CAREMANI, MARCO
 Distribuzione geografica
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Continente #
NA - Nord America 3.640
EU - Europa 2.737
AS - Asia 1.607
SA - Sud America 136
Continente sconosciuto - Info sul continente non disponibili 113
AF - Africa 34
OC - Oceania 21
Totale 8.288
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Nazione #
US - Stati Uniti d'America 3.565
PL - Polonia 1.023
RU - Federazione Russa 637
IT - Italia 592
SG - Singapore 391
CN - Cina 377
HK - Hong Kong 374
VN - Vietnam 146
IE - Irlanda 126
KR - Corea 116
SE - Svezia 93
BR - Brasile 89
FR - Francia 74
BD - Bangladesh 49
DE - Germania 46
IN - India 46
CA - Canada 40
FI - Finlandia 36
GB - Regno Unito 35
ID - Indonesia 29
NL - Olanda 21
TR - Turchia 21
AU - Australia 20
BE - Belgio 13
MX - Messico 13
AR - Argentina 12
DK - Danimarca 12
UA - Ucraina 11
EC - Ecuador 9
ES - Italia 9
IQ - Iraq 9
ZA - Sudafrica 8
CL - Cile 7
JP - Giappone 7
NG - Nigeria 7
UZ - Uzbekistan 7
VE - Venezuela 7
PE - Perù 6
PK - Pakistan 6
CI - Costa d'Avorio 5
CO - Colombia 4
SA - Arabia Saudita 4
DZ - Algeria 3
GT - Guatemala 3
HN - Honduras 3
IL - Israele 3
JO - Giordania 3
MA - Marocco 3
PH - Filippine 3
SV - El Salvador 3
TT - Trinidad e Tobago 3
AT - Austria 2
BJ - Benin 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
JM - Giamaica 2
MY - Malesia 2
NP - Nepal 2
PR - Porto Rico 2
TH - Thailandia 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
AO - Angola 1
AZ - Azerbaigian 1
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
EE - Estonia 1
EG - Egitto 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
KN - Saint Kitts e Nevis 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MU - Mauritius 1
PW - Palau 1
QA - Qatar 1
RS - Serbia 1
TN - Tunisia 1
YT - Mayotte 1
Totale 8.175
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Città #
Warsaw 1.022
Santa Clara 994
Ashburn 408
Hong Kong 344
Fairfield 325
Singapore 295
San Jose 151
Florence 145
Seattle 136
Woodbridge 132
Dublin 122
Seoul 116
Chandler 113
Houston 106
Milan 105
Cambridge 102
Council Bluffs 91
Beijing 86
Ann Arbor 85
Hefei 84
Wilmington 77
Lawrence 44
Altamura 40
Los Angeles 37
Lauterbourg 34
Buffalo 33
Ho Chi Minh City 33
Princeton 33
Rome 33
Dong Ket 29
Mumbai 29
Jakarta 26
Dallas 25
Phoenix 24
San Diego 24
Hanoi 23
The Dalles 23
Boston 22
Paris 21
Moscow 19
Boardman 18
Jacksonville 18
New York 16
Melbourne 15
Medford 14
Brussels 13
Clifton 13
Shanghai 13
Munich 12
Kent 11
Montreal 11
Frankfurt am Main 10
Rufina 10
Lappeenranta 9
Naples 9
Orem 9
Helsinki 8
São Paulo 8
Toronto 8
Bologna 7
Haiphong 7
Hillsboro 7
London 7
Redondo Beach 7
San Francisco 7
Sansepolcro 7
Abuja 6
Bengaluru 6
Lima 6
Santiago 6
Tashkent 6
Abidjan 5
Atlanta 5
Da Nang 5
Hangzhou 5
Izmir 5
Pescara 5
Philadelphia 5
Sydney 5
Verona 5
Andover 4
Ankara 4
Baghdad 4
Bergamo 4
Catania 4
Chicago 4
Denver 4
Genoa 4
Guangzhou 4
Guayaquil 4
Miami 4
Miano 4
Newark 4
Saronno 4
Shijiazhuang 4
Tokyo 4
Amsterdam 3
Bari 3
Brooklyn 3
Bắc Giang 3
Totale 6.016
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Nome #
The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site. 368
Inotropic interventions do not change the resting state of myosin motors during cardiac diastole 368
Low-force transitions in single titin molecules reflect a memory of contractile history 360
Force and number of myosin motors during muscle shortening and the coupling with the release of the ATP hydrolysis products 322
Muscle thixotropy: more than just cross-bridges? 317
Orthovanadate and orthophosphate inhibit muscle force via two different pathways of the myosin ATPase cycle 305
Low temperature traps myosin motors of mammalian muscle in a refractory state that prevents activation 289
Myopalladin promotes muscle growth through modulation of the serum response factor pathway 269
The size and speed of the working stroke of cardiac myosin in situ. 263
Thick Filament Mechano-Sensing in Skeletal and Cardiac Muscles: A Common Mechanism Able to Adapt the Energetic Cost of the Contraction to the Task 251
Thick Filament Length Changes in Muscle Have Both Elastic and Structural Components 248
Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments 243
The force of the myosin motor sets cooperativity in thin filament activation of skeletal muscles 242
Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal muscle 242
Effect of inorganic phosphate on the force and number of myosin cross-bridges during the isometric contraction of permeabilized muscle fibers from rabbit psoas. 237
Myosin filament activation in the heart is tuned to the mechanical task 226
The contributions of filaments and cross-bridges to sarcomere compliance in skeletal muscle 208
Mechanical parameters of the molecular motor myosin II determined in permeabilised fibres from slow and fast skeletal muscles of the rabbit 207
A mechanical model of the half-sarcomere which includes the contribution of titin 205
Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing 202
Titin activates myosin filaments in skeletal muscle by switching from an extensible spring to a mechanical rectifier 201
Muscle Thixotropy: More than Just Cross-Bridges? Response to Comment by Campbell and Lakie 192
Nebulin plays a direct role in promoting strong actin-myosin interactions 190
Orthophosphate increases the efficiency of slow muscle-myosin isoform in the presence of omecamtiv mecarbil 188
Sarcomere level mechanics of the fast skeletal muscle of the medaka fish larva 187
A Kinetic Model that Explains the Effect of Inorganic Phosphate on the Mechanics and Energetics of Isometric Contraction of Fast Skeletal Muscle. 184
An integrated picture of the structural pathways controlling the heart performance 182
Force and kinetics of fast and slow muscle myosin determined with a synthetic sarcomere–like nanomachine 180
The force and stiffness of myosin motors in the isometric twitch of a cardiac trabecula and the effect of the extracellular calcium concentration 175
Anisotropic Elasticity of the Myosin Motor in Muscle 173
Dependence of myosin filament structure on intracellular calcium concentration in skeletal muscle 154
Matching Mechanics and Energetics of Muscle Contraction Suggests Unconventional Chemomechanical Coupling during the Actin-Myosin Interaction 148
Stiffness and fraction of myosin motors responsible for active force in permeabilized muscle fibers from rabbit psoas 143
The anti-steatosic effect of sulfo-adenosylmethionine (SAMe) in various forms of chronic hepatopathy. Multicentric research 137
Allosteric modulation of cardiac myosin mechanics and kinetics by the conjugated omega-7,9 trans-fat rumenic acid 136
The Mechanism of Modulation of Cardiac Force by Temperature 132
Creatine transporter (SLC6A8) knockout mice exhibit reduced muscle performance, disrupted mitochondrial Ca2+ homeostasis, and severe muscle atrophy 126
Ising models of cooperativity in muscle contraction 70
Multiple pathways of the actin-myosin cycle in energy transduction and the release of orthophosphate in muscle 18
Totale 8.288
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Categoria #
all - tutte 21.870
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 21.870
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022239 0 0 35 4 15 6 7 16 34 20 43 59
2022/2023576 56 127 32 34 42 90 74 25 57 17 10 12
2023/2024276 12 24 39 16 34 30 4 51 9 16 13 28
2024/20252.376 66 185 119 248 759 437 59 103 179 55 70 96
2025/20262.322 195 277 204 105 244 98 287 114 161 194 118 325
2026/2027187 75 52 60 0 0 0 0 0 0 0 0 0
Totale 8.288