IRIS
RANZANI, GUGLIELMINA
 Distribuzione geografica
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Continente #
NA - Nord America 2.831
EU - Europa 2.312
AS - Asia 1.482
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 3
OC - Oceania 1
Totale 6.636
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Nazione #
US - Stati Uniti d'America 2.795
CN - Cina 1.454
IE - Irlanda 648
UA - Ucraina 456
FI - Finlandia 300
DE - Germania 245
IT - Italia 222
SE - Svezia 188
GB - Regno Unito 128
FR - Francia 77
CA - Canada 36
BE - Belgio 29
JP - Giappone 16
RU - Federazione Russa 8
EU - Europa 7
NL - Olanda 5
IN - India 4
SG - Singapore 4
GR - Grecia 3
MU - Mauritius 3
IR - Iran 2
AU - Australia 1
CZ - Repubblica Ceca 1
EE - Estonia 1
HK - Hong Kong 1
MY - Malesia 1
PL - Polonia 1
Totale 6.636
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Città #
Chandler 662
Dublin 648
Jacksonville 504
Nanjing 428
Beijing 173
Nanchang 160
Ashburn 155
Ann Arbor 131
Lawrence 125
Medford 125
Princeton 125
Shenyang 118
Hebei 117
Wilmington 111
Jiaxing 105
Boardman 99
Changsha 87
Helsinki 78
Tianjin 64
Shanghai 59
Hangzhou 54
Pavia 52
Milan 46
Woodbridge 40
Verona 35
Toronto 34
Brussels 28
New York 26
Norwalk 24
Houston 21
Fairfield 17
Tokyo 16
Los Angeles 13
Seattle 12
Auburn Hills 11
Chicago 10
Des Moines 10
Kunming 10
Zhengzhou 10
Latina 9
Dearborn 8
Jinan 8
Falls Church 6
Ningbo 5
Taizhou 5
Tappahannock 5
Guangzhou 4
Lanzhou 4
Rome 4
San Francisco 4
Singapore 4
Washington 4
Berlin 3
Catania 3
Florence 3
Urbino 3
Ansbach 2
Ardabil 2
Asti 2
Beregazzo con Figliaro 2
Bologna 2
Borås 2
College Park 2
Como 2
Fuzhou 2
Gunzenhausen 2
Noale 2
Padova 2
Parma 2
Pesaro 2
Redmond 2
Redwood City 2
Shenzhen 2
Torino 2
Almere Stad 1
Amsterdam 1
Bathgate 1
Blainville 1
Brno 1
Busto Arsizio 1
Cagliari 1
Cambridge 1
Canberra 1
Changchun 1
Chongqing 1
Comiso 1
Esslingen am Neckar 1
Fairfax 1
Falkenstein 1
Gallarate 1
Gandhi Nagar 1
Geislingen an der Steige 1
Groningen 1
Haikou 1
Hefei 1
Kemerovo 1
L'aquila 1
Las Vegas 1
London 1
Monza 1
Totale 4.687
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Nome #
Caratterizzazione funzionale di mutazioni del gene MYH associate a poliposi adenomatosa familiare del colon. 113
Caratterizzazione citogenetico-molecolare di estese delezioni di APC in pazienti con poliposi 105
Analysis and clinical implications of p53 gene mutations and human papillomavirus type 16 and 18 infection in primary adenocarcinoma of the uterine cervix 101
“COMBING” DI SINGOLE MOLECOLE DI DNA PER IDENTIFICARE RIARRANGIAMENTI DEL LOCUS APC UMANO 101
Molecular-cytogenetic characterization of APC (Adenomatous Polyposis Coli) gene deletions by means of “DNA combing” 77
Ricerca di mutazioni del gene MYH in pazienti con poliposi attenuata ed in soggetti di controllo, italiani e greci. 76
Caratterizzazione di delezioni del gene APC in pazienti con poliposi adenomatosa familiare del colon 76
Understanding the role of the Q338H MUTYH variant in oxidative damage repair. 75
Effects of topoisomerase II inhibitors on gastric cancer cells characterized by different genetic lesions 74
Characterization of mutations in the base excision repair MYH (MUTYH) gene associated with familial adenomatous polyposis. 74
Analysis and clinical implications of K-ras gene mutations and infection with human papillomavirus types 16 and 18 in primary adenocarcinoma of the uterine cervix 74
MUTYH mutations associated with familial adenomatous polyposis: functional characterization by a mammalian cell-based assay 74
Oxycodone pain management in cytochrome p450-impaired patients. 74
CARATTERIZZAZIONE CITOGENETICO-MOLECOLARE DI DELEZIONI DEL GENE APC (ADENOMATOUS POLYPOSIS COLI) MEDIANTE “DNA COMBING” 71
How and why to screen for CYP2D6 interindividual variability in patients under pharmacological treatments 71
Elevata espressione costitutiva di un trascritto del gene APC dovuto a splicing alternativo tra gli esoni 10 e 15 in pazienti con poliposi. 70
K-ras gene mutations: an unfavorable prognostic marker in stage I lung adenocarcinoma 68
Shifts of Faecal Microbiota During Sporadic Colorectal Carcinogenesis 67
Microsatellite instability in intestinal- and diffuse-type gastric carcinoma 64
Cytokine gene polymorphisms in gastric cancer patients from two Italian areas at high and low cancer prevalence 64
Cancer incidence in eastern Adriatic isolates, Croatia: examples from the islands of Krk, Cres, Losinj, Rab and Pag 64
APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations 64
Oxidative DNA damage drives carcinogenesis in MUTYH-associated-polyposis by specific mutations of mitochondrial and MAPK genes. 64
A study of ten red cell enzymatic markers in the Naples' population. Report of a new GPT variant phenotype. 63
The polymorphism of red cell uridine monophosphate kinase in two samples of the Italian population 63
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis 63
Analysis and clinical implications of p53 gene mutations and human papillomavirus type 16 and 18 infection in primary adenocarcinoma of the uterine cervix. 62
Rapid assessment of replication error phenotype in gastric cancer 62
Loss of heterozygosity and K-ras gene mutations in gastric cancer 62
A study of several genetic biochemical markers in Sherpas with description of some variant phenotypes 62
Analisi mediante MLPA del gene APC in pazienti italiani e greci con diagnosi di poliposi attenuata. 62
Gut Microbiota Analysis in Postoperative Lynch Syndrome Patients 62
Intraductal papillary-mucinous tumours represent a distinct group of pancreatic neoplasms: an investigation of tumour cell differentiation and K-ras, p53 and c-erbB-2 abnormalities in 26 patients. 61
Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach. 61
Molecular combing for the detection of rearrangements involving the human APC locus 61
Functional analysis and case-control study of -160C/A polymorphism in the E-cadherin gene promoter: association with cancer risk 61
Genetic variability at COMT but not at OPRM1 and UGT2B7 loci modulates morphine analgesic response in acute postoperative pain. 61
A novel endonuclease of human cells specific for single-stranded DNA 61
F-Cell distribution in normals and in Heterocellular HPFH (Swiss Type) 61
Intestinal and diffuse gastric cancers arise in a different background of Helicobacter pylori gastritis through different gene involvement 60
Red cell and serum polymorphisms in the Oltrepò Pavese population (northern Italy) 60
A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. 60
Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome. 60
Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition 60
Genetic events in sporadic colorectal adenomas; K-ras and p53 heterozygous mutations are not sufficient for malignant progression 60
Genetica molecolare dei tumori e nuovi approcci terapeutici. 59
Involvement of MYH in colorectal polyposis: where are we? 59
p53 codon 72 polymorphism does not affect the risk of cervical cancer in patients from northern Italy 59
Genetics of colorectal polyps 59
Frameshift mutations of human gastrin receptor gene (hGARE) in gastrointestinal cancers with microsatellite instability 59
Primary retroperitoneal mucinous cystoadenocarcinomas: an immunohistochemical and molecular study 59
APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes 58
Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis 58
Ki-ras and p53 gene mutations in pancreatic ductal carcinoma: a relationship with tumor phenotype and survival 56
Influence of COMT Val158Met Polymorphism on Alzheimer's Disease and Mild Cognitive Impairment in Italian Patients. 56
K-ras and p53 gene mutations in pancreatic cancer: ductal and nonductal tumors progress through different genetic lesions 56
Somatic frameshift mutations in the Bloom syndrome BLM gene are frequent in sporadic gastric carcinomas with microsatellite mutator phenotype 56
Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumors 55
Subtyping of phosphoglucomutase locus 1 (PGM1) polymorphism in some populations of Rwanda: description of variant phenotypes, "haplotype" frequencies, and linkage disequilibrium data 55
Surname as 'cancer risk' in extreme isolates: example from the island of Lastovo, Croatia 55
Colorectal Adenomatous Polyposis: Heterogeneity of Susceptibility Gene Mutations and Phenotypes in a Cohort of Italian Patients 55
Absence of microsatellite instability in breast carcinomas with both p53 and c-erbB-2 alterations 54
Red cell glyoxalase I polymorphism in Italians. Report of a variant phenotype 54
A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype 54
Effect of apoptogenic stimuli on colon carcinoma cell lines with a different c-myc expression level 53
MUTYH-associated polyposis (MAP), the syndrome implicating Base Excision Repair in inherited predisposition to colorectal tumors 53
Oxidative damage repair and protein-protein interactions of the Q338H MUTYH polymorphic variant 53
Heterogeneous protooncogene amplification correlates with tumor progression and presence of metastases in gastric cancer patients 52
The polymorphism of red cell esterase D in Italy 52
An analysis of red cell enzymatic markers in the province of Bologna (Italy) 52
Genetic pattern, histological structure, and cellular phenotype in early and advanced gastric cancers: evidence for structure-related genetic subsets and for loss of glandular structure during progression of some tumors 52
Microsatellite instability and mutations of p53 and TGF-beta RII genes in gastric cancer 51
Study on aneuploidy and p53 mutations in astrocytomas 51
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH 51
Molecular mechanisms involved in the pathogenesis of gastric carcinoma: interactions between genetic alterations, cellular phenotype and cancer histotype 51
A study of several red cell enzyme markers in two samples of the Italian population. Report of new CA1 and PGD variant phenotypes 49
Understanding the role of a polymorphic MUTYH variant in oxidative damage repair 49
Morphine metabolism, transport and brain disposition 49
High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis 49
Study of the c-Ha-ras-1 locus polymorphism in an Italian population with high incidence of gastric cancer 48
The significance of p53 mutations in human cancers 48
Population genetic studies in Sikkim 48
Predisposizione genetica ai tumori 48
Drug transporters and renal drug disposition in the newborn 48
Individualizing pain therapy with opioids: The rational approach based on pharmacogenetics and pharmacokinetics 48
p53 gene mutations and protein nuclear accumulation are early events in intestinal type gastric cancer but late events in diffuse type 48
DNA amplification in human gastric carcinomas 47
Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes 47
DNA sequences amplified in cancer cells: an interface between tumor biology and human genome analysis 47
Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer 46
Detection of a CDH1 rare transcript variant in fresh-frozen gastric cancer tissues by chip-based digital PCR 46
Gene amplification and proliferative kinetics in relation to prognosis of patients with gastric carcinoma 45
Digital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer 44
Multigene Panel Testing Increases the Number of Loci Associated with Gastric Cancer Predisposition 44
Subtyping of human red cell phosphoglucomutase locus 1 (PGM1) polymorphism: a third PGM1(1) allele common among Twa Pygmies from North Rwanda 43
Constitutional high expression of an APC mRNA isoform in a subset of attenuated familial adenomatous polyposis patients 43
A 5'-truncated c-myc gene variant not associated with a risk of cancer 43
Interindividual variability of drug transporters: impact on opioid treatment in chronic renal failure 42
E-cadherin downregulation and microRNAs in sporadic intestinal-type gastric cancer 42
Geni oncosoppressori e tumori ereditari 41
Totale 5.908
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Categoria #
all - tutte 24.421
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 24.421
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.741 496 666 5 89 8 91 3 119 4 137 117 6
2020/2021785 89 70 27 83 10 104 3 120 39 109 107 24
2021/2022617 4 8 37 20 12 24 15 49 39 18 81 310
2022/20231.870 201 131 21 148 209 193 2 111 768 15 42 29
2023/2024579 89 117 17 56 52 116 4 49 8 11 21 39
2024/202522 22 0 0 0 0 0 0 0 0 0 0 0
Totale 6.731