ArTS Archivio della ricerca di Trieste

MERONI, GERMANA
 Distribuzione geografica
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Continente #
NA - Nord America 7.103
EU - Europa 3.741
AS - Asia 2.706
SA - Sud America 319
Continente sconosciuto - Info sul continente non disponibili 281
AF - Africa 129
OC - Oceania 16
Totale 14.295
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Nazione #
US - Stati Uniti d'America 6.995
PL - Polonia 1.516
SG - Singapore 999
IT - Italia 632
CN - Cina 586
SE - Svezia 355
VN - Vietnam 270
BR - Brasile 244
HK - Hong Kong 240
UA - Ucraina 218
DE - Germania 175
TR - Turchia 155
FR - Francia 141
FI - Finlandia 132
BD - Bangladesh 121
KR - Corea 111
RU - Federazione Russa 105
GB - Regno Unito 76
BG - Bulgaria 75
IE - Irlanda 74
MA - Marocco 74
IN - India 64
ES - Italia 59
NL - Olanda 52
CA - Canada 46
BE - Belgio 35
JP - Giappone 30
MX - Messico 28
AT - Austria 24
PH - Filippine 17
CO - Colombia 16
ZA - Sudafrica 16
AR - Argentina 14
AU - Australia 14
EU - Europa 14
CH - Svizzera 13
EC - Ecuador 11
ID - Indonesia 11
IQ - Iraq 11
SA - Arabia Saudita 11
KE - Kenya 9
MY - Malesia 9
GR - Grecia 8
UZ - Uzbekistan 8
AE - Emirati Arabi Uniti 7
CL - Cile 7
EG - Egitto 7
PT - Portogallo 7
SN - Senegal 7
VE - Venezuela 7
AL - Albania 6
DZ - Algeria 6
PK - Pakistan 6
SV - El Salvador 6
UY - Uruguay 6
CR - Costa Rica 5
DK - Danimarca 5
DO - Repubblica Dominicana 5
IL - Israele 5
JO - Giordania 5
LT - Lituania 5
PE - Perù 5
PY - Paraguay 5
RO - Romania 5
TH - Thailandia 5
EE - Estonia 4
KZ - Kazakistan 4
NP - Nepal 4
RS - Serbia 4
TT - Trinidad e Tobago 4
TW - Taiwan 4
BO - Bolivia 3
CZ - Repubblica Ceca 3
JM - Giamaica 3
KG - Kirghizistan 3
LK - Sri Lanka 3
NG - Nigeria 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
AZ - Azerbaigian 2
BB - Barbados 2
GA - Gabon 2
GD - Grenada 2
GH - Ghana 2
GT - Guatemala 2
HN - Honduras 2
KH - Cambogia 2
LB - Libano 2
MK - Macedonia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
CY - Cipro 1
ET - Etiopia 1
GE - Georgia 1
HR - Croazia 1
HU - Ungheria 1
Totale 14.016
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Città #
Warsaw 1.445
Ashburn 767
Fairfield 738
Woodbridge 693
Singapore 646
Houston 573
Ann Arbor 538
Chandler 353
Wilmington 329
Seattle 306
San Jose 260
Cambridge 241
Hong Kong 230
Jacksonville 223
Trieste 176
Beijing 139
Princeton 135
Council Bluffs 130
Izmir 125
Boardman 107
Seoul 101
Chicago 93
Los Angeles 82
Sofia 75
Columbus 74
Dublin 72
Casablanca 70
Hanoi 66
Milan 65
Ho Chi Minh City 64
Falls Church 63
Zgierz 62
Lauterbourg 59
Moscow 54
Hefei 53
Santa Clara 49
Grafing 44
Madrid 41
New York 38
Frankfurt am Main 37
San Diego 37
Dallas 33
Rome 31
São Paulo 30
The Dalles 30
Munich 28
Dearborn 26
Memphis 25
Des Moines 24
London 24
Phoenix 24
Buffalo 22
Dong Ket 22
Brussels 20
Shanghai 20
Montreal 19
Redmond 18
Naples 16
Washington 16
Kocaeli 15
Helsinki 14
Mestre 14
Tokyo 14
Miano 13
Orem 13
San Francisco 13
Guangzhou 12
Haiphong 12
Atlanta 11
Düsseldorf 11
Nanjing 11
Nuremberg 11
Bari 10
Denver 10
Mumbai 10
Paris 10
Turku 10
Vienna 10
Zhengzhou 10
Brooklyn 9
Johannesburg 9
Norwalk 9
Catania 8
Edinburgh 8
Kansas City 8
Nairobi 8
Redondo Beach 8
Rio de Janeiro 8
Tashkent 8
Toronto 8
Bremen 7
Charlotte 7
Chennai 7
Dakar 7
Hangzhou 7
Manchester 7
Mexico City 7
Stockholm 7
Tappahannock 7
Tianjin 7
Totale 10.276
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Nome #
TRIM proteins legitimately enter the MAGEic RING 468
Intranasal administration of recombinant TRAIL down-regulates CXCL-1/KC in an ovalbumin-induced airway inflammation murine model 413
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance 400
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation 382
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation. 370
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells 354
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa 349
Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene 340
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H 319
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis 312
TRIM E3 Ubiquitin Ligases in Rare Genetic Disorders 254
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability 250
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene 246
A structure-function study of MID1 mutations associated with a mild Opitz phenotype 240
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum 228
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle 222
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease") 221
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES 220
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome 216
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development 215
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY 210
Transcriptome-driven integrative exploration of functional state of ureter tissue affected by CAKUT 210
Functional interactions between ubiquitin E2 enzymes and TRIM proteins 204
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region 199
MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells 196
Molecular classification of nodal metastasis in primary larynx squamous cell carcinoma 195
Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? 193
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 193
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata 191
PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblasts 190
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35 187
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome 187
FUNCTIONAL-ANALYSIS OF THE HUMAN LECITHIN-CHOLESTEROL ACYL TRANSFERASE GENE PROMOTER 185
A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia 184
TRIM9 is specifically expressed in the embryonic and adult nervous system 183
TRIMming p53’s anticancer activity 183
The human ROX gene: Genomic structure and mutation analysis in human breast tumors 181
Motifs resembling hepatocyte nuclear factor 1 and activator protein 3 mediate the tissue specificity of the human plasminogen gene 181
MID1 Mutation Screening in a Large Cohort of Opitz G/BBB Syndrome Patients: Twenty-nine Novel Mutations Identified 180
NUCLEOTIDE-SEQUENCE OF THE CDNA FOR LECITHIN-CHOLESTEROL ACYL TRANSFERASE (LCAT) FROM THE RAT 178
TRIM32 ubiquitin E3 ligase, one enzyme for several pathologies: From muscular dystrophy to tumours 176
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids 174
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndrome 173
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues 171
MID1 mutations in patients with X-linked Opitz G/BBB syndrome 169
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctata 168
The MID1 gene product in physiology and disease 168
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA 164
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties 162
TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases 162
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 161
The tripartite motif family identifies cell compartments 160
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase 160
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H 159
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5 delta 157
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases 151
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) 150
Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis 147
Midline 1 controls polarization and migration of murine cytotoxic T cells 145
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 142
TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation 142
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease 142
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe disease 140
The sulfatase gene family 137
Comprehensive ubiquitome analysis reveals persistent mitochondrial remodeling disruptions from doxorubicin-induced cardiotoxicity in aged CD-1 male mice 132
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4 118
null 111
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 106
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and Spermatogenesis 106
null 96
TRIM32 controls timely cell cycle exit in muscular differentiation through downregulation of c-Myc mRNA 17
Totale 14.295
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Categoria #
all - tutte 40.410
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 40.410
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022801 0 0 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
2023/2024567 35 34 32 32 52 126 54 92 5 19 42 44
2024/20251.451 29 48 62 132 199 132 100 93 196 188 125 147
2025/20263.508 360 139 133 285 253 311 522 155 442 467 254 187
2026/2027435 141 169 125 0 0 0 0 0 0 0 0 0
Totale 14.295