CHIERICHETTI, MARTA
 Distribuzione geografica
Continente #
AS - Asia 5.328
EU - Europa 4.558
NA - Nord America 4.210
SA - Sud America 410
AF - Africa 150
OC - Oceania 57
Continente sconosciuto - Info sul continente non disponibili 1
Totale 14.714
Nazione #
US - Stati Uniti d'America 4.028
CN - Cina 1.561
SG - Singapore 1.506
IT - Italia 1.503
DE - Germania 1.110
HK - Hong Kong 506
VN - Vietnam 498
GB - Regno Unito 440
BR - Brasile 316
IN - India 299
RU - Federazione Russa 287
FR - Francia 231
NL - Olanda 212
SE - Svezia 192
KR - Corea 189
JP - Giappone 184
BD - Bangladesh 163
CA - Canada 115
ID - Indonesia 100
FI - Finlandia 91
DK - Danimarca 85
TR - Turchia 85
CI - Costa d'Avorio 76
IE - Irlanda 72
TW - Taiwan 64
BE - Belgio 54
AU - Australia 53
ES - Italia 51
AT - Austria 41
MX - Messico 41
PL - Polonia 40
AR - Argentina 32
CH - Svizzera 31
ZA - Sudafrica 28
IQ - Iraq 21
UA - Ucraina 21
IL - Israele 18
PK - Pakistan 18
EC - Ecuador 17
PH - Filippine 17
SI - Slovenia 14
CO - Colombia 13
HU - Ungheria 12
SA - Arabia Saudita 11
EG - Egitto 10
CL - Cile 9
MO - Macao, regione amministrativa speciale della Cina 9
MY - Malesia 9
GR - Grecia 8
KE - Kenya 8
UZ - Uzbekistan 8
IR - Iran 7
LT - Lituania 7
LU - Lussemburgo 7
MA - Marocco 7
VE - Venezuela 7
NO - Norvegia 6
NP - Nepal 6
RO - Romania 6
AE - Emirati Arabi Uniti 5
CZ - Repubblica Ceca 5
PE - Perù 5
PY - Paraguay 5
SC - Seychelles 5
TH - Thailandia 5
AD - Andorra 4
AL - Albania 4
CR - Costa Rica 4
GE - Georgia 4
JO - Giordania 4
LB - Libano 4
NZ - Nuova Zelanda 4
PT - Portogallo 4
TN - Tunisia 4
AZ - Azerbaigian 3
BO - Bolivia 3
CY - Cipro 3
ET - Etiopia 3
GT - Guatemala 3
HR - Croazia 3
JM - Giamaica 3
KZ - Kazakistan 3
LV - Lettonia 3
MT - Malta 3
NI - Nicaragua 3
PR - Porto Rico 3
RS - Serbia 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BH - Bahrain 2
BW - Botswana 2
DZ - Algeria 2
EE - Estonia 2
KG - Kirghizistan 2
MM - Myanmar 2
PA - Panama 2
PS - Palestinian Territory 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
Totale 14.691
Città #
Singapore 847
Ashburn 602
Milan 530
Hanover 476
Hong Kong 396
San Jose 349
Frankfurt am Main 334
Hefei 237
Beijing 236
Dallas 216
Southend 208
Council Bluffs 178
Chandler 173
New York 155
Los Angeles 144
Ho Chi Minh City 142
Santa Clara 138
Hanoi 123
Bengaluru 102
Seoul 102
Jakarta 85
Munich 85
Fairfield 83
Abidjan 76
Lauterbourg 76
Dublin 70
Chicago 63
Moscow 59
Istanbul 56
Princeton 56
Guangzhou 55
Tokyo 55
Rome 52
Shanghai 52
Buffalo 51
Helsinki 50
Seattle 50
Boardman 49
Phoenix 49
Ann Arbor 48
Philadelphia 48
The Dalles 48
Cambridge 43
Wilmington 41
Da Nang 40
Atlanta 39
Nuremberg 39
Taichung 37
Redwood City 35
Houston 34
Irvine 34
Cangzhou 33
Montreal 33
Turin 33
Magenta 31
Boston 30
Woodbridge 30
Delhi 29
Dearborn 28
Naples 28
São Paulo 28
Amsterdam 27
Dong Ket 26
Indianapolis 26
Genoa 25
Honolulu 25
Warsaw 24
Mumbai 23
Vienna 23
Grafing 22
London 22
Medford 22
Brooklyn 21
Haiphong 21
Turku 21
Tianjin 20
Toronto 20
Bologna 19
Chennai 19
Lappeenranta 19
Madrid 19
Fuzhou 18
Johannesburg 18
Des Moines 17
Padova 17
Zhengzhou 17
Berlin 16
Düsseldorf 16
Trento 16
Washington 16
Basingstoke 15
Madison 15
Melbourne 15
Mexico City 15
Reston 15
Brussels 14
Florence 14
Ljubljana 14
San Francisco 14
Yokohama 14
Totale 8.389
Nome #
Autophagic and Proteasomal Mediated Removal of Mutant Androgen Receptor in Muscle Models of Spinal and Bulbar Muscular Atrophy 548
Retinoic Acid Downregulates HSPB8 Gene Expression in Human Breast Cancer Cells MCF-7 466
Analysis of the autophagic response in models of KIF5A-related neurodegeneration 290
Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives 277
Bicalutamide and Trehalose Ameliorate Spinal and Bulbar Muscular Atrophy Pathology in Mice 274
Molecules capable to induce neuroprotection via lysophagy activation 267
The role of Extracellular Vesicles (EVs) in Amyotrophic Lateral Sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) 265
The regulation of the small heat shock protein B8 in misfolding protein diseases causing motoneuronal and muscle cell death 259
HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies 251
A Crucial Role for the Protein Quality Control System in Motor Neuron Diseases 244
Molecular mechanisms in KIF5A-related neurodegeneration 236
Small heat shock protein B8: from cell functions to its involvement in diseases and potential therapeutic applications 235
TDP-43 PROTEINOPATHIES: THE ROLE OF EXTRACELLULAR VESICLES 234
Alternative Translation Initiation as a novel strategy to block toxicity of the mutant Androgen Receptor in SBMA 231
Motor neuron degeneration in spinal and bulbar muscular atrophy: molecular approaches to counteract mutant androgen receptor neurotoxicity 229
Multiple Roles of Transforming Growth Factor Beta in Amyotrophic Lateral Sclerosis 227
RAN translated C9ORF72 arginine rich poly-dipeptides alter gene transcription in ALS/FTD cell model 226
Generation of novel induced pluripotent stem cell models for the study of spinocerebellar ataxia type 17 223
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) 221
BAG1 assists the degradation of neurotoxic proteins related to motor neuron diseases counteracting dynein-mediated autophagy alteration 220
Pathogenic variants of Valosin Containing Protein induce lysosomal damage and transcriptional activation of autophagy regulators in neuronal cells 213
Extracellular vesicles and the secretion of TDP species in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD) 210
Valosin Containing Protein (VCP): A Multistep Regulator of Autophagy 207
VCP mutants cause lysosomal alterations and autophagy induction in ALS-neuronal model 206
The clearance of aggregated TDP-43 responsible for ALS/FTD diseases 205
Bicalutamide and Trehalose as a therapeutic approach for SBMA 203
Effect of Hspb8 deletion in the skeletal muscle of a mouse model for Amyotrophic Lateral Sclerosis 200
Neurodegenerative Disease-Associated TDP-43 Fragments Are Extracellularly Secreted with CASA Complex Proteins 194
How PQC inhibition modulates miRNA loading in large and small extracellular vesicles 192
VCP modulation rescues C9ORF72 pathological features in ALS-neuronal models 192
STUB1 mutants effect on TBP behavior in digenic spinocerebellar ataxia type 17 191
The BAG1 molecular chaperone regulators prevent ALS related neurotoxic misfolded proteins accumulation via proteasome and chaperone mediated autophagy 189
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders 186
Mechanism of paroxetine-mediated autophagic induction in cell models of ALS/FTD 186
VCP ALS-mutants induce lysosomal damage and autophagy activation 186
Insights on human small heat shock proteins and their alterations in diseases 183
C9ORF72 arginine rich poly-dipeptides induce transcriptional alterations in ALS/FTD cell model 178
Identification of HSPB8 modulators counteracting misfolded protein accumulation in neurodegenerative diseases 175
Extracellular vesicles cooperate with PQC system for the clearance of TDP-43 species associated with ALS and FTD 174
Differentiation of isogenic iPSC reporter lines to motoneurons as tools for familial and sporadic amyotrophic lateral sclerosis 174
Alternative translation initiatin as a novel strategy to block toxicity of the mutant androgen receptor in SBMA 172
Mutations in VCP induce lysosomal alterations and autophagy activation in ALS neuronal models 171
The role of autophagy-lysosomal pathway in motor neuron diseases 170
Chaperone-assisted selective autophagy in Health and Disease 169
Targeting androgen receptor stability and degradation: approaches for developing a therapy for spinal and bulbar muscular atrophy 166
VCP mutants induce lysosomal damage and autophagy activation in amyotrophic lateral sclerosis (ALS) 166
Shared behaviours of KIF5A frameshift mutants in neurodevelopment and neurodegeneration 165
Investigating the molecular mechanisms involved in KIF5A-related neurodegeneration 163
The nucleotide exchange factor BAG1 prevents neurotoxic misfolded proteins accumulation via proteasome and chaperone mediated autophagy 163
Insights into KIF5A-related pathways to neurodegeneration 162
One gene, many phenotypes: investigating KIF5A-linked neurodegeneration mechanisms 160
Mutant Androgen Receptor Alternative Translation Initiation as novel strategy to block toxicity in SBMA. 157
VCP autophagic modulation rescues C9ORF72 pathological features in ALS-neuronal models 152
The role of extracellular vesicles in the removal of aggregated TDP43 responsible for ALS/FTD diseases 152
Lysosome quality control in health and neurodegenerative diseases 150
Proteotoxic responses in amyotrophic lateral sclerosis 149
Molecular defects in KIF5A-linked neurodegenerative and neurodevelopmental diseases 146
Extracellular vesicles and their role in TDP-43 proteinopathies 142
The Role of Small Heat Shock Proteins in Protein Misfolding Associated Motoneuron Diseases 141
The role of extracellular vesicles in the removal of aggregated TDP-43 responsible for ALS/FTD diseases 141
Frameshift mutations in the Heat Shock Protein B8 share common pathogenic mechanisms and impair proteostasis 139
Analysis of the pathogenetic mechanisms involved in KIF5A-related neurodegenerative disorders 138
Large and small extracellular vesicles may contribute to the propagation of ALS and FTD carrying toxic TDP species and potentially harmful miRNAs 137
INSIGHTS INTO MITOCHONDRIAL DYSFUNCTION IN SPINAL AND BULBAR MUSCULAR ATROPHY THROUGH IPSC-DERIVED SKELETAL MUSCLE MODELS 137
Innovative high throughput screening identifies HSPB8 modulators counteracting misfolded protein accumulation in neurodegenerative diseases 136
Unveiling novel players in HSPB8 pathology caused by frameshift mutations 132
Insights into the neurodegenerative mechanisms associated with KIF5A mutations 131
One gene, many phenotypes: altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative and neurodevelopmental disorders 129
The role of extracellular vesicles in TDP-43 proteinopathies 127
Shared mechanisms of pathogenicity of frameshift mutations in the heat shock protein B8 associated with neuromyopathies 126
Androgen receptor with an elongated polyglutamine tract dysregulates muscle expression of myo-miRs and of their target genes. 123
Frameshift mutations in the heat shock protein B8 cause its aggregation and impair proteostasis in neuromyopathies 121
Modulating VCP to mitigate pathological mechanisms related to C9ORF72 mutation in ALS 120
One gene, many phenotypes: the role of KIF5A in neurodegenerative and neurodevelopmental diseases 116
The role of tetraspanins in extracellular vesicle-mediated clearance of insoluble TDP-43 116
Shared behaviours of KIF5A frameshift mutants in neurodevelopment and neurodegeneration 93
Mechanism of paroxetine-mediated autophagic induction in cell models of amyotrophic lateral sclerosis and frontotemporal dementia 93
The alternative androgen receptor isoform a mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy 84
Neuromyopathy-associated frameshift mutations in the heat shock protein b8 cause its aggregation and protostasis impairment 78
Impairment of lysosomal quality control in Huntington disease 72
Trehalose and bicalutamide as a possible therapeutic approach for spinal and bulbar muscular atrophy 64
MUSCLE MITOCHONDRIAL DYSFUNCTIONS AND SYSTEMIC LIPIDOMIC REMODELING IN SBMA 63
Strategies to promote the expression of the androgen receptor AR-A isoform lacking the polyglutamine tract in spinal and bulbar muscular atrophy 59
COMMON AND NOVEL MOLECULAR MECHANISMS OF FRAMESHIFT MUTATIONS CAUSING HSPB8 PATHOLOGY 57
Aberrant interplay between the mutant androgen receptor and GLI3: highlighting a potential neurodevelopmental weakness in Kennedy’s Disease 40
FAK signaling pathways are modulated by HSPB8 and BAG3 in breast cancer 25
Interplay between GLI3 and ARpolyQ in SBMA: friend or foe? 24
Unraveling the Interaction between TBP and STUB1 in the Pathogenesis of SCA17-DI 14
Sex-dependent chaperone-assisted selective autophagy (CASA) activity in ALS glial cells 13
Sex-dependent chaperone-assisted selective autophagy (CASA) activity in ALS astrocytes and microglia 12
Exploring the Role of CHIP in the Pathogenesis of Digenic Spinocerebellar Ataxia Type 17 8
The role of CHIP in the pathogenesis of repeat expansion diseases 7
VCP modulation ameliorates pathological features in C9orf72 models 1
Tetraspanins and their role in the removal of TDP-43 insoluble species via extracellular vesicles 1
The role of tetraspanins in extracellular vesicle-mediated clearance of insoluble TDP-43 1
Totale 15.161
Categoria #
all - tutte 45.413
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 45.413


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021182 0 0 0 0 0 0 0 0 0 0 24 158
2021/20221.258 59 85 82 106 100 105 122 97 133 121 108 140
2022/20231.013 71 135 67 65 69 141 72 92 114 26 92 69
2023/20241.980 64 130 211 329 374 74 119 110 71 154 187 157
2024/20253.170 96 204 121 358 297 156 155 304 166 370 319 624
2025/20266.782 643 586 650 601 697 402 977 327 678 573 648 0
Totale 15.161