CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
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Continente #
NA - Nord America 7.332
EU - Europa 5.125
AS - Asia 3.332
SA - Sud America 478
Continente sconosciuto - Info sul continente non disponibili 91
AF - Africa 90
OC - Oceania 13
Totale 16.461
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Nazione #
US - Stati Uniti d'America 7.154
RU - Federazione Russa 1.855
SG - Singapore 1.321
GB - Regno Unito 1.179
CN - Cina 1.049
IT - Italia 455
BR - Brasile 368
SE - Svezia 306
VN - Vietnam 299
DE - Germania 288
FR - Francia 271
FI - Finlandia 255
HK - Hong Kong 234
IE - Irlanda 221
KR - Corea 95
CA - Canada 87
UA - Ucraina 63
IN - India 52
BE - Belgio 51
JP - Giappone 51
BD - Bangladesh 49
AR - Argentina 45
NL - Olanda 43
ID - Indonesia 35
TR - Turchia 34
PL - Polonia 28
MX - Messico 27
IQ - Iraq 25
ZA - Sudafrica 24
ES - Italia 20
NG - Nigeria 17
GT - Guatemala 16
EC - Ecuador 15
VE - Venezuela 14
AU - Australia 13
PY - Paraguay 11
CR - Costa Rica 10
EG - Egitto 10
PK - Pakistan 10
SA - Arabia Saudita 10
AT - Austria 9
CH - Svizzera 9
CW - ???statistics.table.value.countryCode.CW??? 9
TN - Tunisia 9
CZ - Repubblica Ceca 8
IL - Israele 8
LT - Lituania 8
BJ - Benin 7
CL - Cile 7
CO - Colombia 7
KZ - Kazakistan 7
LV - Lettonia 7
MA - Marocco 7
MY - Malesia 7
SV - El Salvador 7
JM - Giamaica 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
AZ - Azerbaigian 5
IR - Iran 5
JO - Giordania 5
KE - Kenya 5
NO - Norvegia 5
PE - Perù 5
DK - Danimarca 4
EE - Estonia 4
GR - Grecia 4
HN - Honduras 4
PH - Filippine 4
PR - Porto Rico 4
BG - Bulgaria 3
HR - Croazia 3
NP - Nepal 3
PA - Panama 3
PT - Portogallo 3
RS - Serbia 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
BO - Bolivia 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EU - Europa 2
GD - Grenada 2
GP - Guadalupe 2
KG - Kirghizistan 2
LB - Libano 2
LU - Lussemburgo 2
LY - Libia 2
MD - Moldavia 2
MK - Macedonia 2
MN - Mongolia 2
NI - Nicaragua 2
OM - Oman 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TG - Togo 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
Totale 16.366
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Città #
Dallas 1.244
Ashburn 1.054
Southend 992
Singapore 696
Moscow 634
Chandler 588
San Jose 533
Jacksonville 497
Ann Arbor 315
Woodbridge 279
Hong Kong 229
Dublin 222
Verona 215
Beijing 189
Council Bluffs 168
New York 159
Houston 155
The Dalles 133
Los Angeles 104
Ho Chi Minh City 100
Wilmington 90
Jinan 88
Helsinki 85
Lawrence 78
Princeton 77
Munich 76
Hanoi 74
Nanjing 66
São Paulo 64
Shenyang 59
Santa Clara 55
Brussels 51
Tianjin 49
Hebei 45
Tokyo 43
Buffalo 40
Columbus 39
Turku 39
Boardman 37
Sindelfingen 36
Haikou 33
San Francisco 31
Ningbo 30
Orem 30
Montreal 29
Changsha 28
London 28
Hangzhou 27
Nanchang 27
Redondo Beach 27
Milan 26
Seattle 26
Zhengzhou 26
Frankfurt am Main 24
Denver 23
Jakarta 23
Chennai 22
Brooklyn 21
Guangzhou 21
Jiaxing 21
Redmond 21
Atlanta 20
Bologna 20
Warsaw 20
Phoenix 18
Toronto 18
Stockholm 17
Taizhou 17
Johannesburg 16
Rio de Janeiro 16
Rome 16
Taiyuan 16
Amsterdam 15
Chicago 15
Düsseldorf 15
Falls Church 15
Seoul 15
Da Nang 14
Norwalk 14
Abuja 13
Annandale 13
Auburn Hills 13
Dong Ket 13
Lancaster 13
Dearborn 12
Kent 12
Paris 12
Philadelphia 12
Washington 12
Boston 11
Falkenstein 11
Lanzhou 10
Lappeenranta 10
Mumbai 10
Baghdad 9
Guatemala City 9
Naples 9
Redwood City 9
Willemstad 9
Cairo 8
Totale 10.768
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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 324
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 315
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 293
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 281
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 280
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 270
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 269
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 269
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 264
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 261
HDAC9 gene is overexpressed in stroke patients 261
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. 259
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 257
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 257
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 257
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 251
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 245
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 244
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 237
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 237
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 223
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 223
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 221
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 220
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 219
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 218
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 214
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 213
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 208
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 207
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 206
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 206
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 206
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 203
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 202
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 201
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 200
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 200
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. 200
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 197
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 196
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 193
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 189
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 187
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 187
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 187
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 185
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 185
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 184
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 182
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 182
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 179
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 178
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 173
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 172
Splicing mutation causes infantile Sandhoff disease 171
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 168
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 167
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 167
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 160
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 159
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 159
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 158
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 156
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 151
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)) 149
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 148
Expression of FBXW11 in normal and disease-associated osteogenic cells 144
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 144
Osteogenesis Imperfecta at the beginning of bone and joint decade 144
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 142
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 142
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 142
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 141
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 140
Mutations associated with very late-onset metachromatic leukodystrophy. 134
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 134
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 124
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 121
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 111
Adult-onset MLD: A gene mutation with isolated polyneuropathy 106
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 92
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 36
null 35
Totale 16.461
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Categoria #
all - tutte 50.302
article - articoli 41.163
book - libri 0
conference - conferenze 8.532
curatela - curatele 0
other - altro 607
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 100.604
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022462 0 0 0 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
2026/20271.162 58 131 276 697 0 0 0 0 0 0 0 0
Totale 16.461