CARRA, Serena
 Distribuzione geografica
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Continente #
NA - Nord America 14.376
AS - Asia 7.255
EU - Europa 5.539
SA - Sud America 898
Continente sconosciuto - Info sul continente non disponibili 248
AF - Africa 130
OC - Oceania 28
Totale 28.474
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Nazione #
US - Stati Uniti d'America 14.076
SG - Singapore 2.598
CN - Cina 1.762
GB - Regno Unito 1.563
IT - Italia 1.561
HK - Hong Kong 897
BR - Brasile 706
VN - Vietnam 569
DE - Germania 477
SE - Svezia 458
BD - Bangladesh 452
FI - Finlandia 274
FR - Francia 245
UA - Ucraina 245
KR - Corea 209
RU - Federazione Russa 205
CA - Canada 159
TR - Turchia 154
IN - India 142
ID - Indonesia 131
BG - Bulgaria 104
NL - Olanda 86
MX - Messico 70
AR - Argentina 65
JP - Giappone 51
IE - Irlanda 38
ZA - Sudafrica 38
IQ - Iraq 37
PL - Polonia 35
AT - Austria 34
CH - Svizzera 31
LT - Lituania 31
MY - Malesia 30
BE - Belgio 28
AE - Emirati Arabi Uniti 27
ES - Italia 27
CO - Colombia 26
EC - Ecuador 24
MA - Marocco 24
PK - Pakistan 24
SA - Arabia Saudita 24
AU - Australia 22
CZ - Repubblica Ceca 22
CL - Cile 21
IL - Israele 18
PY - Paraguay 18
CR - Costa Rica 16
GR - Grecia 16
PH - Filippine 16
VE - Venezuela 15
EG - Egitto 13
JO - Giordania 11
KE - Kenya 11
RO - Romania 11
TW - Taiwan 10
UZ - Uzbekistan 10
NP - Nepal 9
PE - Perù 9
EU - Europa 8
TN - Tunisia 8
AZ - Azerbaigian 7
BO - Bolivia 7
DO - Repubblica Dominicana 7
IR - Iran 7
JM - Giamaica 7
KZ - Kazakistan 7
LB - Libano 7
TH - Thailandia 7
BH - Bahrain 6
BZ - Belize 6
HN - Honduras 6
NO - Norvegia 6
PR - Porto Rico 6
UY - Uruguay 6
AL - Albania 5
DK - Danimarca 5
DZ - Algeria 5
GE - Georgia 5
HU - Ungheria 5
NZ - Nuova Zelanda 5
OM - Oman 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
SN - Senegal 5
SV - El Salvador 5
ET - Etiopia 4
KG - Kirghizistan 4
RS - Serbia 4
SY - Repubblica araba siriana 4
AM - Armenia 3
AO - Angola 3
CI - Costa d'Avorio 3
CY - Cipro 3
NG - Nigeria 3
NI - Nicaragua 3
PA - Panama 3
XK - ???statistics.table.value.countryCode.XK??? 3
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BY - Bielorussia 2
Totale 28.194
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Città #
Singapore 1.764
Ashburn 1.410
Fairfield 1.400
Santa Clara 1.316
Southend 999
Hong Kong 884
Woodbridge 710
San Jose 682
Houston 605
Chandler 603
Council Bluffs 529
Hefei 509
Seattle 508
Jacksonville 448
Cambridge 434
Wilmington 423
Beijing 362
Dearborn 330
Ann Arbor 304
Modena 293
London 280
Nyköping 277
Los Angeles 251
The Dalles 231
Ho Chi Minh City 180
Seoul 176
Milan 172
Helsinki 167
New York 146
Chicago 140
Hanoi 134
San Diego 130
Jakarta 108
Princeton 102
Sofia 102
Lauterbourg 99
Munich 96
Buffalo 92
Columbus 88
Rome 85
Eugene 84
Moscow 80
Shanghai 68
São Paulo 68
Dallas 59
Redwood City 49
Bologna 47
Boardman 46
Phoenix 46
Salt Lake City 46
Izmir 45
Orem 44
Tokyo 39
Dublin 37
Falls Church 36
Toronto 36
Frankfurt am Main 35
Guangzhou 34
Brooklyn 30
Cardiff 29
Tampa 28
Amsterdam 27
Padova 27
Bremen 26
Da Nang 26
Montreal 26
Norwalk 26
Nuremberg 26
Atlanta 25
Parma 25
Warsaw 25
Haiphong 23
Dong Ket 22
Nanjing 22
Chennai 21
Mexico City 21
Rio de Janeiro 21
Turku 21
Baghdad 20
Brno 20
Manchester 20
Redondo Beach 20
Reggio Emilia 20
Vancouver 20
Johannesburg 19
Naples 19
San Francisco 19
Ankara 18
Denver 18
Kent 18
Birmingham 17
Brasília 17
Florence 17
Stockholm 17
Boston 16
Brussels 16
Provo 16
Bari 15
Belo Horizonte 15
Kunming 15
Totale 19.357
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Nome #
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 482
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 410
Chronic treatment with desipramine and fluoxetine modulate BDNF, CaMKK alpha and CaMKK beta mRNA levels in the hippocampus of transgenic mice expressing antisense RNA against the glucocorticoid receptor 399
Granulostasis: Protein Quality Control of RNP Granules 380
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 378
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 360
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 353
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 353
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 342
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 341
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 337
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 336
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 323
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 322
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 320
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins 320
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 317
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 317
ALS and FTD: Where RNA metabolism meets protein quality control 313
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 312
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 311
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 308
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 307
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 306
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 306
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 303
Autophagy researchers 301
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 299
Small heat shock proteins: multifaceted proteins with important implications for life 296
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 289
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 289
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 284
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 281
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 280
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 278
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 277
The Role of the Protein Quality Control System in SBMA 276
Characterization of the R7S mutation of Heat Shock Protein HSPB3 and of two novel mutations found in patients suffering of myopathy: understanding the mechanisms leading to disease. 276
The regulation of the autophagic network and its implications for human disease 275
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 275
CHARACTERIZATION OF THE R7S MUTATION OF HEAT SHOCK PROTEIN HSPB3 AND TWO NOVEL MUTATIONS FOUND IN PATIENTS SUFFERING OF MYOPATHY: UNDERSTANDING THE MECHANISMS LEADING TO DISEASE. 274
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 274
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 273
Characterization of the R7S mutation of Heat Shock Protein HSPB3 and of two novel mutations found in patients suffering of myopathy: understanding the mechanisms leading to disease. 270
Quality Control of Membraneless Organelles 269
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 266
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 262
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 261
Small heat shock proteins, protein degradation and protein aggregation diseases. 258
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 258
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 258
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 256
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 256
Studying heat shock proteins through single-molecule mechanical manipulation 254
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 253
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 253
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 252
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 252
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 252
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 251
Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial 246
The growing world of small heat shock proteins: from structure to functions 244
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype 239
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 239
Guidelines for the use and interpretation of assays for monitoring autophagy. 235
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 232
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 231
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 229
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 228
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 226
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 225
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 220
Characterization of the myopathy associated BAG3 P209L mutation 219
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 214
Protein products of nonstop mRNA disrupt nucleolar homeostasis 214
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 214
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 210
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 209
Small Heat Shock Proteins in Neurodegenerative Diseases. 208
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 202
Human Small Heat Shock Protein B8 Inhibits Protein Aggregation without Affecting the Native Folding Process 200
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 199
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 198
HSPB6: A lipid-dependent molecular chaperone inhibits α-synuclein aggregation 194
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 193
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 190
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 188
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 186
Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia 185
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 183
HspB8 prevents aberrant phase transitions of FUS by chaperoning its folded RNA binding domain 183
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 183
Regulation of physiological and pathological condensates by molecular chaperones 179
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 179
Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses 178
A shared fate for nuclear and cytosolic inclusions 175
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 173
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 173
Investigating the interplay between the protein quality control system, molecular chaperones and stress granules: from cell stress response to disease 165
Motoneuron and muscle selective removal of ALS-related misfolded proteins. 164
Totale 26.186
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Categoria #
all - tutte 108.357
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 108.357
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.819 0 189 221 92 44 100 95 121 234 175 357 191
2022/20231.746 186 158 176 155 167 260 24 183 256 29 88 64
2023/20241.241 45 68 71 148 227 60 129 184 35 47 74 153
2024/20254.876 141 79 76 340 760 881 355 304 518 196 491 735
2025/20269.658 586 313 755 907 1.451 592 1.206 499 923 898 831 697
2026/2027956 318 638 0 0 0 0 0 0 0 0 0 0
Totale 28.474