SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

LOMBARDI, Silvia
 Distribuzione geografica
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Continente #
EU - Europa 1.303
NA - Nord America 212
AS - Asia 37
SA - Sud America 1
Totale 1.553
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Nazione #
FR - Francia 1.192
US - Stati Uniti d'America 210
IT - Italia 39
DE - Germania 22
SE - Svezia 18
CN - Cina 17
NO - Norvegia 6
DK - Danimarca 5
IN - India 5
JP - Giappone 4
AE - Emirati Arabi Uniti 3
GB - Regno Unito 3
NL - Olanda 3
VN - Vietnam 3
CA - Canada 2
IE - Irlanda 2
MD - Moldavia 2
PH - Filippine 2
PL - Polonia 2
RU - Federazione Russa 2
UA - Ucraina 2
AT - Austria 1
BR - Brasile 1
ES - Italia 1
GR - Grecia 1
HK - Hong Kong 1
HU - Ungheria 1
KR - Corea 1
PK - Pakistan 1
RS - Serbia 1
Totale 1.553
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Città #
Paris 258
Santa Cruz 30
Stockholm 18
Fairfield 16
Bremen 12
Ashburn 11
Chicago 11
Shanghai 10
Buffalo 9
Des Moines 7
Ferrara 7
New York 7
Seattle 7
New Haven 6
Oslo 6
Ann Arbor 5
Boardman 5
Copenhagen 5
Houston 5
Milan 5
Padova 4
San Diego 4
Woodbridge 4
Amsterdam 3
Bologna 3
Clearwater 3
Columbus 3
Dong Ket 3
Ferrara di Monte Baldo 3
Frankfurt am Main 3
Wilmington 3
Cambridge 2
Dublin 2
Las Vegas 2
Miami 2
Portland 2
Tokyo 2
Toronto 2
Utsukushigaoka 2
Warsaw 2
Albignasego 1
Amgaon 1
Andover 1
Argenteuil 1
Athens 1
Augsburg 1
Bloomfield 1
Budapest 1
Camponogara 1
Cassano Magnago 1
Central 1
Cona 1
Council Bluffs 1
Dallas 1
Florence 1
Flushing 1
Fremont 1
Glenview 1
Graz 1
Gurgaon 1
Holly Springs 1
Hyderabad 1
Kanpur 1
Lake Forest 1
Leesburg 1
Lombard 1
Los Angeles 1
Madrid 1
Madurai 1
Mainz 1
Nagold 1
Napoli 1
Pozzuoli 1
Presque Isle 1
Provo 1
Racale 1
Recife 1
Riva 1
Saint Petersburg 1
Santa Clara 1
Scranton 1
Secaucus 1
Vicenza 1
Villanova Del Ghebbo 1
Totale 538
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Nome #
A strategy with chaperone-like compounds to restore expression of factor IX variants affected by frequent missense mutations causing hemophilia B, file e309ade5-6bd5-3969-e053-3a05fe0a2c94 1.135
Translational readthrough of GLA nonsense mutations suggests dominant-negative effects exerted by the interaction of wild-type and missense variants, file e309ade4-8f47-3969-e053-3a05fe0a2c94 70
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation, file e309ade3-1d7c-3969-e053-3a05fe0a2c94 59
Fusion of engineered albumin with factor IX Padua extends half-life and improves coagulant activity, file e309ade4-a41d-3969-e053-3a05fe0a2c94 47
Exploring spontaneous readthrough over recurrent F8 nonsense mutations: potential correlation with inhibitor risk?, file e309ade4-8508-3969-e053-3a05fe0a2c94 42
Rational engineering of a novel factor IX albumin fusion protein results in enhanced coagulant activity and pharmacokinetic profile, file e309ade4-ae44-3969-e053-3a05fe0a2c94 25
Exon-Specific U1snRNA-Mediated Rescue of Splicing and Missense Changes in Hemophilia A, file e309ade4-92c0-3969-e053-3a05fe0a2c94 19
Molecular insights into determinants of translational readthrough and implications for nonsense suppression approaches, file e309ade2-f80d-3969-e053-3a05fe0a2c94 15
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I, file e309ade2-96d4-3969-e053-3a05fe0a2c94 14
A next-generation rFVIIa fusion protein with enhanced half-life as a novel by-passing tool in hemophilia, file e309ade4-aca2-3969-e053-3a05fe0a2c94 13
An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics, file e309ade4-bd31-3969-e053-3a05fe0a2c94 11
Design of a novel factor IX albumin fusion protein with enhanced coagulant activity and pharmacokinetic profile, file e309ade4-cf12-3969-e053-3a05fe0a2c94 11
Detection of Residual Factor VIII Levels Reveals the Occurrence of Readthrough Over the Majority of F8 Nonsense Mutations, file e309ade4-a18b-3969-e053-3a05fe0a2c94 10
Design of a novel factor IX variant with enhanced procoagulant activity and half-life, file e309ade4-ae43-3969-e053-3a05fe0a2c94 10
An exon-specific small nuclear u1 rna (Exspeu1) improves hepatic otc expression in a splicing-defective spf /ash mouse model of ornithine transcarbamylase deficiency, file e309ade2-e3b4-3969-e053-3a05fe0a2c94 9
Rescue of multiple Haemophilia A-causing mutations by a single ExSpeU1: the importance of the genomic context, file e309ade4-8689-3969-e053-3a05fe0a2c94 9
Fusion of engineered albumin with factor IX Padua extends half-life and improves coagulant activity, file e309ade4-7a0c-3969-e053-3a05fe0a2c94 8
Deep molecular mechanisms of F8 exon 19 variants and translational approaches in Hemophilia A, file 01e33b6e-5e4b-4d19-9732-f26e7f907dd7 7
Spontaneous readthrough over recurrent F8 nonsense mutations is associated with residual factor VIII levels: implications for inhibitor risk?, file e309ade4-97bf-3969-e053-3a05fe0a2c94 7
Dissection of pleiotropic effects of variants in and adjacent to F8 exon 19 and rescue of mRNA splicing and protein function, file e309ade4-9d59-3969-e053-3a05fe0a2c94 6
The chaperone-like compound sodium phenylbutyrate improves intracellular trafficking, secretion and coagulant activity of factor IX impaired by the frequent p.R294Q mutation, file e309ade5-7c15-3969-e053-3a05fe0a2c94 6
Targeted molecular strategies for X-linked genetic disorders: the paradigmatic models of Fabry disease and Haemophilias, file e309ade5-94de-3969-e053-3a05fe0a2c94 6
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association, file 5fbac144-86d9-453d-8ae2-bfb235899756 5
The carboxyl-terminal region of human coagulation factor X as a novel naturally-occuring linker for fusion strategies, file e309ade5-7369-3969-e053-3a05fe0a2c94 5
Dissection of pleiotropic effects of variants in and adjacent to F8 exon 19 and rescue of mRNA splicing and protein function, file cad5b000-f0b2-4650-a42f-202ecc40146c 3
Comparative Analysis Of Residual Factor VIII Expression from Recurrent F8 Nonsense Mutations Indicates that Localization in the B- domain Favours Readthrough- mediated Protein Output, file e78c85f4-6fa2-41b4-aa52-0b73eb64b1c3 3
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency, file e309ade1-2b7b-3969-e053-3a05fe0a2c94 1
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies, file e309ade2-af05-3969-e053-3a05fe0a2c94 1
Readthrough-mediated functional suppression of homozygous nonsense mutations accounts for variable bleeding phenotypes in factor VII deficiency, file e309ade5-5f09-3969-e053-3a05fe0a2c94 1
Translation termination codons in protein synthesis and disease, file e5d8ab22-da6d-4cc7-b340-d2f37766661a 1
Totale 1.559
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Categoria #
all - tutte 4.202
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1
Totale 4.203
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202126 0 0 0 0 0 0 7 4 1 2 1 11
2021/2022117 10 12 8 3 8 4 3 6 2 16 36 9
2022/2023145 7 9 26 19 20 20 5 9 9 5 10 6
2023/20241.271 2 8 6 0 9 616 417 114 58 38 3 0
Totale 1.559