CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 3.647
EU - Europa 2.649
AS - Asia 2.004
SA - Sud America 202
AF - Africa 36
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.549
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Nazione #
US - Stati Uniti d'America 3.596
RU - Federazione Russa 957
SG - Singapore 932
CN - Cina 529
GB - Regno Unito 495
SE - Svezia 221
DE - Germania 175
IE - Irlanda 175
IT - Italia 173
BR - Brasile 166
HK - Hong Kong 162
FI - Finlandia 154
VN - Vietnam 150
FR - Francia 130
KR - Corea 68
UA - Ucraina 56
BE - Belgio 34
IN - India 30
NL - Olanda 30
BD - Bangladesh 28
CA - Canada 27
JP - Giappone 20
TR - Turchia 19
MX - Messico 15
IQ - Iraq 13
AR - Argentina 12
ID - Indonesia 12
PL - Polonia 12
ZA - Sudafrica 11
ES - Italia 9
NG - Nigeria 9
AU - Australia 8
EC - Ecuador 8
UZ - Uzbekistan 8
SA - Arabia Saudita 6
MA - Marocco 5
PH - Filippine 5
PK - Pakistan 5
JO - Giordania 4
PE - Perù 4
PY - Paraguay 4
AT - Austria 3
BO - Bolivia 3
CL - Cile 3
ET - Etiopia 3
KZ - Kazakistan 3
LV - Lettonia 3
AE - Emirati Arabi Uniti 2
CR - Costa Rica 2
EG - Egitto 2
GR - Grecia 2
LI - Liechtenstein 2
LT - Lituania 2
MY - Malesia 2
PA - Panama 2
RO - Romania 2
RS - Serbia 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
CO - Colombia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DZ - Algeria 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
IR - Iran 1
KE - Kenya 1
LU - Lussemburgo 1
LY - Libia 1
MS - Montserrat 1
MT - Malta 1
NI - Nicaragua 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SI - Slovenia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.549
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Città #
Singapore 523
Jacksonville 479
Southend 366
Ashburn 348
Chandler 342
Dallas 341
Moscow 327
Woodbridge 252
San Jose 246
Ann Arbor 182
Dublin 175
Hong Kong 160
Houston 130
Verona 104
The Dalles 98
New York 89
Wilmington 79
Los Angeles 58
Lawrence 57
Princeton 57
Beijing 56
Ho Chi Minh City 51
Nanjing 48
Hanoi 39
Kent 39
Munich 39
Jinan 34
Shenyang 33
Helsinki 32
Buffalo 31
Boardman 30
Tianjin 28
Columbus 27
Falls Church 26
Sindelfingen 26
Nanchang 22
Santa Clara 22
Council Bluffs 21
Brussels 20
Hebei 20
Ningbo 20
Tokyo 19
Turku 17
São Paulo 16
Changsha 15
Haikou 15
Philadelphia 14
Waanrode 14
London 13
San Francisco 13
Guangzhou 12
Hangzhou 12
Jiaxing 12
Milan 12
Norwalk 12
Orem 12
Zhengzhou 12
Amsterdam 11
Chicago 11
Redmond 11
Seoul 11
Chennai 10
Frankfurt am Main 10
Redondo Beach 10
Seattle 10
Brooklyn 9
Jakarta 9
Poplar 9
Rio de Janeiro 9
Toronto 9
Da Nang 8
Johannesburg 8
Montreal 8
Mumbai 8
Stockholm 8
Taizhou 8
Tashkent 8
Warsaw 8
Abuja 7
Denver 7
Lancaster 7
Melbourne 7
Taiyuan 7
Ansbach 6
Atlanta 6
Auburn Hills 6
Barnet 6
Belo Horizonte 6
Düsseldorf 6
Phoenix 6
Ankara 5
Dearborn 5
Erbil 5
Hải Dương 5
Mexico City 5
Baghdad 4
Boston 4
Fairfield 4
Haiphong 4
León 4
Totale 5.612
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Nome #
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 259
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 249
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 228
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 224
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 209
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 204
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 202
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. 193
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 188
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 182
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 179
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 174
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 173
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 172
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 172
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 168
Analysis of published PKD1 gene sequence variants. 167
Alport syndrome: the point of view of a pediatric nephrologist 165
Tracking disease genes by reverse genetics 163
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 160
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 158
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 157
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 156
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 155
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 154
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 152
Capitolo 1: Genetica umana: una prospettiva 152
Capitolo 2: Le cellule e la divisione cellulare 151
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 149
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 147
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 147
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 146
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 146
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 146
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 144
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 133
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 130
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 129
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 129
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 126
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 124
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 122
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 121
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 118
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 117
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 112
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 111
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 111
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 109
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 109
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 103
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 102
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 100
Genetics and nephro-uropathies 99
Pregnancy, microchimerism and autoimmunity: An update 91
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 90
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 87
Totale 8.564
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Categoria #
all - tutte 27.294
article - articoli 25.857
book - libri 0
conference - conferenze 573
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 864
Totale 54.588
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202117 0 0 0 0 0 0 0 0 0 0 0 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
2025/20263.340 264 183 279 493 845 264 380 162 185 196 38 51
Totale 8.564