SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

BERNARDI, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 37.341
AS - Asia 20.108
EU - Europa 12.526
SA - Sud America 3.053
Continente sconosciuto - Info sul continente non disponibili 734
AF - Africa 464
OC - Oceania 45
AN - Antartide 1
Totale 74.272
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Nazione #
US - Stati Uniti d'America 36.459
SG - Singapore 7.447
CN - Cina 5.025
FI - Finlandia 2.585
BR - Brasile 2.365
VN - Vietnam 2.336
DE - Germania 2.094
IT - Italia 1.977
UA - Ucraina 1.762
HK - Hong Kong 1.572
TR - Turchia 1.138
GB - Regno Unito 1.058
FR - Francia 628
BD - Bangladesh 568
PL - Polonia 564
JP - Giappone 531
SE - Svezia 501
RU - Federazione Russa 499
CA - Canada 431
IN - India 381
MX - Messico 317
ID - Indonesia 258
AR - Argentina 239
ZA - Sudafrica 170
NL - Olanda 166
ES - Italia 141
IQ - Iraq 141
BE - Belgio 107
EC - Ecuador 107
CO - Colombia 94
PK - Pakistan 93
VE - Venezuela 82
UZ - Uzbekistan 72
MY - Malesia 70
CZ - Repubblica Ceca 64
MA - Marocco 63
AT - Austria 61
LT - Lituania 60
SA - Arabia Saudita 57
CL - Cile 54
PH - Filippine 53
KE - Kenya 52
IR - Iran 40
AU - Australia 38
PY - Paraguay 38
PE - Perù 36
CH - Svizzera 35
TN - Tunisia 35
IE - Irlanda 34
JO - Giordania 34
AE - Emirati Arabi Uniti 33
DZ - Algeria 33
NP - Nepal 31
JM - Giamaica 29
IL - Israele 25
RO - Romania 23
CR - Costa Rica 22
AL - Albania 21
AZ - Azerbaigian 21
KR - Corea 21
UY - Uruguay 21
ET - Etiopia 20
EG - Egitto 19
PT - Portogallo 19
TH - Thailandia 19
TW - Taiwan 19
GR - Grecia 18
BG - Bulgaria 14
KZ - Kazakistan 14
OM - Oman 14
PS - Palestinian Territory 14
DO - Repubblica Dominicana 13
RS - Serbia 13
SN - Senegal 13
EU - Europa 12
NO - Norvegia 12
TT - Trinidad e Tobago 12
BO - Bolivia 11
NG - Nigeria 11
GE - Georgia 10
LB - Libano 10
BH - Bahrain 9
HN - Honduras 9
KG - Kirghizistan 9
PA - Panama 9
SK - Slovacchia (Repubblica Slovacca) 9
SV - El Salvador 9
DK - Danimarca 8
GT - Guatemala 8
HU - Ungheria 8
KW - Kuwait 8
BY - Bielorussia 7
CI - Costa d'Avorio 7
NZ - Nuova Zelanda 7
BA - Bosnia-Erzegovina 6
NI - Nicaragua 6
AF - Afghanistan, Repubblica islamica di 5
AO - Angola 5
BW - Botswana 5
GA - Gabon 5
Totale 73.438
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Città #
Singapore 4.566
Ashburn 3.827
Woodbridge 2.989
Fairfield 2.929
San Jose 2.319
Helsinki 2.130
Houston 1.931
Chandler 1.929
Jacksonville 1.840
Santa Clara 1.664
Hong Kong 1.532
Beijing 1.520
Ann Arbor 1.407
Seattle 1.212
Wilmington 1.115
Dallas 969
Cambridge 962
Ho Chi Minh City 796
New York 712
Izmir 633
Nanjing 572
Los Angeles 570
Warsaw 544
Hanoi 540
Ferrara 531
Munich 519
Tokyo 504
Princeton 438
Boardman 407
Council Bluffs 389
Lauterbourg 370
The Dalles 298
San Diego 277
Milan 259
São Paulo 243
Shanghai 221
Mexico City 208
Orem 191
Nanchang 174
Dearborn 173
Shenyang 171
Jakarta 170
Buffalo 164
London 163
Bremen 162
Toronto 154
Tianjin 142
Chicago 141
Brooklyn 120
Hebei 120
Montreal 115
Hefei 112
Jiaxing 110
Rome 110
Da Nang 106
Frankfurt am Main 105
Falls Church 104
Changsha 101
Denver 100
Turku 99
Brussels 98
Chennai 98
Johannesburg 97
Haiphong 91
Atlanta 86
Redwood City 86
Jinan 83
Phoenix 80
Moscow 76
Falkenstein 75
Norwalk 75
Rio de Janeiro 75
San Mateo 71
Stockholm 71
Amsterdam 69
San Francisco 69
Kunming 68
Manchester 66
Mountain View 65
Guangzhou 64
Tashkent 64
Poplar 60
Belo Horizonte 58
Nuremberg 58
Baghdad 57
Düsseldorf 57
Curitiba 53
Zhengzhou 50
Auburn Hills 49
Biên Hòa 48
Bologna 48
Boston 48
Brno 48
Hải Dương 46
Des Moines 44
Dong Ket 44
Nairobi 44
Addison 42
Brasília 42
Philadelphia 42
Totale 49.544
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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 2.051
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System 428
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients 361
Are Plasma Levels of Vascular Adhesion Protein-1 Associated Both with Cerebral Microbleeds in Multiple Sclerosis and Intracerebral Haemorrhages in Stroke? 324
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency 309
AN EXON-SPECIFIC U1 SMALL NUCLEAR RNA (snRNA) STRATEGY TO CORRECT SPLICING MUTATIONS ASSOCIATED TO HEMOPHILIA B 306
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis 304
Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotides 300
An exon-specific U1snRNA induces a robust factor IX activity in mice expressing multiple human FIX splicing mutants 297
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study 291
An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes 289
Ricerche metodologiche sul dosaggio del cofattore Ristocetinico per la diagnosi di morbo di von Willebrand. 283
Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy 282
Tailoring the CRISPR system to transactivate coagulation gene promoters in normal and mutated contexts 273
A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates 265
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 263
VITAMIN K-INDUCED MODIFICATION OF COAGULATION PHENOTYPE IN VKORC1 HOMOZYGOUS DEFICIENCY 259
Hemostasis biomarkers in multiple sclerosis 259
Characterization of a deleted Y chromosome in a male with Turner stigmata 258
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family 257
A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease 254
U1-snRNA-mediated rescue of mRNA processing in severe factor VII deficiency 254
Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis 252
U1snRNA-mediated rescue of mRNA processing in severe factor VII deficiency 251
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease 250
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects 249
Factor XI rs2036914 gene polymorphism and occurrence of adverse events after percutaneous coronary intervention. A prospective evaluation. 249
Angiotensin-converting enzyme insertion/deletion polymorphism and risk of restenosis after directional coronary atherectomy followed by stent implantation 248
Genetic determinants of activated factor VII antithrombin complex plasma concentration include tissue factor, factor VII and endothelial protein C receptor gene variants 248
Attività sulla emostasi di alcune piante della medicina tradizionale indiana 245
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 244
Chronic sleep deprivation markedly reduces coagulation factor VII expression 244
Calmodulin expression distinguishes the smooth muscle cell population of human carotid plaque 244
Responsiveness of hemophilia B- causing non sense mutations to ribosome readthrough-inducing drugs strictly depends on the nucleotide and prrotein context 244
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype 243
Stimulation of P2 (P2X7) receptors in human dendritic cells induces the release of tissue factor-bearing microparticles. 241
Analisi dei multimeri del fattore von Willebrand mediante doppia immunoprecipitazione dopo elettroforesi su gel di agarosio. 241
Membrane binding and anticoagulant properties of protein S natural variants 240
Coagulation Factor XII Levels and Intrinsic Thrombin Generation in Multiple Sclerosis 240
High-density lipoprotein cholesterol is associated with multiple sclerosis fatigue: A fatigue-metabolism nexus? 239
Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant 239
The carboxyl-terminal region is not essential for secreted and functional levels of coagulation factor X 237
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 234
A NEW DISEASE-CAUSING MUTATION IN THE GAP-RELATED DOMAIN OF THE NF1 GENE 232
Moderate alcohol intake and hemostatic and inflammatory markers in middle-aged women: a controlled study 232
Daily and circadian rhythms of tissue factor pathway inhibitor and factor VII activity 231
A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA. 231
Evidence for an overlapping role of clock and npas2 transcription factors in liver circadian oscillators 230
A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE 229
Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis 223
c-myc oncogene alterations in human thyroid carcinomas. 223
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 222
Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation 222
An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects 221
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile 220
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency 220
The effectiveness of Robot-Assisted Gait Training versus conventional therapy on mobility in severely disabled progressIve MultiplE sclerosis patients (RAGTIME): Study protocol for a randomized controlled trial 220
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the italian population 219
A unique exon specific U1snRNA rescues different haemophilia B - causing splicing-defective factor IX variants in mice 219
Effective hemostasis during minor surgery in a case of hereditary combined deficiency of vitamin K-dependent clotting factors 218
TRATTAMENTO E PREVENZIONE DI MALATTIE CARDIOVASCOLARI CON ACIDO ERUCICO E METODI DIAGNOSTICI CORRELATI 218
Aberrant splicing reverts a potentially lethal coagulation deficiency caused by a +1g/t splicing mutation 217
Factor II Activity is Similarly Increased in Patients With Elevated Apolipoprotein CIII and in Carriers of the Factor II 20210A Allele 216
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 214
Temporal variations of coagulation factor VII activity in mice are influenced by lighting regime 213
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia 213
FXIII levels and genotypes in myocardial infarction: a potential novel prognostic biomarker? 213
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation 213
Asymmetric processing of mutant factor X Arg386Cys reveals differences between intrinsic and extrinsic pathway activation 213
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function 211
Calmodulin Is a Marker of a Distinct Smooth Muscle Cell Population Recruited by Plaque-Derived Macrophages from the Human Carotid Artery Media 211
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition 211
The dominant-negative von Willebrand factor gene deletion p.P1127-C1948delinsR: Molecular mechanism and modulation 210
Crosstalk between hemostasis inhibitors and cholesterol biomarkers in multiple sclerosis 209
A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg) 209
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers 209
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease 209
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X 209
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 204
Specific factor IX mRNA and protein features favor drug-induced readthrough over recurrent nonsense mutations 204
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glul02Lys) in the second EGF‐like domain 203
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala(223)Val MTHFR) in patients with inherited thrombophilic coagulation defects 203
Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations 203
Correction of aberrant splicing causing haemophilia B through the combination of compensatory U1snRNAs and antisense oligonucleotides 203
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene 203
The carboxyl-terminal region of human coagulation factor X as a novel naturally-occuring linker for fusion strategies 203
Performance prediction models based on anthropometric, genetic and psychological traits of Croatian sprinters 202
A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject 200
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 200
Plasma levels of soluble NCAM in multiple sclerosis 200
A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease 199
Human protein S circulates in plasma partially bund to LDL and HDL: do PS-lipoprotein complexes mediate PS delivery within atherosclerotic plaque? 199
Factor VII mutant V154G models a zymogen-like form of factor VIIa 198
The complete impairment of factor VII gene expression by the IVS6+1g/t mutation is compatible with a severe but not lethal bleeding disorder 198
Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency 197
Interaction of occupational posture, lifestyle and genetic components of thrombophilia 196
Circadian rhythms in mouse blood coagulation 195
Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency 195
Residual factor VII activity and different hemorrhagic phenotypes in CRM+ factor VII deficiencies (Gly331Ser and Gly283Ser) 195
CRISPR activation on coagulation F7 or F8 promoters potentiate trascriptional activity in the normal and mutated gene context 195
Totale 25.314
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Categoria #
all - tutte 326.731
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.132
Totale 328.863
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224.434 245 482 276 246 261 178 206 211 138 344 391 1.456
2022/20234.440 488 342 109 583 726 661 211 356 543 39 244 138
2023/20242.348 203 277 110 81 166 433 65 154 59 56 64 680
2024/20259.468 266 186 817 272 1.175 920 242 468 1.492 1.197 1.356 1.077
2025/202629.867 2.588 1.191 2.610 3.726 4.020 1.831 3.329 1.476 4.398 2.817 1.231 650
2026/2027667 667 0 0 0 0 0 0 0 0 0 0 0
Totale 74.272