CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 2.791
EU - Europa 1.688
AS - Asia 1.237
SA - Sud America 142
OC - Oceania 9
AF - Africa 8
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.877
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Nazione #
US - Stati Uniti d'America 2.765
SG - Singapore 586
GB - Regno Unito 469
CN - Cina 409
SE - Svezia 216
IE - Irlanda 175
DE - Germania 168
FI - Finlandia 152
HK - Hong Kong 150
RU - Federazione Russa 140
BR - Brasile 130
FR - Francia 125
IT - Italia 105
UA - Ucraina 55
KR - Corea 35
BE - Belgio 34
NL - Olanda 19
CA - Canada 16
TR - Turchia 10
AU - Australia 8
BD - Bangladesh 8
IN - India 7
PL - Polonia 6
VN - Vietnam 5
AR - Argentina 4
EC - Ecuador 4
MX - Messico 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AT - Austria 3
IQ - Iraq 3
JP - Giappone 3
ZA - Sudafrica 3
BO - Bolivia 2
CR - Costa Rica 2
EG - Egitto 2
ES - Italia 2
ID - Indonesia 2
KZ - Kazakistan 2
LI - Liechtenstein 2
LT - Lituania 2
LV - Lettonia 2
PK - Pakistan 2
RO - Romania 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
CL - Cile 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
HU - Ungheria 1
IM - Isola di Man 1
IR - Iran 1
JO - Giordania 1
LU - Lussemburgo 1
MA - Marocco 1
MS - Montserrat 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 5.877
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Città #
Jacksonville 478
Southend 366
Chandler 342
Dallas 310
Singapore 283
Woodbridge 252
Ann Arbor 182
Dublin 175
Hong Kong 150
Houston 124
Ashburn 99
Wilmington 79
New York 68
Lawrence 57
Princeton 57
Nanjing 48
Verona 45
Kent 39
Munich 38
Beijing 37
Los Angeles 35
Jinan 34
Shenyang 33
Boardman 30
Helsinki 30
Columbus 27
The Dalles 27
Falls Church 26
Sindelfingen 26
Tianjin 23
Nanchang 22
Brussels 20
Hebei 20
Ningbo 20
Buffalo 19
Turku 17
Changsha 15
Haikou 15
Waanrode 14
Philadelphia 13
Jiaxing 12
Norwalk 12
Zhengzhou 12
Hangzhou 11
Milan 11
Redmond 11
Seoul 11
São Paulo 11
Guangzhou 10
Moscow 10
Council Bluffs 9
San Francisco 9
Chicago 8
Santa Clara 8
Seattle 8
Taizhou 8
Lancaster 7
Melbourne 7
Taiyuan 7
Ansbach 6
Auburn Hills 6
Düsseldorf 6
London 6
Toronto 6
Brooklyn 5
Dearborn 5
Frankfurt am Main 5
Phoenix 5
Rio de Janeiro 5
Belo Horizonte 4
Fairfield 4
Tashkent 4
Warsaw 4
Amsterdam 3
Bologna 3
Charlotte 3
Edinburgh 3
Fortaleza 3
Fuzhou 3
Ho Chi Minh City 3
Lonigo 3
Montreal 3
Redondo Beach 3
Stockholm 3
Tappahannock 3
Tokyo 3
Treviso 3
Washington 3
Ypsilanti 3
Atlanta 2
Belgrade 2
Boston 2
Bucharest 2
Chions 2
Cinisello Balsamo 2
Curitiba 2
Denver 2
Detroit 2
Erbil 2
Feira de Santana 2
Totale 4.018
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Nome #
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 164
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 163
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 157
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 155
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 135
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 127
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 125
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. 124
Tracking disease genes by reverse genetics 122
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 120
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 120
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 119
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 119
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 118
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 117
Alport syndrome: the point of view of a pediatric nephrologist 117
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 112
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 109
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 109
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 106
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 106
Capitolo 1: Genetica umana: una prospettiva 105
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 103
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 103
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 103
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 103
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 102
Capitolo 2: Le cellule e la divisione cellulare 102
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 101
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 101
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 101
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 100
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 99
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 97
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 96
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 95
Analysis of published PKD1 gene sequence variants. 95
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 94
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 94
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 94
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 93
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 91
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 89
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 87
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 85
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 84
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 83
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 82
Genetics and nephro-uropathies 81
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 80
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 79
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 78
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 77
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 73
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 68
Pregnancy, microchimerism and autoimmunity: An update 66
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 64
Totale 5.892
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Categoria #
all - tutte 20.597
article - articoli 19.507
book - libri 0
conference - conferenze 433
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 657
Totale 41.194
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021417 0 0 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
2024/20251.144 88 77 23 183 63 10 46 60 198 64 116 216
2025/2026668 264 183 221 0 0 0 0 0 0 0 0 0
Totale 5.892