SCALET, Daniela
 Distribuzione geografica
Continente #
NA - Nord America 700
EU - Europa 275
AS - Asia 145
SA - Sud America 1
Totale 1.121
Nazione #
US - Stati Uniti d'America 689
CN - Cina 79
IT - Italia 76
DE - Germania 45
PL - Polonia 44
GB - Regno Unito 42
TR - Turchia 29
UA - Ucraina 25
SE - Svezia 14
SG - Singapore 12
BE - Belgio 11
CA - Canada 11
ID - Indonesia 8
VN - Vietnam 7
FI - Finlandia 6
IN - India 4
CZ - Repubblica Ceca 3
NL - Olanda 3
ES - Italia 2
HK - Hong Kong 2
KR - Corea 2
RO - Romania 2
RU - Federazione Russa 2
EC - Ecuador 1
IR - Iran 1
TH - Thailandia 1
Totale 1.121
Città #
Fairfield 89
Woodbridge 82
Ann Arbor 66
Houston 56
Ashburn 53
Chandler 50
Warsaw 44
Wilmington 37
Ferrara 35
Jacksonville 32
Seattle 29
Cambridge 27
Beijing 25
Izmir 21
Munich 19
Nanjing 17
Mcallen 11
Princeton 11
Boardman 9
Bremen 9
Brussels 9
Montréal 8
Dong Ket 7
Jakarta 7
Shanghai 7
Falls Church 6
Milan 6
Redwood City 6
Shenyang 6
Singapore 6
Des Moines 5
New York 5
Cagliari 4
Hebei 4
Nanchang 4
San Diego 4
Andover 3
Brno 3
Changsha 3
London 3
Lusia 3
San Mateo 3
Toronto 3
Bologna 2
Dearborn 2
Gloucester 2
Kunming 2
Leawood 2
Mountain View 2
Norwalk 2
Tianjin 2
Waanrode 2
Auburn Hills 1
Augusta 1
Barcelona 1
Chicago 1
Edinburgh 1
Genoa 1
Grugliasco 1
Guangzhou 1
Haikou 1
Hangzhou 1
Hyderabad 1
Indiana 1
Ithaca 1
Jiaxing 1
Merano 1
Minerbio 1
Monmouth Junction 1
Moscow 1
Ningbo 1
Noale 1
Orange 1
Quito 1
Southend 1
Treviso 1
Trieste 1
Wuhan 1
Totale 881
Nome #
Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy 179
An exon-specific U1snRNA induces a robust factor IX activity in mice expressing multiple human FIX splicing mutants 170
Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotides 166
Genetic determinants of activated factor VII antithrombin complex plasma concentration include tissue factor, factor VII and endothelial protein C receptor gene variants 130
A unique exon specific U1snRNA rescues different haemophilia B - causing splicing-defective factor IX variants in mice 95
Disease-causing variants of the conserved+2T of 5 ' splice sites can be rescued by engineered U1snRNAs 84
The somatic FAH C.1061C>A change counteracts the frequent FAH c.1062+5G>A mutation and permits U1snRNA-based splicing correction 82
Correction of aberrant splicing causing haemophilia B through the combination of compensatory U1snRNAs and antisense oligonucleotides 80
Rescue of missense and splicing mutations in Haemophilia A by a unique Exon Specific U1snRNA 67
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I 59
Regulation of exon definition by intrinsic elements and by combination of tailored U1snRNA with antisense oligonucleotides 51
Totale 1.163
Categoria #
all - tutte 4.972
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 4.972


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020245 34 9 15 24 16 28 22 16 24 24 22 11
2020/2021285 18 12 13 15 8 23 41 28 16 66 33 12
2021/2022138 8 18 1 6 5 8 9 3 6 12 8 54
2022/2023146 15 10 10 17 21 14 13 15 14 1 13 3
2023/202477 2 9 0 1 5 13 4 15 1 1 1 25
2024/20256 6 0 0 0 0 0 0 0 0 0 0 0
Totale 1.163