IRIS
SUSCA, Francesco Claudio
 Distribuzione geografica
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Continente #
NA - Nord America 3.750
AS - Asia 1.502
EU - Europa 1.311
SA - Sud America 374
AF - Africa 117
OC - Oceania 2
Totale 7.056
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Nazione #
US - Stati Uniti d'America 3.695
SG - Singapore 651
CN - Cina 377
BR - Brasile 307
SE - Svezia 242
IT - Italia 204
RU - Federazione Russa 188
HK - Hong Kong 163
DE - Germania 152
UA - Ucraina 123
FI - Finlandia 109
VN - Vietnam 95
GB - Regno Unito 81
FR - Francia 76
CI - Costa d'Avorio 69
BE - Belgio 51
IN - India 48
BD - Bangladesh 31
CA - Canada 24
ID - Indonesia 21
AR - Argentina 19
ZA - Sudafrica 19
MX - Messico 18
PL - Polonia 16
VE - Venezuela 16
IQ - Iraq 15
IE - Irlanda 14
PK - Pakistan 14
TR - Turchia 13
CO - Colombia 11
JP - Giappone 11
CZ - Repubblica Ceca 10
EC - Ecuador 10
NL - Olanda 10
ES - Italia 9
PH - Filippine 9
EG - Egitto 8
IR - Iran 7
SA - Arabia Saudita 7
TN - Tunisia 7
UZ - Uzbekistan 7
CL - Cile 4
HN - Honduras 4
LT - Lituania 4
MA - Marocco 4
OM - Oman 4
AL - Albania 3
AT - Austria 3
ET - Etiopia 3
HU - Ungheria 3
JM - Giamaica 3
JO - Giordania 3
MY - Malesia 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GE - Georgia 2
IL - Israele 2
KE - Kenya 2
KR - Corea 2
NP - Nepal 2
PE - Perù 2
PS - Palestinian Territory 2
PY - Paraguay 2
QA - Qatar 2
RS - Serbia 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
EE - Estonia 1
GT - Guatemala 1
HR - Croazia 1
IS - Islanda 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LV - Lettonia 1
ME - Montenegro 1
MN - Mongolia 1
NI - Nicaragua 1
RO - Romania 1
SN - Senegal 1
SO - Somalia 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
Totale 7.056
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Città #
Ashburn 393
Fairfield 391
Singapore 357
Chandler 312
Jacksonville 275
Woodbridge 261
Houston 193
Nyköping 187
San Jose 170
Seattle 166
Hong Kong 163
Cambridge 149
Ann Arbor 147
Beijing 118
Wilmington 115
Abidjan 69
Nanjing 69
Roxbury 61
New York 60
Lawrence 59
Lauterbourg 57
Los Angeles 51
Helsinki 43
Des Moines 41
Bari 38
Boardman 36
Inglewood 36
Princeton 33
Leuven 28
Munich 28
São Paulo 28
Dallas 24
Brooklyn 23
Hanoi 23
Ho Chi Minh City 23
Brussels 18
San Diego 18
Dearborn 17
Jiaxing 17
Santa Clara 17
Nanchang 16
Buffalo 15
San Francisco 14
Dublin 13
Falkenstein 13
London 12
Moscow 12
Rome 12
Council Bluffs 11
Shenyang 11
Tokyo 11
Chennai 10
Warsaw 10
Jakarta 9
Johannesburg 9
Orem 9
Torino 9
Turku 9
Dong Ket 8
Guangzhou 8
Hebei 8
Montreal 8
Phoenix 8
Pune 8
Tianjin 8
Toronto 8
Belo Horizonte 7
Boston 7
Caracas 7
Chicago 7
Frankfurt am Main 7
Mexico City 7
Nuremberg 7
Poplar 7
Redwood City 7
Rio de Janeiro 7
Atlanta 6
Dhaka 6
Guarulhos 6
Jinan 6
Manchester 6
Milan 6
Mumbai 6
Olomouc 6
Washington 6
Zhengzhou 6
Ardabil 5
Baghdad 5
Buenos Aires 5
Cairo 5
Changsha 5
Chieti 5
Denver 5
Falls Church 5
Medellín 5
New Delhi 5
Salt Lake City 5
Shanghai 5
Stockholm 5
Bisceglie 4
Totale 4.782
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Nome #
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 173
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 169
Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells 168
An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite 154
Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines 153
Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme 153
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 152
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study 151
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 151
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects 150
Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors 146
COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation 140
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation 140
Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family 137
Nine novel APC mutations in Italian FAP patients 134
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in NMD efficiency 134
Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians 132
17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures 132
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 129
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. 120
Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes 118
DEPRESSED LEVEL OF NATURAL-KILLER CELLS IN CANCER FAMILY SYNDROME 116
SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome 115
A novel cell type-specific role of p38alpha in the control of autophagy and cell death in colorectal cancer cells 112
Trisomy 13 mosaicism in a phenotypically normal child: description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age 112
FAMILIAL ADENOMATOUS POLYPOSIS - IDENTIFICATION OF A NEW FRAMESHIFT MUTATION OF THE APC GENE IN AN ITALIAN FAMILY 112
Infertility in carriers of two bisatellited marker chromosomes 110
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. 109
Comparision of the cell growth of amniotic fluid samples in different culture media - how to obtain the best results at the lowest costs 108
CANCER FAMILY SYNDROME: REPORT ON A GENETIC STUDIES IN A FAMILY 107
Linkage studies in Italian families with familial adenomatous polyposis 106
A novel genetic variant in the wfs1 gene in a patient with partial uniparental mero‐isodisomy of chromosome 4 105
Two B1 and B2 bradykinin receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 104
ANALISI MOLECOLARE E FUNZIONALE DEL RECETTORE MC1R NEL MELANOMA MALIGNO 104
Benefit of serum screening, maternal age and ultrasound scans in amniocentesis-a six year survey 102
A novel cell type-specific role of p38a in the control of autophagy and cell death in colorectal cancer cells. 100
Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients 99
Esiste un’influenza dei polimorfismi dell’enzima epossi-idrolasi microsomiale(mEH) sui marcatori citogenetici di danno genotossico? 99
Caratterizzazione di geni coinvolti nei processi di trasformazione neoplastica. 99
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects 99
EXCLUSION OF THE APC GENE AS THE CAUSE OF A VARIANT FORM OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) 98
Age-associated increase of micronuclei, sister chromatid exchange and sex chromosomeaneuploidy in human lymphocytes with special look at 100 year old subjects 98
Duplication of 9p11.2-p13.1:a benign cytogenetic variant 97
Characterisation of chromosomal aberrations of amniotic fluid cells occurring in culture and its meaning 90
null 88
Ganglioma arising in a Peutz-Jeghers patient:a case report with molecular implications 87
CORRELATION BETWEEN VASCULAR INFLAMMATION MARKERS, DIASTOLIC DYSFUNCTION AND CARDIOVASCULAR RISK IN PATIENTS WITH TAKAYASU ARTERITIS 86
The influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on gentoxic and cancerogenic process 86
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene 86
Relation between detoxification enzyme polymorphism and genotoxic cytogenetic biomarkers 84
The familial adenomatous polyposis region exhibits many different haplotypes 84
De novo balanced chromosome rearrangements in prenatal diagnosis 84
Cytogenetics and molecular studies in infertile males 81
Molecular characterization of novel melanoma cell lines 81
Two B1 and B2 receptor antagonists fail to inhibit the Ca2+ response elicited by bradykinin in human skin fibroblasts 78
The Ultrasound Detection of Chromosomal Anomalies Vs Maternal Age and Serum Screening – six year survey 72
Sindrome di Holt-Oram: Valutazione cardiologica, Radiologica e Genetica 72
null 68
Xq deletion and premature ovarian failure 65
Identification of a new frameshift mutation of the APC gene in an Italian family 59
Exclusion of the APC gene as a variant form of familial adenomatous polyposis 59
Mutazioni del gene STK11 nella sindrome di Peutz- Jeghers (PJS) e nel cancro colorettale sporadico. 58
MOLECULAR AND FUNCTIONAL ANALYSIS OF MC1R RECEPTOR IN MALIGNANT MELANOMA 56
Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers and its possible repercussion on genotoxic and cancerogeic process 53
The Italian external quality assessment scheme in classical cytogenetics: four years of activity 43
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer 37
Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids 37
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients 34
null 33
null 27
null 16
Totale 7.151
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Categoria #
all - tutte 29.474
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 29.474
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021189 0 0 0 0 0 0 0 0 0 109 39 41
2021/2022479 28 57 6 22 12 27 30 27 25 46 93 106
2022/2023841 104 94 61 83 87 133 3 103 138 9 18 8
2023/2024306 19 62 14 28 44 70 5 24 1 11 0 28
2024/20251.069 34 11 85 34 37 84 134 93 41 47 163 306
2025/20261.994 304 141 159 234 310 118 245 61 210 212 0 0
Totale 7.151