IRIS
SUSCA, Francesco Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 2.977
EU - Europa 782
AS - Asia 242
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 4.004
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Nazione #
US - Stati Uniti d'America 2.977
SE - Svezia 238
CN - Cina 216
IT - Italia 148
UA - Ucraina 117
DE - Germania 95
FI - Finlandia 73
GB - Regno Unito 52
BE - Belgio 18
IE - Irlanda 12
IN - India 11
FR - Francia 9
VN - Vietnam 8
RU - Federazione Russa 7
IR - Iran 6
NL - Olanda 6
HU - Ungheria 2
SI - Slovenia 2
AU - Australia 1
CH - Svizzera 1
CL - Cile 1
CZ - Repubblica Ceca 1
ES - Italia 1
KE - Kenya 1
TW - Taiwan 1
Totale 4.004
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Città #
Fairfield 398
Chandler 313
Jacksonville 270
Woodbridge 265
Ashburn 231
Houston 194
Nyköping 188
Seattle 168
Cambridge 151
Ann Arbor 148
Wilmington 121
Nanjing 68
Roxbury 60
Lawrence 59
Beijing 56
Des Moines 41
New York 39
Inglewood 35
Boardman 33
Princeton 33
Bari 26
San Diego 18
Helsinki 17
Jiaxing 17
Dearborn 16
Nanchang 16
Brussels 14
Brooklyn 12
Dublin 12
Shenyang 11
London 10
Torino 9
Dong Ket 8
Hebei 8
Pune 8
Tianjin 8
Redwood City 7
Rome 7
Bisceglie 6
Los Angeles 6
Washington 6
Ardabil 5
Chieti 5
Falls Church 5
Jinan 5
San Francisco 5
Zhengzhou 5
Changsha 4
Guangzhou 4
Milan 4
Perugia 4
Romanengo 4
Waanrode 4
Barletta 3
Hefei 3
Kilburn 3
Kunming 3
Leawood 3
Mumbai 3
Norwalk 3
Acton 2
Andria 2
Auburn Hills 2
Brescia 2
Grafing 2
Hounslow 2
Indiana 2
Ljubljana 2
Ningbo 2
Paris 2
San Mateo 2
Terlizzi 2
Turin 2
Tübingen 2
Valenzano 2
Altopascio 1
Augusta 1
Baotou 1
Bergamo 1
Brno 1
Budapest 1
Canelli 1
Carpi 1
Chiswick 1
Cisternino 1
Edinburgh 1
Ercolano 1
Esslingen am Neckar 1
Guiyang 1
Hangzhou 1
Introdacqua 1
Islington 1
Lanzhou 1
Marcon 1
Martina Franca 1
Meda 1
Melbourne 1
Mestre 1
Miami Beach 1
Modugno 1
Totale 3.243
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Nome #
Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells 111
Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme 110
Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines 101
An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite 97
Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians 97
Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors 97
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 96
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 95
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 94
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 91
Nine novel APC mutations in Italian FAP patients 90
Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes 89
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 89
null 88
Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors 88
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 87
COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation 85
SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome 84
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 80
Trisomy 13 mosaicism in a phenotypically normal child: description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age 78
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 78
Two B1 and B2 bradykinin receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 77
Infertility in carriers of two bisatellited marker chromosomes 76
De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly. 75
Linkage studies in Italian families with familial adenomatous polyposis 74
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 73
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 70
Duplication of 9p11.2-p13.1:a benign cytogenetic variant 70
null 68
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 63
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 62
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 61
17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures 58
The influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on gentoxic and cancerogenic process 57
De novo balanced chromosome rearrangements in prenatal diagnosis 55
Benefit of serum screening, maternal age and ultrasound scans in amniocentesis-a six year survey 54
Comparision of the cell growth of amniotic fluid samples in different culture media - how to obtain the best results at the lowest costs 52
The familial adenomatous polyposis region exhibits many different haplotypes 52
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene 52
Two B1 and B2 receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 51
Molecular characterization of novel melanoma cell lines 51
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 50
Ganglioma arising in a Peutz-Jeghers patient:a case report with molecular implications 50
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 49
Relation between detoxification enzyme polymorphism and genotoxic cytogenetic biomarkers 46
The Ultrasound Detection of Chromosomal Anomalies Vs Maternal Age and Serum Screening – six year survey 42
null 42
Cytogenetics and molecular studies in infertile males 40
Identification of a new frameshift mutation of the APC gene in an Italian family 40
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 40
Age-associated increase of micronuclei, sister chromatid exchange and sex chromosomeaneuploidy in human lymphocytes with special look at 100 year old subjects 39
Characterisation of chromosomal aberrations of amniotic fluid cells occurring in culture and its meaning 38
A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells 37
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 34
null 33
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects 33
Sindrome di Holt-Oram: Valutazione cardiologica, Radiologica e Genetica 31
A novel genetic variant in the wfs1 gene in a patient with partial uniparental mero‐isodisomy of chromosome 4 31
Caratterizzazione di geni coinvolti nei processi di trasformazione neoplastica. 28
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 28
null 27
A novel cell type-specific role of p38a in the control of autophagy and cell death in colorectal cancer cells. 26
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on genotoxic and cancerogeic process 24
null 16
Mutazioni del gene STK11 nella sindrome di Peutz- Jeghers (PJS) e nel cancro colorettale sporadico. 16
The Italian external quality assessment scheme in classical cytogenetics: four years of activity 14
Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids 13
MOLECULAR AND FUNCTIONAL ANALYSIS OF MC1R RECEPTOR IN MALIGNANT MELANOMA 13
null 11
CORRELATION BETWEEN VASCULAR INFLAMMATION MARKERS, DIASTOLIC DYSFUNCTION AND CARDIOVASCULAR RISK IN PATIENTS WITH TAKAYASU ARTERITIS 10
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 6
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer 3
Totale 4.086
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Categoria #
all - tutte 15.790
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 15.790
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019287 0 0 0 0 0 0 0 0 0 0 145 142
2019/20201.065 185 74 26 89 108 62 116 84 129 53 105 34
2020/2021651 61 39 45 39 100 20 62 38 58 108 40 41
2021/2022476 28 57 6 21 12 28 30 25 26 46 92 105
2022/2023847 104 94 62 83 87 134 3 106 138 9 19 8
2023/2024281 19 62 14 28 44 74 5 23 1 11 0 0
Totale 4.086