CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 2.274
EU - Europa 1.595
AS - Asia 889
SA - Sud America 74
OC - Oceania 9
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.844
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Nazione #
US - Stati Uniti d'America 2.266
GB - Regno Unito 464
SG - Singapore 429
CN - Cina 387
SE - Svezia 213
IE - Irlanda 174
RU - Federazione Russa 138
FI - Finlandia 134
DE - Germania 130
FR - Francia 120
IT - Italia 102
BR - Brasile 65
UA - Ucraina 54
BE - Belgio 34
HK - Hong Kong 32
NL - Olanda 14
KR - Corea 12
TR - Turchia 9
AU - Australia 8
CA - Canada 6
AR - Argentina 3
EC - Ecuador 3
UZ - Uzbekistan 3
AT - Austria 2
IN - India 2
KZ - Kazakistan 2
LI - Liechtenstein 2
LV - Lettonia 2
PK - Pakistan 2
PL - Polonia 2
RS - Serbia 2
VN - Vietnam 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BO - Bolivia 1
BY - Bielorussia 1
CL - Cile 1
EG - Egitto 1
ES - Italia 1
GR - Grecia 1
HU - Ungheria 1
IM - Isola di Man 1
IR - Iran 1
JO - Giordania 1
JP - Giappone 1
LT - Lituania 1
LU - Lussemburgo 1
MS - Montserrat 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
SA - Arabia Saudita 1
TN - Tunisia 1
Totale 4.844
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Città #
Jacksonville 478
Southend 366
Chandler 342
Singapore 253
Woodbridge 252
Ann Arbor 182
Dublin 174
Houston 124
Ashburn 88
Wilmington 79
New York 59
Lawrence 57
Princeton 57
Nanjing 48
Verona 45
Kent 39
Beijing 36
Jinan 33
Shenyang 33
Hong Kong 32
Boardman 30
Helsinki 30
Falls Church 26
Sindelfingen 26
Tianjin 23
Nanchang 22
Brussels 20
Hebei 20
Ningbo 20
Changsha 15
Haikou 15
Waanrode 14
Philadelphia 13
Jiaxing 12
Los Angeles 12
Norwalk 12
Zhengzhou 12
Hangzhou 11
Milan 11
Redmond 11
Guangzhou 10
Moscow 10
Seoul 10
Council Bluffs 9
Taizhou 8
Lancaster 7
Melbourne 7
Taiyuan 7
The Dalles 7
Ansbach 6
Auburn Hills 6
Dallas 6
Düsseldorf 6
San Francisco 6
Seattle 6
Chicago 5
Dearborn 5
São Paulo 5
Toronto 5
Fairfield 4
Frankfurt am Main 4
London 4
Bologna 3
Edinburgh 3
Fuzhou 3
Lonigo 3
Rio de Janeiro 3
Santa Clara 3
Tappahannock 3
Tashkent 3
Treviso 3
Washington 3
Ypsilanti 3
Belgrade 2
Chions 2
Cinisello Balsamo 2
Fortaleza 2
Goiânia 2
Groningen 2
Ho Chi Minh City 2
Itajaí 2
Lanzhou 2
Leawood 2
Munich 2
Naples 2
Penza 2
Ribeirão Preto 2
Riga 2
Riva 2
Salvador 2
San Diego 2
Vicenza 2
Almaty 1
Amman 1
Amsterdam 1
Astana 1
Athens 1
Auckland 1
Avellaneda 1
Baku 1
Totale 3.354
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Nome #
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 131
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 130
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 126
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 119
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 110
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 108
Tracking disease genes by reverse genetics 107
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 105
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 105
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 102
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 100
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 99
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 99
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 98
Alport syndrome: the point of view of a pediatric nephrologist 96
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 95
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 93
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 91
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 91
Capitolo 1: Genetica umana: una prospettiva 91
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 89
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 89
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. 88
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 87
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 87
Capitolo 2: Le cellule e la divisione cellulare 86
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 85
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 84
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 84
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 84
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 83
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 83
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 81
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 78
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 78
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 77
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 76
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 75
Analysis of published PKD1 gene sequence variants. 75
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 74
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 74
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 74
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 73
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 73
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 73
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 72
Genetics and nephro-uropathies 69
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 68
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 67
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 65
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 65
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 63
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 63
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 59
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 58
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 52
Pregnancy, microchimerism and autoimmunity: An update 52
Totale 4.859
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Categoria #
all - tutte 16.884
article - articoli 15.974
book - libri 0
conference - conferenze 357
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 553
Totale 33.768
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020157 0 0 0 0 0 0 0 0 0 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
2024/2025779 88 77 23 183 63 10 46 60 198 31 0 0
Totale 4.859