IRIS
NASTI, SABINA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 2.797
Totale 2.797
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 2.797
Totale 2.797
Salva come PNG Salva come JPEG
Città #
Genova 2.217
Rapallo 339
Genoa 233
Bordighera 8
Totale 2.797
Salva come PNG Salva come JPEG
Nome #
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. 153
Mutation Analysis of PRKAR1A Gene in a Patient with Atrial Myxoma 147
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 132
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 132
C242T polymorphism in CYBA gene (p22phox) and risk of coronary artery disease in a population of Caucasian Italians 131
Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the p53 PIN3 A2-Pro72 Haplotype. 130
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. 128
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLDmutation in Brenner tumor 126
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. 125
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. 122
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. 118
Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. 116
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma 116
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study 115
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. 114
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) 103
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 100
Hereditary trichilemmal cysts: A proposal for the assessment of diagnostic clinical criteria 92
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma 86
ANALISI GENOME-WIDE PER LA SUSCETTIBILITÀ AL MELANOMA: NUOVI LOCICHE CONFERMANO IL RUOLO DEI GENI DELLA PIGMENTAZIONE 85
MC1R variation and melanoma risk in relation to host/clinical and environmental factors in CDKN2A positive and negative melanoma patients. 81
Identification of a SUFU germline mutation in a family with Gorlin syndrome 80
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas 77
Features associated with germline CDKN2A mutations: A GenoMEL study of melanoma-prone families from three continents 74
Predicting the risk of pancreatic cancer: on CDKN2A mutations in the melanoma-pancreatic cancer syndrome in Italy 72
CDKN2A/p16INK4a 5’UTR variants in melanoma and pancreatic cancer predisposition: lost in translation, somewhere 49
Molecular characterisation of Italian Nevoid Basal Cell Carcinoma Syndrome patients 45
Totale 2.849
Salva come PNG Salva come JPEG
Categoria #
all - tutte 7.369
article - articoli 6.963
book - libri 0
conference - conferenze 406
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 14.738
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019187 0 0 0 0 0 0 0 0 0 36 86 65
2019/2020801 36 20 50 67 83 78 119 55 65 124 75 29
2020/2021189 11 36 12 21 15 9 5 21 12 23 11 13
2021/2022383 11 32 28 58 22 24 30 79 16 32 15 36
2022/2023391 31 41 2 50 77 45 2 31 42 3 63 4
2023/2024188 7 27 2 24 15 53 16 10 31 3 0 0
Totale 2.849