CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 3.008
EU - Europa 2.443
AS - Asia 1.520
SA - Sud America 169
AF - Africa 18
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.169
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.971
RU - Federazione Russa 866
SG - Singapore 676
CN - Cina 499
GB - Regno Unito 481
SE - Svezia 219
IE - Irlanda 175
DE - Germania 169
FI - Finlandia 152
HK - Hong Kong 151
BR - Brasile 147
FR - Francia 125
IT - Italia 106
VN - Vietnam 63
UA - Ucraina 55
KR - Corea 37
BE - Belgio 34
NL - Olanda 23
CA - Canada 21
IN - India 19
BD - Bangladesh 13
JP - Giappone 13
TR - Turchia 12
ID - Indonesia 10
MX - Messico 10
PL - Polonia 10
ZA - Sudafrica 10
AR - Argentina 8
AU - Australia 8
ES - Italia 6
EC - Ecuador 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AT - Austria 3
IQ - Iraq 3
MA - Marocco 3
PE - Perù 3
PK - Pakistan 3
PY - Paraguay 3
AE - Emirati Arabi Uniti 2
BO - Bolivia 2
CL - Cile 2
CR - Costa Rica 2
EG - Egitto 2
KZ - Kazakistan 2
LI - Liechtenstein 2
LT - Lituania 2
LV - Lettonia 2
PH - Filippine 2
RO - Romania 2
RS - Serbia 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
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
IR - Iran 1
JO - Giordania 1
KE - Kenya 1
LU - Lussemburgo 1
MS - Montserrat 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 7.169
Salva come PNG Salva come JPEG
Città #
Jacksonville 478
Southend 366
Chandler 342
Dallas 340
Moscow 301
Singapore 287
Woodbridge 252
Ann Arbor 182
Dublin 175
Ashburn 158
Hong Kong 151
Houston 127
New York 82
Wilmington 79
Lawrence 57
Princeton 57
Beijing 56
Los Angeles 54
Nanjing 48
Verona 45
Kent 39
Munich 38
Jinan 34
Shenyang 33
Boardman 30
Helsinki 30
Ho Chi Minh City 28
Columbus 27
The Dalles 27
Tianjin 27
Falls Church 26
Sindelfingen 26
Buffalo 25
Nanchang 22
Brussels 20
Hebei 20
Ningbo 20
Turku 17
Santa Clara 16
Changsha 15
Haikou 15
Waanrode 14
Philadelphia 13
São Paulo 13
Tokyo 13
Guangzhou 12
Hangzhou 12
Hanoi 12
Jiaxing 12
Norwalk 12
Zhengzhou 12
Milan 11
Redmond 11
Seoul 11
Redondo Beach 10
Brooklyn 9
Council Bluffs 9
Poplar 9
San Francisco 9
Seattle 9
Chicago 8
Johannesburg 8
London 8
Taizhou 8
Toronto 8
Amsterdam 7
Chennai 7
Jakarta 7
Lancaster 7
Melbourne 7
Taiyuan 7
Warsaw 7
Ansbach 6
Auburn Hills 6
Düsseldorf 6
Montreal 6
Mumbai 6
Stockholm 6
Dearborn 5
Denver 5
Frankfurt am Main 5
Hải Dương 5
Phoenix 5
Rio de Janeiro 5
Atlanta 4
Belo Horizonte 4
Boston 4
Fairfield 4
Mexico City 4
Orem 4
Porto Alegre 4
Tashkent 4
Ankara 3
Bologna 3
Charlotte 3
Edinburgh 3
Elk Grove Village 3
Fortaleza 3
Fuzhou 3
Lonigo 3
Totale 4.596
Salva come PNG Salva come JPEG
Nome #
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 216
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 210
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 200
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 186
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 174
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 171
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 165
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. 161
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 158
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 158
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 153
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 151
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 144
Alport syndrome: the point of view of a pediatric nephrologist 141
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 140
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 139
Tracking disease genes by reverse genetics 138
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 138
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 137
Capitolo 2: Le cellule e la divisione cellulare 135
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 133
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 133
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 132
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 131
Capitolo 1: Genetica umana: una prospettiva 130
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 129
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 129
Analysis of published PKD1 gene sequence variants. 129
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 127
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 123
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 122
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 119
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 119
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 116
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 115
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 115
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 108
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 108
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 108
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 106
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 105
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 104
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 100
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 97
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 96
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 96
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 93
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 91
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 90
Genetics and nephro-uropathies 90
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 90
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 89
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 89
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 83
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 77
Pregnancy, microchimerism and autoimmunity: An update 76
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 71
Totale 7.184
Salva come PNG Salva come JPEG
Categoria #
all - tutte 23.295
article - articoli 22.040
book - libri 0
conference - conferenze 494
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 761
Totale 46.590
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021336 0 0 0 0 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
2025/20261.960 264 183 279 493 741 0 0 0 0 0 0 0
Totale 7.184