GOMEZ, Maria Macarena
 Distribuzione geografica
Continente #
NA - Nord America 3.219
EU - Europa 2.874
AS - Asia 1.568
SA - Sud America 164
AF - Africa 16
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 3
Totale 7.856
Nazione #
US - Stati Uniti d'America 3.201
GB - Regno Unito 1.105
CN - Cina 824
SG - Singapore 594
SE - Svezia 289
IT - Italia 271
FR - Francia 237
IE - Irlanda 216
FI - Finlandia 198
RU - Federazione Russa 194
DE - Germania 183
BR - Brasile 142
UA - Ucraina 57
BE - Belgio 50
NL - Olanda 27
HK - Hong Kong 24
KR - Corea 21
VN - Vietnam 21
TR - Turchia 18
ID - Indonesia 13
AU - Australia 12
JP - Giappone 12
CA - Canada 11
AR - Argentina 8
IN - India 6
EC - Ecuador 5
IL - Israele 5
LV - Lettonia 5
AT - Austria 4
AZ - Azerbaigian 4
CZ - Repubblica Ceca 4
AE - Emirati Arabi Uniti 3
CH - Svizzera 3
CO - Colombia 3
EG - Egitto 3
ES - Italia 3
IR - Iran 3
KZ - Kazakistan 3
LT - Lituania 3
MA - Marocco 3
MX - Messico 3
NO - Norvegia 3
ZA - Sudafrica 3
AL - Albania 2
BG - Bulgaria 2
CL - Cile 2
DK - Danimarca 2
EE - Estonia 2
EU - Europa 2
HR - Croazia 2
IQ - Iraq 2
KE - Kenya 2
KG - Kirghizistan 2
LU - Lussemburgo 2
MN - Mongolia 2
PA - Panama 2
PK - Pakistan 2
PL - Polonia 2
PY - Paraguay 2
TG - Togo 2
TN - Tunisia 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BO - Bolivia 1
BY - Bielorussia 1
CR - Costa Rica 1
GE - Georgia 1
GR - Grecia 1
IM - Isola di Man 1
JM - Giamaica 1
JO - Giordania 1
ME - Montenegro 1
MK - Macedonia 1
MY - Malesia 1
NP - Nepal 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
VE - Venezuela 1
Totale 7.856
Città #
Southend 992
Chandler 588
Jacksonville 494
Singapore 345
Ann Arbor 315
Woodbridge 279
Ashburn 234
Dublin 216
Beijing 141
Houston 141
Verona 126
New York 103
Wilmington 89
Jinan 87
Lawrence 77
Princeton 77
Helsinki 74
Nanjing 66
Shenyang 58
Brussels 50
Hebei 45
Tianjin 37
Boardman 36
Sindelfingen 36
Haikou 33
Ningbo 30
Nanchang 27
Changsha 25
Hangzhou 25
Zhengzhou 25
Hong Kong 24
Jiaxing 21
Redmond 21
Seattle 20
Bologna 17
San Francisco 17
Taizhou 17
Milan 16
Taiyuan 16
Council Bluffs 15
Düsseldorf 15
Falls Church 15
Guangzhou 15
Santa Clara 14
Auburn Hills 13
Dallas 13
Dong Ket 13
Lancaster 13
Norwalk 13
Seoul 13
Dearborn 12
Los Angeles 12
São Paulo 12
Kent 11
Lanzhou 10
Jakarta 9
Moscow 9
Redwood City 9
Washington 9
Fairfield 8
Melbourne 8
Rio de Janeiro 8
Rome 8
Tokyo 8
Chicago 7
Fuzhou 7
Philadelphia 7
Detroit 6
Dongguan 6
Frankfurt am Main 6
London 6
Edinburgh 5
Leawood 5
Ottawa 5
Riga 5
Toronto 5
Amsterdam 4
Baku 4
Cagliari 4
Clearwater 4
Mehlingen 4
Riva 4
Tombolo 4
Belo Horizonte 3
Bogotá 3
Brno 3
Buenos Aires 3
Cairo 3
Città Di Castello 3
Curitiba 3
Fortaleza 3
Guayaquil 3
Lappeenranta 3
Leeds 3
Lonigo 3
Munich 3
Naples 3
Nuremberg 3
Oslo 3
Paris 3
Totale 5.474
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 169
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 165
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 146
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 141
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 136
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 134
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 134
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 134
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 132
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 130
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 129
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. 128
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 128
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 125
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 125
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 124
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 124
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 121
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 117
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 116
Splicing mutation causes infantile Sandhoff disease 116
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 116
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 111
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 110
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 110
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 109
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 108
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 107
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 107
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 105
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 105
HDAC9 gene is overexpressed in stroke patients 105
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 105
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 103
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 102
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 102
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 101
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 101
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 101
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 100
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 100
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 99
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 99
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 97
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)) 96
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 96
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 96
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 96
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 93
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 93
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 91
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 90
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 90
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 87
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 87
Mutations associated with very late-onset metachromatic leukodystrophy. 85
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. 85
Osteogenesis Imperfecta at the beginning of bone and joint decade 83
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 83
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 83
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 82
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 82
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 81
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 80
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 78
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 78
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 76
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 74
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 71
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 70
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 66
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 63
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 57
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 51
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 51
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 49
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 44
Expression of FBXW11 in normal and disease-associated osteogenic cells 39
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 36
null 35
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 23
Adult-onset MLD: A gene mutation with isolated polyneuropathy 21
New Axes of Interaction in Circ_0079593/miR-516b-5p Network in Melanoma Metastasis Cell Lines 15
Totale 7.933
Categoria #
all - tutte 26.780
article - articoli 21.857
book - libri 0
conference - conferenze 4.624
curatela - curatele 0
other - altro 299
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 53.560


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020242 0 0 0 0 0 0 0 0 0 81 60 101
2020/2021815 128 139 53 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
2024/20251.276 112 120 66 291 110 52 142 91 291 1 0 0
Totale 7.933