TESTA, Maria Francesca
 Distribuzione geografica
Continente #
NA - Nord America 359
EU - Europa 90
AS - Asia 78
AF - Africa 2
Totale 529
Nazione #
US - Stati Uniti d'America 357
IT - Italia 42
CN - Cina 32
SG - Singapore 19
DE - Germania 13
CZ - Repubblica Ceca 9
ID - Indonesia 9
SE - Svezia 6
TR - Turchia 6
FI - Finlandia 5
IQ - Iraq 5
FR - Francia 4
RU - Federazione Russa 4
UA - Ucraina 4
HK - Hong Kong 3
CA - Canada 2
NG - Nigeria 2
TW - Taiwan 2
CH - Svizzera 1
GB - Regno Unito 1
IN - India 1
JP - Giappone 1
NO - Norvegia 1
Totale 529
Città #
Fairfield 50
Chandler 48
New York 26
Ferrara 25
Ashburn 22
Seattle 22
Wilmington 18
Houston 16
Cambridge 15
Woodbridge 14
Shanghai 12
Singapore 12
Princeton 10
Jakarta 9
Brno 8
San Diego 8
Bremen 7
Los Angeles 7
Milan 7
Izmir 6
Baghdad 5
Dearborn 5
Redwood City 5
Bologna 4
Helsinki 4
Jacksonville 4
Rochester 4
San Mateo 4
Kunming 3
Nanjing 3
Ann Arbor 2
Beijing 2
Florence 2
Henderson 2
Hong Kong 2
Jiaxing 2
Lagos 2
Monmouth Junction 2
Moscow 2
Munich 2
Padova 2
Shenyang 2
Taipei 2
Toronto 2
Worcester 2
Andover 1
Boardman 1
Central District 1
Changsha 1
Dallas 1
Ferrara di Monte Baldo 1
Guangzhou 1
Jinan 1
Kanpur 1
Lappeenranta 1
Leawood 1
London 1
Mountain View 1
Mégevette 1
Nanchang 1
Norwalk 1
Olomouc 1
Orange 1
Oslo 1
Piemonte 1
Sayreville 1
Tokyo 1
Washington 1
Totale 436
Nome #
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 101
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 88
TRPP2 dysfunction decreases ATP-evoked calcium, induces cell aggregation and stimulates proliferation in T lymphocytes 77
Exploring spontaneous readthrough over recurrent F8 nonsense mutations: potential correlation with inhibitor risk? 46
Molecular insights into determinants of translational readthrough and implications for nonsense suppression approaches 38
Detection of Residual Factor VIII Levels Reveals the Occurrence of Readthrough Over the Majority of F8 Nonsense Mutations 38
Translation termination codons in protein synthesis and disease 34
An advanced method for the small-scale production of high-quality minicircle DNA 32
Spontaneous readthrough over recurrent F8 nonsense mutations is associated with residual factor VIII levels: implications for inhibitor risk? 31
Comparative Analysis Of Residual Factor VIII Expression from Recurrent F8 Nonsense Mutations Indicates that Localization in the B- domain Favours Readthrough- mediated Protein Output 21
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association 21
A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia 16
An engineered factor X variant as a novel by-passing agent for hemophilia 14
The p.P1127S pathogenic variant lowers von Willebrand factor levels through higher affinity for the macrophagic scavenger receptor LRP1: Clinical phenotype and pathogenic mechanisms 11
Engineered suppressor tRNAs as a novel correction approach for recurrent hemophilia A-causing nonsense mutations 6
An integrated multi-tool analysis contributes elements to interpreting unclassified factor IX missense variants associated with haemophilia B 1
Totale 575
Categoria #
all - tutte 4.178
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 193
Totale 4.371


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202081 0 5 2 10 6 13 16 12 9 4 1 3
2020/202170 4 4 1 3 1 5 18 14 3 4 12 1
2021/202280 17 7 1 6 1 3 1 2 4 7 3 28
2022/2023115 11 14 5 9 16 8 11 11 14 2 4 10
2023/2024128 6 6 7 1 4 33 4 10 10 4 5 38
2024/202531 23 8 0 0 0 0 0 0 0 0 0 0
Totale 575