BONCOMPAGNI, SIMONA
 Distribuzione geografica
Continente #
NA - Nord America 4.166
AS - Asia 2.674
EU - Europa 2.460
SA - Sud America 302
AF - Africa 42
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 9.654
Nazione #
US - Stati Uniti d'America 4.068
SG - Singapore 1.033
CN - Cina 760
IT - Italia 478
IE - Irlanda 348
UA - Ucraina 298
RU - Federazione Russa 291
SE - Svezia 277
VN - Vietnam 262
BR - Brasile 249
TR - Turchia 241
GB - Regno Unito 223
FR - Francia 186
DE - Germania 175
IN - India 130
HK - Hong Kong 72
FI - Finlandia 68
BD - Bangladesh 48
CA - Canada 48
MX - Messico 33
JP - Giappone 24
ZA - Sudafrica 22
PL - Polonia 19
IQ - Iraq 18
AR - Argentina 17
BE - Belgio 17
AT - Austria 16
ES - Italia 15
VE - Venezuela 14
KR - Corea 12
NL - Olanda 11
SA - Arabia Saudita 11
PK - Pakistan 10
CZ - Repubblica Ceca 8
IR - Iran 8
EC - Ecuador 7
LT - Lituania 7
AU - Australia 6
CL - Cile 6
UZ - Uzbekistan 6
EG - Egitto 5
IL - Israele 5
MA - Marocco 5
PH - Filippine 5
CO - Colombia 4
EU - Europa 4
ID - Indonesia 4
KZ - Kazakistan 4
NI - Nicaragua 4
NO - Norvegia 4
OM - Oman 4
GR - Grecia 3
JM - Giamaica 3
MY - Malesia 3
SN - Senegal 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AO - Angola 2
BO - Bolivia 2
CH - Svizzera 2
CR - Costa Rica 2
DZ - Algeria 2
EE - Estonia 2
JO - Giordania 2
PE - Perù 2
PT - Portogallo 2
RO - Romania 2
RS - Serbia 2
AZ - Azerbaigian 1
BG - Bulgaria 1
BZ - Belize 1
CG - Congo 1
CU - Cuba 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GE - Georgia 1
GP - Guadalupe 1
HN - Honduras 1
KE - Kenya 1
LB - Libano 1
LV - Lettonia 1
ML - Mali 1
MN - Mongolia 1
NP - Nepal 1
PA - Panama 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 9.654
Città #
Singapore 749
San Jose 579
Chandler 509
Jacksonville 371
Dublin 341
Ashburn 250
Beijing 223
Dearborn 215
Dallas 159
Princeton 149
Izmir 134
Southend 134
Nanjing 112
Chieti 102
Council Bluffs 91
Ho Chi Minh City 90
Los Angeles 89
The Dalles 86
Ann Arbor 82
Altamura 77
Santa Clara 75
Wilmington 70
Hong Kong 69
Boardman 58
Cambridge 57
New York 48
Dong Ket 44
Nanchang 44
Hanoi 42
Buffalo 40
Tongling 40
São Paulo 34
Pescara 32
Shenyang 29
Munich 28
Woodbridge 28
Moscow 27
Redondo Beach 22
Tokyo 20
Nuremberg 19
Teramo 19
Kunming 18
Hefei 17
Brussels 16
Changsha 16
Hebei 16
Mexico City 16
Orem 16
Phoenix 16
Tianjin 16
Houston 15
San Mateo 15
Toronto 15
Warsaw 15
Chennai 14
Jiaxing 14
Milan 14
Rome 14
Frankfurt am Main 13
Lappeenranta 13
Montreal 13
Poplar 13
Boston 12
Seoul 12
Ankara 11
Augusta 11
Denver 11
Johannesburg 11
Padova 11
Brooklyn 10
Chicago 10
Dhaka 10
Falls Church 10
Helsinki 10
Redwood City 10
Washington 10
Baghdad 9
Leawood 9
London 9
Mumbai 9
Seattle 9
Shanghai 9
Stockholm 9
Belo Horizonte 8
Manchester 8
Norwalk 8
Rio de Janeiro 8
Vienna 8
Brno 7
Haiphong 7
Jinan 7
Perugia 7
Philadelphia 7
Atlanta 6
Auburn Hills 6
Bắc Ninh 6
Can Tho 6
Changchun 6
Hangzhou 6
Lanzhou 6
Totale 6.031
Nome #
Exercise-dependent formation of new junctions that promote STIM1-Orai1 assembly in skeletal muscle 195
Novel zwitterionic Natural Deep Eutectic Solvents as environmentally friendly media for spontaneous self-assembly of gold nanoparticles 183
Gold nanoparticles as scaffolds for poor water soluble and difficult to vehiculate antiparkinson codrugs 180
Aerobic Training Prevents Heatstrokes in Calsequestrin-1 Knockout Mice by Reducing Oxidative Stress 175
Addendum: Exercise-dependent formation of new junctions that promote STIM1-Orai1 assembly in skeletal muscle 172
A sub-population of rat muscle fibers maintains an assessable excitation-contraction coupling mechanism after long-standing denervation, despite lost contractility 166
Strenuous exercise triggers a life-threatening response in mice susceptible to malignant hyperthermia 162
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene ( RYR2) 160
Age-dependent uncoupling of mitochondria from Ca2+ release units in skeletal muscle 160
Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity 158
Growth associated protein 43 is expressed in skeletal muscle fibers and is localized in proximity of mitochondria and calcium release units. 156
Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy 155
Age-dependent oxidative stress and functional capacity of human skeletal muscle satellite cells 150
The mitochondrial calcium uniporter controls skeletal muscle trophism in vivo 149
Antioxidant Treatment Reduces Formation of Structural Cores and Improves Muscle Function in RYR1 Y522S/WT Mice 149
Estrogens Protect Calsequestrin-1 Knockout Mice from Lethal Hyperthermic Episodes by Reducing Oxidative Stress in Muscle 145
The contribution of reactive oxygen species to sarcopenia and muscle ageing 142
THE NEURONAL GROWTH ASSOCIATED PROTEIN 43 IS EXPRESSED IN SKELETAL MUSCLE FIBERS CLOSE TO MITOCHONDRIA AND CALCIUM RELEASE UNITS. 142
Muscle activity prevents the uncoupling of mitochondria from Ca2+ Release Units induced by ageing and disuse 141
Gold nanoparticles as scaffolds for new antiparkinson prodrugs 140
Membrane glucocorticoid receptors are localised in the extracellular matrix and signal through the MAPK pathway in mammalian skeletal muscle fibres 140
Muscle Expression of SOD1 G93A Triggers the Dismantlement of Neuromuscular Junction via PKC-Theta 139
Persistent Muscle Fiber Regeneration in Long Term Denervation. Past, Present, Future 137
Progressive disorganization of the excitation-contraction coupling apparatus in ageing human skeletal muscle as revealed by electron microscopy: A possible role in the decline of muscle performance 135
Atrophy, but not necrosis, in rabbit skeletal muscle denervated for periods up to one year. 135
Kinetic evaluation of the effect of layer by layer deposition of polyeletrolytes on the stability of POPC liposomes 134
Mechanical parameters of the molecular motor myosin II determined in permeabilised fibres from slow and fast skeletal muscles of the rabbit 133
Role of Mitofusin-2 in mitochondrial localization and calcium uptake in skeletal muscle 132
Effects of chronic electrical stimulation on long-term denervated muscles of the rabbit hind limb 132
Unexpected structural and functional consequences of the R33Q homozygous mutation in cardiac calsequestrin. A complex arrhythmogenic cascade in a knock-in mouse model. 131
Home-based functional electrical stimulation rescues permanently denervated muscles in paraplegic patients with complete lower motor neuron lesion. 131
Liposomes entrapping β-cyclodextrin/ibuprofen inclusion complex: Role of the host and the guest on the bilayer integrity and microviscosity 131
Calcium entry units (CEUs): perspectives in skeletal muscle function and disease 129
Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction 129
An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. 126
Single Delivery of an Adeno-Associated Viral Construct to Transfer the CASQ2 Gene to Knock-In Mice Affected by Catecholaminergic Polymorphic Ventricular Tachycardia Is Able to Cure the Disease From Birth to Advanced Age 125
Pre-assembled Ca2+ entry units and constitutively active Ca2+ entry in skeletal muscle of calsequestrin-1 knockout mice 125
Long-Term Exercise Reduces Formation of Tubular Aggregates and Promotes Maintenance of Ca 2+ Entry Units in Aged Muscle 121
Mitochondria are linked to calcium stores in striated muscle by developmentally regulated tethering structures 119
Sequential stages in the gradual formation and accumulation of tubular aggregates in aging fast twitch muscle: SERCA and Calsequestrin involvement. 119
Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin-1. 118
Mitochondrial superoxide flashes: metabolic biomarkers of skeletal muscle activity and disease 117
Atrophy-resistant fibers in permanent peripheral denervation of human skeletal muscle. 116
Lifelong Physical Exercise Delays Age-Associated Skeletal Muscle Decline. 116
DRP1-mediated mitochondrial shape controls calcium homeostasis and muscle mass 116
Role of STIM1/ORAI1-mediated store-operated Ca2+ entry in skeletal muscle physiology and disease 115
Abnormal Propagation of Calcium Waves and Ultrastructural Remodeling in Recessive Catecholaminergic Polymorphic Ventricular Tachycardia. 113
Stable muscle atrophy in long-term paraplegics with complete upper motor neuron lesion from 3- to 20-year SCI 112
Characterization and temporal development of cores in a mouse model of malignant hyperthermia. 111
Viral gene transfer rescues arrhythmogenic phenotype and ultrastructural abnormalities in adult calsequestrin-null mice with inherited arrhythmias. 111
Transverse tubule remodeling enhances orai1-dependent Ca2+ entry in skeletal muscle 110
Orai1-dependent calcium entry promotes skeletal muscle growth and limits fatigue 109
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 109
RyR1 S-Nitrosylation Underlies Environmental Heat Stroke and Sudden Death in Y522S RyR1 Knockin Mice 107
The use of CalciumOrange-5N as a specific marker of mitochondrial Ca2+ in mouse skeletal muscle fibers. 106
Ageing Causes Ultrastructural Modification to Calcium Release Units and Mitochondria in Cardiomyocytes 105
Long-term denervation in humans causes degeneration of both contractile and excitation-contraction coupling apparatus, which is reversible by functional electrical stimulation (FES): a role for myofiber regeneration? 103
Structural differentiation of skeletal muscle fibers in absence of innervation in humans. 102
Triadin/Junctin double null mouse reveals a differential role for Triadin and Junctin in anchoring CASQ to the jSR and regulating Ca(2+) homeostasis 102
Fine-tuning of POPC liposomal leakage by the use of β-cyclodextrin and several hydrophobic guests 102
Differential impact of mitochondrial positioning on mitochondrial Ca2+ uptake and Ca2+ spark suppression in skeletal muscle. 101
Constitutive assembly of Ca2+ entry units in soleus muscle from calsequestrin knockout mice 101
Diaphragm Fatigue in SMNΔ7 Mice and Its Molecular Determinants: An Underestimated Issue 100
Layer-by-layer deposition of shortened nanotubes or polyethylene glycol-derivatized nanotubes on liposomes: A tool for increasing liposome stability 98
Sarcoplasmic reticulum-mitochondrial symbiosis: bidirectional signaling in skeletal muscle 98
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 98
SARS-CoV-2 ORF3a accessory protein is a water-permeable channel that induces lysosome swelling 97
Mice expressing T4826I-RYR1 are viable but exhibit sex- andgenotype-dependent susceptibility to malignant hyperthermia and muscle damage. 93
Skeletal muscle mTORC1 regulates neuromuscular junction stability 93
Functional electrical stimulation: A possible strategy to improve muscle function in central core disease? 93
Electron Microscopy (EM) Analysis of Collagen Fibers in the Peri-Implant Soft Tissues around Two Different Abutments 89
The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging. 88
Creatine transporter (SLC6A8) knockout mice exhibit reduced muscle performance, disrupted mitochondrial Ca2+ homeostasis, and severe muscle atrophy 86
Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation 83
Post-natal heart adaptation in a knock-in mouse model of calsequestrin 2-linked recessive catecholaminergic polymorphic ventricular tachycardia 81
Physical and functional cross talk between endo-sarcoplasmic reticulum and mitochondria in skeletal muscle 80
Mitochondrial dysfunction in skeletal muscle of amyloid precursor protein-overexpressing mice 79
The evolution of the mitochondria-to-calcium release units relationship in vertebrate skeletal muscles. 77
SEPN1-related myopathy depends on the oxidoreductase ERO1A and is druggable with the chemical chaperone TUDCA 76
Ablation of palladin in adult heart causes dilated cardiomyopathy associated with intercalated disc abnormalities 73
An Orai1 gain-of-function tubular aggregate myopathy mouse model phenocopies key features of the human disease 71
Improper Remodeling of Organelles Deputed to Ca 2+ Handling and Aerobic ATP Production Underlies Muscle Dysfunction in Ageing 71
Loss of Calpain 3 dysregulates store‐operated calcium entry and its exercise response in mice 70
An aged-related structural study of DHPR tetrads in peripheral couplings of human skeletal muscle 70
Parvalbumin affects skeletal muscle trophism through modulation of mitochondrial calcium uptake 62
Mitochondria can substitute for parvalbumin to lower cytosolic calcium levels in the murine fast skeletal muscle 59
Program with last minute abstracts of the Padua Days on Muscle and Mobility Medicine, 27 February – 2 March, 2024 (2024Pdm3) 27
Effects of Titanium Dioxide Nanoparticles on Porcine Prepubertal Sertoli Cells: An “In Vitro” Study 21
Ergothioneine supplementation improves pup phenotype and survival in a murine model of spinal muscular atrophy 13
"Balancing" children’s physical risks: relationship between balance and risk propensity in developmental age of an Italian children group 11
Correction: Gambelunghe et al. Redox-Sensitive Glyoxalase 1 Up-Regulation Is Crucial for Protecting Human Lung Cells from Gold Nanoparticles Toxicity. Antioxidants 2020, 9, 697 10
Totale 10.252
Categoria #
all - tutte 41.359
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 41.359


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202171 0 0 0 0 0 0 0 0 0 0 0 71
2021/2022441 10 20 2 114 26 12 12 31 21 19 48 126
2022/20231.324 107 191 54 171 135 228 68 96 185 13 39 37
2023/2024514 37 26 41 26 24 144 125 11 4 16 6 54
2024/20251.398 76 203 152 40 35 78 103 87 145 92 188 199
2025/20263.470 243 201 309 367 281 194 664 188 395 337 173 118
Totale 10.252