IRIS
SUSCA, Francesco Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 2.985
EU - Europa 803
AS - Asia 287
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 4.078
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Nazione #
US - Stati Uniti d'America 2.985
CN - Cina 238
SE - Svezia 238
IT - Italia 152
UA - Ucraina 117
DE - Germania 104
FI - Finlandia 73
GB - Regno Unito 52
SG - Singapore 23
BE - Belgio 18
IE - Irlanda 12
IN - India 11
CZ - Repubblica Ceca 9
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
ES - Italia 1
KE - Kenya 1
TW - Taiwan 1
Totale 4.078
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Città #
Fairfield 398
Chandler 313
Jacksonville 270
Woodbridge 265
Ashburn 232
Houston 194
Nyköping 188
Seattle 168
Cambridge 151
Ann Arbor 148
Wilmington 121
Nanjing 68
Roxbury 60
Lawrence 59
Beijing 57
Des Moines 41
New York 39
Boardman 35
Inglewood 35
Princeton 33
Bari 28
Jiaxing 18
San Diego 18
Helsinki 17
Dearborn 16
Nanchang 16
Brussels 14
Singapore 14
Brooklyn 12
Dublin 12
Shenyang 11
London 10
Los Angeles 9
Munich 9
Rome 9
Torino 9
Dong Ket 8
Hebei 8
Pune 8
Tianjin 8
Guangzhou 7
Redwood City 7
Bisceglie 6
Washington 6
Ardabil 5
Chieti 5
Falls Church 5
Jinan 5
Olomouc 5
San Francisco 5
Zhengzhou 5
Brno 4
Changsha 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
Hangzhou 2
Heze 2
Hounslow 2
Indiana 2
Ljubljana 2
Ningbo 2
Paris 2
San Mateo 2
Shanghai 2
Terlizzi 2
Turin 2
Tübingen 2
Valenzano 2
Altopascio 1
Augusta 1
Baotou 1
Bergamo 1
Budapest 1
Canelli 1
Carpi 1
Chiswick 1
Cisternino 1
Edinburgh 1
Ercolano 1
Esslingen am Neckar 1
Guiyang 1
Introdacqua 1
Islington 1
Lanzhou 1
Marcon 1
Martina Franca 1
Totale 3.289
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Nome #
Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme 112
Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells 111
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 101
Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines 101
Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians 99
An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite 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
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 96
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 96
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 93
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 90
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 90
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 89
null 88
Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors 88
COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation 87
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 81
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. 76
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 76
Linkage studies in Italian families with familial adenomatous polyposis 74
Duplication of 9p11.2-p13.1:a benign cytogenetic variant 71
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 70
null 68
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 64
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 62
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 62
The influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on gentoxic and cancerogenic process 58
17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures 58
Comparision of the cell growth of amniotic fluid samples in different culture media - how to obtain the best results at the lowest costs 55
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
The familial adenomatous polyposis region exhibits many different haplotypes 54
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene 53
Two B1 and B2 receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 52
Molecular characterization of novel melanoma cell lines 51
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 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
Relation between detoxification enzyme polymorphism and genotoxic cytogenetic biomarkers 48
The Ultrasound Detection of Chromosomal Anomalies Vs Maternal Age and Serum Screening – six year survey 42
Cytogenetics and molecular studies in infertile males 42
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 42
null 42
A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells 41
Identification of a new frameshift mutation of the APC gene in an Italian family 40
Age-associated increase of micronuclei, sister chromatid exchange and sex chromosomeaneuploidy in human lymphocytes with special look at 100 year old subjects 40
Characterisation of chromosomal aberrations of amniotic fluid cells occurring in culture and its meaning 40
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 36
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects 34
A novel genetic variant in the wfs1 gene in a patient with partial uniparental mero‐isodisomy of chromosome 4 34
Sindrome di Holt-Oram: Valutazione cardiologica, Radiologica e Genetica 33
null 33
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 30
A novel cell type-specific role of p38a in the control of autophagy and cell death in colorectal cancer cells. 29
Caratterizzazione di geni coinvolti nei processi di trasformazione neoplastica. 28
null 27
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on genotoxic and cancerogeic process 24
Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids 17
Mutazioni del gene STK11 nella sindrome di Peutz- Jeghers (PJS) e nel cancro colorettale sporadico. 17
null 16
The Italian external quality assessment scheme in classical cytogenetics: four years of activity 15
MOLECULAR AND FUNCTIONAL ANALYSIS OF MC1R RECEPTOR IN MALIGNANT MELANOMA 14
CORRELATION BETWEEN VASCULAR INFLAMMATION MARKERS, DIASTOLIC DYSFUNCTION AND CARDIOVASCULAR RISK IN PATIENTS WITH TAKAYASU ARTERITIS 12
null 11
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 4
Totale 4.160
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Categoria #
all - tutte 17.224
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 17.224
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020880 0 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
2023/2024309 19 62 14 28 44 74 5 23 1 11 0 28
2024/202546 37 9 0 0 0 0 0 0 0 0 0 0
Totale 4.160