ArTS Archivio della ricerca di Trieste

MERONI, GERMANA
 Distribuzione geografica
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Continente #
NA - Nord America 6.595
EU - Europa 3.617
AS - Asia 2.586
SA - Sud America 306
AF - Africa 129
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 14
Totale 13.266
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Nazione #
US - Stati Uniti d'America 6.528
PL - Polonia 1.513
SG - Singapore 993
CN - Cina 577
IT - Italia 526
SE - Svezia 355
VN - Vietnam 269
BR - Brasile 241
HK - Hong Kong 236
UA - Ucraina 218
DE - Germania 175
TR - Turchia 155
FR - Francia 137
FI - Finlandia 131
KR - Corea 110
RU - Federazione Russa 105
BG - Bulgaria 75
GB - Regno Unito 74
IE - Irlanda 74
MA - Marocco 74
IN - India 64
ES - Italia 59
NL - Olanda 50
BE - Belgio 35
JP - Giappone 30
CA - Canada 26
MX - Messico 26
BD - Bangladesh 25
AT - Austria 24
PH - Filippine 16
ZA - Sudafrica 16
AR - Argentina 14
EU - Europa 14
CH - Svizzera 13
AU - Australia 12
CO - Colombia 11
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
EG - Egitto 7
SN - Senegal 7
CL - Cile 6
DZ - Algeria 6
PK - Pakistan 6
PT - Portogallo 6
VE - Venezuela 6
AL - Albania 5
JO - Giordania 5
LT - Lituania 5
PY - Paraguay 5
TH - Thailandia 5
UY - Uruguay 5
DK - Danimarca 4
DO - Repubblica Dominicana 4
EE - Estonia 4
IL - Israele 4
KZ - Kazakistan 4
NP - Nepal 4
PE - Perù 4
RO - Romania 4
RS - Serbia 4
TW - Taiwan 4
BO - Bolivia 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
CR - Costa Rica 2
CZ - Repubblica Ceca 2
GA - Gabon 2
GD - Grenada 2
GH - Ghana 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
CY - Cipro 1
ET - Etiopia 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
Totale 13.253
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Città #
Warsaw 1.445
Fairfield 738
Woodbridge 692
Ashburn 688
Singapore 643
Houston 570
Ann Arbor 538
Chandler 353
Wilmington 328
Seattle 305
San Jose 256
Cambridge 240
Hong Kong 226
Jacksonville 222
Trieste 165
Beijing 132
Princeton 132
Izmir 125
Boardman 107
Seoul 101
Chicago 87
Sofia 75
Dublin 72
Casablanca 70
Columbus 67
Hanoi 65
Los Angeles 65
Ho Chi Minh City 64
Falls Church 63
Zgierz 62
Lauterbourg 59
Milan 54
Moscow 54
Hefei 53
Grafing 44
Madrid 41
Frankfurt am Main 37
San Diego 37
Santa Clara 33
Dallas 29
São Paulo 29
The Dalles 29
Munich 28
Council Bluffs 27
Dearborn 26
New York 25
Des Moines 23
London 23
Rome 23
Dong Ket 22
Phoenix 22
Brussels 20
Shanghai 20
Memphis 19
Redmond 18
Buffalo 15
Kocaeli 15
Mestre 14
Tokyo 14
Helsinki 13
Miano 13
Montreal 13
Washington 13
Guangzhou 12
Haiphong 12
Orem 12
Düsseldorf 11
Nanjing 11
Naples 11
Nuremberg 11
Bari 10
Mumbai 10
San Francisco 10
Turku 10
Vienna 10
Zhengzhou 10
Atlanta 9
Denver 9
Johannesburg 9
Norwalk 9
Edinburgh 8
Kansas City 8
Nairobi 8
Paris 8
Redondo Beach 8
Tashkent 8
Bremen 7
Chennai 7
Dakar 7
Hangzhou 7
Rio de Janeiro 7
Stockholm 7
Tappahannock 7
Tianjin 7
Amsterdam 6
Ankara 6
Baghdad 6
Da Nang 6
Dhaka 6
Hyderabad 6
Totale 9.917
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Nome #
TRIM proteins legitimately enter the MAGEic RING 464
Intranasal administration of recombinant TRAIL down-regulates CXCL-1/KC in an ovalbumin-induced airway inflammation murine model 408
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance 389
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation 373
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation. 353
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells 345
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa 341
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H 312
Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene 304
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis 300
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability 244
TRIM E3 Ubiquitin Ligases in Rare Genetic Disorders 244
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene 227
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum 216
A structure-function study of MID1 mutations associated with a mild Opitz phenotype 216
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease") 213
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY 206
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle 206
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES 204
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome 202
Functional interactions between ubiquitin E2 enzymes and TRIM proteins 201
Transcriptome-driven integrative exploration of functional state of ureter tissue affected by CAKUT 201
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development 197
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata 189
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region 188
Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? 187
MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells 186
Molecular classification of nodal metastasis in primary larynx squamous cell carcinoma 186
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
TRIM9 is specifically expressed in the embryonic and adult nervous system 178
FUNCTIONAL-ANALYSIS OF THE HUMAN LECITHIN-CHOLESTEROL ACYL TRANSFERASE GENE PROMOTER 177
A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia 174
Motifs resembling hepatocyte nuclear factor 1 and activator protein 3 mediate the tissue specificity of the human plasminogen gene 173
NUCLEOTIDE-SEQUENCE OF THE CDNA FOR LECITHIN-CHOLESTEROL ACYL TRANSFERASE (LCAT) FROM THE RAT 173
The human ROX gene: Genomic structure and mutation analysis in human breast tumors 172
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndrome 171
TRIM32 ubiquitin E3 ligase, one enzyme for several pathologies: From muscular dystrophy to tumours 170
TRIMming p53’s anticancer activity 170
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 167
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids 164
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome 163
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues 160
TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases 158
MID1 Mutation Screening in a Large Cohort of Opitz G/BBB Syndrome Patients: Twenty-nine Novel Mutations Identified 157
MID1 mutations in patients with X-linked Opitz G/BBB syndrome 156
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties 155
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctata 154
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA 153
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H 152
The MID1 gene product in physiology and disease 152
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 151
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase 151
The tripartite motif family identifies cell compartments 148
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5 delta 144
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) 142
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases 142
Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis 140
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe disease 133
Midline 1 controls polarization and migration of murine cytotoxic T cells 133
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease 133
The sulfatase gene family 130
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 129
TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation 126
null 111
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and Spermatogenesis 101
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4 100
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 99
null 96
Comprehensive ubiquitome analysis reveals persistent mitochondrial remodeling disruptions from doxorubicin-induced cardiotoxicity in aged CD-1 male mice 93
Totale 13.525
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Categoria #
all - tutte 36.789
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 36.789
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021155 0 0 0 0 0 0 0 0 0 0 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
2023/2024567 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
2025/20263.173 360 139 133 285 253 311 522 155 442 467 106 0
Totale 13.525