CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 3.738
EU - Europa 2.663
AS - Asia 2.016
SA - Sud America 207
AF - Africa 36
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 9
Totale 8.686
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Nazione #
US - Stati Uniti d'America 3.677
RU - Federazione Russa 957
SG - Singapore 933
CN - Cina 534
GB - Regno Unito 495
SE - Svezia 221
IT - Italia 185
DE - Germania 176
IE - Irlanda 175
BR - Brasile 167
HK - Hong Kong 163
FI - Finlandia 154
VN - Vietnam 151
FR - Francia 130
KR - Corea 69
UA - Ucraina 56
BE - Belgio 34
BD - Bangladesh 31
IN - India 30
NL - Olanda 30
CA - Canada 29
JP - Giappone 20
TR - Turchia 19
MX - Messico 15
AR - Argentina 13
IQ - Iraq 13
ID - Indonesia 12
PL - Polonia 12
ZA - Sudafrica 11
EC - Ecuador 9
ES - Italia 9
NG - Nigeria 9
AU - Australia 8
UZ - Uzbekistan 8
CR - Costa Rica 6
SA - Arabia Saudita 6
MA - Marocco 5
PH - Filippine 5
PK - Pakistan 5
CL - Cile 4
JM - Giamaica 4
JO - Giordania 4
PE - Perù 4
PY - Paraguay 4
AT - Austria 3
BO - Bolivia 3
ET - Etiopia 3
KZ - Kazakistan 3
LV - Lettonia 3
AE - Emirati Arabi Uniti 2
CO - Colombia 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
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
IS - Islanda 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 8.671
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Città #
Singapore 523
Jacksonville 479
Southend 366
Ashburn 351
Chandler 342
Dallas 342
Moscow 327
Woodbridge 252
San Jose 249
Ann Arbor 182
Dublin 175
Hong Kong 161
Houston 130
Verona 104
The Dalles 98
New York 90
Wilmington 79
Council Bluffs 71
Beijing 59
Los Angeles 58
Lawrence 57
Princeton 57
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
Brussels 20
Hebei 20
Ningbo 20
Tokyo 19
Milan 17
Turku 17
Philadelphia 16
São Paulo 16
Changsha 15
Haikou 15
Waanrode 14
London 13
San Francisco 13
Chicago 12
Guangzhou 12
Hangzhou 12
Jiaxing 12
Norwalk 12
Orem 12
Seoul 12
Zhengzhou 12
Amsterdam 11
Frankfurt am Main 11
Redmond 11
Brooklyn 10
Chennai 10
Redondo Beach 10
Seattle 10
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
Phoenix 7
Taiyuan 7
Ansbach 6
Atlanta 6
Auburn Hills 6
Barnet 6
Belo Horizonte 6
Düsseldorf 6
Rome 6
Ankara 5
Dearborn 5
Erbil 5
Hải Dương 5
Mexico City 5
Baghdad 4
Bologna 4
Boston 4
Fairfield 4
Totale 5.688
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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. 260
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 250
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 229
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 226
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 212
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 210
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 206
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. 194
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 190
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 180
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 177
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 176
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 174
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 173
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 172
Analysis of published PKD1 gene sequence variants. 171
Alport syndrome: the point of view of a pediatric nephrologist 168
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 167
Tracking disease genes by reverse genetics 166
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 162
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 161
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 159
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 159
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 156
Capitolo 1: Genetica umana: una prospettiva 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 153
Capitolo 2: Le cellule e la divisione cellulare 152
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 151
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 150
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 149
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 148
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 147
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 146
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 145
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 134
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 132
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 131
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 130
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 129
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 125
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 124
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 122
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 122
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 121
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 114
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 112
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 112
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 112
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 111
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 104
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 103
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 103
Genetics and nephro-uropathies 100
Pregnancy, microchimerism and autoimmunity: An update 92
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 91
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 87
Totale 8.686
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Categoria #
all - tutte 28.438
article - articoli 26.944
book - libri 0
conference - conferenze 597
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 897
Totale 56.876
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022387 0 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
2025/20263.342 264 183 279 493 845 264 380 162 185 196 38 53
2026/2027120 37 83 0 0 0 0 0 0 0 0 0 0
Totale 8.686