CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
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Continente #
NA - Nord America 4.783
EU - Europa 3.101
AS - Asia 2.211
SA - Sud America 318
AF - Africa 28
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 10.457
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Nazione #
US - Stati Uniti d'America 4.741
GB - Regno Unito 1.117
CN - Cina 889
SG - Singapore 841
SE - Svezia 291
IT - Italia 281
BR - Brasile 278
DE - Germania 273
FR - Francia 253
FI - Finlandia 243
RU - Federazione Russa 221
HK - Hong Kong 218
IE - Irlanda 217
UA - Ucraina 60
KR - Corea 59
VN - Vietnam 58
BE - Belgio 50
NL - Olanda 29
JP - Giappone 26
CA - Canada 23
ID - Indonesia 21
TR - Turchia 21
IN - India 18
AR - Argentina 16
AU - Australia 13
MX - Messico 11
PL - Polonia 10
AT - Austria 9
EC - Ecuador 9
ZA - Sudafrica 9
BD - Bangladesh 7
CZ - Repubblica Ceca 7
IL - Israele 7
AZ - Azerbaigian 5
IQ - Iraq 5
LV - Lettonia 5
SA - Arabia Saudita 5
CL - Cile 4
EG - Egitto 4
JO - Giordania 4
KE - Kenya 4
KZ - Kazakistan 4
NO - Norvegia 4
PK - Pakistan 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
CH - Svizzera 3
CO - Colombia 3
DK - Danimarca 3
ES - Italia 3
IR - Iran 3
LT - Lituania 3
MA - Marocco 3
NP - Nepal 3
PY - Paraguay 3
TN - Tunisia 3
UZ - Uzbekistan 3
AL - Albania 2
BO - Bolivia 2
CR - Costa Rica 2
EE - Estonia 2
EU - Europa 2
HR - Croazia 2
KG - Kirghizistan 2
LU - Lussemburgo 2
MN - Mongolia 2
PA - Panama 2
SN - Senegal 2
TG - Togo 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
DZ - Algeria 1
GD - Grenada 1
GE - Georgia 1
GR - Grecia 1
HN - Honduras 1
IM - Isola di Man 1
JM - Giamaica 1
ME - Montenegro 1
MK - Macedonia 1
MY - Malesia 1
PE - Perù 1
PS - Palestinian Territory 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
Totale 10.457
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Città #
Dallas 1.202
Southend 992
Chandler 588
Jacksonville 494
Singapore 387
Ann Arbor 315
Woodbridge 279
Ashburn 275
Hong Kong 218
Dublin 217
Beijing 150
Houston 143
Verona 126
New York 106
Wilmington 89
Jinan 88
Lawrence 77
Princeton 77
Helsinki 75
Munich 75
Nanjing 66
Shenyang 59
Los Angeles 51
Brussels 50
Hebei 45
Tianjin 39
Turku 39
Columbus 38
Boardman 36
Sindelfingen 36
The Dalles 36
Haikou 33
Buffalo 30
Ningbo 30
Changsha 27
Nanchang 27
Hangzhou 26
Zhengzhou 26
San Francisco 25
Santa Clara 25
São Paulo 25
Redondo Beach 23
Council Bluffs 22
Seattle 22
Jiaxing 21
Redmond 21
Tokyo 21
Bologna 19
Guangzhou 19
Milan 18
Taizhou 17
Taiyuan 16
Düsseldorf 15
Falls Church 15
Ho Chi Minh City 15
Jakarta 15
Rio de Janeiro 14
Seoul 14
Auburn Hills 13
Dong Ket 13
Lancaster 13
Norwalk 13
Dearborn 12
Frankfurt am Main 12
Chicago 11
Hanoi 11
Kent 11
Falkenstein 10
Lanzhou 10
Moscow 10
Redwood City 9
Washington 9
Brooklyn 8
Fairfield 8
Lappeenranta 8
London 8
Melbourne 8
Rome 8
Detroit 7
Fuzhou 7
Nuremberg 7
Philadelphia 7
Warsaw 7
Dongguan 6
Fortaleza 6
Ottawa 6
Toronto 6
Atlanta 5
Cotia 5
Edinburgh 5
Guayaquil 5
Leawood 5
Montreal 5
Mumbai 5
Phoenix 5
Riga 5
Amman 4
Amsterdam 4
Baku 4
Belo Horizonte 4
Totale 7.374
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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 221
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 212
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 202
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 202
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 180
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 179
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 179
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 176
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 170
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 167
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 166
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 166
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. 163
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 162
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 161
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 161
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 160
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 160
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 157
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 148
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 146
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 144
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 140
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 139
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 139
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 139
Splicing mutation causes infantile Sandhoff disease 137
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 136
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 134
HDAC9 gene is overexpressed in stroke patients 133
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 132
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 132
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 131
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 131
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 129
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 129
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 127
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 127
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 127
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 127
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. 127
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 126
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 126
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 126
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 125
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 124
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 122
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 122
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 122
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)) 116
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 115
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 115
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 114
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 112
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 112
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 112
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 112
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 109
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 108
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 107
Osteogenesis Imperfecta at the beginning of bone and joint decade 106
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 106
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 106
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 105
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 104
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 103
Mutations associated with very late-onset metachromatic leukodystrophy. 102
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 102
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 100
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 93
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 92
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 91
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 89
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 87
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 86
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 82
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 81
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 73
Expression of FBXW11 in normal and disease-associated osteogenic cells 63
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 56
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 54
Adult-onset MLD: A gene mutation with isolated polyneuropathy 51
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 45
null 35
Totale 10.535
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Categoria #
all - tutte 34.995
article - articoli 28.738
book - libri 0
conference - conferenze 5.889
curatela - curatele 0
other - altro 368
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 69.990
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021495 0 0 0 73 82 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
2025/20261.972 416 406 1.076 74 0 0 0 0 0 0 0 0
Totale 10.535