SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESE, Mattia
 Distribuzione geografica
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Continente #
NA - Nord America 1.732
AS - Asia 561
EU - Europa 525
SA - Sud America 5
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.827
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Nazione #
US - Stati Uniti d'America 1.719
CN - Cina 230
IT - Italia 216
SG - Singapore 152
DE - Germania 67
TR - Turchia 56
ID - Indonesia 54
PL - Polonia 53
UA - Ucraina 46
GB - Regno Unito 32
SE - Svezia 32
FI - Finlandia 16
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
BR - Brasile 5
NL - Olanda 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 2.827
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Città #
Chandler 212
Fairfield 195
Santa Clara 165
Singapore 132
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 32
Milan 25
Bremen 22
Los Angeles 16
Nanchang 14
Redwood City 12
Guangzhou 11
San Diego 11
Brussels 10
Dong Ket 10
Helsinki 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
Falkenstein 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 2.226
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Nome #
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency 171
Akt-mediated phosphorylation of MICU1 regulates mitochondrial Ca 2+ levels and tumor growth 153
Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based Therapeutics 142
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 133
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation 117
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 109
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 109
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies 107
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition 102
Secretion of wild-type factor IX upon readthrough over F9 pre-peptide nonsense mutations causing hemophilia B 98
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 80
A strategy with chaperone-like compounds to restore expression of factor IX variants affected by frequent missense mutations causing hemophilia B 77
The chaperone-like compound sodium phenylbutyrate improves intracellular trafficking, secretion and coagulant activity of factor IX impaired by the frequent p.R294Q mutation 73
An optimized in vitro expression platform identifies Haemophilia B nonsense mutations, and thus patients, eligible for therapeutic drug-induced readthrough 72
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I 72
An exon-specific small nuclear u1 rna (Exspeu1) improves hepatic otc expression in a splicing-defective spf /ash mouse model of ornithine transcarbamylase deficiency 63
A next-generation rFVIIa fusion protein with enhanced half-life as a novel by-passing tool in hemophilia 63
Mutation-specific contributions to trace factor X levels account for a life-threating phenotype in a compound heterozygous factor X deficient patient 61
Exploring chaperone-like compounds as innovative therapeutic correction approach for factor IX missense mutations causing type I Haemophilia B 61
An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics 59
Fusion of engineered albumin with factor IX Padua extends half-life and improves coagulant activity 58
Identification of novel mechanisms underlying functional response to drug-induced readthrough of haemophilia B nonsense mutations 57
Rational engineering of a novel factor IX albumin fusion protein results in enhanced coagulant activity and pharmacokinetic profile 55
Exploring chaperone-like compounds as innovative therapeutic strategy for Hemophilia B 51
Design of a novel factor IX albumin fusion protein with enhanced coagulant activity and pharmacokinetic profile 50
Next generation factor VIIa with enhanced half-life 48
Detection of Residual Factor VIII Levels Reveals the Occurrence of Readthrough Over the Majority of F8 Nonsense Mutations 48
Readthrough-mediated functional suppression of homozygous nonsense mutations accounts for variable bleeding phenotypes in factor VII deficiency 47
An advanced method for the small-scale production of high-quality minicircle DNA 43
Design of a novel factor IX variant with enhanced procoagulant activity and half-life 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 39
Spontaneous readthrough over recurrent F8 nonsense mutations is associated with residual factor VIII levels: implications for inhibitor risk? 39
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association 35
Comparative Analysis Of Residual Factor VIII Expression from Recurrent F8 Nonsense Mutations Indicates that Localization in the B- domain Favours Readthrough- mediated Protein Output 33
Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domains 33
Suppression of “leaky” nonsense mutations by ribosome readthrough accounts for residual factor IX levels in Haemophilia B patients 19
Totale 2.972
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Categoria #
all - tutte 17.167
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 17.167
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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
2024/2025436 36 20 97 29 130 124 0 0 0 0 0 0
Totale 2.972