ArTS Archivio della ricerca di Trieste

MERONI, GERMANA
 Distribuzione geografica
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Continente #
NA - Nord America 6.791
EU - Europa 3.693
AS - Asia 2.685
SA - Sud America 313
AF - Africa 129
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 14
Totale 13.644
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Nazione #
US - Stati Uniti d'America 6.704
PL - Polonia 1.514
SG - Singapore 995
IT - Italia 590
CN - Cina 580
SE - Svezia 355
VN - Vietnam 269
BR - Brasile 243
HK - Hong Kong 238
UA - Ucraina 218
DE - Germania 175
TR - Turchia 155
FR - Francia 139
FI - Finlandia 132
BD - Bangladesh 116
KR - Corea 110
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 51
CA - Canada 36
BE - Belgio 35
JP - Giappone 30
MX - Messico 27
AT - Austria 24
PH - Filippine 16
ZA - Sudafrica 16
AR - Argentina 14
EU - Europa 14
CH - Svizzera 13
CO - Colombia 13
AU - Australia 12
ID - Indonesia 11
IQ - Iraq 11
EC - Ecuador 10
SA - Arabia Saudita 10
KE - Kenya 9
MY - Malesia 9
GR - Grecia 8
UZ - Uzbekistan 8
AE - Emirati Arabi Uniti 7
CL - Cile 7
EG - Egitto 7
SN - Senegal 7
AL - Albania 6
DZ - Algeria 6
PK - Pakistan 6
PT - Portogallo 6
UY - Uruguay 6
VE - Venezuela 6
DK - Danimarca 5
IL - Israele 5
JO - Giordania 5
LT - Lituania 5
PE - Perù 5
PY - Paraguay 5
RO - Romania 5
SV - El Salvador 5
TH - Thailandia 5
CR - Costa Rica 4
DO - Repubblica Dominicana 4
EE - Estonia 4
KZ - Kazakistan 4
NP - Nepal 4
RS - Serbia 4
TW - Taiwan 4
BO - Bolivia 3
CZ - Repubblica Ceca 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
KH - Cambogia 2
LB - Libano 2
MK - Macedonia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
TT - Trinidad e Tobago 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
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
Totale 13.629
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Città #
Warsaw 1.445
Fairfield 738
Ashburn 722
Woodbridge 692
Singapore 643
Houston 571
Ann Arbor 538
Chandler 353
Wilmington 328
Seattle 305
San Jose 257
Cambridge 240
Hong Kong 228
Jacksonville 222
Trieste 168
Beijing 134
Princeton 132
Izmir 125
Boardman 107
Seoul 101
Chicago 91
Los Angeles 77
Sofia 75
Dublin 72
Casablanca 70
Columbus 67
Hanoi 65
Ho Chi Minh City 64
Falls Church 63
Zgierz 62
Milan 60
Lauterbourg 59
Moscow 54
Hefei 53
Grafing 44
Council Bluffs 41
Madrid 41
Santa Clara 41
Frankfurt am Main 37
San Diego 37
New York 35
Dallas 31
São Paulo 30
The Dalles 29
Munich 28
Rome 28
Dearborn 26
Des Moines 24
London 24
Memphis 24
Phoenix 23
Buffalo 22
Dong Ket 22
Brussels 20
Shanghai 20
Redmond 18
Montreal 16
Kocaeli 15
Naples 15
Washington 15
Helsinki 14
Mestre 14
Tokyo 14
Miano 13
Guangzhou 12
Haiphong 12
Orem 12
Atlanta 11
Düsseldorf 11
Nanjing 11
Nuremberg 11
Bari 10
Mumbai 10
San Francisco 10
Turku 10
Vienna 10
Zhengzhou 10
Denver 9
Johannesburg 9
Norwalk 9
Edinburgh 8
Kansas City 8
Nairobi 8
Paris 8
Redondo Beach 8
Tashkent 8
Toronto 8
Bremen 7
Charlotte 7
Chennai 7
Dakar 7
Hangzhou 7
Manchester 7
Rio de Janeiro 7
Stockholm 7
Tappahannock 7
Tianjin 7
Amsterdam 6
Ankara 6
Baghdad 6
Totale 10.053
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Nome #
TRIM proteins legitimately enter the MAGEic RING 467
Intranasal administration of recombinant TRAIL down-regulates CXCL-1/KC in an ovalbumin-induced airway inflammation murine model 410
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance 393
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation 376
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation. 361
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells 350
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa 347
Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene 317
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H 316
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis 305
TRIM E3 Ubiquitin Ligases in Rare Genetic Disorders 249
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability 248
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene 229
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum 225
A structure-function study of MID1 mutations associated with a mild Opitz phenotype 222
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease") 215
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES 214
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development 213
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle 213
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome 211
Transcriptome-driven integrative exploration of functional state of ureter tissue affected by CAKUT 209
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY 207
Functional interactions between ubiquitin E2 enzymes and TRIM proteins 202
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region 197
MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells 190
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata 190
Molecular classification of nodal metastasis in primary larynx squamous cell carcinoma 188
Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? 188
PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblasts 186
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35 186
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 186
FUNCTIONAL-ANALYSIS OF THE HUMAN LECITHIN-CHOLESTEROL ACYL TRANSFERASE GENE PROMOTER 180
TRIM9 is specifically expressed in the embryonic and adult nervous system 179
A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia 178
TRIMming p53’s anticancer activity 178
MID1 Mutation Screening in a Large Cohort of Opitz G/BBB Syndrome Patients: Twenty-nine Novel Mutations Identified 177
The human ROX gene: Genomic structure and mutation analysis in human breast tumors 174
Motifs resembling hepatocyte nuclear factor 1 and activator protein 3 mediate the tissue specificity of the human plasminogen gene 174
TRIM32 ubiquitin E3 ligase, one enzyme for several pathologies: From muscular dystrophy to tumours 174
NUCLEOTIDE-SEQUENCE OF THE CDNA FOR LECITHIN-CHOLESTEROL ACYL TRANSFERASE (LCAT) FROM THE RAT 173
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndrome 172
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome 170
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids 167
The MID1 gene product in physiology and disease 166
MID1 mutations in patients with X-linked Opitz G/BBB syndrome 165
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctata 164
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues 164
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA 159
TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases 158
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties 156
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H 154
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 154
The tripartite motif family identifies cell compartments 154
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase 152
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5 delta 151
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases 147
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) 145
Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis 144
Midline 1 controls polarization and migration of murine cytotoxic T cells 138
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease 137
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe disease 135
TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation 135
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 134
The sulfatase gene family 132
Comprehensive ubiquitome analysis reveals persistent mitochondrial remodeling disruptions from doxorubicin-induced cardiotoxicity in aged CD-1 male mice 125
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4 115
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 102
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and Spermatogenesis 101
null 96
TRIM32 controls timely cell cycle exit in muscular differentiation through downregulation of c-Myc mRNA 4
Totale 13.904
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Categoria #
all - tutte 38.466
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 38.466
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2023/2024567 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
2026/202744 44 0 0 0 0 0 0 0 0 0 0 0
Totale 13.904