “PTENhamartoma tumor syndrome” 133
Identification of nine novel APC transcript: Enhanced Expression o the truncated APC Transcript Includine a Novel Exon during Colon Carcinogenesis 132
Genetics, diagnosis and management of colorectal cancer (Review) 132
Evidence for coupling of alternative splicing and nonsense-mediated mRNA decay in the regulation of a new APC transcript bearing nonsense codon 131
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 131
“Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana” 130
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 130
Identification of seven novel mutations in HNPCC Patients 129
Mutazioni germinali nel gene APC in pazienti argentini affetti da FAP. 129
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype 127
“Analisi molecolare del gene STK11 in 10 so9getti affetti da Sindrome di Peutz-Jeghers”. 126
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 126
Molecular diagnosis of the APC gene in 42 Argentinean FAP patients. 125
Identificazione di splicing alternativi e splicing aberranti nella regione 5' del gene APC. 124
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis. 124
The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care 124
A novel Mbo II polymorphism in exon 15 of the human adenomatous polyposis coli gene 123
The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue 123
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression 123
CHIRURGIA ONCOLOGICA COLO-RETTALE DNA GUIDATA 122
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 122
Mir-137 targets the 3′ untranslated region of msh2: Potential implications in lynch syndrome-related colorectal cancer 122
Interleukin-10 Receptor Down-Expression in Early-Onset Inflammatory Bowel Disease: A Case-Report 121
Growth-arrested dependence of aldolase A L-type mRNA expression in rodent cell lines. 119
Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment 119
Inhibition of interleukin-6-induced matrix metalloproteinase-2 expression and invasive ability of lemon peel polyphenol extract in human primary colon cancer cells 119
Basi molecolari del cancro colorettale ereditario non poliposico. 118
Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature 118
Identification of a novel exon in the APC gene and novel APC transcripts derived from alternative and aberrant splicing 117
Identification of molecular defects responsible for Familial Adenomatous Polyposis. 117
A potential role of il-6/il-6r in the development and management of colon cancer 117
Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome. 117
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 116
Identification of novel mutations in HNPCC patients 114
Molecular analysis of APC mutations in familial adenomatous polyposis 114
Colo-rectal cancer: Importance of molecular diagnosis for clinical approach 113
Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion 113
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 113
Genetics, diagnosis and treatment of lynch syndrome: Old lessons and current challenges (Review) 112
Synergistic Effects of Low-Risk Variant Alleles in Cancer Predisposition 111
Molecular defects in a Turcot family with autosomal recessive inheritance 110
Association of ‘minor’mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer: probability of synergistic effects 110
Familial Adenomatosus Polyposis Coli: five novel mutation in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients 109
Evidence for autosomal recessive inheritanceof Turcot Syndrome 109
The molecular basis of familial adenomatous polyposis in 20 families from campania: an update 109
“Minor” mismatch repair genes involvement in genetic predisposition to lynch syndrome. 108
Role of Alu-sequences in susceptibility to large genomic rearrangements in Southern Italian families with Lynch Syndrome 108
‘‘Minor’’ mismatch repair genes involvement in geneticpredisposition to Lynch sindrome 108
Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis 108
"Turcot syndrome: evidence for autosomal recessive inheritance". 107
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds. 106
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 106
Regulation of aldolase a L-type mRNA expression in rodent cell lines during differentiation 105
The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations. 104
Microsatellite instability in patients with early onset of colorectal. 104
Association of "minor" mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer:probability of synergistic effects 104
The Epithelial to Mesenchymal Transition in Colorectal Cancer Progression: The Emerging Role of Succinate Dehydrogenase Alterations and Succinate Accumulation 103
REAL-TIME PCR QUANTIFICATION OF HUMAN DKC1 EXPRESSION IN COLORECTAL CANCER 103
“New mutations in HNPCC families and protein expression in patients with high-frequency microsatellite instability” 103
Expression of truncated spliced variants of adenomatous poliposis coli gene is modulated by nonsense-mediated decay 103
Microsatellite instability in patients with early onset of colorectal. 103
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 103
Molecular Genetic Analysis of the Adenomatous Polyposis Coli (APC) Gene in Familial Polyposis Colorectal Cancer 102
Detection of compound heterozygous PMS2 gene mutations in a Turcot family 100
Promising colorectal cancer biomarkers for precision prevention and therapy 100
Analisi molecolare dei geni “minori” del MisMatch Repair mediante DHPLC: identificazione di 15 nuove mutazioni. 99
MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer 99
Microsatellite instability in patients with early onset of colorectal 98
LiCI inhibits cell growth of spheroid colon cancer cell cultures expressing CD133 and CD44v6 markers at the membrane level 98
Caratterizzazione molecolare di pazienti FAP negativi per mutazioni troncanti del gene APC 97
Germline mutations in the APC gene in 71 Argentinean patients with familial adenomatous polyposis syndrome: 14 novel mutations 97
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 97
Isolation and molecular characterization of primary epithelial-mesenchymal colon cancer cell cultures 97
“Evidence for autosomal recessive inheritanceof Turcot Syndrome” 95
Novel Implications in Molecular Diagnosis of Lynch Syndrome 95
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 93
Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion 91
Chirurgia oncologica colo-rettale <> 91
Sporadic pediatric severe familial adenomatous polyposis: A case report 89
Genetica e Cancro 88
Molecular Analysis of Genes Responsible for Familial Adenomatous Polyposis and Hereditary Non Polyposis Colorectal Cancer 88
Genetica e cancro in Trattato di Chirurgia Oncologica 86
Three submicroscopic delections at the APC locus and their rapid detection by quantitative-PCR analysis 85
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. 85
SALT-INDUCIBLE KINASE 1 MESSENGER ALTERATIONS ARE INVOLVED IN COLORECTAL TUMORIGENESIS 85
Totale 11.638
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Categoria #
all - tutte 46.078
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 46.078
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022880 0 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
2025/20266.565 731 373 751 654 1.345 208 749 313 756 482 110 93
2026/202789 73 16 0 0 0 0 0 0 0 0 0 0
Totale 13.994