IRIS
IZZO, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 4.058
EU - Europa 2.956
AS - Asia 1.253
AF - Africa 50
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 4
Totale 8.325
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Nazione #
US - Stati Uniti d'America 3.987
IT - Italia 1.231
SG - Singapore 633
CN - Cina 537
UA - Ucraina 411
FR - Francia 304
FI - Finlandia 230
DE - Germania 213
IE - Irlanda 191
NL - Olanda 178
SE - Svezia 93
CA - Canada 71
GB - Regno Unito 62
CI - Costa d'Avorio 49
IN - India 36
VN - Vietnam 28
BE - Belgio 19
CZ - Repubblica Ceca 10
TR - Turchia 7
CH - Svizzera 5
ES - Italia 4
EU - Europa 4
HK - Hong Kong 4
IR - Iran 3
BR - Brasile 2
CL - Cile 2
KR - Corea 2
SM - San Marino 2
LY - Libia 1
ME - Montenegro 1
MY - Malesia 1
PH - Filippine 1
PL - Polonia 1
RO - Romania 1
TW - Taiwan 1
Totale 8.325
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Città #
Chandler 714
Singapore 513
Jacksonville 458
Princeton 227
Millbury 210
Napoli 208
Naples 194
Amsterdam 164
Nanjing 159
Wilmington 129
Beijing 117
Ashburn 110
Santa Clara 110
Boston 102
Cagliari 84
Ottawa 67
Nanchang 62
Norwalk 50
Des Moines 35
Falls Church 34
Shenyang 32
Woodbridge 32
Dublin 30
Dong Ket 28
Hebei 28
Boardman 25
Tianjin 24
Pune 23
Changsha 22
Jiaxing 22
Rome 22
Ann Arbor 21
Kronberg 21
Kunming 21
Redwood City 21
Milan 18
Seattle 18
Waanrode 18
Lawrence 15
Cardito 14
Formia 13
Caserta 12
Orange 11
Washington 11
Hangzhou 10
Los Angeles 10
Redmond 9
Sarno 9
Turin 9
Dearborn 8
Brno 7
Houston 7
Pozzuoli 7
Shanghai 7
Fairfield 6
Gavirate 6
Lanzhou 6
Munich 6
Salerno 6
Casalnuovo Di Napoli 5
Giugliano In Campania 5
Montecorvino Rovella 5
Nürnberg 5
Parabiago 5
Portici 5
Postiglione 5
Brescia 4
Castellammare Di Stabia 4
Changchun 4
Dallas 4
Fremont 4
Indiana 4
Potenza 4
Reggio Calabria 4
San Giorgio A Cremano 4
Sant'antonio Abate 4
Simi Valley 4
Bacoli 3
Campoli del Monte Taburno 3
Catanzaro 3
Chicago 3
Chieti 3
Edinburgh 3
Gothenburg 3
Helsinki 3
Hong Kong 3
Maddaloni 3
Ningbo 3
Nola 3
Oristano 3
Palermo 3
Perugia 3
Prague 3
Sammichele Di Bari 3
San Francisco 3
Springfield 3
Verona 3
Altamura 2
Ardabil 2
Augusta 2
Totale 4.507
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Nome #
Biochimica del pancreas 148
ALLELE-SPECIFIC TRANSCRIPTIONAL ACTIVITY OF THE VARIABLE NUMBER OF TANDEM REPEATS OF THE INDUCIBLE NITRIC OXIDE SYNTHASE GENE IS ASSOCIATED WITH IDIOPATHIC ACHALASIA 103
Basi molecolari delle emoglobinopatie ed approcci diagnostici attraverso le metodologie del DNA ricombinante 94
Identificazione di tre nuove mutazioni del gene LKB1/STK11 associate all’insorgenza della syndrome di Peutz-Jeghers. 89
Analisi molecolare del gene della poliposi adenomatosa del colon (APC) in pazienti affetti da poliposi adenomatosa familiare /FAP): diagnosi presintomatica nelle famiglie a rischio 82
GATA-1 isoforms differently contribute to the production and compartmentation of reactive oxygen species in the myeloid leukemia cell line K562 79
Il promotore distale del gene dell'aldolasi A è regolato da un repressore trascrizionale (p97) 78
Analisi quantitativa dell’espressione di un nuovo trascritto del gene APC nel corso del differenziamento e della tumorigenesi colorettale 70
Correlazione tra mutanti del fattore trascrizionale GATA-1 e livelli di espressione della proteina del tumore di Wilms in neonati con sindrome di Down affetti da disordine mieloproliferativo transitorio. 69
Molecular Basis of Thalassemia 69
L'arginina metiltransferasi PRMT5 partecipa alla repressione trascrizionale del gene dell'aldolasi A umana mediata dalla "zinc-finger protein" ZNF224 67
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 62
Differential expression and cellular localization of ZNF224 and ZNF255, two isoforms of the Kruppel-like zinc-finger protein family 60
A sporadic case of hemophilia A detected by RFLP analysis 57
Over-Expressed GATA-1S, the Short Isoform of the Hematopoietic Transcriptional Factor GATA-1, Inhibits Ferroptosis in K562 Myeloid Leukemia Cells by Preventing Lipid Peroxidation 56
Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome. 56
Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript 55
Genetics, diagnosis and management of colorectal cancer (Review) 54
CHIRURGIA ONCOLOGICA COLO-RETTALE DNA GUIDATA 53
ZNF224: Structure and role of a multifunctional KRAB-ZFP protein 52
The Kruppel-like zinc-finger protein ZNF224 represses aldolase A gene transcription by interacting with the KAP-1 co-repressor protein 51
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 51
WT1-mediated repression of the proapoptotic transcription factor ZNF224 is triggered by the BCR-ABL oncogene 51
Cloning of several cDNA segments coding for human liver proteins. 49
Biochemical and functional interaction between ZNF224 and ZNF255, two members of the Kruppel-like zinc-finger protein family and WT1 protein isoforms. 49
The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care 49
Hb Federico II, a novel haemoglobin variant (beta 106 Leu->Val) associated with a beta thalassemia phenotype. 48
ZNF 224, a novel KRAB-zinc finger protein represses transcription through functional interaction with the corepressor KAP-1. 47
Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases 47
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 47
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression 47
Identification of a transcriptional factor involved in gamma globin gene expression 46
Familial Adenomatosus Polyposis Coli: five novel mutation in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients 46
A proteomic approach for the identification of ZNF224 interacting partners 46
Analisi molecolare e correlazioni genotipo-fenotipo per la consulenza genetica delle emoglobinopatie 46
Identificazione di una delezione intragenica del gene LKB1/STK11 in un soggetto affetto da sindrome di Peutz-Jeghers mediata da sequenze Alu 46
Meccanismi molecolari coinvolti nella trasformazione leucemica in disordini mieloproliferativi transitori. 46
Characterization of a silencer that modulates transcription of the human distal aldolase A promoter 45
A novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications 45
Screening of families with adenomatous polyposis syndrome in Campania: experience of five years 45
Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana 45
The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue 45
A novel zinc finger transcriptional repressor, ZNF224, interacts with the negative regulatory element (AldA-NRE) and inhibits gene expression 44
“Una nuova mutazione nel gene STK11 è associate all’insorgenza della syndrome di peutz-Jeghers in una famiglia campana” 44
Interleukin-10 receptor down-expression in early-onset inflammatory bowel disease: a case-report 44
Lithium chloride increases sensitivity to photon irradiation treatment in primary mesenchymal colon cancer cells 44
The Kruppel like zinc finger protein,ZNF224, is a novel trascriptional co-regulator of WT1 44
A sporadic case of hemophilia A detected by RFLP analysis 43
A unique origin for the Sicilian (__)°-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysis. 43
Functional characterization and expression of ZNF224, a novel KRAB-ZNF transcriptional repressor. 43
Clinical and anamnestic evaluation rôle for the diagnosis and treatment of families affected by Lynch syndrome. Case report and review of the literature 43
Carrier detection of hemophilia A and B 42
MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer 42
Transfer RNA methyltransferases: properties and role in the maturation of tRNA 41
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis. 41
WT1 and its molecular partners modulate bag3 gene expression 41
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 41
Andamento dei livelli di GATA-1 e WT-1 in corso di emopatie pediatriche 41
Aldolase gene and protein families: structure, expression and pathophysiology. 40
Cold shock domain protein A (CSDA) acts as repressor factor of gamma globin gene expression in vivo. 40
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 40
BCR-ABL decreases expression of the proapoptotic factor ZNF224 via the PI3K-Akt signalling pathway 40
The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations. 39
“Analisi molecolare del gene STK11 in 10 so9getti affetti da Sindrome di Peutz-Jeghers”. 39
Mutazioni germinali nel gene APC in pazienti argentini affetti da FAP. 39
Evidence for coupling of alternative splicing and nonsense-mediated mRNA decay in the regulation of a new APC transcript bearing nonsense codon 39
Role of GATA-1 isoforms in transient mieloproliferative disease associated with Down Syndrome 39
Chirurgia oncologica colo-rettale <> 39
A novel Mbo II polymorphism in exon 15 of the human adenomatous polyposis coli gene 39
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 39
Detection of four novel mutations in the iduronate-2-sulphatase gene 38
Identification of a novel exon in the APC gene and novel APC transcripts derived from alternative and aberrant splicing 38
Caratterizzazione molecolare di pazienti FAP negativi per mutazioni troncanti del gene APC 38
A novel Mediterranean “delta-beta thalassemia” phenotype due to a complex combination of three globin gene mutations. 38
Association of "minor" mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer:probability of synergistic effects 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
Identificazione di splicing alternativi e splicing aberranti nella regione 5' del gene APC. 37
The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience. 37
Detection of new mutations in hMLH1 gene in five out of ten Italian Hereditary Non Polyposis Colorectal Cancer (HNPCC) families 37
Interleukin-10 Receptor Down-Expression in Early-Onset Inflammatory Bowel Disease: A Case-Report 37
Colo-rectal cancer: Importance of molecular diagnosis for clinical approach 37
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds 36
A new human species of aldolase A mRNA from fibroblasts 36
Molecular diagnosis of the APC gene in 42 Argentinean FAP patients. 36
Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors 36
A potential role of il-6/il-6r in the development and management of colon cancer 36
Diagnosi di malattie genetiche: emofilia A e B 35
A rare case of compound heterozygosity for d+ thalassemia and Hb Neapolis (Dhonburi) associated with an atypical b-thalassemia phenotype. 35
Identification of seven novel mutations in HNPCC Patients 35
Identification of nine novel APC transcript: Enhanced Expression o the truncated APC Transcript Includine a Novel Exon during Colon Carcinogenesis 35
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 35
Identification of novel mutations in HNPCC patients 34
Basi molecolari del cancro colorettale ereditario non poliposico. 34
Identification of alternative and aberrant splicing in the 5' region of the APC gene. 34
Genetic and Clinical Characterisation of Familial Adenomatous Polyposis: Populations Based Studies. 34
Role of the Cold Shock Domain Protein A in the transcriptional regulation of HBG expression 34
Impaired beta-globin mRNA stability is responsible of a beta-thalassemic phenotype associated with Hb Federico II [beta-106 (G8) Leu’Val)]. 34
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the “PTENhamartoma tumor syndrome” 34
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 34
Totale 4.720
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Categoria #
all - tutte 34.699
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 34.699
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020665 0 0 83 34 123 44 7 15 12 62 102 183
2020/20211.060 32 83 116 112 114 139 94 19 139 21 149 42
2021/20221.519 39 4 12 18 22 108 36 58 185 122 407 508
2022/20231.720 250 171 40 88 203 201 16 177 291 180 74 29
2023/20241.136 48 169 164 65 62 103 11 197 25 30 173 89
2024/2025801 380 408 13 0 0 0 0 0 0 0 0 0
Totale 8.640