CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
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Continente #
NA - Nord America 5.302
EU - Europa 4.814
AS - Asia 2.862
SA - Sud America 408
AF - Africa 52
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 13.454
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Nazione #
US - Stati Uniti d'America 5.228
RU - Federazione Russa 1.849
SG - Singapore 1.177
GB - Regno Unito 1.146
CN - Cina 1.008
BR - Brasile 329
SE - Svezia 304
IT - Italia 283
DE - Germania 274
FR - Francia 254
FI - Finlandia 245
HK - Hong Kong 218
IE - Irlanda 217
VN - Vietnam 180
KR - Corea 68
UA - Ucraina 60
BE - Belgio 50
CA - Canada 41
JP - Giappone 40
IN - India 36
AR - Argentina 34
NL - Olanda 33
TR - Turchia 27
PL - Polonia 25
ID - Indonesia 23
MX - Messico 22
ZA - Sudafrica 20
BD - Bangladesh 15
ES - Italia 14
AU - Australia 13
IQ - Iraq 13
EC - Ecuador 10
AT - Austria 9
PY - Paraguay 9
VE - Venezuela 8
BJ - Benin 7
CZ - Repubblica Ceca 7
IL - Israele 7
EG - Egitto 6
LT - Lituania 6
PK - Pakistan 6
AZ - Azerbaigian 5
KZ - Kazakistan 5
LV - Lettonia 5
SA - Arabia Saudita 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
CH - Svizzera 4
CL - Cile 4
CO - Colombia 4
IR - Iran 4
JO - Giordania 4
KE - Kenya 4
MA - Marocco 4
NO - Norvegia 4
PE - Perù 4
AL - Albania 3
BG - Bulgaria 3
DK - Danimarca 3
NP - Nepal 3
UY - Uruguay 3
UZ - Uzbekistan 3
BO - Bolivia 2
CR - Costa Rica 2
EE - Estonia 2
EU - Europa 2
GT - Guatemala 2
HR - Croazia 2
KG - Kirghizistan 2
LU - Lussemburgo 2
MD - Moldavia 2
MN - Mongolia 2
MY - Malesia 2
PA - Panama 2
SN - Senegal 2
TG - Togo 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
IM - Isola di Man 1
JM - Giamaica 1
KW - Kuwait 1
LB - Libano 1
ME - Montenegro 1
MK - Macedonia 1
NG - Nigeria 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
Totale 13.454
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Città #
Dallas 1.203
Southend 992
Moscow 634
Chandler 588
Singapore 584
Jacksonville 494
Ashburn 448
Ann Arbor 315
Woodbridge 279
Hong Kong 218
Dublin 217
Beijing 181
Houston 149
New York 139
Verona 126
Wilmington 89
Jinan 88
Los Angeles 86
The Dalles 78
Lawrence 77
Princeton 77
Helsinki 75
Munich 75
Nanjing 66
Shenyang 59
Ho Chi Minh City 58
Brussels 50
Tianjin 49
Hebei 45
São Paulo 44
Hanoi 41
Turku 39
Columbus 38
Boardman 36
Sindelfingen 36
Tokyo 35
Haikou 33
Buffalo 31
Santa Clara 31
Ningbo 30
Changsha 28
Hangzhou 27
Nanchang 27
Council Bluffs 26
Redondo Beach 26
San Francisco 26
Zhengzhou 26
Seattle 24
Guangzhou 21
Jiaxing 21
London 21
Redmond 21
Bologna 19
Denver 18
Milan 18
Montreal 18
Warsaw 18
Chennai 17
Taizhou 17
Brooklyn 16
Stockholm 16
Taiyuan 16
Düsseldorf 15
Falls Church 15
Jakarta 15
Phoenix 14
Rio de Janeiro 14
Seoul 14
Atlanta 13
Auburn Hills 13
Dong Ket 13
Johannesburg 13
Lancaster 13
Norwalk 13
Orem 13
Chicago 12
Dearborn 12
Frankfurt am Main 12
Boston 11
Falkenstein 11
Kent 11
Lanzhou 10
Lappeenranta 10
Rome 10
San Jose 10
Mumbai 9
Redwood City 9
Toronto 9
Washington 9
Amsterdam 8
Da Nang 8
Fairfield 8
Melbourne 8
Ankara 7
Biên Hòa 7
Cotonou 7
Detroit 7
Fuzhou 7
Nuremberg 7
Philadelphia 7
Totale 8.804
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Nome #
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 269
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 266
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 261
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 253
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain 239
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 226
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 226
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 225
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 221
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 220
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 216
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 213
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 213
TLR4 -2604G>A variant confers differential DNA binding capacity to transcription factors of the GATA family and alters gene expression in peripheral blood of atherosclerotic patients. 207
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 206
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 205
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 203
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 197
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 197
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 192
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 189
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 184
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 181
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 181
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 181
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 178
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 177
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 176
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 175
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 174
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 174
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 173
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 171
HDAC9 gene is overexpressed in stroke patients 170
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 169
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 169
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 169
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. 168
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 165
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation 164
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 159
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 158
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 157
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 157
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 156
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 154
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 154
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene 150
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 150
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 150
Splicing mutation causes infantile Sandhoff disease 149
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 149
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 147
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 145
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 145
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 144
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 140
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 137
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 135
Upregulation of miR-34a-5p, miR-20a-3p and miR-29a-3p by onconase in A375 melanoma cells correlates with the downregulation of specific onco-proteins 132
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 131
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation acid show different phenotypes; description of a novel null-type mutation (Human Genetics (1998) 102 (459-463)) 128
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 127
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 127
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 127
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 126
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 124
Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II Osteogenesis Imperfecta dramatically affects the mineralization of bone 124
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 121
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 120
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 118
Osteogenesis Imperfecta at the beginning of bone and joint decade 117
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 115
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 115
Mutations associated with very late-onset metachromatic leukodystrophy. 114
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 114
Expression of FBXW11 in normal and disease-associated osteogenic cells 113
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 107
Melanoma risk alleles are associated with down-regulation of the MTAP gene and hyper-methylation of a CpG Island upstream of the gene in dermal fibroblasts 90
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 89
Sex-dependent interaction of PTGS2 with miR-146a as risk factor for melanoma and the impact of sex hormones in gene expression in skin cells 87
Adult-onset MLD: A gene mutation with isolated polyneuropathy 82
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 70
null 35
Totale 13.532
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Categoria #
all - tutte 40.239
article - articoli 32.988
book - libri 0
conference - conferenze 6.847
curatela - curatele 0
other - altro 404
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 80.478
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021340 0 0 0 0 0 66 19 72 62 13 72 36
2021/2022741 63 211 5 84 16 24 14 39 39 19 51 176
2022/20231.592 105 185 150 267 138 363 20 105 185 8 47 19
2023/2024864 24 56 77 118 120 161 50 57 10 32 107 52
2024/20251.906 112 120 66 291 110 52 142 91 291 84 169 378
2025/20264.969 416 406 1.076 1.049 1.643 379 0 0 0 0 0 0
Totale 13.532