CATALOGO DEI PRODOTTI DELLA RICERCA

TURCO, Alberto
 Distribuzione geografica
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Continente #
NA - Nord America 4.233
EU - Europa 2.691
AS - Asia 2.022
SA - Sud America 219
AF - Africa 37
Continente sconosciuto - Info sul continente non disponibili 20
OC - Oceania 9
Totale 9.231
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Nazione #
US - Stati Uniti d'America 4.119
RU - Federazione Russa 959
SG - Singapore 933
CN - Cina 535
GB - Regno Unito 501
SE - Svezia 221
IT - Italia 201
DE - Germania 177
IE - Irlanda 175
BR - Brasile 173
HK - Hong Kong 163
FI - Finlandia 154
VN - Vietnam 151
FR - Francia 131
KR - Corea 69
UA - Ucraina 56
CA - Canada 53
BE - Belgio 34
BD - Bangladesh 32
IN - India 30
NL - Olanda 30
JP - Giappone 20
TR - Turchia 20
MX - Messico 16
AR - Argentina 13
ID - Indonesia 13
IQ - Iraq 13
EC - Ecuador 12
PL - Polonia 12
ZA - Sudafrica 11
CR - Costa Rica 10
ES - Italia 9
NG - Nigeria 9
NI - Nicaragua 9
AU - Australia 8
UZ - Uzbekistan 8
SA - Arabia Saudita 6
GT - Guatemala 5
MA - Marocco 5
PH - Filippine 5
PK - Pakistan 5
TT - Trinidad e Tobago 5
CL - Cile 4
CO - Colombia 4
JM - Giamaica 4
JO - Giordania 4
PE - Perù 4
PY - Paraguay 4
AT - Austria 3
BO - Bolivia 3
CW - ???statistics.table.value.countryCode.CW??? 3
ET - Etiopia 3
IL - Israele 3
KZ - Kazakistan 3
LV - Lettonia 3
PA - Panama 3
PR - Porto Rico 3
SV - El Salvador 3
AE - Emirati Arabi Uniti 2
BA - Bosnia-Erzegovina 2
EG - Egitto 2
GR - Grecia 2
LI - Liechtenstein 2
LT - Lituania 2
MY - Malesia 2
RO - Romania 2
RS - Serbia 2
TN - Tunisia 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BB - Barbados 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
EE - Estonia 1
HU - Ungheria 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
NO - Norvegia 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SC - Seychelles 1
SI - Slovenia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 9.216
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Città #
Singapore 523
Ashburn 509
Jacksonville 480
Southend 366
Dallas 352
Chandler 342
Moscow 327
San Jose 295
Woodbridge 252
Ann Arbor 182
Dublin 175
Hong Kong 161
Houston 131
Verona 104
The Dalles 98
New York 93
Wilmington 79
Council Bluffs 71
Beijing 60
Los Angeles 60
Lawrence 57
Princeton 57
Ho Chi Minh City 51
Nanjing 48
Hanoi 39
Kent 39
Munich 39
Jinan 34
Shenyang 33
Buffalo 32
Helsinki 32
Annandale 31
Boardman 30
Santa Clara 29
Columbus 28
Tianjin 28
Falls Church 26
Sindelfingen 26
Nanchang 22
Brussels 20
Hebei 20
Ningbo 20
São Paulo 20
Tokyo 19
Milan 18
Philadelphia 18
Turku 17
Brooklyn 15
Changsha 15
Haikou 15
Waanrode 14
Chicago 13
London 13
Norwalk 13
San Francisco 13
Frankfurt am Main 12
Guangzhou 12
Hangzhou 12
Jiaxing 12
Orem 12
Seoul 12
Toronto 12
Zhengzhou 12
Amsterdam 11
Montreal 11
Redmond 11
Chennai 10
Redondo Beach 10
Seattle 10
Jakarta 9
Phoenix 9
Poplar 9
Rio de Janeiro 9
Bologna 8
Da Nang 8
Denver 8
Johannesburg 8
Managua 8
Mumbai 8
Rome 8
Stockholm 8
Taizhou 8
Tashkent 8
Warsaw 8
Abuja 7
Lancaster 7
Melbourne 7
San José 7
Taiyuan 7
Ansbach 6
Atlanta 6
Auburn Hills 6
Barnet 6
Belo Horizonte 6
Düsseldorf 6
Las Vegas 6
Ankara 5
Boston 5
Dearborn 5
Erbil 5
Totale 5.984
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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. 272
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 257
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 239
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 239
Autosomal dominant polycystic kidney disease: clinical and genetic aspects 220
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 215
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 214
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. 201
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 197
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 193
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 192
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 187
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 186
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes 184
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 182
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 180
Analysis of published PKD1 gene sequence variants. 177
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families 176
Tracking disease genes by reverse genetics 176
A mild phenotype of incontinentia pigmenti in a male child: DNA confirmation of a somatic mosaicism 175
Alport syndrome--is there a genotype-phenotype relationship? [editorial] 174
Alport syndrome: the point of view of a pediatric nephrologist 174
Capitolo 1: Genetica umana: una prospettiva 171
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome 170
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 169
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 167
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 165
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 164
Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. 163
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 160
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 159
Capitolo 2: Le cellule e la divisione cellulare 157
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene 156
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers 156
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes 153
ERRONOUS GENETIC RISK ASSESMENT OF ALPORT SYNDROME 144
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction 140
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 140
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 139
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease 139
Genetica e clinica della malattia policistica renale autosomica dominante (ADPKD): recenti acquisizioni su una malattia molto frequente e poco conosciuta 136
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia 135
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP) 133
Renin-angiotensin system (RAS) DNA polymorphisms and TGFbeta1-mediated fibrogenetic pathway gene expression studies in primary IgA naphropathy (Berger’s disease). 133
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers 130
Evidence against the reported linkage of the cutaneous melanoma dysplastic nevus syndrome locus to chromosome 1p36. 127
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's Syndrome 124
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome 120
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects 119
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 117
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families 113
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA) 111
Malformazioni renali non cistiche ad espressione fenotipica variabile : descrizione di una famiglia 109
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease 108
Genetics and nephro-uropathies 105
Pregnancy, microchimerism and autoimmunity: An update 97
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndome 92
Totale 9.231
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Categoria #
all - tutte 30.181
article - articoli 28.590
book - libri 0
conference - conferenze 630
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 961
Totale 60.362
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022264 0 0 0 0 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
2026/2027665 37 83 165 356 24 0 0 0 0 0 0 0
Totale 9.231