CARRA, Serena
 Distribuzione geografica
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Continente #
NA - Nord America 9.771
EU - Europa 3.868
AS - Asia 1.990
SA - Sud America 135
AF - Africa 15
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 10
Totale 15.799
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Nazione #
US - Stati Uniti d'America 9.738
GB - Regno Unito 1.202
IT - Italia 917
SG - Singapore 705
CN - Cina 506
HK - Hong Kong 402
SE - Svezia 394
DE - Germania 370
UA - Ucraina 217
RU - Federazione Russa 186
FI - Finlandia 151
BR - Brasile 124
TR - Turchia 116
BG - Bulgaria 102
FR - Francia 96
ID - Indonesia 91
IN - India 43
NL - Olanda 42
IE - Irlanda 27
LT - Lituania 26
BE - Belgio 25
VN - Vietnam 24
CZ - Repubblica Ceca 22
AT - Austria 21
CH - Svizzera 21
MY - Malesia 21
CA - Canada 20
KR - Corea 19
GR - Grecia 11
JP - Giappone 11
ES - Italia 9
IL - Israele 9
EU - Europa 8
AU - Australia 7
IR - Iran 7
PK - Pakistan 7
NO - Norvegia 6
HU - Ungheria 5
MX - Messico 5
BZ - Belize 4
DK - Danimarca 4
KZ - Kazakistan 4
MA - Marocco 4
RO - Romania 4
AE - Emirati Arabi Uniti 3
EG - Egitto 3
NZ - Nuova Zelanda 3
SA - Arabia Saudita 3
TW - Taiwan 3
ZA - Sudafrica 3
AR - Argentina 2
AZ - Azerbaigian 2
BD - Bangladesh 2
CO - Colombia 2
CR - Costa Rica 2
CY - Cipro 2
KG - Kirghizistan 2
KH - Cambogia 2
PH - Filippine 2
PL - Polonia 2
SK - Slovacchia (Repubblica Slovacca) 2
VE - Venezuela 2
ZM - Zambia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CL - Cile 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
IQ - Iraq 1
IS - Islanda 1
JM - Giamaica 1
KE - Kenya 1
LB - Libano 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
PT - Portogallo 1
PY - Paraguay 1
SN - Senegal 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 15.799
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Città #
Fairfield 1.400
Santa Clara 1.171
Southend 999
Woodbridge 709
Ashburn 675
Chandler 603
Houston 593
Seattle 497
Jacksonville 444
Cambridge 433
Wilmington 414
Hong Kong 397
Singapore 341
Dearborn 329
Ann Arbor 304
Nyköping 276
Modena 265
Beijing 135
San Diego 125
Princeton 102
Sofia 101
Jakarta 91
Eugene 84
Moscow 77
Helsinki 74
Council Bluffs 67
Milan 60
Redwood City 49
New York 47
Izmir 43
London 43
Rome 40
Falls Church 36
Bologna 30
Munich 29
Shanghai 29
Padova 27
Boardman 26
Bremen 26
Dublin 26
Norwalk 26
Nuremberg 23
Dong Ket 22
Amsterdam 21
Hefei 21
Nanjing 21
Brno 20
Los Angeles 19
Parma 19
Phoenix 17
Brussels 16
Provo 16
Frankfurt am Main 15
São Paulo 15
Chicago 14
Florence 14
Guangzhou 14
Kunming 12
San Mateo 12
Des Moines 11
Kilburn 11
Oldenburg 11
San Jose 11
Toronto 11
Tübingen 11
Wuhan 11
Reggio Emilia 10
Dongguan 9
Magenta 9
Segrate 9
Trieste 9
Fremont 8
Lappeenranta 8
Napoli 8
Rochester 8
Bari 7
Chiswick 7
Dalseong-gun 7
Heidelberg 7
Turin 7
Vienna 7
Würzburg 7
Zurich 7
Hebei 6
Indiana 6
Nanchang 6
Perugia 6
Piacenza 6
Redmond 6
Ulm 6
Zhengzhou 6
Augusta 5
Buffalo 5
Hounslow 5
Islington 5
Istanbul 5
Jinan 5
Mainz 5
Paris 5
Reggio Nell'emilia 5
Totale 11.858
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Nome #
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 278
Granulostasis: Protein Quality Control of RNP Granules 263
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism 255
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins 255
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin 248
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function 247
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8 241
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function 230
Altered regulation of CREB by chronic antidepressant administration in the brain of transgenic mice with impaired glucocorticoid receptor function. 225
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats. 224
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity. 222
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3) 220
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity 216
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks 213
Small heat shock proteins: multifaceted proteins with important implications for life 213
The role of the heat shock protein B8 (HSPB8) in motoneuron diseases 208
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response 206
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling 204
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases 201
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells 199
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 198
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain. 193
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. 193
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice 193
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 193
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. 192
Autophagy researchers 192
The Role of the Protein Quality Control System in SBMA 190
The regulation of the autophagic network and its implications for human disease 187
Specific protein homeostatic functions of small heat-shock proteins increase lifespan 187
Tdp-25 Routing to Autophagy and Proteasome Ameliorates its Aggregation in Amyotrophic Lateral Sclerosis Target Cells 185
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. 183
Quality Control of Membraneless Organelles 182
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 180
Proteostasis and ALS: Protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 178
Small heat shock proteins, protein degradation and protein aggregation diseases. 177
The small heat shock protein B8 (HSPB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). 177
ALS and FTD: Where RNA metabolism meets protein quality control 177
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins. 175
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies. 171
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. 171
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. 170
Autophagic and proteasomal mediated removal of mutant androgen receptor in muscle models of spinal and bulbar muscular atrophy 169
The growing world of small heat shock proteins: from structure to functions 166
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. 165
A role of small heat shock protein B8 (HSPB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. 164
Role of HSPB8 in the Proteostasis Network: From Protein Synthesis to Protein Degradation and Beyond 163
Guidelines for the use and interpretation of assays for monitoring autophagy. 163
OVEREXPRESSION OF HSPB8 PROTECTS AGAINST TDP43-MEDIATED TOXICITY IN DROSOPHILA 159
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. 159
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 158
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch 158
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. 157
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. 154
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. 153
Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases 150
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly 146
VCP AND AUTOPHAGOLYSOSOMAL PATHWAY: GUARDIANS OF PROTEOSTASIS AND STRESS GRANULE DYNAMICS. UNRAVELING THEIR IMPLICATIONS IN ALS 145
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. 142
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017 142
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 140
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 138
Characterization of the myopathy associated BAG3 P209L mutation 136
BAG3 induces the sequestration of ubiquitinated proteins into cytoplasmic puncta and re-routes them to autophagy upon proteasomal impairment 136
Studying heat shock proteins through single-molecule mechanical manipulation 136
Role of HspB1 and HspB8 in hereditary peripheral neuropathies: beyond the chaperone function 135
HspB8 and Bag3: A new chaperone complex targeting misfolded proteins to macroautophagy 134
CYTOPROTECTIVE FUNCTIONS OF SMALL STRESS PROTEINS IN PROTEIN CONFORMATIONAL DISEASES 128
Small Heat Shock Proteins in Neurodegenerative Diseases. 127
The Regulation of the Small Heat Shock Protein B8 in Misfolding Protein Diseases Causing Motoneuronal and Muscle Cell Death 126
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. 123
Structural and functional diversities between members of the human HspB, HspH, HspA, and DnaJ chaperones families. 120
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes 120
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: Implications for protein quality control and viral factory degradation? 118
HspB8 participates in protein quality control by a non chaperone-like mechanism that requires eIF2alpha phosphorylation. 117
BAG3-mediated re-routing of protein degradation towards autophagy upon proteasomal impairment 116
SENSING AND REROUTING OF PROTEIN DEGRADATION TOWARDS AUTOPHAGY UPON PROTEASOMAL IMPAIRMENT 114
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor 111
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 109
Nucleolus: A Liquid Droplet Compartment for Misbehaving Proteins 108
Upregulation of HSPB8 as potential therapeutic approach in familial and sporadic ALS 106
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 102
Motoneuron and muscle selective removal of ALS-related misfolded proteins. 96
Investigating the interplay between the protein quality control system, molecular chaperones and stress granules: from cell stress response to disease 95
Characterization of the interplay between the protein quality control and the stress granule response: implication in neurodegenerative diseases 95
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes 95
Implications of HSPBs and BAG3 in neuro/muscular-protein aggregate diseases 94
Upregulation of HSPB8 as potential therapeutic approach in Amyotrophic Lateral Sclerosis 85
Protein products of nonstop mRNA disrupt nucleolar homeostasis 84
Impairment of the Protein Quality Control System Affects Stress Granule Response and Dynamics 83
Inhibition of autophagy, lysosome and VCP alters stress granule morphology and composition 82
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones 82
Implications of HSPBs and BAG3 in protein aggregate neuro/muscular diseases 80
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 77
SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study 72
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype 64
Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial 59
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis 56
HSPB6: A lipid-dependent molecular chaperone inhibits α-synuclein aggregation 56
The beauty and complexity of the small heat shock proteins: a report on the proceedings of the fourth workshop on small heat shock proteins 56
Totale 15.536
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Categoria #
all - tutte 69.383
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 69.383
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020673 0 0 0 0 0 0 0 0 286 112 169 106
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
2024/20253.044 141 79 76 340 760 881 355 304 108 0 0 0
Totale 16.028