MARTONI, Elena
 Distribuzione geografica
Continente #
NA - Nord America 1.102
EU - Europa 544
AS - Asia 144
AF - Africa 1
Totale 1.791
Nazione #
US - Stati Uniti d'America 1.100
PL - Polonia 306
CN - Cina 94
DE - Germania 54
UA - Ucraina 54
TR - Turchia 43
IT - Italia 42
GB - Regno Unito 29
SE - Svezia 23
FI - Finlandia 16
RU - Federazione Russa 6
BE - Belgio 5
VN - Vietnam 4
ES - Italia 3
NL - Olanda 3
CA - Canada 2
FR - Francia 2
IN - India 2
EG - Egitto 1
GR - Grecia 1
IR - Iran 1
Totale 1.791
Città #
Warsaw 306
Fairfield 149
Woodbridge 130
Ann Arbor 107
Chandler 96
Houston 96
Ashburn 78
Seattle 61
Jacksonville 59
Cambridge 49
Wilmington 48
Beijing 27
Izmir 26
Nanjing 18
Milan 16
San Diego 16
New York 15
Princeton 15
Boardman 12
Bremen 12
Shanghai 12
Ferrara 9
Dearborn 7
Nanchang 7
Brussels 5
Shenyang 5
Tianjin 5
Cagliari 4
Helsinki 4
San Mateo 4
Washington 4
Changsha 3
Des Moines 3
Dong Ket 3
Falls Church 3
Ferrara di Monte Baldo 3
Norwalk 3
Borgo Val di Taro 2
Hangzhou 2
Hebei 2
Hefei 2
Jiaxing 2
Leawood 2
Madrid 2
Mountain View 2
Ningbo 2
Orange 2
Redwood City 2
Zhengzhou 2
Addison 1
Antalya 1
Auburn Hills 1
Augusta 1
Bologna 1
Cairo 1
Changchun 1
Chicago 1
Fuzhou 1
Groningen 1
Guarda Veneta 1
Hanoi 1
Hounslow 1
Irkutsk 1
Jinan 1
Kunming 1
London 1
Los Angeles 1
Montreal 1
New Bedfont 1
Philadelphia 1
Phoenix 1
Prescot 1
Rueil-Malmaison 1
Taizhou 1
Toronto 1
Wakefield 1
Wandsworth 1
Totale 1.472
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 319
Whole transcriptome expression profiling in collagen VI myopathies KO mice reveals muscle-specific fingerprints and arises the role of circadian clock genes as myopathy biomarkers 182
Macrophages: a minimally invasive tool for monitoring collagen VI myopathies 140
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse 135
null 131
Autosomal recessive myosclerosis myopathy is a collagen VI disorder 118
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies 117
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 111
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 111
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 109
Transcriptional behavior of DMD gene duplications in DMD/BMD males 105
Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy 103
Autosomal recessive Bethlem myopathy 101
Nanoparticle-Mediated Delivery of Antisense Oligoribonucleotides Allows Restoration of Dystrophin Expression in the mdx Mouse 17
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 11
Totale 1.810
Categoria #
all - tutte 5.408
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 5.408


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019149 0 0 0 0 0 0 0 0 0 0 57 92
2019/2020453 59 23 22 64 32 49 41 45 40 46 18 14
2020/2021263 27 26 14 27 31 18 18 24 9 26 30 13
2021/2022189 3 13 18 4 6 5 26 9 6 13 24 62
2022/2023230 17 25 1 36 49 22 19 13 23 4 10 11
2023/202492 4 16 13 0 13 25 2 15 2 2 0 0
Totale 1.810