DE ROSA, MARINA
 Distribuzione geografica
Continente #
NA - Nord America 2.158
EU - Europa 1.362
AS - Asia 733
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 4.281
Nazione #
US - Stati Uniti d'America 2.120
IT - Italia 551
SG - Singapore 409
CN - Cina 283
FR - Francia 199
IE - Irlanda 134
UA - Ucraina 119
FI - Finlandia 110
NL - Olanda 95
DE - Germania 63
CA - Canada 38
SE - Svezia 29
GB - Regno Unito 28
CI - Costa d'Avorio 25
IN - India 25
BE - Belgio 21
VN - Vietnam 8
TR - Turchia 6
CH - Svizzera 2
CZ - Repubblica Ceca 2
ES - Italia 2
EU - Europa 2
LU - Lussemburgo 2
ME - Montenegro 2
AU - Australia 1
HK - Hong Kong 1
IR - Iran 1
MD - Moldavia 1
RO - Romania 1
RU - Federazione Russa 1
Totale 4.281
Città #
Chandler 423
Singapore 348
Jacksonville 153
Naples 133
Santa Clara 112
Princeton 106
Millbury 97
Nanjing 83
Amsterdam 82
Ashburn 67
Napoli 66
Beijing 61
Wilmington 58
Boston 48
Ottawa 35
Nanchang 29
Des Moines 27
Norwalk 26
Woodbridge 21
Waanrode 20
Dublin 19
Hebei 19
Pune 18
Shenyang 18
Falls Church 16
Redwood City 16
Lawrence 14
Milan 14
Ann Arbor 13
Seattle 13
Tianjin 13
Changsha 12
Kunming 12
Boardman 11
Jiaxing 11
Rome 10
Dong Ket 8
Kronberg 7
Pompei 7
Sarno 7
Los Angeles 6
Brescia 5
Fairfield 5
Hangzhou 5
Montecorvino Rovella 5
Orange 5
Portici 5
Redmond 5
Salerno 5
Washington 5
Cardito 4
Casalnuovo di Napoli 4
Changchun 4
Ercolano 4
Falerna 4
Menlo Park 4
Pozzuoli 4
Campoli del Monte Taburno 3
Lanzhou 3
Oristano 3
Piemonte 3
San Giorgio A Cremano 3
Verona 3
Acerenza 2
Belfast 2
Bern 2
Caserta 2
Castellammare Di Stabia 2
Clifton 2
Cusano Mutri 2
Dallas 2
Eboli 2
Edinburgh 2
Helsinki 2
Houston 2
Lappeenranta 2
Legnano 2
Luxembourg 2
Marano di Napoli 2
Ningbo 2
Nola 2
Podgorica 2
Prague 2
Procida 2
San Francisco 2
Shanghai 2
Toronto 2
Torre Annunziata 2
Villaricca 2
Alvignano 1
Andover 1
Arezzo 1
Ariano Irpino 1
Augusta 1
Bacoli 1
Bergamo 1
Brindisi 1
Brussels 1
Busto Arsizio 1
Caivano 1
Totale 2.413
Nome #
Identificazione di tre nuove mutazioni del gene LKB1/STK11 associate all’insorgenza della syndrome di Peutz-Jeghers. 94
Analisi quantitativa dell’espressione di un nuovo trascritto del gene APC nel corso del differenziamento e della tumorigenesi colorettale 73
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 64
Dyskerin Downregulation Can Induce ER Stress and Promote Autophagy via AKT-mTOR Signaling Deregulation 62
Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome. 60
CHIRURGIA ONCOLOGICA COLO-RETTALE DNA GUIDATA 57
Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript 57
Genetics, diagnosis and management of colorectal cancer (Review) 55
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 52
Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature 50
The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care 50
Lithium chloride increases sensitivity to photon irradiation treatment in primary mesenchymal colon cancer cells 50
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 49
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype 49
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression 49
Familial Adenomatosus Polyposis Coli: five novel mutation in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients 48
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 47
Identificazione di una delezione intragenica del gene LKB1/STK11 in un soggetto affetto da sindrome di Peutz-Jeghers mediata da sequenze Alu 47
Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana 47
The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue 47
Interleukin-10 receptor down-expression in early-onset inflammatory bowel disease: a case-report 46
MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer 46
“Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana” 45
A novel Mbo II polymorphism in exon 15 of the human adenomatous polyposis coli gene 44
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis. 42
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 42
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 42
Evidence for coupling of alternative splicing and nonsense-mediated mRNA decay in the regulation of a new APC transcript bearing nonsense codon 41
The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations. 40
“Analisi molecolare del gene STK11 in 10 so9getti affetti da Sindrome di Peutz-Jeghers”. 40
Mutazioni germinali nel gene APC in pazienti argentini affetti da FAP. 40
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 40
Identification of a novel exon in the APC gene and novel APC transcripts derived from alternative and aberrant splicing 39
Caratterizzazione molecolare di pazienti FAP negativi per mutazioni troncanti del gene APC 39
Association of "minor" mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer:probability of synergistic effects 39
Chirurgia oncologica colo-rettale <> 39
Interleukin-10 Receptor Down-Expression in Early-Onset Inflammatory Bowel Disease: A Case-Report 39
A potential role of il-6/il-6r in the development and management of colon cancer 39
Identificazione di splicing alternativi e splicing aberranti nella regione 5' del gene APC. 38
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 38
Colo-rectal cancer: Importance of molecular diagnosis for clinical approach 38
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome 38
A novel MboII polymorphism in exon 15 of the human adenomatous polyposis coli gene. 37
Molecular diagnosis of the APC gene in 42 Argentinean FAP patients. 37
Identification of nine novel APC transcript: Enhanced Expression o the truncated APC Transcript Includine a Novel Exon during Colon Carcinogenesis 37
The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience. 37
Mir-137 targets the 3′ untranslated region of msh2: Potential implications in lynch syndrome-related colorectal cancer 37
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds 36
Basi molecolari del cancro colorettale ereditario non poliposico. 36
Identification of seven novel mutations in HNPCC Patients 36
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the “PTENhamartoma tumor syndrome” 36
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 36
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 36
Inhibition of interleukin-6-induced matrix metalloproteinase-2 expression and invasive ability of lemon peel polyphenol extract in human primary colon cancer cells 36
Identification of novel mutations in HNPCC patients 35
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 35
Genetic and Clinical Characterisation of Familial Adenomatous Polyposis: Populations Based Studies. 35
Microsatellite instability in patients with early onset of colorectal. 35
Three submicroscopic delections at the APC locus and their rapid detection by quantitative-PCR analysis 34
Genetics, diagnosis and treatment of lynch syndrome: Old lessons and current challenges (Review) 34
Cell-cycle dependence of aldolase A L-type mRNA expression in rodents cell lines 34
Identification of molecular defects responsible for Familial Adenomatous Polyposis. 34
“Minor” mismatch repair genes involvement in genetic predisposition to lynch syndrome. 34
Familial adenomatous polyposis coli: five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients. Mutations in brief no. 225. Online 33
Analisi molecolare dei geni “minori” del MisMatch Repair mediante DHPLC: identificazione di 15 nuove mutazioni. 33
Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion 33
Isolation and molecular characterization of primary epithelial-mesenchymal colon cancer cell cultures 33
Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation. 33
The Mutation Spectrum of the APC Gene in FAP Patients from Southern Italy: Detection of Known and Four Novel Mutations 32
Microsatellite instability in patients with early onset of colorectal. 32
Detection of compound heterozygous PMS2 gene mutations in a Turcot family 32
"Turcot syndrome: evidence for autosomal recessive inheritance". 32
Association of ‘minor’mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer: probability of synergistic effects 31
Autophagy genes variants and pediatric Crohn's disease phenotype: a single-center experience. 31
LiCI inhibits cell growth of spheroid colon cancer cell cultures expressing CD133 and CD44v6 markers at the membrane level 31
REAL-TIME PCR QUANTIFICATION OF HUMAN DKC1 EXPRESSION IN COLORECTAL CANCER 30
Three novel germline mutations in the adenomatous polyposis coli gene. 30
The molecular basis of familial adenomatous polyposis in 20 families from campania: an update 30
Growth-arrested dependence of aldolase A L-type mRNA expression in rodent cell lines. 29
Evidence for a recessive inheritance of Turcot’s syndrome caused by compound heterozygous mutations within the PMS2 gene 29
"Colo-rectal cancer: importance of Molecular Analysis for clinical approach". 29
“New mutations in HNPCC families and protein expression in patients with high-frequency microsatellite instability” 29
Role of Alu-sequences in susceptibility to large genomic rearrangements in Southern Italian families with Lynch Syndrome 29
Expression of truncated spliced variants of adenomatous polyposis coli gene is modulated by nonsense-mediated deay 29
Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment 29
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome 29
Novel MSH2 splice-site mutation in a young patient with Lynch syndrome 29
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds. 28
Molecular Genetic Analysis of the Adenomatous Polyposis Coli (APC) Gene in Familial Polyposis Colorectal Cancer 28
Regulation of aldolase a L-type mRNA expression in rodent cell lines during differentiation 28
Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis 28
Novel Implications in Molecular Diagnosis of Lynch Syndrome 28
The Epithelial to Mesenchymal Transition in Colorectal Cancer Progression: The Emerging Role of Succinate Dehydrogenase Alterations and Succinate Accumulation 27
Molecular defects in a Turcot family with autosomal recessive inheritance 27
Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome. 27
Genetica e Cancro 26
Expression of truncated spliced variants of adenomatous poliposis coli gene is modulated by nonsense-mediated decay 26
“Genetic and Clinical Characterisation of Familial Adenomatous Polyposis: Populations Based Studies”. 26
Promising colorectal cancer biomarkers for precision prevention and therapy 26
Sporadic pediatric severe familial adenomatous polyposis: A case report 26
Totale 3.836
Categoria #
all - tutte 20.263
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 20.263


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020218 0 0 0 0 39 15 2 7 7 25 53 70
2020/2021423 21 27 46 44 45 55 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
2024/2025644 203 233 24 41 143 0 0 0 0 0 0 0
Totale 4.509