LOMBARDI, VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 1.757
EU - Europa 594
AS - Asia 248
AF - Africa 84
OC - Oceania 26
SA - Sud America 23
Continente sconosciuto - Info sul continente non disponibili 5
Totale 2.737
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Nazione #
US - Stati Uniti d'America 1.715
IT - Italia 192
CN - Cina 83
IE - Irlanda 71
GB - Regno Unito 68
FR - Francia 58
VN - Vietnam 57
DE - Germania 52
CA - Canada 41
ET - Etiopia 34
PL - Polonia 34
RU - Federazione Russa 28
ZA - Sudafrica 28
JP - Giappone 25
AU - Australia 21
IN - India 18
UA - Ucraina 15
TR - Turchia 13
NL - Olanda 12
ES - Italia 9
SE - Svezia 9
BR - Brasile 8
PK - Pakistan 8
CZ - Repubblica Ceca 7
IR - Iran 7
SG - Singapore 7
CL - Cile 6
FI - Finlandia 6
LK - Sri Lanka 6
HU - Ungheria 5
NO - Norvegia 5
NZ - Nuova Zelanda 5
PH - Filippine 5
CO - Colombia 4
EU - Europa 4
GH - Ghana 4
ID - Indonesia 4
KE - Kenya 4
NG - Nigeria 4
BE - Belgio 3
DK - Danimarca 3
DZ - Algeria 3
KR - Corea 3
LT - Lituania 3
RO - Romania 3
TW - Taiwan 3
ZW - Zimbabwe 3
AE - Emirati Arabi Uniti 2
BD - Bangladesh 2
CH - Svizzera 2
HR - Croazia 2
PE - Perù 2
SA - Arabia Saudita 2
TH - Thailandia 2
TZ - Tanzania 2
UY - Uruguay 2
A1 - Anonimo 1
AT - Austria 1
EC - Ecuador 1
EE - Estonia 1
EG - Egitto 1
GR - Grecia 1
HK - Hong Kong 1
LV - Lettonia 1
MD - Moldavia 1
MX - Messico 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
UG - Uganda 1
Totale 2.737
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Città #
Fairfield 225
Santa Cruz 142
Buffalo 122
Woodbridge 117
Houston 113
Ashburn 106
Seattle 102
Florence 97
Cambridge 73
Dublin 68
Dong Ket 54
Ann Arbor 53
Wilmington 49
Beijing 31
Warsaw 30
Mountain View 27
San Diego 22
Chicago 21
Clearwater 19
Muizenberg 18
Saint Petersburg 16
Wuhan 16
Las Vegas 14
Phoenix 13
Council Bluffs 11
Dearborn 11
Los Angeles 11
Ottawa 11
London 10
University Park 10
Anguillara Sabazia 9
Henderson 9
Toronto 9
Herndon 8
Lake Forest 8
Hangzhou 7
Paris 7
San Francisco 7
Shanghai 7
Dallas 6
Istanbul 6
Jacksonville 6
New York 6
Provo 6
San Jose 6
Bengaluru 5
Chengdu 5
Helsinki 5
Riva 5
Rufina 5
Silverton 5
Singapore 5
Atlanta 4
Boardman 4
Boulder 4
Büdelsdorf 4
Castle Hill 4
Elk Grove Village 4
Lubbock 4
Mcallen 4
Milpitas 4
Munich 4
Valencia 4
Xian 4
Yellow Springs 4
Andover 3
Barcelona 3
Busto Arsizio 3
Durban 3
Easton 3
Frankfurt Am Main 3
Grenoble 3
Hamburg 3
Milan 3
Montréal 3
Mumbai 3
Nanjing 3
Oxford 3
Pittsburgh 3
Polska 3
Poole 3
Shawinigan 3
Solna 3
Taipei 3
Worcester 3
Zhengzhou 3
Bangalore 2
Bangkok 2
Bogotá 2
Brescia 2
Bursa 2
Castelldefels 2
Cheyenne 2
Città Di Castello 2
College Park 2
Columbia 2
Copenhagen 2
Des Moines 2
Downers Grove 2
Dubuque 2
Totale 1.897
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Nome #
Mechanism of force generation by myosin heads in skeletal muscle, file e398c378-9c61-179a-e053-3705fe0a4cff 586
Elastic bending and active tilting of myosin heads during muscle contraction, file e398c378-96d2-179a-e053-3705fe0a4cff 193
Force and number of myosin motors during muscle shortening and the coupling with the release of the ATP hydrolysis products, file e398c379-af8f-179a-e053-3705fe0a4cff 157
An AT-barrier mechanically controls DNA reannealing under tension, file e398c37a-b97c-179a-e053-3705fe0a4cff 149
Low temperature traps myosin motors of mammalian muscle in a refractory state that prevents activation, file e398c37e-e1c7-179a-e053-3705fe0a4cff 142
The conformation of myosin head domains in rigor muscle determined by X-ray interference., file e398c378-9372-179a-e053-3705fe0a4cff 138
The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site., file e398c379-cf34-179a-e053-3705fe0a4cff 138
Inotropic interventions do not change the resting state of myosin motors during cardiac diastole, file e398c37e-0857-179a-e053-3705fe0a4cff 133
Thick Filament Mechano-Sensing in Skeletal and Cardiac Muscles: A Common Mechanism Able to Adapt the Energetic Cost of the Contraction to the Task, file e398c37d-c885-179a-e053-3705fe0a4cff 131
A myosin II nanomachine mimicking the striated muscle, file e398c37d-70c0-179a-e053-3705fe0a4cff 122
Thick Filament Length Changes in Muscle Have Both Elastic and Structural Components, file e398c37e-53f9-179a-e053-3705fe0a4cff 116
Orthovanadate and orthophosphate inhibit muscle force via two different pathways of the myosin ATPase cycle, file e398c378-cbc0-179a-e053-3705fe0a4cff 115
Low-force transitions in single titin molecules reflect a memory of contractile history, file e398c37a-9042-179a-e053-3705fe0a4cff 105
Motion of myosin head domains during activation and force development in skeletal muscle, file e398c378-b6fd-179a-e053-3705fe0a4cff 97
Orthophosphate increases the efficiency of slow muscle-myosin isoform in the presence of omecamtiv mecarbil, file e398c37f-656a-179a-e053-3705fe0a4cff 69
Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing, file e398c380-b7dc-179a-e053-3705fe0a4cff 68
Piconewton-millisencond force steps reveal the transition kinetics and mechanism of the double stranded DNA elongation, file e398c378-cbc9-179a-e053-3705fe0a4cff 54
Muscle thixotropy: more than just cross-bridges?, file e398c37a-9849-179a-e053-3705fe0a4cff 50
Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing, file e398c380-b7dd-179a-e053-3705fe0a4cff 47
An integrated in vitro and in situ study of kinetics ofmyosin II from frog skeletal muscle, file e398c378-bfd5-179a-e053-3705fe0a4cff 38
Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments, file e398c382-2ec5-179a-e053-3705fe0a4cff 31
Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal muscle, file e398c37b-b489-179a-e053-3705fe0a4cff 29
An integrated in vitro and in situ study of kinetics ofmyosin II from frog skeletal muscle, file e398c378-bfd6-179a-e053-3705fe0a4cff 28
Response to 'Crossbridge recruitment by stretching does not invalidate force spectroscopy experiments in living skeletal muscle fibres, file e398c378-b1b6-179a-e053-3705fe0a4cff 26
The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site., file e398c37a-0bcd-179a-e053-3705fe0a4cff 19
Titin activates myosin filaments in skeletal muscle by switching from an extensible spring to a mechanical rectifier, file 67e16619-b06c-41f6-b19d-02c9fc1fbda8 16
Review: The XXXIII European Muscle Coference: Elba Sept. 04., file e398c378-8948-179a-e053-3705fe0a4cff 13
Low-force transitions in single titin molecules reflect a memory of contractile history, file e398c37b-5157-179a-e053-3705fe0a4cff 11
Motion of myosin head domains during activation and force development in skeletal muscle, file e398c378-b6fe-179a-e053-3705fe0a4cff 8
Piconewton-millisencond force steps reveal the transition kinetics and mechanism of the double stranded DNA elongation, file e398c378-cbca-179a-e053-3705fe0a4cff 6
Myosin filament activation in the heart is tuned to the mechanical task, file e398c37b-aeea-179a-e053-3705fe0a4cff 5
Myosin motors that cannot bind actin leave their folded OFF state on activation of skeletal muscle, file e398c381-8933-179a-e053-3705fe0a4cff 5
Orthovanadate and orthophosphate inhibit muscle force via two different pathways of the myosin ATPase cycle, file e398c378-cbc2-179a-e053-3705fe0a4cff 4
Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments, file e398c379-a9ed-179a-e053-3705fe0a4cff 4
New techniques in linear and non-linear laser optics in muscle research., file e398c378-8d1d-179a-e053-3705fe0a4cff 2
Probing myosin structural conformation in vivo by second-harmonic generation microscopy., file e398c378-ba91-179a-e053-3705fe0a4cff 2
Mechanics of myosin function in white muscle fibres of the dogfish Scyliorhinus canicula, file e398c378-de4e-179a-e053-3705fe0a4cff 2
Sarcomere-length dependence of myosin filament structure in skeletal muscle fibres of the frog, file e398c37a-123b-179a-e053-3705fe0a4cff 2
The non-linear elasticity of the muscle sarcomere and the compliance of myosin motors, file e398c37a-123d-179a-e053-3705fe0a4cff 2
Contracting striated muscle has a dynamic I-band spring with an undamped stiffness 100 times larger than the passive stiffness, file e398c37e-f176-179a-e053-3705fe0a4cff 2
Structural changes in myosin motors and filaments during relaxation of skeletal muscle, file e398c378-c545-179a-e053-3705fe0a4cff 1
Mechanics of myosin function in white muscle fibres of the dogfish Scyliorhinus canicula, file e398c378-d6d9-179a-e053-3705fe0a4cff 1
The myofilament elasticity and its effect on kinetics of force generation by the myosin motor, file e398c378-f478-179a-e053-3705fe0a4cff 1
Is muscle powered by springs or motors?, file e398c37a-a7ac-179a-e053-3705fe0a4cff 1
The force and stiffness of myosin motors in the isometric twitch of a cardiac trabecula and the effect of the extracellular calcium concentration, file e398c37d-b2e9-179a-e053-3705fe0a4cff 1
Totale 2.870
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Categoria #
all - tutte 5.859
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 5.859
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019192 0 0 0 0 0 0 0 0 0 47 85 60
2019/2020611 57 44 23 54 74 70 49 61 73 37 35 34
2020/2021473 31 44 42 26 38 44 43 45 28 26 50 56
2021/2022598 62 33 51 65 58 21 29 22 33 24 143 57
2022/2023459 24 23 136 76 24 35 69 13 15 16 24 4
2023/2024123 4 4 22 12 18 6 18 24 7 8 0 0
Totale 2.870