CARRA, Serena
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 12.732
AS - Asia 6.728
EU - Europa 5.138
SA - Sud America 884
AF - Africa 128
OC - Oceania 26
Continente sconosciuto - Info sul continente non disponibili 12
Totale 25.648
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 12.534
SG - Singapore 2.544
CN - Cina 1.703
GB - Regno Unito 1.561
IT - Italia 1.190
HK - Hong Kong 884
BR - Brasile 699
VN - Vietnam 568
DE - Germania 473
SE - Svezia 457
FI - Finlandia 274
UA - Ucraina 245
FR - Francia 243
KR - Corea 206
RU - Federazione Russa 205
TR - Turchia 153
IN - India 141
ID - Indonesia 127
BG - Bulgaria 103
CA - Canada 90
NL - Olanda 76
BD - Bangladesh 72
MX - Messico 66
AR - Argentina 63
JP - Giappone 46
IE - Irlanda 38
IQ - Iraq 37
ZA - Sudafrica 37
AT - Austria 34
PL - Polonia 32
LT - Lituania 31
MY - Malesia 29
BE - Belgio 28
CH - Svizzera 28
AE - Emirati Arabi Uniti 26
ES - Italia 26
CO - Colombia 25
EC - Ecuador 24
MA - Marocco 24
PK - Pakistan 24
SA - Arabia Saudita 24
CZ - Repubblica Ceca 22
AU - Australia 20
CL - Cile 19
IL - Israele 18
PY - Paraguay 18
GR - Grecia 15
PH - Filippine 15
VE - Venezuela 14
EG - Egitto 13
JO - Giordania 11
KE - Kenya 11
RO - Romania 11
TW - Taiwan 10
UZ - Uzbekistan 10
PE - Perù 9
CR - Costa Rica 8
EU - Europa 8
NP - Nepal 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
UY - Uruguay 6
DK - Danimarca 5
DZ - Algeria 5
HU - Ungheria 5
NZ - Nuova Zelanda 5
OM - Oman 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
SN - Senegal 5
AL - Albania 4
ET - Etiopia 4
GE - Georgia 4
JM - Giamaica 4
KG - Kirghizistan 4
PR - Porto Rico 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
BY - Bielorussia 2
KH - Cambogia 2
LY - Libia 2
ML - Mali 2
Totale 25.616
Salva come PNG Salva come JPEG
Città #
Singapore 1.744
Fairfield 1.400
Santa Clara 1.232
Ashburn 1.203
Southend 999
Hong Kong 873
Woodbridge 709
Chandler 603
Houston 601
Hefei 509
Seattle 505
San Jose 481
Jacksonville 444
Cambridge 434
Wilmington 422
Beijing 345
Dearborn 330
Ann Arbor 304
Modena 289
London 279
Nyköping 277
Council Bluffs 238
The Dalles 224
Los Angeles 183
Ho Chi Minh City 179
Seoul 173
Helsinki 167
Hanoi 134
Chicago 132
San Diego 127
Jakarta 108
Princeton 102
Sofia 102
Lauterbourg 99
Milan 97
Munich 96
New York 96
Eugene 84
Moscow 80
Shanghai 67
São Paulo 67
Buffalo 65
Rome 57
Redwood City 49
Izmir 45
Salt Lake City 45
Columbus 41
Bologna 39
Orem 38
Dublin 37
Falls Church 36
Tokyo 35
Frankfurt am Main 34
Guangzhou 34
Phoenix 32
Dallas 31
Cardiff 29
Amsterdam 27
Boardman 27
Padova 27
Tampa 27
Bremen 26
Da Nang 26
Norwalk 26
Nuremberg 26
Brooklyn 25
Parma 25
Haiphong 23
Warsaw 23
Dong Ket 22
Toronto 22
Chennai 21
Nanjing 21
Rio de Janeiro 21
Turku 21
Baghdad 20
Brno 20
Manchester 20
Redondo Beach 20
Mexico City 19
Reggio Emilia 19
Ankara 18
Atlanta 18
Johannesburg 18
Kent 18
Birmingham 17
Brasília 17
Montreal 17
San Francisco 17
Brussels 16
Provo 16
Stockholm 16
Belo Horizonte 15
Kunming 15
Lappeenranta 15
Boston 14
Campinas 14
Elk Grove Village 14
Florence 14
Vancouver 14
Totale 18.042
Salva come PNG Salva come JPEG
Nome #
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 387
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 374
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 373
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 366
Granulostasis: Protein Quality Control of RNP Granules 345
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 343
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 328
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 320
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 316
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 313
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 312
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 311
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 300
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 300
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 297
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 296
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 295
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 295
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins 293
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 291
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 288
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 287
Autophagy researchers 286
Small heat shock proteins: multifaceted proteins with important implications for life 278
ALS and FTD: Where RNA metabolism meets protein quality control 278
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 274
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 274
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 264
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 264
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. 264
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 263
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 261
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 259
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 258
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 258
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 257
The Role of the Protein Quality Control System in SBMA 257
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 255
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 255
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. 253
Quality Control of Membraneless Organelles 252
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 248
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. 247
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 246
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 244
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 243
The regulation of the autophagic network and its implications for human disease 243
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 242
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 242
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 239
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 239
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 238
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 236
Small heat shock proteins, protein degradation and protein aggregation diseases. 232
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 231
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 231
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 230
Guidelines for the use and interpretation of assays for monitoring autophagy. 230
Studying heat shock proteins through single-molecule mechanical manipulation 230
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 226
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 225
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 225
The growing world of small heat shock proteins: from structure to functions 221
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 218
Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial 208
Characterization of the myopathy associated BAG3 P209L mutation 208
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 206
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 204
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 203
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 203
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 199
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 198
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 196
Small Heat Shock Proteins in Neurodegenerative Diseases. 194
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 193
Protein products of nonstop mRNA disrupt nucleolar homeostasis 191
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 190
HSPB6: A lipid-dependent molecular chaperone inhibits α-synuclein aggregation 189
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 185
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 184
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype 181
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 180
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 180
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 180
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 177
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 176
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 172
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 171
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 170
A shared fate for nuclear and cytosolic inclusions 170
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 168
Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia 167
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 167
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 167
HspB8 prevents aberrant phase transitions of FUS by chaperoning its folded RNA binding domain 158
Motoneuron and muscle selective removal of ALS-related misfolded proteins. 155
Implications of HSPBs and BAG3 in neuro/muscular-protein aggregate diseases 154
Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses 153
Investigating the interplay between the protein quality control system, molecular chaperones and stress granules: from cell stress response to disease 153
Inhibition of autophagy, lysosome and VCP alters stress granule morphology and composition 151
Totale 23.947
Salva come PNG Salva come JPEG
Categoria #
all - tutte 96.673
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 96.673
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021800 0 0 0 0 0 0 0 0 0 452 191 157
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
2025/20268.021 586 313 755 907 1.451 592 1.206 499 923 789 0 0
Totale 25.881