GOMEZ, Maria Macarena
 Distribuzione geografica
Continente #
NA - Nord America 3.050
EU - Europa 2.661
AS - Asia 773
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 3
SA - Sud America 3
AF - Africa 1
Totale 6.499
Nazione #
US - Stati Uniti d'America 3.045
GB - Regno Unito 1.101
CN - Cina 722
SE - Svezia 288
FR - Francia 237
IT - Italia 232
IE - Irlanda 222
FI - Finlandia 185
DE - Germania 178
BE - Belgio 111
UA - Ucraina 55
VN - Vietnam 19
NL - Olanda 14
TR - Turchia 10
AU - Australia 8
RU - Federazione Russa 8
CA - Canada 5
IN - India 5
CZ - Repubblica Ceca 4
IL - Israele 4
CH - Svizzera 3
ES - Italia 3
ID - Indonesia 3
AL - Albania 2
BR - Brasile 2
DK - Danimarca 2
EU - Europa 2
HR - Croazia 2
IR - Iran 2
JP - Giappone 2
LV - Lettonia 2
MN - Mongolia 2
NO - Norvegia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AT - Austria 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
CL - Cile 1
EE - Estonia 1
EG - Egitto 1
GR - Grecia 1
IM - Isola di Man 1
LU - Lussemburgo 1
ME - Montenegro 1
MK - Macedonia 1
NP - Nepal 1
PL - Polonia 1
SA - Arabia Saudita 1
Totale 6.499
Città #
Southend 992
Chandler 588
Jacksonville 494
Ann Arbor 315
Woodbridge 279
Dublin 222
Ashburn 205
Houston 141
Beijing 122
Verona 120
Brussels 111
New York 102
Wilmington 89
Jinan 87
Lawrence 77
Princeton 77
Nanjing 66
Helsinki 61
Shenyang 58
Hebei 45
Tianjin 37
Sindelfingen 36
Haikou 33
Ningbo 30
Boardman 28
Nanchang 27
Changsha 25
Hangzhou 25
Zhengzhou 25
Jiaxing 21
Redmond 21
Seattle 20
San Francisco 17
Taizhou 17
Bologna 16
Milan 16
Taiyuan 16
Düsseldorf 15
Falls Church 15
Philadelphia 14
Auburn Hills 13
Dong Ket 13
Norwalk 13
Chicago 12
Dearborn 12
Guangzhou 12
Lancaster 12
Lanzhou 10
Redwood City 9
Washington 9
Fairfield 8
Fuzhou 7
Detroit 6
Hanover 6
Los Angeles 6
Edinburgh 5
Frankfurt am Main 5
Leawood 5
Cagliari 4
Clearwater 4
Dongguan 4
Mehlingen 4
Melbourne 4
Riva 4
Tombolo 4
Toronto 4
Brno 3
Città Di Castello 3
Lappeenranta 3
Leeds 3
London 3
Lonigo 3
Naples 3
Paris 3
Ypsilanti 3
Berlin 2
Chions 2
Copenhagen 2
Eboli 2
Ede 2
Haifa 2
Henderson 2
Kemerovo 2
Madrid 2
Mumbai 2
Newbury Park 2
Oslo 2
Pedrengo 2
Pescara 2
Riga 2
Sant'Ambrogio di Valpolicella 2
Aarau 1
Adelaide 1
Alatri 1
Ardabil 1
Augusta 1
Avezzano 1
Baku 1
Boydton 1
Breganze 1
Totale 4.968
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 144
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 141
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 127
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 123
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 119
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 118
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 118
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 116
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 115
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 112
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 112
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia. 111
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 109
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 109
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. 108
Splicing mutation causes infantile Sandhoff disease 107
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 107
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 106
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 106
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 103
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 97
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 97
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 97
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 97
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 95
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 95
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 94
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 91
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 91
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 90
CD45 and Multiple Sclerosis: the exon 4 C77G polymorphism and new markers 90
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 89
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 88
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 88
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 87
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)) 86
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 86
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 86
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 84
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 84
HDAC9 gene is overexpressed in stroke patients 84
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 84
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 83
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 82
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 80
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 79
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 78
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 77
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 76
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 76
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 75
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 74
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 74
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 73
Mutations associated with very late-onset metachromatic leukodystrophy. 72
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 72
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 69
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 69
Osteogenesis Imperfecta at the beginning of bone and joint decade 67
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 67
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 67
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 64
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 62
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. 62
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 61
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 59
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 57
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 55
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 52
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 47
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 47
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 47
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 42
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 40
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 37
null 35
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 28
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 27
Expression of FBXW11 in normal and disease-associated osteogenic cells 26
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 23
Adult-onset MLD: A gene mutation with isolated polyneuropathy 1
Totale 6.573
Categoria #
all - tutte 17.146
article - articoli 13.973
book - libri 0
conference - conferenze 2.993
curatela - curatele 0
other - altro 180
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 34.292


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201959 0 0 0 0 0 0 0 0 9 15 19 16
2019/2020814 86 28 2 77 115 72 108 56 28 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
2022/20231.649 105 185 150 267 138 363 32 108 193 21 54 33
2023/2024723 35 62 82 132 136 161 50 57 8 0 0 0
Totale 6.573