CATALOGO DEI PRODOTTI DELLA RICERCA

GOMEZ, Maria Macarena
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 2582
EU - Europa 2374
AS - Asia 702
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 3
SA - Sud America 2
AF - Africa 1
Totale 5670
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2577
GB - Regno Unito 1093
CN - Cina 652
SE - Svezia 288
FR - Francia 237
IT - Italia 211
IE - Irlanda 168
FI - Finlandia 122
DE - Germania 102
BE - Belgio 58
UA - Ucraina 55
VN - Vietnam 19
NL - Olanda 12
TR - Turchia 10
RU - Federazione Russa 8
AU - Australia 6
CA - Canada 5
IN - India 5
IL - Israele 4
CH - Svizzera 3
ES - Italia 3
ID - Indonesia 3
AL - Albania 2
DK - Danimarca 2
EU - Europa 2
HR - Croazia 2
IR - Iran 2
JP - Giappone 2
MN - Mongolia 2
NO - Norvegia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BR - Brasile 1
CL - Cile 1
EE - Estonia 1
EG - Egitto 1
GR - Grecia 1
IM - Isola di Man 1
LU - Lussemburgo 1
NP - Nepal 1
SA - Arabia Saudita 1
Totale 5670
Salva come PNG Salva come JPEG
Città #
Southend 992
Chandler 588
Jacksonville 494
Ann Arbor 315
Woodbridge 279
Dublin 168
Houston 141
Verona 120
Beijing 90
Wilmington 89
Jinan 87
Lawrence 77
Princeton 77
Nanjing 66
Ashburn 60
Brussels 58
Shenyang 58
Hebei 45
Tianjin 37
Haikou 33
Ningbo 30
Boardman 28
Nanchang 27
Changsha 25
Hangzhou 25
Zhengzhou 25
Jiaxing 21
Redmond 21
San Francisco 17
Taizhou 17
Bologna 16
Taiyuan 16
Düsseldorf 15
Falls Church 15
Milan 15
Auburn Hills 13
Dong Ket 13
Norwalk 13
Dearborn 12
Guangzhou 12
Lancaster 12
Lanzhou 10
Philadelphia 10
Redwood City 9
Fairfield 8
Fuzhou 7
Detroit 6
Los Angeles 6
Chicago 5
Leawood 5
Clearwater 4
New York 4
Riva 4
Tombolo 4
Toronto 4
Città Di Castello 3
Leeds 3
London 3
Lonigo 3
Melbourne 3
Paris 3
Ypsilanti 3
Berlin 2
Chions 2
Copenhagen 2
Haifa 2
Henderson 2
Kemerovo 2
Madrid 2
Mumbai 2
Oslo 2
Pescara 2
Sant'Ambrogio di Valpolicella 2
Aarau 1
Alatri 1
Ardabil 1
Augusta 1
Avezzano 1
Baku 1
Breganze 1
Büdelsdorf 1
Cairo 1
Canberra 1
Cerea 1
Changle 1
Chaoyang 1
Cupertino 1
Delhi 1
Douglas 1
El Cajon 1
Helsinki 1
Isola Della Scala 1
Istanbul 1
Jastrebarsko 1
Kharkov 1
Modesto 1
Modica 1
Monmouth Junction 1
Montréal 1
Novokuznetsk 1
Totale 4418
Salva come PNG Salva come JPEG
Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 129
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 129
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 115
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 110
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 106
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 105
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 103
Molecular detection of bacterial RNA in atheromatous plaques of patients with stroke 103
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 103
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 102
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 99
Splicing mutation causes infantile Sandhoff disease 98
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 96
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 96
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation 96
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy 94
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia. 93
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 92
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 89
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. 89
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 88
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 86
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 85
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 85
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 84
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 83
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 82
CD45 and Multiple Sclerosis: the exon 4 C77G polymorphism and new markers 82
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 82
High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia. 81
Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients 80
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 80
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 79
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)) 79
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 79
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 78
HDAC9 gene is overexpressed in stroke patients 78
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 76
Multiple self-healing squamous epithelioma in different ethnic groups: More than a founder mutation disorder? 75
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 75
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 75
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 74
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 73
Clinical, microbiologic and radiologic assessment of soft and hard tissues surrounding zygomatic implants: a retrospective study 71
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 70
Recurring familial epithelioma of Ferguson Smith in an eleven - year old child: case report. 69
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 68
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 66
Espressione dei geni COX-2, EP4, TLR4 e ACE nella placca carotidea sintomatica 66
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 66
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 65
Primary IgA nephropathy is more severe in TGF-ss1 high secretor patients 65
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 65
Expression of circulating miR-17-92 cluster and HDAC9 gene in atherosclerotic patients with unstable and stable carotid plaques 64
Mutations associated with very late-onset metachromatic leukodystrophy. 63
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 62
Osteogenesis Imperfecta at the beginning of bone and joint decade 62
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 61
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 61
Studio di associazione in coronaropatia e di espressione in vitro del promotore del gene PLA2G7. 60
Differenze di espressione genica di COX-2 e TLR4 nel sangue periferico di pazienti con ictus cardioembolico e aterosclerotico 59
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood 58
Two new highly polymorphic markers in the 3’UTR region of the PLA2G7 gene 57
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. 53
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 51
Rehabilitation and biomarkers of stroke recovery: study protocol for a randomized controlled trial 48
Up-regulated serum miR-128-3p in progressive and relapse-free multiple sclerosis patients 43
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 43
Polymorphism analysis in cox-2 gene regulatory regions in non-melanoma skin cancer after transplantation 39
Espressione dei geni HDAC9 e TWIST1. Possibili biomarcatori di vulnerabilità della placca carotidea? 39
Regulation of microRNAs in satellite cell renewal, muscle function, sarcopenia and the role of exercise 39
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 38
null 35
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure 34
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression 34
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 28
Human melanoma cells differentially express RNASEL/RNase-L and miR-146a-5p under sex hormonal stimulation 19
miR-146a-5p impairs melanoma resistance to kinase inhibitors by targeting COX2 and regulating NFkB-mediated inflammatory mediators 19
La sovraespressione di TLR4 nel sangue periferico correla con l’espressione di COX-2 nei pazienti con ictus ischemico 16
Totale 5742
Salva come PNG Salva come JPEG
Categoria #
all - tutte 10213
article - articoli 8355
book - libri 0
conference - conferenze 1763
curatela - curatele 0
other - altro 95
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 20426
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201827 0000 00 00 071010
2018/2019473 83312714 5461 9423 9151916
2019/2020814 8628277 11572 10856 288160101
2020/2021815 1281395373 8266 1972 62137236
2021/2022741 63211584 1624 1439 391951176
2022/20231541 105185150267 138363 32108 193000
Totale 5742