LINARI, MARCO
 Distribuzione geografica
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Continente #
NA - Nord America 7.532
EU - Europa 5.133
AS - Asia 2.851
SA - Sud America 234
Continente sconosciuto - Info sul continente non disponibili 150
AF - Africa 65
OC - Oceania 44
Totale 16.009
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Nazione #
US - Stati Uniti d'America 7.401
PL - Polonia 1.813
RU - Federazione Russa 1.216
IT - Italia 923
SG - Singapore 769
HK - Hong Kong 728
CN - Cina 588
SE - Svezia 302
IE - Irlanda 291
VN - Vietnam 268
KR - Corea 198
BR - Brasile 170
FR - Francia 142
DE - Germania 138
UA - Ucraina 89
CA - Canada 84
FI - Finlandia 83
IN - India 68
GB - Regno Unito 54
BD - Bangladesh 53
TR - Turchia 44
AU - Australia 43
ID - Indonesia 34
NL - Olanda 28
MX - Messico 19
ZA - Sudafrica 18
IQ - Iraq 17
JP - Giappone 16
EC - Ecuador 15
AR - Argentina 14
DK - Danimarca 12
ES - Italia 12
BE - Belgio 11
NG - Nigeria 11
PE - Perù 10
CO - Colombia 8
PK - Pakistan 8
UZ - Uzbekistan 8
VE - Venezuela 8
CI - Costa d'Avorio 7
CL - Cile 7
MA - Marocco 7
NP - Nepal 6
PH - Filippine 6
IL - Israele 5
JO - Giordania 5
JM - Giamaica 4
MY - Malesia 4
SN - Senegal 4
SV - El Salvador 4
TT - Trinidad e Tobago 4
BJ - Benin 3
CH - Svizzera 3
DZ - Algeria 3
EU - Europa 3
GT - Guatemala 3
LB - Libano 3
OM - Oman 3
PR - Porto Rico 3
SA - Arabia Saudita 3
SC - Seychelles 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
BH - Bahrain 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
EE - Estonia 2
EG - Egitto 2
GE - Georgia 2
IR - Iran 2
KE - Kenya 2
LT - Lituania 2
RO - Romania 2
TH - Thailandia 2
TW - Taiwan 2
AI - Anguilla 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
CZ - Repubblica Ceca 1
ET - Etiopia 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
HR - Croazia 1
HT - Haiti 1
HU - Ungheria 1
KN - Saint Kitts e Nevis 1
KW - Kuwait 1
KZ - Kazakistan 1
MU - Mauritius 1
NI - Nicaragua 1
PA - Panama 1
PW - Palau 1
QA - Qatar 1
Totale 15.860
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Città #
Santa Clara 2.048
Warsaw 1.812
Ashburn 756
Fairfield 712
Hong Kong 660
Singapore 582
Chandler 313
Woodbridge 298
Dublin 285
Seattle 283
Cambridge 248
Houston 241
San Jose 233
Seoul 197
Wilmington 190
Florence 172
Milan 169
Jacksonville 162
Beijing 140
Council Bluffs 122
Ann Arbor 116
Hefei 112
Lawrence 91
Altamura 87
Buffalo 87
Princeton 73
Lauterbourg 72
Rome 72
Ho Chi Minh City 68
Los Angeles 68
The Dalles 61
Dallas 50
Boston 49
Boardman 48
Dong Ket 42
San Diego 42
Mumbai 40
Hanoi 39
Melbourne 39
Medford 38
Paris 36
Moscow 34
Jakarta 31
Phoenix 25
New York 24
Shanghai 24
Izmir 23
Munich 22
Toronto 20
Falls Church 19
Kent 18
Montreal 16
Naples 15
Norwalk 15
Atlanta 14
Orem 14
Redondo Beach 14
Tokyo 14
Bologna 13
Da Nang 13
Frankfurt am Main 13
Miano 13
Figino 12
Haiphong 12
Helsinki 12
São Paulo 12
Vancouver 12
Austin 11
Brussels 11
Columbus 11
Abuja 10
Chicago 10
Clifton 10
Johannesburg 10
London 10
Rufina 10
Guangzhou 9
Hillsboro 9
Palermo 9
San Francisco 9
Vaiano 9
Bochum 8
Lima 8
Pescara 8
Redwood City 8
Verona 8
West Jordan 8
Abidjan 7
Amsterdam 7
Baghdad 7
Bengaluru 7
Brooklyn 7
Genoa 7
Lappeenranta 7
Sansepolcro 7
Stockholm 7
Tashkent 7
Istanbul 6
Rio de Janeiro 6
Santiago 6
Totale 11.681
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Nome #
Motion of myosin head domains during activation and force development in skeletal muscle 369
Inotropic interventions do not change the resting state of myosin motors during cardiac diastole 367
The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site. 366
Effects of myosin heavy chain (MHC) plasticity induced by HMGCoA-reductase inhibition on skeletal muscle functions 361
Energy storage during stretch of active single fibres from frog skeletal muscle 359
Low-force transitions in single titin molecules reflect a memory of contractile history 358
Mechanism of force generation by myosin heads in skeletal muscle 339
Force and number of myosin motors during muscle shortening and the coupling with the release of the ATP hydrolysis products 321
Muscle thixotropy: more than just cross-bridges? 316
The conformation of myosin head domains in rigor muscle determined by X-ray interference. 311
Elastic bending and active tilting of myosin heads during muscle contraction 309
Orthovanadate and orthophosphate inhibit muscle force via two different pathways of the myosin ATPase cycle 304
Low temperature traps myosin motors of mammalian muscle in a refractory state that prevents activation 285
Myopalladin promotes muscle growth through modulation of the serum response factor pathway 268
The size and speed of the working stroke of cardiac myosin in situ. 262
Thick Filament Mechano-Sensing in Skeletal and Cardiac Muscles: A Common Mechanism Able to Adapt the Energetic Cost of the Contraction to the Task 250
Thick Filament Length Changes in Muscle Have Both Elastic and Structural Components 245
Rapid regeneration of the actin-myosin power stroke in contracting muscle 241
Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments 241
The force of the myosin motor sets cooperativity in thin filament activation of skeletal muscles 239
Effect of inorganic phosphate on the force and number of myosin cross-bridges during the isometric contraction of permeabilized muscle fibers from rabbit psoas. 235
Myosin filament activation in the heart is tuned to the mechanical task 225
Skeletal muscle performance determined by modulation of number of myosin motors rather than motor force or stroke size 210
Skeletal muscle resists stretch by rapid binding of the second motor domain of myosin to actin 205
The contributions of filaments and cross-bridges to sarcomere compliance in skeletal muscle 205
Mechanics of myosin function in white muscle fibres of the dogfish Scyliorhinus canicula 201
New techniques in linear and non-linear laser optics in muscle research. 200
Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing 200
Titin activates myosin filaments in skeletal muscle by switching from an extensible spring to a mechanical rectifier 199
The myosin motor in muscle generates a smaller and slower working stroke at higher load 198
Structural changes in the myosin filament and cross-bridges during active force development in single intact frog muscle fibres: stiffness and X-ray diffraction measurements. 192
The mechanism of the resistance to stretch of isometrically contracting single muscle fibres 191
Sarcomere-length dependence of myosin filament structure in skeletal muscle fibres of the frog 191
Muscle Thixotropy: More than Just Cross-Bridges? Response to Comment by Campbell and Lakie 190
Nebulin plays a direct role in promoting strong actin-myosin interactions 189
The structural basis of the increase in isometric force production with temperature in frog skeletal muscle 189
Energy storage during stretch of active single fibres 187
A combined mechanical and X-ray diffraction study of stretch potentiation in single frog muscle fibres 187
Orthophosphate increases the efficiency of slow muscle-myosin isoform in the presence of omecamtiv mecarbil 187
Structural changes in myosin motors and filaments during relaxation of skeletal muscle 184
Cross-bridge detachment and attachment following a step stretch imposed on active single frog muscle fibres 184
The myofilament elasticity and its effect on kinetics of force generation by the myosin motor 182
Sarcomere level mechanics of the fast skeletal muscle of the medaka fish larva 181
Ca-activation and stretch-activation in insect flight muscle 181
A Kinetic Model that Explains the Effect of Inorganic Phosphate on the Mechanics and Energetics of Isometric Contraction of Fast Skeletal Muscle. 181
An integrated picture of the structural pathways controlling the heart performance 180
The effect of myofilament compliance on kinetics of force generation by myosin motors in muscle 180
Force and kinetics of fast and slow muscle myosin determined with a synthetic sarcomere–like nanomachine 179
Interference x-ray diffraction from single muscle cells reveals the molecular basis of muscle braking 178
Probing myosin structural conformation in vivo by second-harmonic generation microscopy. 177
Temperature dependence of the force-generating process in single fibres from frog skeletal muscle. 174
The force and stiffness of myosin motors in the isometric twitch of a cardiac trabecula and the effect of the extracellular calcium concentration 172
Structural and molecular conformation of myosin in intact muscle fibers by second harmonic generation 171
Kinetics of regeneration of cross-bridge power stroke in shortening muscle 169
Functional imaging of skeletal muscle fiber in different physiological states by Second Harmonic Generation 167
Comparison of energy output during ramp and staircase shortening in frog muscle fibres 166
Structural dynamics of the skeletal muscle fiber by second harmonic generation 166
Study of skeletal muscle cross-bridge population dynamics by Second Harmonic Generation 164
Structure-function relation of the myosin motor in striated muscle 160
X-ray diffraction studies of the contractile mechanism in single muscle fibres 158
Dependence of myosin filament structure on intracellular calcium concentration in skeletal muscle 152
Functional imaging of muscle cells by Second Harmonic Generation - art. no. 60891I 151
Changes in conformation of myosin heads during the development of isometric contraction and rapid shortening in single frog muscle fibres 149
Matching Mechanics and Energetics of Muscle Contraction Suggests Unconventional Chemomechanical Coupling during the Actin-Myosin Interaction 148
The stiffness of skeletal muscle in isometric contraction and rigor: the fraction of myosin heads bound to actin 147
The mechanism of the force response to stretch in human skinned muscle fibres with different myosin isoforms 147
Interference fine structure and sarcomere length dependence of the axial X-ray pattern from active single muscle fibres 144
Cross-bridge kinetics studied with staircase shortening in single fibres from frog skeletal muscle 144
Myosin head movements during isometric contraction and shortening at high speed studied by X-ray diffraction on single muscle fibres 143
Stiffness and fraction of myosin motors responsible for active force in permeabilized muscle fibers from rabbit psoas 142
Myosin motors that cannot bind actin leave their folded OFF state on activation of skeletal muscle 140
Mechanical and energy characteristics during shortening in isolated type-1 muscle fibres from Xenopus laevis studied at maximal and submaximal activation 139
The effect of hypertonicity on force generation in tetanized single fibres from frog skeletal muscle 131
The Mechanism of Modulation of Cardiac Force by Temperature 128
Creatine transporter (SLC6A8) knockout mice exhibit reduced muscle performance, disrupted mitochondrial Ca2+ homeostasis, and severe muscle atrophy 126
Straightening Out the Elasticity of Myosin Cross-Bridges 126
Tension transient during steady lengthening of tetanized muscle fibres of the frog 122
Ising models of cooperativity in muscle contraction 68
Multiple pathways of the actin-myosin cycle in energy transduction and the release of orthophosphate in muscle 16
Totale 16.009
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Categoria #
all - tutte 40.447
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 40.447
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022554 0 55 50 9 44 24 25 31 35 29 123 129
2022/20231.330 124 276 67 87 111 223 176 77 124 25 25 15
2023/2024504 23 50 82 25 70 53 12 92 18 24 19 36
2024/20254.517 133 344 203 500 1.570 855 60 224 302 102 120 104
2025/20264.115 379 492 313 152 433 180 561 209 285 372 137 602
2026/2027232 145 87 0 0 0 0 0 0 0 0 0 0
Totale 16.009