CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 2.136
EU - Europa 1.389
AS - Asia 366
OC - Oceania 4
SA - Sud America 3
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.900
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Nazione #
US - Stati Uniti d'America 2.130
GB - Regno Unito 451
CN - Cina 341
SE - Svezia 209
IE - Irlanda 161
FI - Finlandia 125
DE - Germania 123
FR - Francia 118
IT - Italia 88
UA - Ucraina 52
BE - Belgio 30
NL - Olanda 12
KR - Corea 10
TR - Turchia 9
RU - Federazione Russa 7
AU - Australia 4
CA - Canada 4
IN - India 2
LI - Liechtenstein 2
PL - Polonia 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
BA - Bosnia-Erzegovina 1
CL - Cile 1
EC - Ecuador 1
EG - Egitto 1
ES - Italia 1
GR - Grecia 1
HU - Ungheria 1
IM - Isola di Man 1
IR - Iran 1
LU - Lussemburgo 1
LV - Lettonia 1
MS - Montserrat 1
PA - Panama 1
PH - Filippine 1
SA - Arabia Saudita 1
SG - Singapore 1
Totale 3.900
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Città #
Jacksonville 468
Southend 363
Chandler 336
Woodbridge 252
Ann Arbor 182
Dublin 161
Houston 114
Ashburn 81
Wilmington 78
New York 59
Lawrence 56
Princeton 56
Nanjing 47
Verona 44
Jinan 33
Shenyang 32
Beijing 31
Boardman 29
Falls Church 26
Sindelfingen 26
Helsinki 23
Tianjin 23
Nanchang 21
Hebei 20
Ningbo 20
Brussels 16
Changsha 15
Haikou 14
Waanrode 14
Jiaxing 12
Norwalk 12
Philadelphia 12
Zhengzhou 12
Hangzhou 11
Los Angeles 11
Milan 11
Redmond 11
Seoul 10
Guangzhou 8
Taizhou 8
Lancaster 7
Taiyuan 7
Ansbach 6
Auburn Hills 6
Düsseldorf 6
San Francisco 6
Seattle 6
Chicago 5
Dearborn 5
Fairfield 4
Frankfurt am Main 4
Toronto 4
Bologna 3
Edinburgh 3
Lonigo 3
Melbourne 3
Tappahannock 3
Treviso 3
Washington 3
Ypsilanti 3
Belgrade 2
Chions 2
Fuzhou 2
Groningen 2
Lanzhou 2
Leawood 2
London 2
Penza 2
Riva 2
San Diego 2
Vicenza 2
Athens 1
Berlin 1
Breganze 1
Budapest 1
Cairo 1
Canberra 1
Cerea 1
Charlotte 1
Clearwater 1
Cleveland 1
Dallas 1
Denver 1
Des Moines 1
Douglas 1
Falkenstein 1
Grafing 1
Guayaquil 1
Gunzenhausen 1
Henderson 1
Kilburn 1
Makati 1
Miami 1
Mumbai 1
Perugia 1
Phoenix 1
Redwood City 1
Richmond 1
Riga 1
Riyadh 1
Totale 2.899
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Nome #
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 114
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 108
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 104
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 97
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 96
Tracking disease genes by reverse genetics 92
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 89
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 88
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 85
Alport syndrome: the point of view of a pediatric nephrologist 83
A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family 82
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 81
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 81
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 79
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 78
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 77
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 77
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 77
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 76
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 75
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 75
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 74
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney disease 72
Clinical value of PCR in diagnosis and follow-up of leukaemia and lymphoma: report of the Third Workshop of the Molecular Biology/BMT Study Group 71
Capitolo 1: Genetica umana: una prospettiva 71
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 70
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 70
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 70
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 69
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 Gene 68
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 68
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 67
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 65
Capitolo 2: Le cellule e la divisione cellulare 64
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an update 63
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 62
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. 62
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 61
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 60
Genetics and nephro-uropathies 60
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 59
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 58
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 57
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 56
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 56
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 56
Analysis of published PKD1 gene sequence variants. 56
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 54
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 54
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 54
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 51
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologoue is deleted in mice with kidney and retinal defect. 50
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 50
Pregnancy microchimerism and autoimmunity:an update 42
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 41
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 40
Totale 3.915
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Categoria #
all - tutte 11.310
article - articoli 10.710
book - libri 0
conference - conferenze 229
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 371
Totale 22.620
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201937 0 0 0 0 0 0 0 0 0 0 24 13
2019/2020492 67 4 3 52 23 85 42 50 12 52 18 84
2020/2021548 52 85 28 52 61 70 4 50 52 2 75 17
2021/2022402 23 77 2 40 18 23 8 21 25 10 44 111
2022/2023996 69 99 92 151 103 232 24 70 98 3 42 13
2023/2024345 13 51 38 46 57 78 15 29 4 14 0 0
Totale 3.915