RECONDITI, MASSIMO
 Distribuzione geografica
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Continente #
NA - Nord America 5.909
EU - Europa 3.543
AS - Asia 2.373
SA - Sud America 220
Continente sconosciuto - Info sul continente non disponibili 128
AF - Africa 54
OC - Oceania 26
Totale 12.253
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Nazione #
US - Stati Uniti d'America 5.796
RU - Federazione Russa 994
PL - Polonia 822
IT - Italia 793
SG - Singapore 624
HK - Hong Kong 616
CN - Cina 502
IE - Irlanda 234
VN - Vietnam 210
SE - Svezia 208
KR - Corea 172
BR - Brasile 161
FR - Francia 141
DE - Germania 117
CA - Canada 72
UA - Ucraina 70
FI - Finlandia 68
IN - India 56
BD - Bangladesh 55
GB - Regno Unito 44
ID - Indonesia 28
TR - Turchia 28
AU - Australia 25
NL - Olanda 18
MX - Messico 16
AR - Argentina 15
EC - Ecuador 15
IQ - Iraq 15
JP - Giappone 12
ZA - Sudafrica 12
PE - Perù 11
NG - Nigeria 10
ES - Italia 9
CO - Colombia 7
MA - Marocco 7
VE - Venezuela 7
BE - Belgio 6
PH - Filippine 6
UZ - Uzbekistan 6
CI - Costa d'Avorio 5
JM - Giamaica 5
MY - Malesia 5
PK - Pakistan 5
SA - Arabia Saudita 5
IL - Israele 4
JO - Giordania 4
NP - Nepal 4
BJ - Benin 3
CH - Svizzera 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
SC - Seychelles 3
SV - El Salvador 3
TT - Trinidad e Tobago 3
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
CL - Cile 2
DK - Danimarca 2
HN - Honduras 2
HR - Croazia 2
KZ - Kazakistan 2
LB - Libano 2
PA - Panama 2
PR - Porto Rico 2
SK - Slovacchia (Repubblica Slovacca) 2
AO - Angola 1
AZ - Azerbaigian 1
BY - Bielorussia 1
CG - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
CZ - Repubblica Ceca 1
EE - Estonia 1
EG - Egitto 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GH - Ghana 1
GR - Grecia 1
GT - Guatemala 1
IR - Iran 1
KE - Kenya 1
KN - Saint Kitts e Nevis 1
KW - Kuwait 1
LT - Lituania 1
LU - Lussemburgo 1
MU - Mauritius 1
MV - Maldive 1
OM - Oman 1
PT - Portogallo 1
PW - Palau 1
PY - Paraguay 1
QA - Qatar 1
RS - Serbia 1
SN - Senegal 1
TH - Thailandia 1
TN - Tunisia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 12.125
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Città #
Santa Clara 1.654
Warsaw 821
Ashburn 589
Hong Kong 565
Fairfield 532
Singapore 478
Woodbridge 239
Chandler 231
Dublin 226
Cambridge 197
Seattle 196
Houston 187
San Jose 171
Seoul 170
Wilmington 162
Florence 159
Milan 146
Jacksonville 121
Hefei 111
Beijing 105
Council Bluffs 97
Buffalo 77
Altamura 74
Lawrence 74
Ann Arbor 68
Ho Chi Minh City 58
Lauterbourg 58
Princeton 58
Los Angeles 56
Rome 51
Boston 47
Paris 47
The Dalles 46
Boardman 43
San Diego 37
Dallas 35
Hanoi 33
Mumbai 33
Medford 25
Jakarta 24
Munich 24
Melbourne 23
Shanghai 22
Dong Ket 21
Moscow 21
New York 17
Naples 16
Norwalk 16
Phoenix 16
Kent 15
Atlanta 14
Orem 14
Toronto 14
Bologna 13
Lappeenranta 13
São Paulo 13
Clifton 12
Falls Church 12
Izmir 12
Montreal 12
Vancouver 12
Helsinki 11
Columbus 10
Da Nang 10
Frankfurt am Main 10
Haiphong 10
Miano 10
Redondo Beach 10
Tokyo 10
West Jordan 10
Abuja 9
Figino 9
London 9
Baghdad 8
Bochum 8
Chicago 8
Lima 8
Andover 7
Rufina 7
San Francisco 7
Verona 7
Boydton 6
Brussels 6
Guangzhou 6
Guayaquil 6
Pescara 6
Rio de Janeiro 6
Turin 6
Vaiano 6
Abidjan 5
Bari 5
Bengaluru 5
Brooklyn 5
Bắc Ninh 5
Genoa 5
Hillsboro 5
Johannesburg 5
Palermo 5
Poplar 5
Redwood City 5
Totale 8.714
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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
Mechanism of force generation by myosin heads in skeletal muscle 339
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
Low temperature traps myosin motors of mammalian muscle in a refractory state that prevents activation 287
The size and speed of the working stroke of cardiac myosin in situ. 262
Conformation of the myosin motor during force generation in skeletal muscle 255
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
Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal 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
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
A mechanical model of the half-sarcomere which includes the contribution of titin 203
Mechanics of myosin function in white muscle fibres of the dogfish Scyliorhinus canicula 201
Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing 201
Titin activates myosin filaments in skeletal muscle by switching from an extensible spring to a mechanical rectifier 200
The myosin motor in muscle generates a smaller and slower working stroke at higher load 198
Is muscle powered by springs or motors? 196
Contracting striated muscle has a dynamic I-band spring with an undamped stiffness 100 times larger than the passive stiffness 195
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
The structural basis of the increase in isometric force production with temperature in frog skeletal muscle 189
Convergent evolutionary pathways toward energy saving in muscle? 189
A combined mechanical and X-ray diffraction study of stretch potentiation in single frog muscle fibres 187
The non-linear elasticity of the muscle sarcomere and the compliance of myosin motors 185
Cross-bridge detachment and attachment following a step stretch imposed on active single frog muscle fibres 185
Structural changes in myosin motors and filaments during relaxation of skeletal muscle 184
The myofilament elasticity and its effect on kinetics of force generation by the myosin motor 183
Sarcomere level mechanics of the fast skeletal muscle of the medaka fish larva 182
An integrated picture of the structural pathways controlling the heart performance 181
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
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
X-ray interference studies of crossbridge action in muscle contraction: evidence from quick releases. 171
Anisotropic Elasticity of the Myosin Motor in Muscle 170
Distribution of crossbridge states in contracting muscle 169
X-ray interference studies of crossbridge action in muscle contraction: evidence from muscles during steady shortening. 169
Recent improvements in small angle x-ray diffraction for the study of muscle physiology 166
Structure-function relation of the myosin motor in striated muscle 160
X-ray diffraction studies of the contractile mechanism in single muscle fibres 158
IRIDE: Interdisciplinary research infrastructure based on dual electron linacs and lasers 158
Reverse actin sliding triggers strong myosin binding that moves tropomyosin 153
Dependence of myosin filament structure on intracellular calcium concentration in skeletal muscle 152
Editorial to the Special Issue "Molecular Motors: From Single Molecules to Cooperative and Regulatory Mechanisms In Vivo" 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
Myosin head movements during isometric contraction and shortening at high speed studied by X-ray diffraction on single muscle fibres 143
Myosin motors that cannot bind actin leave their folded OFF state on activation of skeletal muscle 140
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
There is no experimental evidence for non-linear myofilament elasticity in skeletal muscle. 112
The Baraitser-Winter Cerebrofrontofacial Syndrome Recurrent R196H Variant in Cytoplasmic β-Actin Impairs Its Cellular Polymerization and Stability 63
null 61
X-ray interference evidence concerning the range of crossbridge movement and backbone contributions to the meridional pattern 56
Multiple pathways of the actin-myosin cycle in energy transduction and the release of orthophosphate in muscle 16
Totale 12.253
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Categoria #
all - tutte 32.491
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 32.491
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022441 0 47 29 6 40 21 20 20 37 23 93 105
2022/20231.038 85 228 67 66 76 177 137 56 87 22 23 14
2023/2024386 13 47 64 25 60 25 6 72 16 24 14 20
2024/20253.760 105 269 159 415 1.274 682 68 172 311 95 104 106
2025/20263.358 294 425 294 168 331 165 453 187 198 265 121 457
2026/2027198 126 72 0 0 0 0 0 0 0 0 0 0
Totale 12.253