CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 6.162
EU - Europa 5.028
AS - Asia 3.278
SA - Sud America 451
AF - Africa 89
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 15.024
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.068
RU - Federazione Russa 1.849
SG - Singapore 1.311
GB - Regno Unito 1.174
CN - Cina 1.041
IT - Italia 390
BR - Brasile 352
SE - Svezia 305
VN - Vietnam 298
DE - Germania 285
FR - Francia 266
FI - Finlandia 255
HK - Hong Kong 233
IE - Irlanda 221
KR - Corea 95
UA - Ucraina 62
IN - India 52
BE - Belgio 51
CA - Canada 51
JP - Giappone 51
AR - Argentina 44
NL - Olanda 40
TR - Turchia 33
ID - Indonesia 32
BD - Bangladesh 28
PL - Polonia 28
IQ - Iraq 25
MX - Messico 25
ZA - Sudafrica 24
ES - Italia 18
NG - Nigeria 17
AU - Australia 13
EC - Ecuador 12
EG - Egitto 10
PY - Paraguay 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
LV - Lettonia 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
AZ - Azerbaigian 5
CO - Colombia 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
RS - Serbia 3
UY - Uruguay 3
BO - Bolivia 2
CR - Costa Rica 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
PT - Portogallo 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 15.016
Salva come PNG Salva come JPEG
Città #
Dallas 1.206
Southend 992
Singapore 696
Ashburn 663
Moscow 634
Chandler 588
Jacksonville 495
San Jose 442
Ann Arbor 315
Woodbridge 279
Hong Kong 228
Dublin 221
Verona 214
Beijing 183
Houston 152
New York 151
The Dalles 133
Ho Chi Minh City 100
Los Angeles 94
Wilmington 89
Jinan 88
Helsinki 85
Lawrence 77
Princeton 77
Munich 76
Hanoi 73
Nanjing 66
Shenyang 59
Brussels 51
São Paulo 50
Tianjin 49
Hebei 45
Tokyo 43
Turku 39
Columbus 38
Santa Clara 38
Boardman 37
Buffalo 36
Sindelfingen 36
Council Bluffs 33
Haikou 33
Ningbo 30
Orem 30
Changsha 28
London 28
San Francisco 28
Hangzhou 27
Nanchang 27
Redondo Beach 27
Montreal 26
Zhengzhou 26
Seattle 24
Jakarta 23
Chennai 22
Frankfurt am Main 21
Guangzhou 21
Jiaxing 21
Redmond 21
Warsaw 20
Bologna 19
Denver 18
Milan 18
Stockholm 17
Taizhou 17
Brooklyn 16
Johannesburg 16
Rio de Janeiro 16
Taiyuan 16
Amsterdam 15
Atlanta 15
Düsseldorf 15
Falls Church 15
Seoul 15
Da Nang 14
Phoenix 14
Abuja 13
Auburn Hills 13
Chicago 13
Dong Ket 13
Lancaster 13
Norwalk 13
Dearborn 12
Paris 12
Boston 11
Falkenstein 11
Kent 11
Lanzhou 10
Lappeenranta 10
Mumbai 10
Rome 10
Toronto 10
Baghdad 9
Redwood City 9
Washington 9
Cairo 8
City of London 8
Fairfield 8
Melbourne 8
Philadelphia 8
Ankara 7
Totale 9.969
Salva come PNG Salva come JPEG
Nome #
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 301
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 292
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 284
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 268
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 261
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 256
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 251
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 248
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 248
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 246
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 244
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 233
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 232
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. 230
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 228
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 227
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 226
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 224
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 214
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 212
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 212
HDAC9 gene is overexpressed in stroke patients 203
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 202
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 201
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 200
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 200
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 198
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 198
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 197
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 196
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 194
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 193
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. 192
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 192
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 192
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 191
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 188
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 187
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 187
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 185
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 184
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 178
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 176
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 171
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 169
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 169
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 169
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 169
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 169
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 167
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 167
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 165
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 162
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 162
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 161
Splicing mutation causes infantile Sandhoff disease 158
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 157
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 156
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 151
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 151
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 148
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 146
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 145
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 138
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 137
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 135
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 135
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 135
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)) 134
Expression of FBXW11 in normal and disease-associated osteogenic cells 133
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 133
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 132
Osteogenesis Imperfecta at the beginning of bone and joint decade 131
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 130
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 130
Mutations associated with very late-onset metachromatic leukodystrophy. 127
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 123
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 118
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 111
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 106
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 102
Adult-onset MLD: A gene mutation with isolated polyneuropathy 96
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 82
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 17
Totale 15.103
Salva come PNG Salva come JPEG
Categoria #
all - tutte 43.285
article - articoli 35.482
book - libri 0
conference - conferenze 7.372
curatela - curatele 0
other - altro 431
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 86.570
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021121 0 0 0 0 0 0 0 0 0 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
2025/20266.540 416 406 1.076 1.049 1.643 411 533 265 448 293 0 0
Totale 15.103