ArTS Archivio della ricerca di Trieste

MERONI, GERMANA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.231
EU - Europa 2.791
AS - Asia 490
Continente sconosciuto - Info sul continente non disponibili 16
SA - Sud America 16
OC - Oceania 11
AF - Africa 6
Totale 8.561
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.218
PL - Polonia 1.418
SE - Svezia 350
IT - Italia 320
UA - Ucraina 211
CN - Cina 186
TR - Turchia 141
FI - Finlandia 110
HK - Hong Kong 93
DE - Germania 81
BG - Bulgaria 75
IE - Irlanda 69
ES - Italia 42
BE - Belgio 31
VN - Vietnam 24
GB - Regno Unito 19
EU - Europa 14
NL - Olanda 14
FR - Francia 13
CA - Canada 12
BR - Brasile 11
AU - Australia 10
CH - Svizzera 8
JP - Giappone 8
IN - India 7
RU - Federazione Russa 5
KR - Corea 4
MY - Malesia 4
RS - Serbia 4
SN - Senegal 4
AE - Emirati Arabi Uniti 3
BD - Bangladesh 3
CL - Cile 3
EE - Estonia 3
PH - Filippine 3
PT - Portogallo 3
RO - Romania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
AT - Austria 2
DK - Danimarca 2
ID - Indonesia 2
SG - Singapore 2
AL - Albania 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
EG - Egitto 1
GE - Georgia 1
GR - Grecia 1
HR - Croazia 1
HU - Ungheria 1
KZ - Kazakistan 1
LI - Liechtenstein 1
LK - Sri Lanka 1
MC - Monaco 1
MD - Moldavia 1
MX - Messico 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
SA - Arabia Saudita 1
TH - Thailandia 1
TW - Taiwan 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 8.561
Salva come PNG Salva come JPEG
Città #
Warsaw 1.418
Fairfield 738
Woodbridge 692
Houston 565
Ann Arbor 538
Ashburn 406
Chandler 353
Wilmington 328
Seattle 303
Cambridge 240
Jacksonville 219
Trieste 149
Princeton 132
Izmir 124
Hong Kong 90
Sofia 75
Dublin 67
Falls Church 63
Beijing 55
Grafing 44
Madrid 40
Boardman 38
San Diego 37
Dearborn 26
Dong Ket 22
Brussels 20
Des Moines 20
Redmond 18
Milan 17
Phoenix 16
Kocaeli 15
Mestre 14
Washington 13
Los Angeles 11
Shanghai 10
Chicago 9
Norwalk 9
São Paulo 9
Edinburgh 8
San Francisco 8
Bremen 7
Hefei 7
Helsinki 7
Nanjing 7
Rome 7
Tappahannock 7
Guangzhou 6
Toronto 6
Waanrode 6
Kunming 5
London 5
Zhengzhou 5
Belgrade 4
Cividale del Friuli 4
Dakar 4
Düsseldorf 4
Indiana 4
Montpellier 4
Nanchang 4
Seoul 4
Sydney 4
Tokyo 4
Augusta 3
Belpasso 3
Berlin 3
Bern 3
Buffalo 3
Chions 3
Dongguan 3
Fremont 3
Gießen 3
Kuala Lumpur 3
Manila 3
Montreal 3
Redwood City 3
Sacile 3
Spin 3
Stockholm 3
Tallinn 3
Andover 2
Atlanta 2
Baotou 2
Bengaluru 2
Binetto 2
Bisceglie 2
Brooklyn 2
Capurso 2
Catania 2
Champigny-sur-Marne 2
Dubai 2
Estarreja 2
Florence 2
Fuzhou 2
Groningen 2
Jakarta 2
Jinan 2
Leipzig 2
Menlo Park 2
Naples 2
Napoli 2
Totale 7.167
Salva come PNG Salva come JPEG
Nome #
TRIM proteins legitimately enter the MAGEic RING 400
Intranasal administration of recombinant TRAIL down-regulates CXCL-1/KC in an ovalbumin-induced airway inflammation murine model 326
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation 321
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance 314
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells 302
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa 291
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation. 250
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H 230
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis 213
Transcriptome-driven integrative exploration of functional state of ureter tissue affected by CAKUT 164
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene 163
Functional interactions between ubiquitin E2 enzymes and TRIM proteins 162
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability 148
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle 147
Molecular classification of nodal metastasis in primary larynx squamous cell carcinoma 145
PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblasts 145
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES 143
Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? 141
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development 138
TRIM9 is specifically expressed in the embryonic and adult nervous system 137
MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells 135
NUCLEOTIDE-SEQUENCE OF THE CDNA FOR LECITHIN-CHOLESTEROL ACYL TRANSFERASE (LCAT) FROM THE RAT 135
A structure-function study of MID1 mutations associated with a mild Opitz phenotype 132
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease") 132
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome 132
FUNCTIONAL-ANALYSIS OF THE HUMAN LECITHIN-CHOLESTEROL ACYL TRANSFERASE GENE PROMOTER 131
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor 129
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum 127
The human ROX gene: Genomic structure and mutation analysis in human breast tumors 125
TRIM32 ubiquitin E3 ligase, one enzyme for several pathologies: From muscular dystrophy to tumours 122
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties 121
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY 120
Motifs resembling hepatocyte nuclear factor 1 and activator protein 3 mediate the tissue specificity of the human plasminogen gene 120
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35 120
MID1 Mutation Screening in a Large Cohort of Opitz G/BBB Syndrome Patients: Twenty-nine Novel Mutations Identified 116
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctata 115
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region 115
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata 113
MID1 mutations in patients with X-linked Opitz G/BBB syndrome 111
null 111
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase 111
TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases 110
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H 104
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndrome 104
The tripartite motif family identifies cell compartments 100
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) 99
Midline 1 controls polarization and migration of murine cytotoxic T cells 99
Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis 98
null 96
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids 88
A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia 87
The sulfatase gene family 86
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues 85
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe disease 80
TRIMming p53’s anticancer activity 77
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome 68
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5 delta 64
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases 61
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA 55
Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules 54
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4 53
The MID1 gene product in physiology and disease 52
TRIM E3 Ubiquitin Ligases in Rare Genetic Disorders 48
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease 47
Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene 43
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and Spermatogenesis 38
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 34
TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation 23
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs 9
Totale 8.815
Salva come PNG Salva come JPEG
Categoria #
all - tutte 19.987
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 19.987
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019575 0 0 0 0 0 0 0 0 0 0 366 209
2019/20202.245 122 132 154 424 162 239 208 206 187 155 137 119
2020/20211.067 118 88 58 154 90 82 75 103 43 101 42 113
2021/2022883 16 66 28 63 44 115 79 35 138 111 47 141
2022/20231.240 181 149 92 143 140 203 7 80 124 6 83 32
2023/2024481 35 34 32 32 52 126 54 92 5 19 0 0
Totale 8.815