CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
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Continente #
NA - Nord America 6.461
EU - Europa 5.069
AS - Asia 3.316
SA - Sud America 456
AF - Africa 89
Continente sconosciuto - Info sul continente non disponibili 82
OC - Oceania 13
Totale 15.486
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Nazione #
US - Stati Uniti d'America 6.357
RU - Federazione Russa 1.849
SG - Singapore 1.320
GB - Regno Unito 1.174
CN - Cina 1.049
IT - Italia 422
BR - Brasile 354
SE - Svezia 306
VN - Vietnam 298
DE - Germania 285
FR - Francia 269
FI - Finlandia 255
HK - Hong Kong 234
IE - Irlanda 221
KR - Corea 95
UA - Ucraina 62
CA - Canada 55
IN - India 52
BE - Belgio 51
JP - Giappone 51
BD - Bangladesh 48
AR - Argentina 45
NL - Olanda 42
TR - Turchia 33
ID - Indonesia 32
PL - Polonia 28
MX - Messico 27
IQ - Iraq 25
ZA - Sudafrica 24
ES - Italia 20
NG - Nigeria 17
AU - Australia 13
EC - Ecuador 12
PY - Paraguay 11
EG - Egitto 10
SA - Arabia Saudita 10
VE - Venezuela 10
AT - Austria 9
CH - Svizzera 9
PK - Pakistan 9
TN - Tunisia 9
CZ - Repubblica Ceca 8
BJ - Benin 7
CL - Cile 7
IL - Israele 7
KZ - Kazakistan 7
LT - Lituania 7
MA - Marocco 7
CO - Colombia 6
LV - Lettonia 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
AZ - Azerbaigian 5
CR - Costa Rica 5
JO - Giordania 5
KE - Kenya 5
NO - Norvegia 5
PE - Perù 5
GR - Grecia 4
IR - Iran 4
BG - Bulgaria 3
DK - Danimarca 3
GT - Guatemala 3
HR - Croazia 3
MY - Malesia 3
NP - Nepal 3
PH - Filippine 3
PT - Portogallo 3
RS - Serbia 3
UY - Uruguay 3
BO - Bolivia 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EE - Estonia 2
EU - Europa 2
GD - Grenada 2
JM - Giamaica 2
KG - Kirghizistan 2
LB - Libano 2
LU - Lussemburgo 2
LY - Libia 2
MD - Moldavia 2
MK - Macedonia 2
MN - Mongolia 2
OM - Oman 2
PA - Panama 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
SV - El Salvador 2
TG - Togo 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
HN - Honduras 1
IM - Isola di Man 1
Totale 15.398
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Città #
Dallas 1.207
Southend 992
Singapore 696
Ashburn 678
Moscow 634
Chandler 588
Jacksonville 495
San Jose 467
Ann Arbor 315
Woodbridge 279
Hong Kong 229
Dublin 221
Verona 214
Beijing 189
Council Bluffs 168
New York 155
Houston 153
The Dalles 133
Ho Chi Minh City 100
Los Angeles 99
Wilmington 90
Jinan 88
Helsinki 85
Lawrence 77
Princeton 77
Munich 76
Hanoi 73
Nanjing 66
Shenyang 59
Brussels 51
São Paulo 51
Santa Clara 50
Tianjin 49
Hebei 45
Tokyo 43
Buffalo 39
Turku 39
Columbus 38
Boardman 37
Sindelfingen 36
Haikou 33
Ningbo 30
Orem 30
Changsha 28
London 28
San Francisco 28
Hangzhou 27
Nanchang 27
Redondo Beach 27
Montreal 26
Zhengzhou 26
Milan 24
Seattle 24
Jakarta 23
Chennai 22
Frankfurt am Main 21
Guangzhou 21
Jiaxing 21
Redmond 21
Denver 20
Warsaw 20
Bologna 19
Brooklyn 17
Stockholm 17
Taizhou 17
Atlanta 16
Johannesburg 16
Rio de Janeiro 16
Taiyuan 16
Amsterdam 15
Düsseldorf 15
Falls Church 15
Seoul 15
Chicago 14
Da Nang 14
Phoenix 14
Abuja 13
Auburn Hills 13
Dong Ket 13
Lancaster 13
Norwalk 13
Rome 13
Dearborn 12
Kent 12
Paris 12
Philadelphia 12
Boston 11
Falkenstein 11
Lanzhou 10
Lappeenranta 10
Mumbai 10
Toronto 10
Washington 10
Baghdad 9
Redwood City 9
Cairo 8
City of London 8
Detroit 8
Fairfield 8
Melbourne 8
Totale 10.200
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Nome #
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 306
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 296
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 286
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 273
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 263
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 260
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 258
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 257
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 252
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 250
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 250
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 249
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 237
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 236
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. 233
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 229
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 229
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 226
HDAC9 gene is overexpressed in stroke patients 221
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 218
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 216
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 216
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
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 206
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 203
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 202
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 202
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 201
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 199
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 199
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 197
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
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 194
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 194
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 193
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 193
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 190
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 190
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 190
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 189
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 181
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 181
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 176
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 176
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 174
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 174
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 174
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 171
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 171
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 170
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 170
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 166
Splicing mutation causes infantile Sandhoff disease 164
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 164
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 164
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 160
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 159
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 154
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 154
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 153
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 151
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 148
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 147
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 142
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 142
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 141
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 138
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)) 137
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 136
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 136
Expression of FBXW11 in normal and disease-associated osteogenic cells 135
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 135
Osteogenesis Imperfecta at the beginning of bone and joint decade 135
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 134
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 132
Mutations associated with very late-onset metachromatic leukodystrophy. 128
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 121
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 115
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 111
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 105
Adult-onset MLD: A gene mutation with isolated polyneuropathy 101
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 88
null 35
Serum Levels of miR-34a-5p, miR-30b-5p, and miR-140-5p Are Associated with Disease Activity and Brain Atrophy in Early Multiple Sclerosis 24
Totale 15.486
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Categoria #
all - tutte 47.493
article - articoli 39.017
book - libri 0
conference - conferenze 8.006
curatela - curatele 0
other - altro 470
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 94.986
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022678 0 211 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
2025/20266.736 416 406 1.076 1.049 1.643 411 533 265 448 304 60 125
2026/2027187 58 129 0 0 0 0 0 0 0 0 0 0
Totale 15.486