CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 2.245
EU - Europa 1.569
AS - Asia 642
OC - Oceania 9
SA - Sud America 3
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.470
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Nazione #
US - Stati Uniti d'America 2.238
GB - Regno Unito 458
CN - Cina 382
SG - Singapore 231
SE - Svezia 213
IE - Irlanda 173
RU - Federazione Russa 137
FI - Finlandia 132
DE - Germania 126
FR - Francia 120
IT - Italia 99
UA - Ucraina 53
BE - Belgio 30
NL - Olanda 13
KR - Corea 10
TR - Turchia 9
AU - Australia 8
CA - Canada 5
HK - Hong Kong 2
IN - India 2
LI - Liechtenstein 2
LV - Lettonia 2
PL - Polonia 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 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
JP - Giappone 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MS - Montserrat 1
NZ - Nuova Zelanda 1
PA - Panama 1
PH - Filippine 1
SA - Arabia Saudita 1
Totale 4.470
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Città #
Jacksonville 478
Southend 366
Chandler 342
Woodbridge 252
Singapore 191
Ann Arbor 182
Dublin 173
Houston 124
Ashburn 88
Wilmington 79
New York 59
Lawrence 57
Princeton 57
Nanjing 48
Verona 44
Kent 39
Beijing 36
Jinan 33
Shenyang 33
Boardman 30
Helsinki 28
Falls Church 26
Sindelfingen 26
Tianjin 23
Nanchang 22
Hebei 20
Ningbo 20
Brussels 16
Changsha 15
Haikou 15
Waanrode 14
Philadelphia 13
Jiaxing 12
Norwalk 12
Zhengzhou 12
Hangzhou 11
Los Angeles 11
Milan 11
Redmond 11
Guangzhou 10
Moscow 10
Seoul 10
Taizhou 8
Lancaster 7
Melbourne 7
Taiyuan 7
Ansbach 6
Auburn Hills 6
Dallas 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
Santa Clara 3
Tappahannock 3
Treviso 3
Washington 3
Ypsilanti 3
Belgrade 2
Chions 2
Cinisello Balsamo 2
Fuzhou 2
Groningen 2
Hong Kong 2
Lanzhou 2
Leawood 2
London 2
Munich 2
Naples 2
Penza 2
Riga 2
Riva 2
San Diego 2
Vicenza 2
Almaty 1
Amsterdam 1
Athens 1
Auckland 1
Baku 1
Berlin 1
Breganze 1
Budapest 1
Cairo 1
Canberra 1
Cerea 1
Charlotte 1
Clearwater 1
Cleveland 1
Denver 1
Des Moines 1
Dongguan 1
Douglas 1
Falkenstein 1
Totale 3.221
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Nome #
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 124
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 120
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 115
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 104
Tracking disease genes by reverse genetics 102
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 102
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 102
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 94
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 93
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 92
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 91
Alport syndrome: the point of view of a pediatric nephrologist 91
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 90
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 90
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 89
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 88
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 87
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 87
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 86
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 85
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 85
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 84
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 81
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 80
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 79
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 79
Capitolo 1: Genetica umana: una prospettiva 79
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 78
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 77
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 76
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 76
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 74
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. 74
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 74
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5 72
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 72
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 72
Capitolo 2: Le cellule e la divisione cellulare 72
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 70
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 68
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 67
Genetics and nephro-uropathies 67
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 67
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 67
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 67
Analysis of published PKD1 gene sequence variants. 66
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 64
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 63
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 63
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 62
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 61
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 60
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologoue is deleted in mice with kidney and retinal defect. 58
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 55
Pregnancy, microchimerism and autoimmunity: An update 49
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 48
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 47
Totale 4.485
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Categoria #
all - tutte 14.754
article - articoli 13.981
book - libri 0
conference - conferenze 303
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 470
Totale 29.508
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020371 0 0 0 0 23 86 42 51 12 53 18 86
2020/2021555 52 86 28 53 62 71 4 51 53 2 76 17
2021/2022410 23 79 2 42 18 23 8 21 26 10 45 113
2022/20231.022 70 100 93 152 105 245 24 71 101 3 43 15
2023/2024444 13 51 38 46 57 78 15 29 4 14 78 21
2024/2025405 88 77 23 183 34 0 0 0 0 0 0 0
Totale 4.485