IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CRIPPA, VALERIA
 Distribuzione geografica
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Continente #
EU - Europa 18.852
NA - Nord America 10.706
AS - Asia 6.147
OC - Oceania 290
SA - Sud America 161
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 8
Totale 36.226
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Nazione #
US - Stati Uniti d'America 10.401
IT - Italia 5.318
DE - Germania 5.216
GB - Regno Unito 4.401
CN - Cina 3.732
SE - Svezia 1.176
KR - Corea 519
IN - India 489
RU - Federazione Russa 380
FR - Francia 378
IE - Irlanda 363
UA - Ucraina 352
JP - Giappone 349
CA - Canada 288
AU - Australia 274
HK - Hong Kong 247
TR - Turchia 227
DK - Danimarca 220
FI - Finlandia 209
NL - Olanda 203
BE - Belgio 158
TW - Taiwan 144
EU - Europa 113
SG - Singapore 87
VN - Vietnam 82
ES - Italia 81
CH - Svizzera 78
CO - Colombia 76
PH - Filippine 65
PL - Polonia 65
GR - Grecia 57
IL - Israele 40
BR - Brasile 39
IR - Iran 35
ID - Indonesia 30
RO - Romania 28
PT - Portogallo 27
AT - Austria 25
MY - Malesia 24
TH - Thailandia 24
CL - Cile 23
NO - Norvegia 22
NZ - Nuova Zelanda 16
HU - Ungheria 15
SI - Slovenia 15
MX - Messico 13
ZA - Sudafrica 12
AL - Albania 11
CZ - Repubblica Ceca 10
EG - Egitto 10
EC - Ecuador 9
ET - Etiopia 9
PK - Pakistan 9
HR - Croazia 8
SC - Seychelles 8
MO - Macao, regione amministrativa speciale della Cina 6
PE - Perù 6
UZ - Uzbekistan 6
AR - Argentina 5
GH - Ghana 5
LU - Lussemburgo 5
ME - Montenegro 5
NG - Nigeria 5
AD - Andorra 4
BG - Bulgaria 4
RS - Serbia 4
AE - Emirati Arabi Uniti 3
BD - Bangladesh 3
KE - Kenya 3
KZ - Kazakistan 3
MM - Myanmar 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
BN - Brunei Darussalam 2
BT - Bhutan 2
IS - Islanda 2
KW - Kuwait 2
LT - Lituania 2
MG - Madagascar 2
ML - Mali 2
QA - Qatar 2
SA - Arabia Saudita 2
SM - San Marino 2
UG - Uganda 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BZ - Belize 1
CU - Cuba 1
CY - Cipro 1
DO - Repubblica Dominicana 1
FK - Isole Falkland (Malvinas) 1
IM - Isola di Man 1
IQ - Iraq 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
MD - Moldavia 1
Totale 36.324
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Città #
Southend 3.748
Hanover 3.195
Milan 973
Chandler 918
Beijing 771
Frankfurt am Main 654
Boise 651
Seattle 569
Ashburn 532
Fairfield 481
Wilmington 467
Princeton 456
Ann Arbor 375
Rome 364
Dublin 356
Hangzhou 336
Shanghai 270
Jacksonville 268
Woodbridge 268
Houston 233
Nanjing 230
Cambridge 218
Grafing 204
Dearborn 203
Redwood City 200
Guangzhou 195
Phoenix 193
Mountain View 189
Hong Kong 162
Redmond 149
Medford 148
Bengaluru 146
New York 143
Des Moines 141
Shenyang 124
Seoul 119
Jinan 115
Turin 109
Boardman 100
Changsha 98
Wuhan 95
Serra 94
Taipei 91
Florence 87
Palermo 86
Andover 82
Bari 82
Berlin 79
Bogotá 74
Helsinki 74
Sakarya 74
Toronto 71
Chengdu 70
Zhengzhou 65
Kiez 62
Padova 62
Tianjin 62
Tokyo 61
Chicago 60
London 60
Nanchang 59
Genoa 58
Istanbul 54
Naples 54
Verona 51
Catania 49
Brussels 48
Sunnyvale 48
Xian 48
Los Angeles 47
Ottawa 47
Philadelphia 47
Somerville 46
Athens 44
Boston 43
San Diego 43
Brescia 42
Bühl 42
Dallas 42
Dong Ket 42
Falls Church 42
Pittsburgh 42
Cottonwood 41
Hebei 41
Magenta 41
Central District 38
Fremont 38
Garden Valley 38
Hefei 38
Rochester 37
Atlanta 36
Kunming 36
Mumbai 35
Jerome 34
Baltimore 33
Perugia 33
Trento 33
Brisbane 32
Eitensheim 32
Jiaxing 32
Totale 22.248
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Nome #
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 3.853
Becker : Il mondo della cellula 3.304
Mutation of the SOD1 in ALS : a gain of a loss of function 1.367
Anti-inflammatory effects of AT1 receptor blockade provide end-organ protection in stroke-prone rats independently from blood pressure fall 1.060
Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration 1.042
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS) 709
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 495
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 441
Autophagic and Proteasomal Mediated Removal of Mutant Androgen Receptor in Muscle Models of Spinal and Bulbar Muscular Atrophy 414
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 403
The role of sex and sex Hormones in Neurodegenerative Diseases 396
FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagy 395
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 394
Transforming Growth Factor beta 1 signaling is altered in the spinal cord and muscle of amyotrophic lateral sclerosis mice and patients 384
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 340
Retinoic Acid Downregulates HSPB8 Gene Expression in Human Breast Cancer Cells MCF-7 314
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 304
HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation 304
L’inibizione dell’attività ATPasica della dineina riduce l’aggregazione di proteine mutate responsabili di Malattie del Motoneurone 247
Differences in protein quality control correlate with phenotype variability in 2 mouse models of familial amyotrophic lateral sclerosis 224
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 222
The Chaperone HSPB8 Reduces the Accumulation of Truncated TDP-43 Species in Cells and Protects Against TDP-43-Mediated Toxicity 221
The anabolic/androgenic steroid nandrolone exacerbates gene expression modifications induced by mutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis 212
HspB8 enhances autophagic degradation of mutant misfolded proteins responsible for motorneuron diseases 197
MISFOLDING PROTEICO E NEURODEGENERAZIONE : STUDIO DEL COINVOLGIMENTO DELLA PROTEINA CHAPERONE HEAT SHOCK PROTEIN B8 196
Effetto dell’espansione del tratto poliglutamminico del recettore degli androgeni sul differenziamento dei motoneuroni 191
Aberrant Autophagic Response in The Muscle of A Knock-in Mouse Model of Spinal and Bulbar Muscular Atrophy 185
The role of Extracellular Vesicles (EVs) in Amyotrophic Lateral Sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) 182
The HSPB8 by complexing with Bag3/Hsc70/CHIP removes mutant SOD1 in models of familiar amyotrophic lateral sclerosis 179
Aggregation and proteasome: the case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy 176
Analysis of the autophagic response in models of KIF5A-related neurodegeneration 174
Proteostasis and ALS : protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 173
Dysregulation of axonal transport and motorneuron diseases 168
A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases 164
THE ANDROGEN RECEPTOR AND ITS PATHOPHYSIOLOGICAL ROLE IN MOTOR NEURONS 164
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 163
L’inibizione dell’attività ATPasica della dineina riduce l’aggregazione del recettore degli androgeni mutato responsabile dell’ Atrofia Muscolare Spinale e Bulbare (SBMA) 160
Role of the Ubiquitin proteasome system and autophagic pathway in the degradation of a mutant PolyQ protein 159
Alterazione della funzione della Superossido Dismutasi di tipo I (SODI) a livello nucleare nella Sclerosi Laterale Amiotrofica Familiare 159
The protein quality control system in motoneuron diseases 157
Alteration of protein folding and degradation in motor neuron diseases : Implications and protective functions of small heat shock proteins 152
Molecules capable to induce neuroprotection via lysophagy activation 152
Alteration of protein folding and degradation in als: protective role of the small heat shock protein B8 151
Synergic prodegradative activity of bicalutamide and trehalose on the mutant androgen receptor responsible for spinal and bulbar muscular atrophy 148
The Role of the Heat Shock Protein B8 (HSPB8) in Motoneuron Diseases 143
17-(ALLYLAMINO)-17-DEMETHOXYGELDANAMYCIN (17 AAG) A PHARMACOLOGICAL APPROACH TO INDUCE DEGRADATION OF MISFOLDED PROTEINS 142
Dual role of testosterone in motoneuronal survival in SBMA 141
Accumulation of motor neuron diseases associated misfolded proteins is counteracted by dynein inhibition 140
The role of dynein mediated transport in the clearance of misfolded proteins responsible for motoneuron diseases 140
RNA molecular signature profiling in PBMCs of sporadic ALS patients: HSP70 overexpression is associated with nuclear SOD1 140
Anti-aggregant and pro-degradative molecules decrease mutant ARpolyQ accumulation in SBMA cell models 139
The regulation of the small heat shock protein B8 in misfolding protein diseases causing motoneuronal and muscle cell death 139
A Crucial Role for the Protein Quality Control System in Motor Neuron Diseases 137
The involvement of cellular degradative systems in the Spinal and bulbar muscular atrophy 136
Alteration of ubiquitin proteasome pathway in a cellular model of familial amyotrophic lateral sclerosis 136
Chaperone Assisted Selective Autophagy (CASA) a potential target for therapeutics in motoneuron diseases 135
TGFbeta1 expression in muscle of mouse model of familial amyotrophic lateral sclerosis 134
Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis 133
Dual role of testosterone in motorneuronal spinal and bulbar muscular atrophy (SBMA) 131
Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives 131
Controllo dell'espressione del recettore degli androgeni: una possibile applicazione per l'Atrofia Muscolare Spinale e Bulbare 130
Induction of oxidative DNA damage in cells expressing mutant Superoxide Dismutase 1 (SOD1) 130
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy 130
Familial Amyotrophic Lateral Sclerosis: Role of mutant forms of SOD1 on Ubiquitin Proteasome Pathway 129
17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy 129
Extracellular vesicles and the secretion of TDP species in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD) 128
ALS-related misfolded protein management in motor neurons and muscle cells 127
Spinal and Bulbar Muscular Atrophy : different approaches to induce ARpolyQ clearance 126
Biochemical behavior of SOD1 in two cell models of familial amyotrophic lateral sclerosis 125
Modultion of the Androgen Receptor promoter :a potential therapeutic approach to Kennedy's disease 125
Amyotrophic Lateral Sclerosis, a non-“cell-autonomous” disease : involvement of muscle cells 123
Alteration of nuclear ROS protection, in models of familial Amyotrophic Lateral Sclerosis (fALS) 122
Inhibition of dynein ATPase activity reduces aggregates formation of misfolded proteins involved in motoneuron diseases 122
Different behaviour of mutant SOD1 in motorneuronal and muscle cellular models of Amyotrophic Lateral Sclerosis 121
Superoxide Dismutase 1 (SOD1) and alteration of nuclear ROS protection in Amyotrophic Lateral Sclerosis (ALS) 121
Motoneuron and muscle-selective removal of ALS-related misfolded proteins 121
Familial amyotrophic lateral sclerosis: role of mutant forms of SOD1 on ubiquitin proteasome pathway 120
Motor neuron degeneration in spinal and bulbar muscular atrophy: molecular approaches to counteract mutant androgen receptor neurotoxicity 120
Inhibition of dynein ATPase activity reduces aggregation of misfolded proteins involved in motoneuron diseases 119
RAN translated C9ORF72 arginine rich poly-dipeptides alter gene transcription in ALS/FTD cell model 119
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 118
Effetto di un modulatore delle chaperones sulle proteine mutate responsabili di malattie del motoneurone 117
Inibizione della migrazione di cellule di carcinoma prostatico umano 117
IN VIVO EVALUATION OF PROTEASOME DYSFUNCTION IN A MOTONEURON CELL LINE AND IN A MOUSE MODEL OF FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS 117
Alteration of the protein quality control system in motor neuron and muscle expressing mutant proteins causing ALS and SBMA 116
Role of altered proteolysis in the degeneration of motor neurons in in vivo and in vitro models of familial amyotrophic lateral sclerosis. Involvement of constitutive and immuno proteasomes and of the autophagy-lysosome pathway 115
Identification of new HSPB8 variants linked to familial Amiotrophic Lateral Sclerosis 115
Meccanismi molecolari alla base di forme familiari della Sclerosi Laterale Amiotrofica 114
Protein aggregation and impairment of Ubiquitin Proteasome Pathway in a cellular model of familial amyotrophic lateral sclerosis 114
Pathophysiological roles of the androgen receptor in motor neurons 114
Pathological Proteins Are Transported by Extracellular Vesicles of Sporadic Amyotrophic Lateral Sclerosis Patients 113
ALS-associeted VCP-mutants lead to lysosome damage 113
Alternative translation initiatin as a novel strategy to block toxicity of the mutant androgen receptor in SBMA 112
CAG/POLYGLN related diseases - the case of spinobulbar muscular atrophy : aggregate formation, dystrophic neurites, neuronal survival 111
Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis 111
TDP25 aggregation in motor neuron and muscle cells is rescued by chaperone overexpression 111
CLEARANCE OF MISFOLDED PROTEINS IN SBMA AND ALS 110
Motorneuron degeneration in Spinal and Bulbar Muscular Atrophy: from the molecular mechanisms to the potential therapeutical approaches 110
The Role of HSPB8, a Component of the Chaperone-Assisted Selective Autophagy Machinery, in Cancer 110
A new approach to downregulate this neurotoxic androgen receptor in spinal and bulbar muscular atrophy 109
Totale 27.546
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Categoria #
all - tutte 78.276
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 78.276
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019735 0 0 0 0 0 0 0 0 0 0 406 329
2019/20204.850 625 253 294 564 375 398 472 348 582 479 295 165
2020/20214.064 251 339 254 280 316 294 213 291 544 367 503 412
2021/20227.298 247 290 358 625 675 732 749 632 768 804 699 719
2022/20235.237 485 497 435 750 531 772 241 347 544 121 314 200
2023/20244.640 185 296 501 1.151 984 244 297 391 224 334 33 0
Totale 37.861