MANNINI, BENEDETTA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 2.820
EU - Europa 2.105
AS - Asia 1.667
SA - Sud America 217
AF - Africa 46
OC - Oceania 26
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.882
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.785
PL - Polonia 763
RU - Federazione Russa 662
SG - Singapore 482
CN - Cina 470
HK - Hong Kong 182
IT - Italia 173
KR - Corea 171
BR - Brasile 163
VN - Vietnam 149
IE - Irlanda 109
SE - Svezia 93
IN - India 83
DE - Germania 73
FI - Finlandia 68
FR - Francia 51
CH - Svizzera 33
GB - Regno Unito 31
ID - Indonesia 27
AU - Australia 26
AR - Argentina 15
CA - Canada 15
JO - Giordania 14
NG - Nigeria 14
TR - Turchia 13
ES - Italia 12
IQ - Iraq 12
JP - Giappone 12
MX - Messico 12
BD - Bangladesh 10
NL - Olanda 10
AE - Emirati Arabi Uniti 9
CO - Colombia 7
EC - Ecuador 7
ZA - Sudafrica 7
PY - Paraguay 6
UA - Ucraina 6
VE - Venezuela 6
BJ - Benin 5
MA - Marocco 5
AL - Albania 4
CL - Cile 4
IL - Israele 4
MY - Malesia 4
PE - Perù 4
UY - Uruguay 4
AM - Armenia 3
AT - Austria 3
CI - Costa d'Avorio 3
DZ - Algeria 3
EG - Egitto 3
LT - Lituania 3
PH - Filippine 3
PK - Pakistan 3
UZ - Uzbekistan 3
CR - Costa Rica 2
ET - Etiopia 2
IR - Iran 2
JM - Giamaica 2
PA - Panama 2
RO - Romania 2
SA - Arabia Saudita 2
TW - Taiwan 2
AF - Afghanistan, Repubblica islamica di 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BW - Botswana 1
CM - Camerun 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
GT - Guatemala 1
HR - Croazia 1
HU - Ungheria 1
KG - Kirghizistan 1
LB - Libano 1
MR - Mauritania 1
NP - Nepal 1
PT - Portogallo 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 6.882
Salva come PNG Salva come JPEG
Città #
Santa Clara 764
Warsaw 763
Ashburn 382
Singapore 364
Hefei 179
Fairfield 177
Hong Kong 162
Seoul 161
Chandler 126
Dublin 109
San Jose 100
Seattle 85
Woodbridge 79
Houston 69
Wilmington 69
Cambridge 66
Council Bluffs 62
Ho Chi Minh City 53
Florence 50
The Dalles 49
Beijing 43
Lawrence 41
Los Angeles 41
Moscow 40
Lauterbourg 38
Altamura 36
Mumbai 28
Buffalo 26
Princeton 26
Hanoi 25
Helsinki 24
Melbourne 24
Pune 24
Munich 23
Ann Arbor 22
Bremen 22
Jakarta 22
Kent 21
Atlanta 20
Boston 20
Dallas 17
Boardman 15
Lappeenranta 15
Shanghai 15
Turku 15
Abuja 14
San Diego 13
Basel 12
Dong Ket 12
Chennai 11
Medford 10
Milwaukee 10
New York 10
Bengaluru 9
Bern 9
Da Nang 9
Haiphong 9
Rome 9
Seongnam 9
São Paulo 9
Barcelona 8
London 8
Milan 8
Norwalk 8
Tokyo 8
Cagliari 7
Clifton 7
Dübendorf 7
Falls Church 7
Frankfurt am Main 7
Jacksonville 7
Orem 7
Abu Dhabi 6
Belo Horizonte 6
Brasília 6
Denver 6
Groningen 6
Phoenix 6
Rio de Janeiro 6
Serra 6
Tianjin 6
Virginia Beach 6
Amman 5
Baghdad 5
Chicago 5
Cotonou 5
Hillsboro 5
Izmir 5
Manchester 5
Paris 5
Guangzhou 4
Montevideo 4
Nuremberg 4
Raleigh 4
Tel Aviv 4
Tirana 4
Toronto 4
Abidjan 3
Asunción 3
Brooklyn 3
Totale 4.893
Salva come PNG Salva come JPEG
Nome #
A causative link between the structure of aberrant protein oligomers and their toxicity 459
Large proteins have a great tendency to aggregate but a low propensity to form amyloid fibrils 341
Effect of molecular chaperones on aberrant protein oligomers in vitro: super- versus sub-stoichiometric chaperone concentrations 299
Early-forming aberrant aggregates in protein deposition diseases: structural characteristics, interaction with molecular chaperones, ability to trigger inflammation 295
Toxic HypF-N oligomers selectively bind the plasma membrane to impair cell adhesion capability 273
Multistep Inhibition of α‑Synuclein Aggregation and Toxicity in Vitro and in Vivo by Trodusquemine 236
The induction of α-helical structure in partially unfolded HypF-N does not affect its aggregation propensity 204
Chaperones as Suppressors of Protein Misfolded Oligomer Toxicity 198
A comparison of the biochemical modifications caused by toxic and non-toxic protein oligomers in cells 191
Amyloid-β oligomer synaptotoxicity is mimicked by oligomers of the model protein HypF-N 189
Molecular mechanisms used by chaperones to reduce the toxicity of aberrant protein oligomers 189
Glycosaminoglycans (GAGs) Suppress the Toxicity of HypF-N Prefibrillar Aggregates 184
Bis(indolyl)phenylmethane derivatives are effective small molecules for inhibition of amyloid fibril formation by hen lysozyme 164
Squalamine and its derivatives modulate the aggregation of amyloid-β and α-synuclein and suppress the toxicity of their oligomers 163
Differential interactome and innate immune response activation of two structurally distinct misfolded protein oligomers 159
SERS Detection of Amyloid Oligomers on Metallorganic-Decorated Plasmonic Beads 158
Aβ oligomers dysregulate calcium homeostasis by mechanosensitive activation of AMPA and NMDA receptors. 155
Salt anions promote the conversion of HypF-N into amyloid-like oligomers and modulate the structure of the oligomers and the monomeric precursor state. 154
Trodusquemine displaces protein misfolded oligomers from cell membranes and abrogates their cytotoxicity through a generic mechanism 152
Distinct responses of human peripheral blood cells to different misfolded protein oligomers 151
Small-molecule sequestration of amyloid-beta. as a drug discovery strategy for Alzheimer's disease 146
Chaperones suppress protein oligomer toxicity: Insight into the molecular mechanism of action 142
Exogenous misfolded protein oligomers can cross the intestinal barrier and cause a disease phenotype in C. elegans 130
The Pathological G51D Mutation in Alpha-Synuclein Oligomers Confers Distinct Structural Attributes and Cellular Toxicity 129
Chaperones suppress the toxicity of aberrant protein aggregates. Molecular insight into the mechanism of action 129
Stabilization and Characterization of Cytotoxic Aβ40 Oligomers Isolated from an Aggregation Reaction in the Presence of Zinc Ions 128
Toxicity of Protein Oligomers Is Rationalized by a Function Combining Size and Surface Hydrophobicity 127
Therapeutic strategies to reduce the toxicity of misfolded protein oligomers 123
A Relationship between the Structures and Neurotoxic Effects of Aβ Oligomers Stabilized by Different Metal Ions 117
Two human metabolites rescue a C. elegans model of Alzheimer’s disease via a cytosolic unfolded protein response 116
Preparation and Characterization of Zn(II)-Stabilized Aβ42 Oligomers 116
Rationally designed antibodies as research tools to study the structure–toxicity relationship of amyloid-β oligomers 114
Proteome-wide observation of the phenomenon of life on the edge of solubility 111
Rational design of a conformation-specific antibody for the quantification of Aβ oligomers 110
A rationally designed bicyclic peptide remodels Aβ42 aggregation in vitro and reduces its toxicity in a worm model of Alzheimer’s disease 107
Delivery of Native Proteins into C. Elegans Using a Transduction Protocol Based on Lipid Vesicles 106
Systematic development of small molecules to inhibit specific microscopic steps of Aβ42 aggregation in Alzheimer's disease 102
Surface-Catalyzed Secondary Nucleation Dominates the Generation of Toxic IAPP Aggregates 100
Structure-Based Discovery of Small-Molecule Inhibitors of the Autocatalytic Proliferation of α-Synuclein Aggregates 99
Single molecule secondary structure determination of proteins through infrared absorption nanospectroscopy 94
Targeting Protein Aggregation in ALS 89
Small Molecule Inhibitors for Precise Inhibition of Alpha-Synuclein Oligomer Generation in Parkinson’s Disease (S32.002) 89
A dopamine metabolite stabilizes neurotoxic amyloid-β oligomers 87
Berberine mitigates neurotoxicity of misfolded protein oligomers by interacting with the cell membrane and subsequent internalization, without altering their structure 40
Totale 6.965
Salva come PNG Salva come JPEG
Categoria #
all - tutte 18.085
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 18.085
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202145 0 0 0 0 0 0 0 0 0 0 19 26
2021/2022162 1 25 16 5 3 7 8 14 10 9 18 46
2022/2023562 37 109 36 52 44 104 66 32 50 3 16 13
2023/2024274 9 28 27 9 9 42 10 50 4 61 14 11
2024/20252.010 49 215 87 266 662 259 41 64 125 41 83 118
2025/20262.416 255 361 338 215 253 109 311 135 198 157 84 0
Totale 6.965