IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

FERRARI, VERONICA
 Distribuzione geografica
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Continente #
AS - Asia 8.383
EU - Europa 7.960
NA - Nord America 7.393
SA - Sud America 609
AF - Africa 205
OC - Oceania 88
Continente sconosciuto - Info sul continente non disponibili 2
Totale 24.640
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Nazione #
US - Stati Uniti d'America 7.088
CN - Cina 2.522
DE - Germania 2.353
SG - Singapore 2.235
IT - Italia 2.075
GB - Regno Unito 1.208
HK - Hong Kong 727
BD - Bangladesh 690
VN - Vietnam 664
BR - Brasile 462
RU - Federazione Russa 439
IN - India 401
SE - Svezia 393
FR - Francia 339
JP - Giappone 293
NL - Olanda 270
KR - Corea 255
CA - Canada 207
IE - Irlanda 154
ID - Indonesia 148
FI - Finlandia 136
DK - Danimarca 133
TR - Turchia 102
CI - Costa d'Avorio 100
AU - Australia 83
BE - Belgio 81
TW - Taiwan 81
ES - Italia 64
PL - Polonia 59
MX - Messico 57
CH - Svizzera 47
AT - Austria 44
AR - Argentina 40
UA - Ucraina 39
ZA - Sudafrica 31
EC - Ecuador 30
IL - Israele 27
IQ - Iraq 27
PH - Filippine 27
PK - Pakistan 27
CL - Cile 24
CO - Colombia 23
IR - Iran 20
EG - Egitto 19
GR - Grecia 18
SA - Arabia Saudita 16
HU - Ungheria 15
SI - Slovenia 15
NP - Nepal 14
MY - Malesia 12
TH - Thailandia 12
UZ - Uzbekistan 12
KE - Kenya 11
MO - Macao, regione amministrativa speciale della Cina 11
MA - Marocco 10
RO - Romania 10
AE - Emirati Arabi Uniti 9
TN - Tunisia 9
VE - Venezuela 9
LT - Lituania 8
LU - Lussemburgo 8
CR - Costa Rica 7
PE - Perù 7
CZ - Repubblica Ceca 6
NO - Norvegia 6
PT - Portogallo 6
PY - Paraguay 6
GT - Guatemala 5
JO - Giordania 5
KZ - Kazakistan 5
LB - Libano 5
NZ - Nuova Zelanda 5
SC - Seychelles 5
AD - Andorra 4
AL - Albania 4
AZ - Azerbaigian 4
BB - Barbados 4
BO - Bolivia 4
DZ - Algeria 4
ET - Etiopia 4
GE - Georgia 4
HR - Croazia 4
RS - Serbia 4
TT - Trinidad e Tobago 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
CY - Cipro 3
HN - Honduras 3
JM - Giamaica 3
KG - Kirghizistan 3
LV - Lettonia 3
MM - Myanmar 3
MT - Malta 3
NG - Nigeria 3
NI - Nicaragua 3
PA - Panama 3
PR - Porto Rico 3
UY - Uruguay 3
BG - Bulgaria 2
BH - Bahrain 2
Totale 24.601
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Città #
Hanover 1.426
Singapore 1.324
Ashburn 973
Southend 807
Milan 675
Hong Kong 586
San Jose 476
Frankfurt am Main 438
Beijing 379
Chandler 350
Council Bluffs 336
Dallas 300
Santa Clara 257
Hefei 256
New York 252
Los Angeles 226
Ho Chi Minh City 198
Fairfield 187
Hanoi 156
Boardman 153
Dublin 151
Wilmington 144
Seoul 139
Princeton 130
Jakarta 127
Bengaluru 126
Ann Arbor 123
Munich 122
Shanghai 122
Lauterbourg 111
Seattle 107
Cambridge 106
Guangzhou 102
Abidjan 100
Phoenix 100
Buffalo 88
Tokyo 88
Moscow 85
Redwood City 85
Rome 85
Chicago 84
Houston 84
Helsinki 79
Dearborn 78
The Dalles 73
Woodbridge 72
Philadelphia 71
Istanbul 60
Nanjing 57
Grafing 55
Medford 53
Cangzhou 51
Nuremberg 50
Naples 49
Turin 48
Atlanta 47
Da Nang 47
Des Moines 47
São Paulo 47
Boston 44
Toronto 42
Shenyang 40
Basingstoke 39
Irvine 39
Tianjin 39
Zhengzhou 39
Amsterdam 38
Delhi 38
Montreal 38
Jinan 37
Taichung 37
Magenta 36
Brooklyn 35
Wuhan 34
Columbus 33
Genoa 33
Mumbai 33
Fuzhou 31
Warsaw 30
Indianapolis 29
San Francisco 28
Haiphong 27
Changsha 26
Chennai 26
Dong Ket 26
Honolulu 26
London 26
Turku 26
Nanchang 25
Vienna 25
Berlin 24
Brussels 24
Quanzhou 24
Florence 23
Lappeenranta 23
Washington 22
Bologna 21
Melbourne 21
Paris 21
Central District 20
Totale 14.396
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Nome #
Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration 1.232
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 560
Autophagic and Proteasomal Mediated Removal of Mutant Androgen Receptor in Muscle Models of Spinal and Bulbar Muscular Atrophy 558
Transforming Growth Factor beta 1 signaling is altered in the spinal cord and muscle of amyotrophic lateral sclerosis mice and patients 541
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 526
Retinoic Acid Downregulates HSPB8 Gene Expression in Human Breast Cancer Cells MCF-7 477
VALOSIN CONTAINING PROTEIN IN AMYOTROPHIC LATERAL SCLEROSIS: NEW INSIGHT IN PATHOLOGICAL MECHANISMS 460
The Role of the Heat Shock Protein B8 (HSPB8) in Motoneuron Diseases 305
Analysis of the autophagic response in models of KIF5A-related neurodegeneration 300
Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives 297
Molecules capable to induce neuroprotection via lysophagy activation 296
Bicalutamide and Trehalose Ameliorate Spinal and Bulbar Muscular Atrophy Pathology in Mice 277
The role of Extracellular Vesicles (EVs) in Amyotrophic Lateral Sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) 276
The regulation of the small heat shock protein B8 in misfolding protein diseases causing motoneuronal and muscle cell death 270
Chaperone Assisted Selective Autophagy (CASA) a potential target for therapeutics in motoneuron diseases 266
HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies 262
Molecular mechanisms in KIF5A-related neurodegeneration 254
A Crucial Role for the Protein Quality Control System in Motor Neuron Diseases 251
BAG1 assists the degradation of neurotoxic proteins related to motor neuron diseases counteracting dynein-mediated autophagy alteration 244
Motor neuron degeneration in spinal and bulbar muscular atrophy: molecular approaches to counteract mutant androgen receptor neurotoxicity 243
Small heat shock protein B8: from cell functions to its involvement in diseases and potential therapeutic applications 242
Generation of novel induced pluripotent stem cell models for the study of spinocerebellar ataxia type 17 240
Alternative Translation Initiation as a novel strategy to block toxicity of the mutant Androgen Receptor in SBMA 239
TDP-43 PROTEINOPATHIES: THE ROLE OF EXTRACELLULAR VESICLES 237
Multiple Roles of Transforming Growth Factor Beta in Amyotrophic Lateral Sclerosis 237
TDP25 aggregation in motor neuron and muscle cells is rescued by chaperone overexpression 232
RAN translated C9ORF72 arginine rich poly-dipeptides alter gene transcription in ALS/FTD cell model 232
Identification of new HSPB8 variants linked to familial Amiotrophic Lateral Sclerosis 228
STIP1 Homology And U-Box Containing Protein 1 (STUB1/CHIP) mutants as a key factor on TATA-box binding protein (TBP) behaviour in digenic spinocerebellar ataxia type 17 (SCA17-DI) 224
Pathogenic variants of Valosin Containing Protein induce lysosomal damage and transcriptional activation of autophagy regulators in neuronal cells 224
Extracellular vesicles and the secretion of TDP species in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD) 219
Effect of Hspb8 deletion in the skeletal muscle of a mouse model for Amyotrophic Lateral Sclerosis 218
The clearance of aggregated TDP-43 responsible for ALS/FTD diseases 216
Valosin Containing Protein (VCP): A Multistep Regulator of Autophagy 215
VCP mutants cause lysosomal alterations and autophagy induction in ALS-neuronal model 214
ALS-associeted VCP-mutants lead to lysosome damage 212
Bicalutamide and Trehalose as a therapeutic approach for SBMA 208
Insights on human small heat shock proteins and their alterations in diseases 206
Chaperone mediated autophagy respond to dynein mediated transport inhibition in motor neuron diseases 206
Neurodegenerative Disease-Associated TDP-43 Fragments Are Extracellularly Secreted with CASA Complex Proteins 206
How PQC inhibition modulates miRNA loading in large and small extracellular vesicles 202
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders 200
Chaperone mediated autophagy responds to macroautophagy inhibition in motor neuron diseases 200
The BAG1 molecular chaperone regulators prevent ALS related neurotoxic misfolded proteins accumulation via proteasome and chaperone mediated autophagy 199
STUB1 mutants effect on TBP behavior in digenic spinocerebellar ataxia type 17 197
VCP modulation rescues C9ORF72 pathological features in ALS-neuronal models 194
Amyotrophic lateral sclerosis related proteins are actively removed by HspB8 193
VCP ALS-mutants induce lysosomal damage and autophagy activation 193
Novel pathogenic mechanism of ALS-associated VCP- mutants 190
Extracellular vesicles cooperate with PQC system for the clearance of TDP-43 species associated with ALS and FTD 189
Mechanism of paroxetine-mediated autophagic induction in cell models of ALS/FTD 188
Clearance of misfolded proteins in motoneuron disease: the case of Spinal and Bulbar Muscular Atrophy 188
C9ORF72 arginine rich poly-dipeptides induce transcriptional alterations in ALS/FTD cell model 186
Differentiation of isogenic iPSC reporter lines to motoneurons as tools for familial and sporadic amyotrophic lateral sclerosis 184
The role of autophagy-lysosomal pathway in motor neuron diseases 183
Mutations in VCP induce lysosomal alterations and autophagy activation in ALS neuronal models 183
Chaperone-assisted selective autophagy in Health and Disease 182
BAG1 prevents misfolded proteins accumulation when autophagy flux is blocked in neurodegenerative disorders 180
Alternative translation initiatin as a novel strategy to block toxicity of the mutant androgen receptor in SBMA 180
Identification of HSPB8 modulators counteracting misfolded protein accumulation in neurodegenerative diseases 177
VCP: a novel regulator of SOD1-G93A clearance in a als model 177
Clearance and transport of misfolded protein responsible for motor neuron diseases (MNDs) 176
The nucleotide exchange factor BAG1 prevents neurotoxic misfolded proteins accumulation via proteasome and chaperone mediated autophagy 176
Investigating the molecular mechanisms involved in KIF5A-related neurodegeneration 175
Shared behaviours of KIF5A frameshift mutants in neurodevelopment and neurodegeneration 174
TDP43 inclusions are re-routes to autophagy by the activity of the small chaperone HspB8 174
The role of Valosin Containing Protein (VCP) in the degradation of neurotoxic protein aggregates in Amyotrophic Lateral Sclerosis 174
Characterization of two new mutations in the small Heat Shock protein B8 HSPB8 and impact in Amyotrophic Lateral Sclerosis cell models 174
VCP mutants induce lysosomal damage and autophagy activation in amyotrophic lateral sclerosis (ALS) 174
One gene, many phenotypes: investigating KIF5A-linked neurodegeneration mechanisms 171
Insights into KIF5A-related pathways to neurodegeneration 170
Targeting androgen receptor stability and degradation: approaches for developing a therapy for spinal and bulbar muscular atrophy 169
Trehalose and bicalutamide as therapeutic agents of Kennedy disease 169
Autophagic removal of aggregating dipeptides produced in C9ORF72 related neurodegenerative diseases 167
Novel role of VCP in the clearance of mutant-SOD1 in als 167
The small heat shock protein B8 at the interplay between the intracellular degradative pathways in motoneuron disease 167
Mutant Androgen Receptor Alternative Translation Initiation as novel strategy to block toxicity in SBMA. 165
Role of the autophagic pathway in a muscle model of Spinal and Bulbar Muscular Atrophy 165
VCP autophagic modulation rescues C9ORF72 pathological features in ALS-neuronal models 162
The role of extracellular vesicles in the removal of aggregated TDP43 responsible for ALS/FTD diseases 161
Autophagy mediated HSPB8 removal of aggregating dipeptides produced in C9ORF72 related neurodegenerative diseases 157
Lysosome quality control in health and neurodegenerative diseases 157
Valosin Containing Protein role in the clearance of toxic mutated-SOD1 aggregates in fALS 156
Motor neuron degeneration in Spinal and Bulbar Muscular Atrophy: molecular approaches to counteract mutant androgen receptor neurotoxicity 155
Design, synthesis and characterization of aryl bis-guanyl hydrazones as RNA binders of C9orf72 G4C2 extended repeats 154
Valosin Containing Protein cooperates in the removal of toxic mutated-SOD-1 aggregates in Neurodegenerative diseases 154
Proteotoxic responses in amyotrophic lateral sclerosis 152
Autophagy Dysfunction in ALS: from Transport to Protein Degradation 152
Molecular defects in KIF5A-linked neurodegenerative and neurodevelopmental diseases 151
Innovative high throughput screening identifies HSPB8 modulators counteracting misfolded protein accumulation in neurodegenerative diseases 151
The chaperone HSPB8 removes insoluble forms of the C9ORF72 RAN translated dipeptides responsible for ALS/FTD 151
Insights into the neurodegenerative mechanisms associated with KIF5A mutations 150
The Role of Small Heat Shock Proteins in Protein Misfolding Associated Motoneuron Diseases 149
The small heat shock protein B8 (HSPB8) removes dipeptides produced in C9ORF72-related neurodegenerative diseases 149
The role of extracellular vesicles in the removal of aggregated TDP-43 responsible for ALS/FTD diseases 149
Extracellular vesicles and their role in TDP-43 proteinopathies 149
Transcriptional alterations induced by polyDPRs overexpression in neuronal cell model 148
Analysis of the pathogenetic mechanisms involved in KIF5A-related neurodegenerative disorders 147
Large and small extracellular vesicles may contribute to the propagation of ALS and FTD carrying toxic TDP species and potentially harmful miRNAs 146
Frameshift mutations in the Heat Shock Protein B8 share common pathogenic mechanisms and impair proteostasis 143
Totale 22.565
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Categoria #
all - tutte 70.688
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 70.688
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021229 0 0 0 0 0 0 0 0 0 0 0 229
2021/20222.772 81 135 140 246 262 294 277 236 281 293 236 291
2022/20231.800 138 207 150 129 147 275 100 150 220 37 146 101
2023/20242.576 95 165 267 400 478 92 136 164 107 181 265 226
2024/20254.348 154 296 161 477 429 215 192 429 206 472 422 895
2025/202610.431 934 737 854 770 1.016 571 1.287 450 942 756 1.443 671
Totale 25.406