CARRA, Serena
 Distribuzione geografica
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Continente #
NA - Nord America 16.428
AS - Asia 7.297
EU - Europa 5.727
SA - Sud America 913
Continente sconosciuto - Info sul continente non disponibili 254
AF - Africa 140
OC - Oceania 28
Totale 30.787
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Nazione #
US - Stati Uniti d'America 15.966
SG - Singapore 2.602
CN - Cina 1.767
IT - Italia 1.653
GB - Regno Unito 1.582
HK - Hong Kong 897
BR - Brasile 713
VN - Vietnam 571
DE - Germania 486
SE - Svezia 460
BD - Bangladesh 458
FI - Finlandia 274
FR - Francia 249
UA - Ucraina 247
RU - Federazione Russa 229
CA - Canada 226
KR - Corea 209
TR - Turchia 156
IN - India 144
ID - Indonesia 132
BG - Bulgaria 104
NL - Olanda 95
MX - Messico 70
AR - Argentina 69
JP - Giappone 53
IE - Irlanda 42
AT - Austria 38
PL - Polonia 38
ZA - Sudafrica 38
IQ - Iraq 37
LT - Lituania 35
CR - Costa Rica 33
IL - Israele 33
ES - Italia 32
CH - Svizzera 31
MY - Malesia 30
BE - Belgio 28
AE - Emirati Arabi Uniti 27
CO - Colombia 27
EC - Ecuador 26
SA - Arabia Saudita 25
MA - Marocco 24
PK - Pakistan 24
AU - Australia 22
CZ - Repubblica Ceca 22
TT - Trinidad e Tobago 22
CL - Cile 21
PY - Paraguay 18
HN - Honduras 17
GR - Grecia 16
PH - Filippine 16
VE - Venezuela 16
SV - El Salvador 15
EG - Egitto 13
JM - Giamaica 13
PR - Porto Rico 13
JO - Giordania 11
KE - Kenya 11
RO - Romania 11
SC - Seychelles 11
TW - Taiwan 10
UZ - Uzbekistan 10
NP - Nepal 9
PE - Perù 9
EU - Europa 8
GP - Guadalupe 8
NI - Nicaragua 8
TH - Thailandia 8
TN - Tunisia 8
AZ - Azerbaigian 7
BO - Bolivia 7
DO - Repubblica Dominicana 7
EE - Estonia 7
IR - Iran 7
KZ - Kazakistan 7
LB - Libano 7
BB - Barbados 6
BH - Bahrain 6
BZ - Belize 6
CW - ???statistics.table.value.countryCode.CW??? 6
DK - Danimarca 6
NO - Norvegia 6
OM - Oman 6
UY - Uruguay 6
AL - Albania 5
DZ - Algeria 5
GE - Georgia 5
HU - Ungheria 5
NZ - Nuova Zelanda 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
SN - Senegal 5
ET - Etiopia 4
GT - Guatemala 4
KG - Kirghizistan 4
RS - Serbia 4
SY - Repubblica araba siriana 4
AM - Armenia 3
AO - Angola 3
CI - Costa d'Avorio 3
Totale 30.492
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Città #
Ashburn 1.836
Singapore 1.765
Fairfield 1.400
Santa Clara 1.348
Southend 999
San Jose 959
Hong Kong 884
Woodbridge 711
Council Bluffs 645
Houston 609
Chandler 603
Seattle 512
Hefei 509
Jacksonville 448
Cambridge 434
Wilmington 423
Beijing 363
Dearborn 330
Ann Arbor 304
Modena 293
London 284
Nyköping 277
Los Angeles 259
The Dalles 252
Milan 181
Ho Chi Minh City 180
Seoul 176
Helsinki 167
New York 160
Chicago 149
Hanoi 135
San Diego 132
Jakarta 108
Princeton 108
Sofia 102
Lauterbourg 99
Buffalo 98
Rome 97
Columbus 96
Munich 96
Austin 89
Eugene 84
Dallas 80
Moscow 80
São Paulo 70
Shanghai 68
Phoenix 56
Round Rock 52
Bologna 51
Orem 49
Redwood City 49
Boardman 47
Salt Lake City 47
Toronto 46
Izmir 45
Brooklyn 43
Tokyo 41
Montreal 39
Dublin 38
Atlanta 37
Falls Church 36
Frankfurt am Main 36
Guangzhou 34
Tampa 32
North Bergen 31
Cardiff 29
Amsterdam 28
Padova 27
Bremen 26
Da Nang 26
Norwalk 26
Nuremberg 26
Warsaw 26
Newark 25
Parma 25
San Francisco 25
San José 24
Haiphong 23
Denver 22
Dong Ket 22
Lakewood 22
Nanjing 22
Naples 22
Vancouver 22
Chennai 21
Mexico City 21
Rio de Janeiro 21
Turku 21
Washington 21
Baghdad 20
Brno 20
Florence 20
Manchester 20
Redondo Beach 20
Reggio Emilia 20
Johannesburg 19
Stockholm 19
Ankara 18
Carrboro 18
Kent 18
Totale 20.596
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Nome #
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 607
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 442
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 408
Granulostasis: Protein Quality Control of RNP Granules 394
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 389
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 388
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 375
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 374
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 363
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 363
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins 359
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 358
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 347
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 342
ALS and FTD: Where RNA metabolism meets protein quality control 337
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 336
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 335
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 332
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 332
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 329
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 327
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. 326
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 323
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 321
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 321
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 321
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 319
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 316
Small heat shock proteins: multifaceted proteins with important implications for life 313
Autophagy researchers 311
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 310
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 306
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 304
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. 303
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 300
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 299
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 299
Quality Control of Membraneless Organelles 298
The Role of the Protein Quality Control System in SBMA 293
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. 292
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 291
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 288
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 288
The regulation of the autophagic network and its implications for human disease 286
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 284
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 283
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 282
Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial 280
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 280
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 279
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 278
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 278
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 278
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 276
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 276
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 276
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 273
Studying heat shock proteins through single-molecule mechanical manipulation 273
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 271
Small heat shock proteins, protein degradation and protein aggregation diseases. 268
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 267
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 266
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype 265
Guidelines for the use and interpretation of assays for monitoring autophagy. 260
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 257
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 257
The growing world of small heat shock proteins: from structure to functions 255
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 248
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 248
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 242
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 240
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 236
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 232
Characterization of the myopathy associated BAG3 P209L mutation 232
Small Heat Shock Proteins in Neurodegenerative Diseases. 230
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 229
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 229
Protein products of nonstop mRNA disrupt nucleolar homeostasis 227
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 222
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 222
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 221
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 216
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 214
Human Small Heat Shock Protein B8 Inhibits Protein Aggregation without Affecting the Native Folding Process 213
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 212
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 210
Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses 206
HSPB6: A lipid-dependent molecular chaperone inhibits α-synuclein aggregation 204
Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia 201
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 200
A shared fate for nuclear and cytosolic inclusions 199
Regulation of physiological and pathological condensates by molecular chaperones 199
HspB8 prevents aberrant phase transitions of FUS by chaperoning its folded RNA binding domain 198
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 195
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 194
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 191
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 191
Phenotypical Characterization of C9ALS Patients from the Emilia Romagna Registry of ALS: A Retrospective Case–Control Study 181
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 181
RNA Molecular Signature Profiling in PBMCs of Sporadic ALS Patients: HSP70 Overexpression Is Associated with Nuclear SOD1 176
Totale 28.166
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Categoria #
all - tutte 115.864
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 115.864
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.317 0 0 0 0 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
2026/20273.269 318 643 996 1.007 305 0 0 0 0 0 0 0
Totale 30.787