CARRA, Serena
 Distribuzione geografica
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Continente #
NA - Nord America 13.623
AS - Asia 7.140
EU - Europa 5.445
SA - Sud America 887
AF - Africa 128
OC - Oceania 28
Continente sconosciuto - Info sul continente non disponibili 12
Totale 27.263
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Nazione #
US - Stati Uniti d'America 13.367
SG - Singapore 2.576
CN - Cina 1.732
GB - Regno Unito 1.561
IT - Italia 1.482
HK - Hong Kong 891
BR - Brasile 701
VN - Vietnam 568
DE - Germania 477
SE - Svezia 457
BD - Bangladesh 402
FI - Finlandia 274
UA - Ucraina 245
FR - Francia 243
KR - Corea 209
RU - Federazione Russa 205
TR - Turchia 154
IN - India 142
CA - Canada 136
ID - Indonesia 127
BG - Bulgaria 104
NL - Olanda 79
MX - Messico 68
AR - Argentina 63
JP - Giappone 50
IE - Irlanda 38
IQ - Iraq 37
ZA - Sudafrica 37
AT - Austria 34
PL - Polonia 33
LT - Lituania 31
CH - Svizzera 30
MY - Malesia 30
BE - Belgio 28
ES - Italia 27
AE - Emirati Arabi Uniti 26
CO - Colombia 25
EC - Ecuador 24
MA - Marocco 24
PK - Pakistan 24
SA - Arabia Saudita 24
AU - Australia 22
CZ - Repubblica Ceca 22
CL - Cile 20
IL - Israele 18
PY - Paraguay 18
GR - Grecia 16
PH - Filippine 16
VE - Venezuela 14
EG - Egitto 13
JO - Giordania 11
KE - Kenya 11
RO - Romania 11
TW - Taiwan 10
UZ - Uzbekistan 10
CR - Costa Rica 9
NP - Nepal 9
PE - Perù 9
EU - Europa 8
TN - Tunisia 8
AZ - Azerbaigian 7
DO - Repubblica Dominicana 7
IR - Iran 7
KZ - Kazakistan 7
LB - Libano 7
TH - Thailandia 7
BH - Bahrain 6
BO - Bolivia 6
BZ - Belize 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
JM - Giamaica 5
NZ - Nuova Zelanda 5
OM - Oman 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
SN - Senegal 5
ET - Etiopia 4
HN - Honduras 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
PA - Panama 3
SV - El Salvador 3
XK - ???statistics.table.value.countryCode.XK??? 3
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BY - Bielorussia 2
KH - Cambogia 2
Totale 27.225
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Città #
Singapore 1.758
Fairfield 1.400
Ashburn 1.337
Santa Clara 1.281
Southend 999
Hong Kong 879
Woodbridge 710
Chandler 603
Houston 603
San Jose 583
Hefei 509
Seattle 507
Jacksonville 446
Cambridge 434
Wilmington 423
Council Bluffs 369
Beijing 350
Dearborn 330
Ann Arbor 304
Modena 293
London 279
Nyköping 277
Los Angeles 237
The Dalles 229
Ho Chi Minh City 179
Seoul 176
Helsinki 167
Milan 153
Chicago 137
New York 135
Hanoi 134
San Diego 129
Jakarta 108
Princeton 102
Sofia 102
Lauterbourg 99
Munich 96
Buffalo 86
Eugene 84
Moscow 80
Rome 80
São Paulo 68
Shanghai 67
Dallas 50
Redwood City 49
Bologna 47
Izmir 45
Salt Lake City 45
Columbus 43
Boardman 42
Orem 42
Phoenix 40
Tokyo 39
Dublin 37
Falls Church 36
Toronto 36
Frankfurt am Main 35
Guangzhou 34
Cardiff 29
Amsterdam 27
Padova 27
Tampa 27
Bremen 26
Brooklyn 26
Da Nang 26
Norwalk 26
Nuremberg 26
Parma 25
Atlanta 23
Haiphong 23
Warsaw 23
Dong Ket 22
Montreal 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 19
Ankara 18
Johannesburg 18
Kent 18
San Francisco 18
Birmingham 17
Brasília 17
Brussels 16
Florence 16
Naples 16
Provo 16
Stockholm 16
Bari 15
Belo Horizonte 15
Denver 15
Kunming 15
Lappeenranta 15
Totale 18.806
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Nome #
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 402
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 395
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 389
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 371
Granulostasis: Protein Quality Control of RNP Granules 366
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 352
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 343
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 341
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 334
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 331
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 330
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 325
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 319
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins 315
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 314
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 312
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 310
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 307
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 306
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 304
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 304
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 298
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 297
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 297
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 296
Autophagy researchers 294
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 294
Small heat shock proteins: multifaceted proteins with important implications for life 290
ALS and FTD: Where RNA metabolism meets protein quality control 288
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 283
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 282
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 276
The Role of the Protein Quality Control System in SBMA 273
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 272
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 271
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 270
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 270
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. 269
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 267
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 264
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 263
The regulation of the autophagic network and its implications for human disease 262
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. 262
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. 259
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 259
Quality Control of Membraneless Organelles 257
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 256
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 252
Small heat shock proteins, protein degradation and protein aggregation diseases. 252
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 252
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 252
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 252
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 249
Studying heat shock proteins through single-molecule mechanical manipulation 248
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 247
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 244
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 244
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 243
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 241
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 240
The growing world of small heat shock proteins: from structure to functions 237
Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial 236
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 234
Guidelines for the use and interpretation of assays for monitoring autophagy. 231
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 224
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 224
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 221
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 220
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 220
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype 219
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 215
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 212
Characterization of the myopathy associated BAG3 P209L mutation 211
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 209
Protein products of nonstop mRNA disrupt nucleolar homeostasis 207
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 207
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 206
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 204
Small Heat Shock Proteins in Neurodegenerative Diseases. 201
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 198
Human Small Heat Shock Protein B8 Inhibits Protein Aggregation without Affecting the Native Folding Process 193
HSPB6: A lipid-dependent molecular chaperone inhibits α-synuclein aggregation 191
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 189
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 188
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 187
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 186
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 182
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 180
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 179
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 177
Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia 176
HspB8 prevents aberrant phase transitions of FUS by chaperoning its folded RNA binding domain 176
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 174
A shared fate for nuclear and cytosolic inclusions 173
Regulation of physiological and pathological condensates by molecular chaperones 172
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 169
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 168
Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses 166
Investigating the interplay between the protein quality control system, molecular chaperones and stress granules: from cell stress response to disease 160
Motoneuron and muscle selective removal of ALS-related misfolded proteins. 158
Totale 25.335
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Categoria #
all - tutte 103.009
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 103.009
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021157 0 0 0 0 0 0 0 0 0 0 0 157
2021/20221.944 125 189 221 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
2025/20269.639 586 313 755 907 1.451 592 1.206 499 923 898 831 678
Totale 27.499