CARRA, Serena
 Distribuzione geografica
Continente #
NA - Nord America 8.408
EU - Europa 3.503
AS - Asia 1.170
SA - Sud America 15
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 9
AF - Africa 3
Totale 13.117
Nazione #
US - Stati Uniti d'America 8.384
GB - Regno Unito 1.193
IT - Italia 850
CN - Cina 448
SE - Svezia 389
DE - Germania 333
HK - Hong Kong 237
UA - Ucraina 215
SG - Singapore 198
FI - Finlandia 148
TR - Turchia 113
BG - Bulgaria 101
FR - Francia 95
ID - Indonesia 46
IN - India 43
IE - Irlanda 26
VN - Vietnam 24
BE - Belgio 23
NL - Olanda 22
CZ - Repubblica Ceca 21
MY - Malesia 21
CH - Svizzera 19
CA - Canada 17
LT - Lituania 14
BR - Brasile 11
GR - Grecia 10
JP - Giappone 10
RU - Federazione Russa 10
ES - Italia 8
EU - Europa 8
IL - Israele 7
KR - Corea 7
AU - Australia 6
AT - Austria 5
NO - Norvegia 5
BZ - Belize 4
DK - Danimarca 4
HU - Ungheria 4
IR - Iran 3
MX - Messico 3
NZ - Nuova Zelanda 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
CO - Colombia 2
CY - Cipro 2
KZ - Kazakistan 2
PH - Filippine 2
PK - Pakistan 2
PL - Polonia 2
RO - Romania 2
ZM - Zambia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
CL - Cile 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
MK - Macedonia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 13.117
Città #
Fairfield 1.400
Southend 999
Woodbridge 709
Ashburn 662
Chandler 603
Houston 593
Seattle 495
Jacksonville 444
Cambridge 431
Wilmington 414
Dearborn 329
Ann Arbor 304
Nyköping 276
Modena 260
Hong Kong 232
Singapore 137
Beijing 132
San Diego 125
Princeton 102
Sofia 100
Eugene 84
Helsinki 72
Redwood City 49
Milan 47
New York 47
Jakarta 46
Izmir 43
London 39
Falls Church 36
Rome 32
Shanghai 27
Boardman 26
Bremen 26
Munich 26
Norwalk 26
Dublin 25
Bologna 24
Padova 24
Dong Ket 22
Brno 20
Hefei 20
Nanjing 20
Phoenix 17
Parma 16
Provo 16
Brussels 14
Chicago 14
Los Angeles 13
Florence 12
Frankfurt am Main 12
Kunming 12
San Mateo 12
Amsterdam 11
Des Moines 11
Kilburn 11
Oldenburg 11
San Jose 11
Tübingen 11
Guangzhou 10
Toronto 10
Magenta 9
Reggio Emilia 9
Segrate 9
Trieste 9
Dongguan 8
Fremont 8
Napoli 8
Rochester 8
Wuhan 8
Bari 7
Chiswick 7
Heidelberg 7
Lappeenranta 7
São Paulo 7
Turin 7
Würzburg 7
Hebei 6
Indiana 6
Nanchang 6
Perugia 6
Redmond 6
Ulm 6
Zurich 6
Augusta 5
Buffalo 5
Hounslow 5
Islington 5
Jinan 5
Reggio Nell'emilia 5
Washington 5
Zhengzhou 5
Belize City 4
Berlin 4
Clearwater 4
Hangzhou 4
Holon 4
Istanbul 4
Jinhua 4
Killwangen 4
L’Aquila 4
Totale 9.995
Nome #
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 254
Granulostasis: Protein Quality Control of RNP Granules 238
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 226
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 223
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 222
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 216
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 211
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 205
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 198
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 198
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 195
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 194
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 193
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 191
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 187
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 185
Small heat shock proteins: multifaceted proteins with important implications for life 184
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 182
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 177
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 175
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 175
The Role of the Protein Quality Control System in SBMA 173
Autophagy researchers 172
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 172
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 171
The regulation of the autophagic network and its implications for human disease 171
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 171
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 170
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 170
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 167
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 166
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 165
Quality Control of Membraneless Organelles 164
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 160
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 155
Small heat shock proteins, protein degradation and protein aggregation diseases. 153
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins. 153
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 150
ALS and FTD: Where RNA metabolism meets protein quality control 149
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 147
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 147
The growing world of small heat shock proteins: from structure to functions 147
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 144
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 142
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 142
Guidelines for the use and interpretation of assays for monitoring autophagy. 141
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 138
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 138
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 137
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 134
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 134
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 132
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 132
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 128
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 124
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. 120
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. 120
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. 120
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 118
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 117
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 116
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 112
Characterization of the myopathy associated BAG3 P209L mutation 111
Studying heat shock proteins through single-molecule mechanical manipulation 111
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 110
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 109
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 106
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 104
Small Heat Shock Proteins in Neurodegenerative Diseases. 103
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 101
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 99
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 98
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 96
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 95
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 91
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 91
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 90
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 86
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 84
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 82
Motoneuron and muscle selective removal of ALS-related misfolded proteins. 78
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 78
Investigating the interplay between the protein quality control system, molecular chaperones and stress granules: from cell stress response to disease 76
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 75
Implications of HSPBs and BAG3 in neuro/muscular-protein aggregate diseases 74
Upregulation of HSPB8 as potential therapeutic approach in Amyotrophic Lateral Sclerosis 68
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 66
Inhibition of autophagy, lysosome and VCP alters stress granule morphology and composition 65
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 65
Impairment of the Protein Quality Control System Affects Stress Granule Response and Dynamics 64
Protein products of nonstop mRNA disrupt nucleolar homeostasis 61
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 60
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 58
Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 44
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 41
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 40
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype 34
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 29
RNA Molecular Signature Profiling in PBMCs of Sporadic ALS Patients: HSP70 Overexpression Is Associated with Nuclear SOD1 28
The beauty and complexity of the small heat shock proteins: a report on the proceedings of the fourth workshop on small heat shock proteins 25
Totale 13.107
Categoria #
all - tutte 59.972
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 59.972


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.334 0 0 0 161 260 440 497 303 286 112 169 106
2020/20212.786 227 75 175 202 320 240 183 421 143 452 191 157
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
2024/2025355 141 79 76 59 0 0 0 0 0 0 0 0
Totale 13.339