SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESE, Mattia
 Distribuzione geografica
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Continente #
NA - Nord America 1.516
EU - Europa 491
AS - Asia 378
SA - Sud America 4
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.393
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Nazione #
US - Stati Uniti d'America 1.508
CN - Cina 209
IT - Italia 204
DE - Germania 62
TR - Turchia 55
PL - Polonia 53
UA - Ucraina 46
SE - Svezia 32
GB - Regno Unito 31
ID - Indonesia 27
SG - Singapore 24
FI - Finlandia 12
BE - Belgio 11
HK - Hong Kong 10
NO - Norvegia 10
VN - Vietnam 10
IR - Iran 9
CZ - Repubblica Ceca 8
JP - Giappone 8
CA - Canada 7
PK - Pakistan 7
KR - Corea 6
FR - Francia 5
NL - Olanda 5
BR - Brasile 4
PT - Portogallo 4
DK - Danimarca 3
GE - Georgia 3
IN - India 3
AU - Australia 2
IL - Israele 2
RU - Federazione Russa 2
TW - Taiwan 2
AT - Austria 1
EU - Europa 1
IE - Irlanda 1
IQ - Iraq 1
MX - Messico 1
MY - Malesia 1
RO - Romania 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 2.393
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Città #
Chandler 212
Fairfield 195
Woodbridge 131
Ferrara 105
Ashburn 102
Seattle 83
Houston 72
Wilmington 71
Cambridge 67
Ann Arbor 64
Warsaw 52
New York 48
Izmir 46
Jacksonville 43
Princeton 43
Shanghai 38
Nanjing 37
Dearborn 34
Beijing 32
Jakarta 25
Milan 25
Bremen 22
Nanchang 14
Singapore 14
Redwood City 12
Guangzhou 11
San Diego 11
Dong Ket 10
Shenyang 10
Boardman 9
Hebei 9
Bologna 8
Jiaxing 8
Brussels 7
Lahore 7
Los Angeles 7
Oslo 7
Toronto 7
Brno 6
Helsinki 6
Kunming 6
London 6
Piemonte 6
Ferrara di Monte Baldo 5
Hong Kong 5
Jinan 5
San Mateo 5
Tianjin 5
Washington 5
Cagliari 4
Castagnole delle Lanze 4
Changsha 4
Des Moines 4
Louvain 4
Ningbo 4
Seocho-gu 4
Zhengzhou 4
Andover 3
Chicago 3
Copenhagen 3
Florence 3
Hangzhou 3
Ipiranga 3
Leawood 3
Munich 3
Norwalk 3
Reading 3
Silveira 3
Augusta 2
Belvedere Spinello 2
Duncan 2
Falls Church 2
Fars 2
Halesowen 2
Hefei 2
Hounslow 2
Imola 2
Olomouc 2
Reggio Emilia 2
Rome 2
Sabz 2
Semnan 2
Tabriz 2
Tel Aviv 2
Worcester 2
Wuhan 2
Zanica 2
Addison 1
Balk 1
Bloemfontein 1
Boxborough 1
Brisbane 1
Cabinteely 1
Cento 1
Chengdu 1
Chiswick 1
Chongqing 1
Dallas 1
Danvers 1
Decatur 1
Totale 1.874
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Nome #
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency 158
Akt-mediated phosphorylation of MICU1 regulates mitochondrial Ca 2+ levels and tumor growth 136
Specific factor IX mRNA and protein features favor drug-induced readthrough over recurrent nonsense mutations 133
Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based Therapeutics 131
Responsiveness of hemophilia B- causing non sense mutations to ribosome readthrough-inducing drugs strictly depends on the nucleotide and prrotein context 122
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation 106
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 99
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies 98
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 98
null 93
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition 89
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 87
Translational readthrough of GLA nonsense mutations suggests dominant-negative effects exerted by the interaction of wild-type and missense variants 74
The carboxyl-terminal region of human coagulation factor X as a novel naturally-occuring linker for fusion strategies 70
An optimized in vitro expression platform identifies Haemophilia B nonsense mutations, and thus patients, eligible for therapeutic drug-induced readthrough 62
A strategy with chaperone-like compounds to restore expression of factor IX variants affected by frequent missense mutations causing hemophilia B 61
The chaperone-like compound sodium phenylbutyrate improves intracellular trafficking, secretion and coagulant activity of factor IX impaired by the frequent p.R294Q mutation 60
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I 59
Mutation-specific contributions to trace factor X levels account for a life-threating phenotype in a compound heterozygous factor X deficient patient 53
An exon-specific small nuclear u1 rna (Exspeu1) improves hepatic otc expression in a splicing-defective spf /ash mouse model of ornithine transcarbamylase deficiency 50
Exploring chaperone-like compounds as innovative therapeutic correction approach for factor IX missense mutations causing type I Haemophilia B 50
A next-generation rFVIIa fusion protein with enhanced half-life as a novel by-passing tool in hemophilia 49
An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics 47
Fusion of engineered albumin with factor IX Padua extends half-life and improves coagulant activity 46
Rational engineering of a novel factor IX albumin fusion protein results in enhanced coagulant activity and pharmacokinetic profile 45
Identification of novel mechanisms underlying functional response to drug-induced readthrough of haemophilia B nonsense mutations 45
Exploring chaperone-like compounds as innovative therapeutic strategy for Hemophilia B 43
Next generation factor VIIa with enhanced half-life 43
Readthrough-mediated functional suppression of homozygous nonsense mutations accounts for variable bleeding phenotypes in factor VII deficiency 39
Design of a novel factor IX albumin fusion protein with enhanced coagulant activity and pharmacokinetic profile 38
Detection of Residual Factor VIII Levels Reveals the Occurrence of Readthrough Over the Majority of F8 Nonsense Mutations 37
Recombinant Expression of F9 Nonsense Mutations and Fix Pharmacokinetics in Hemophilia B 31
Spontaneous readthrough over recurrent F8 nonsense mutations is associated with residual factor VIII levels: implications for inhibitor risk? 30
Design of a novel factor IX variant with enhanced procoagulant activity and half-life 30
An advanced method for the small-scale production of high-quality minicircle DNA 28
Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domains 26
Protein engineering and pharmacological approaches to develop novel treatment strategies for coagulation disorders 25
Comparative Analysis Of Residual Factor VIII Expression from Recurrent F8 Nonsense Mutations Indicates that Localization in the B- domain Favours Readthrough- mediated Protein Output 20
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association 18
Suppression of “leaky” nonsense mutations by ribosome readthrough accounts for residual factor IX levels in Haemophilia B patients 9
Totale 2.538
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Categoria #
all - tutte 12.730
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 12.730
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020477 76 17 13 64 50 75 52 39 46 20 16 9
2020/2021433 19 9 22 24 20 38 58 60 25 66 51 41
2021/2022358 59 35 8 4 21 22 5 12 17 31 21 123
2022/2023436 48 61 12 62 62 50 30 31 42 5 18 15
2023/2024285 10 23 16 4 17 61 15 30 6 9 12 82
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 2.538