CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 2.215
EU - Europa 1.453
AS - Asia 444
OC - Oceania 4
SA - Sud America 3
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.121
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Nazione #
US - Stati Uniti d'America 2.209
GB - Regno Unito 457
CN - Cina 352
SE - Svezia 213
IE - Irlanda 169
FI - Finlandia 127
DE - Germania 124
FR - Francia 120
IT - Italia 88
SG - Singapore 64
UA - Ucraina 53
RU - Federazione Russa 46
BE - Belgio 30
NL - Olanda 13
KR - Corea 10
TR - Turchia 9
AU - Australia 4
CA - Canada 4
HK - Hong Kong 2
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
JP - Giappone 1
KZ - Kazakistan 1
LU - Lussemburgo 1
LV - Lettonia 1
MS - Montserrat 1
PA - Panama 1
PH - Filippine 1
SA - Arabia Saudita 1
Totale 4.121
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Città #
Jacksonville 478
Southend 366
Chandler 342
Woodbridge 252
Ann Arbor 182
Dublin 169
Houston 124
Ashburn 83
Wilmington 79
New York 59
Lawrence 57
Princeton 57
Singapore 51
Nanjing 48
Verona 44
Kent 39
Beijing 36
Jinan 33
Shenyang 33
Boardman 30
Falls Church 26
Sindelfingen 26
Helsinki 23
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
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
Moscow 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
Hong Kong 2
Lanzhou 2
Leawood 2
London 2
Penza 2
Riva 2
San Diego 2
Vicenza 2
Almaty 1
Amsterdam 1
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
Totale 3.045
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Nome #
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 116
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 111
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 106
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 100
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 96
Tracking disease genes by reverse genetics 95
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 92
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 87
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 85
Alport syndrome: the point of view of a pediatric nephrologist 85
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 84
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 83
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 83
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 81
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 80
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 80
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 80
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 79
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 79
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 77
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 76
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 74
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 74
Capitolo 1: Genetica umana: una prospettiva 74
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 73
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 72
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 72
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 71
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 71
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 71
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 70
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 68
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 68
Capitolo 2: Le cellule e la divisione cellulare 67
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 65
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 65
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 64
Genetics and nephro-uropathies 64
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 64
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 63
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. 63
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 61
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 60
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 60
Analysis of published PKD1 gene sequence variants. 60
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 60
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 59
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 58
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 57
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 57
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologoue is deleted in mice with kidney and retinal defect. 54
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 53
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 51
Pregnancy, microchimerism and autoimmunity: An update 45
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 44
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 41
Totale 4.136
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Categoria #
all - tutte 12.668
article - articoli 12.000
book - libri 0
conference - conferenze 254
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 414
Totale 25.336
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020499 68 4 3 53 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
2024/202556 56 0 0 0 0 0 0 0 0 0 0 0
Totale 4.136