SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESE, Mattia
 Distribuzione geografica
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Continente #
NA - Nord America 1.733
AS - Asia 571
EU - Europa 557
SA - Sud America 5
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.870
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Nazione #
US - Stati Uniti d'America 1.720
CN - Cina 235
IT - Italia 218
SG - Singapore 157
DE - Germania 75
TR - Turchia 56
ID - Indonesia 54
PL - Polonia 53
UA - Ucraina 46
FI - Finlandia 36
GB - Regno Unito 33
SE - Svezia 32
BE - Belgio 14
CA - Canada 12
HK - Hong Kong 10
NO - Norvegia 10
PK - Pakistan 10
VN - Vietnam 10
CZ - Repubblica Ceca 9
IR - Iran 9
JP - Giappone 8
FR - Francia 6
KR - Corea 6
NL - Olanda 6
BR - Brasile 5
PT - Portogallo 5
GE - Georgia 4
RU - Federazione Russa 4
DK - Danimarca 3
IN - India 3
AU - Australia 2
IL - Israele 2
LT - Lituania 2
TW - Taiwan 2
AT - Austria 1
EU - Europa 1
IE - Irlanda 1
IQ - Iraq 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MX - Messico 1
MY - Malesia 1
RO - Romania 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 2.870
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Città #
Chandler 212
Fairfield 195
Santa Clara 165
Singapore 137
Woodbridge 131
Ferrara 106
Ashburn 103
Seattle 83
Houston 72
Wilmington 71
Cambridge 67
Ann Arbor 64
Jakarta 52
Warsaw 52
New York 48
Izmir 46
Jacksonville 43
Princeton 43
Shanghai 39
Nanjing 37
Dearborn 34
Beijing 33
Helsinki 30
Milan 25
Bremen 22
Los Angeles 16
Nanchang 15
Redwood City 12
Guangzhou 11
San Diego 11
Brussels 10
Dong Ket 10
Falkenstein 10
Shenyang 10
Toronto 10
Boardman 9
Hebei 9
Bologna 8
Jiaxing 8
Lahore 8
Rome 8
London 7
Oslo 7
Brno 6
Kunming 6
Piemonte 6
Andover 5
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
Munich 4
Ningbo 4
Seocho-gu 4
Zhengzhou 4
Chicago 3
Copenhagen 3
Florence 3
Frankfurt am Main 3
Hangzhou 3
Ipiranga 3
Leawood 3
Moscow 3
Norwalk 3
Reading 3
Silveira 3
Alexandria 2
Augusta 2
Belvedere Spinello 2
Clifton 2
Duncan 2
Falls Church 2
Fars 2
Halesowen 2
Hefei 2
Hounslow 2
Imola 2
Olomouc 2
Ottawa 2
Padova 2
Reggio Emilia 2
Sabz 2
Semnan 2
Shenzhen 2
Tabriz 2
Tel Aviv 2
Worcester 2
Wuhan 2
Zanica 2
Addison 1
Ambrolauri 1
Balk 1
Bishkek 1
Totale 2.261
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Nome #
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency 175
Akt-mediated phosphorylation of MICU1 regulates mitochondrial Ca 2+ levels and tumor growth 154
Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based Therapeutics 143
Specific factor IX mRNA and protein features favor drug-induced readthrough over recurrent nonsense mutations 139
Responsiveness of hemophilia B- causing non sense mutations to ribosome readthrough-inducing drugs strictly depends on the nucleotide and prrotein context 136
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation 118
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 110
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 110
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies 108
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition 103
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 99
null 93
Translational readthrough of GLA nonsense mutations suggests dominant-negative effects exerted by the interaction of wild-type and missense variants 81
The carboxyl-terminal region of human coagulation factor X as a novel naturally-occuring linker for fusion strategies 81
A strategy with chaperone-like compounds to restore expression of factor IX variants affected by frequent missense mutations causing hemophilia B 78
The chaperone-like compound sodium phenylbutyrate improves intracellular trafficking, secretion and coagulant activity of factor IX impaired by the frequent p.R294Q mutation 74
An optimized in vitro expression platform identifies Haemophilia B nonsense mutations, and thus patients, eligible for therapeutic drug-induced readthrough 73
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I 73
An exon-specific small nuclear u1 rna (Exspeu1) improves hepatic otc expression in a splicing-defective spf /ash mouse model of ornithine transcarbamylase deficiency 64
A next-generation rFVIIa fusion protein with enhanced half-life as a novel by-passing tool in hemophilia 64
Mutation-specific contributions to trace factor X levels account for a life-threating phenotype in a compound heterozygous factor X deficient patient 62
Exploring chaperone-like compounds as innovative therapeutic correction approach for factor IX missense mutations causing type I Haemophilia B 62
An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics 60
Fusion of engineered albumin with factor IX Padua extends half-life and improves coagulant activity 59
Identification of novel mechanisms underlying functional response to drug-induced readthrough of haemophilia B nonsense mutations 58
Rational engineering of a novel factor IX albumin fusion protein results in enhanced coagulant activity and pharmacokinetic profile 57
Exploring chaperone-like compounds as innovative therapeutic strategy for Hemophilia B 52
Design of a novel factor IX albumin fusion protein with enhanced coagulant activity and pharmacokinetic profile 51
Readthrough-mediated functional suppression of homozygous nonsense mutations accounts for variable bleeding phenotypes in factor VII deficiency 49
Detection of Residual Factor VIII Levels Reveals the Occurrence of Readthrough Over the Majority of F8 Nonsense Mutations 49
Next generation factor VIIa with enhanced half-life 48
An advanced method for the small-scale production of high-quality minicircle DNA 44
Design of a novel factor IX variant with enhanced procoagulant activity and half-life 42
Spontaneous readthrough over recurrent F8 nonsense mutations is associated with residual factor VIII levels: implications for inhibitor risk? 41
Protein engineering and pharmacological approaches to develop novel treatment strategies for coagulation disorders 41
Recombinant Expression of F9 Nonsense Mutations and Fix Pharmacokinetics in Hemophilia B 40
Comparative Analysis Of Residual Factor VIII Expression from Recurrent F8 Nonsense Mutations Indicates that Localization in the B- domain Favours Readthrough- mediated Protein Output 35
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association 35
Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domains 34
Suppression of “leaky” nonsense mutations by ribosome readthrough accounts for residual factor IX levels in Haemophilia B patients 20
Totale 3.015
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Categoria #
all - tutte 17.517
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 17.517
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020257 0 0 0 0 0 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
2024/2025479 36 20 97 29 130 167 0 0 0 0 0 0
Totale 3.015