IRIS
SORRENTINO, VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 21.246
EU - Europa 14.016
AS - Asia 7.412
SA - Sud America 1.063
AF - Africa 267
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 44.039
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Nazione #
US - Stati Uniti d'America 21.012
GB - Regno Unito 3.321
CN - Cina 2.789
IT - Italia 2.517
RU - Federazione Russa 2.342
SG - Singapore 2.234
IE - Irlanda 1.682
UA - Ucraina 1.103
BR - Brasile 880
SE - Svezia 822
FR - Francia 737
DE - Germania 724
VN - Vietnam 665
HK - Hong Kong 583
KR - Corea 379
FI - Finlandia 353
IN - India 145
BD - Bangladesh 134
CA - Canada 131
TR - Turchia 130
ZA - Sudafrica 114
ES - Italia 92
AR - Argentina 71
NL - Olanda 69
JP - Giappone 63
MX - Messico 54
PL - Polonia 53
NG - Nigeria 47
BE - Belgio 45
IQ - Iraq 43
ID - Indonesia 36
EC - Ecuador 30
AT - Austria 29
CI - Costa d'Avorio 28
SA - Arabia Saudita 25
AU - Australia 24
VE - Venezuela 23
PK - Pakistan 21
KE - Kenya 20
RO - Romania 18
CO - Colombia 17
IR - Iran 17
MA - Marocco 17
CL - Cile 16
AE - Emirati Arabi Uniti 15
NP - Nepal 15
CH - Svizzera 13
EG - Egitto 13
LT - Lituania 13
UZ - Uzbekistan 13
AZ - Azerbaigian 12
CZ - Repubblica Ceca 12
JO - Giordania 10
PY - Paraguay 10
SK - Slovacchia (Repubblica Slovacca) 10
UY - Uruguay 10
MY - Malesia 9
TW - Taiwan 9
CR - Costa Rica 8
HU - Ungheria 8
IL - Israele 8
JM - Giamaica 8
SY - Repubblica araba siriana 8
TN - Tunisia 8
GR - Grecia 7
RS - Serbia 7
SN - Senegal 7
TT - Trinidad e Tobago 7
ET - Etiopia 6
OM - Oman 6
PA - Panama 6
PT - Portogallo 6
AL - Albania 5
DO - Repubblica Dominicana 5
LV - Lettonia 5
BG - Bulgaria 4
DK - Danimarca 4
GT - Guatemala 4
HN - Honduras 4
KG - Kirghizistan 4
KZ - Kazakistan 4
LU - Lussemburgo 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
PH - Filippine 4
PS - Palestinian Territory 4
TH - Thailandia 4
AM - Armenia 3
EU - Europa 3
GE - Georgia 3
HR - Croazia 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
PE - Perù 3
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
BO - Bolivia 2
GD - Grenada 2
KW - Kuwait 2
Totale 44.016
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Città #
Fairfield 2.942
Southend 2.904
Dallas 2.123
Ashburn 1.718
Dublin 1.667
Woodbridge 1.369
Singapore 1.198
Seattle 1.155
Chandler 1.120
Wilmington 1.094
Houston 1.044
Cambridge 1.020
Jacksonville 898
Ann Arbor 683
Milan 678
Moscow 667
Beijing 657
Santa Clara 607
Hong Kong 556
Siena 549
San Jose 446
Hefei 414
Seoul 376
The Dalles 364
Nanjing 327
Princeton 311
Council Bluffs 269
Rome 221
Los Angeles 206
Ho Chi Minh City 199
Lauterbourg 178
Boardman 163
San Diego 148
Helsinki 145
New York 141
Florence 125
Hanoi 123
Menlo Park 118
Buffalo 116
Columbus 113
Nanchang 109
Munich 100
Johannesburg 94
Shenyang 86
San Mateo 84
Dong Ket 82
London 82
Izmir 80
Lancaster 77
São Paulo 77
Shanghai 72
Tianjin 66
Tokyo 55
Figino 51
Toronto 51
Hebei 50
Orem 50
Changsha 49
Kunming 48
San Francisco 47
Málaga 46
Dearborn 45
Washington 45
Frankfurt am Main 43
Warsaw 43
Abuja 41
Jiaxing 40
Hangzhou 39
Zhengzhou 39
Haiphong 38
Brussels 36
Turin 35
Bengaluru 34
Atlanta 31
Brooklyn 31
Phoenix 31
Chicago 30
Jinan 30
Rio de Janeiro 30
Guangzhou 29
Abidjan 28
Da Nang 27
Chennai 26
Denver 25
Norwalk 25
Redondo Beach 25
Montreal 24
Stockholm 24
Venezia 24
Düsseldorf 23
Ningbo 23
Redwood City 23
Belo Horizonte 21
Jakarta 21
Nuremberg 20
Sovicille 19
Amsterdam 18
Brasília 17
Manchester 17
Ankara 16
Totale 31.744
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Nome #
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 472
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 403
Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers 394
A Rett syndrome MECP2 mutation that causes mental retardation in men 375
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 369
A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects 365
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b 356
Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers 353
Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice 348
A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush 344
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q) 337
Not all pericytes are born equal: Pericytes from human adult tissues present different differentiation properties 335
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia 323
The potential of obscurin as a therapeutic target in muscle disorders 312
A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene 311
Yip1B isoform is localized at ER-Golgi intermediate and cis-Golgi compartments and is not required for maintenance of the Golgi structure in skeletal muscle 310
Multi-potent progenitors in freshly isolated and cultured human mesenchymal stem cells: a comparison between adipose and dermal tissue 310
Calcium Homeostasis Is Modified in Skeletal Muscle Fibers of Small Ankyrin1 Knockout Mice 309
Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers 307
Tissue-Specific Cultured Human Pericytes: Perivascular Cells from Smooth Muscle Tissue Have Restricted Mesodermal Differentiation Ability 306
Calsequestrin, a key protein in striated muscle health and disease 306
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles 305
Constant expression of hexose-6-phosphate dehydrogenase during differentiation of human adipose-derived mesenchymal stem cells 303
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 301
Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channels 297
Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle 293
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates 293
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres 292
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy 292
Human pericytes isolated from adipose tissue have better differentiation abilities than their mesenchymal stem cell counterparts 291
Pluripotency regulators in human mesenchymal stem cells: expression of NANOG but not of OCT-4 and SOX-2 290
Identification of cancer stem cells from human glioblastomas: growth and differentiation capabilities and CD133/prominin-1 expression 289
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication 289
Ca2+ release induced by cyclic ADP ribose in mice lacking type 3 ryanodine receptor 284
Functional electrical stimulation: A possible strategy to improve muscle function in central core disease? 284
The sarcoplasmic reticulum: an organized patchwork of specialized domains 283
Ameliorating effects of the immunomodulator 3-(2-ethylphenyl)-5-(3-methoxyphenyl)-1H-1,2,4-triazole in an experimental model of colitis in the rat 283
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients 281
Alteration in calcium handling at the subcellular level in mdx myotubes 276
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene 275
Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity 274
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study 272
Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum 272
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 270
Compound heterozygosity in the GALC gene in a late onset Iranian patient with spastic paraparesis, peripheral neuropathy and leukoencephalopathy 269
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome) 269
The Sarcoplasmic Reticulum of Skeletal Muscle Cells: A Labyrinth of Membrane Contact Sites 269
MECP2 mutation in male patients with non-specific X-linked mental retardation 266
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning 261
C-myc gene effects on cell growth and transformation 260
Molecular interactions with obscurin are involved in the localization of muscle-specific small ankyrin1 isoforms to subcompartments of the sarcoplasmic reticulum 259
The 12 kDa FK506-binding protein, FKBP12, modulates the Ca(2+)-flux properties of the type-3 ryanodine receptor 258
Calcium pools in Ehrlich carcinoma cells. A major, high affinity Ca2+ pool is sensitive to both inositol 1,4,5-trisphosphate and thapsigargin 257
A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells 257
Putative endothelial progenitor cells predict long-term mortality in type-2 diabetes 253
Junctophilin 1 and 2 proteins interact with the L-type Ca2+ channel dihydropyridine receptors (DHPRs) in skeletal muscle 253
Metyrapone prevents cortisone-induced preadipocyte differentiation by depleting luminal NADPH of the endoplasmic reticulum 250
Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain 249
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 247
Levels of circulating CXCR4-positive cells are decreased and negatively correlated with risk factors in cardiac transplant recipients 245
Impaired Intracellular Ca2+ Dynamics, M-Band and Sarcomere Fragility in Skeletal Muscles of Obscurin KO Mice 245
SCN1A mutation associated with atypical Panayiotopoulos syndrome 243
Generalised reduction of putative endothelial progenitors and CXCR4-positive peripheral blood cells in type 2 diabetes. 243
Induction and/or selective retention of proteins in mammalian cells exposed to cycloheximide 242
Mesenchymal stem cells: from the perivascular environment to clinical applications 242
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c 242
The KSR2-calcineurin complex regulates STIM1-ORAI1 dynamics and Store-Operated Calcium Entry (SOCE) 241
Expression of growth arrest-specific (gas) genes in senescent murine cells 236
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene 235
Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T 233
Ca2+ sparks and waves in canine purkinje cells: a triple layered system of Ca2+ activation 232
A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids 232
Properties of ryanodine receptor in rat muscles submitted to unloaded conditions 231
Expression and functional activity of ryanodine receptors (RyRs) during skeletal muscle development 231
Murine obscurin and Obsl1 have functionally redundant roles in sarcolemmal integrity, sarcoplasmic reticulum organization, and muscle metabolism 229
A human amniotic cell line yielding high titres of human fibroblast interferon 228
Muscle Research and Gene Ontology: New standards for improved data integration 228
Mutations in the RYR1 gene in Italian patients at risk for malignant hyperthermia: evidence for a cluster of novel mutations in the C-terminal region 228
RYR2 proteins contribute to the formation of Ca(2+) sparks in smooth muscle 227
Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors 227
Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis 227
Bcl-2 binds to and inhibits ryanodine receptors 226
Ryanodine receptors are expressed and functionally active in mouse spermatogenic cells and their inhibition interferes with spermatogonial differentiation 225
Assembly and dynamics of proteins of the longitudinal and junctional sarcoplasmic reticulum in skeletal muscle cells 224
Cardiac expression of ryanodine receptor subtype 3; a strategic component in the intracellular Ca2 + release system of Purkinje fibers in large mammalian heart 223
Homer proteins and InsP(3) receptors co-localise in the longitudinal sarcoplasmic reticulum of skeletal muscle fibres 221
A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum 219
Cell proliferation inhibited by MyoD1 independently of myogenic differentiation 218
From growth arrest to growth suppression 218
ATP-induced activation of expressed RyR3 at low free calcium 217
Intracellular membrane contact sites in skeletal muscle cells 216
CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy 215
Evidence for the transport of glutathione through ryanodine receptor channel type 1 215
The conserved sites for the FK506-binding proteins in ryanodine receptors and inositol 1,4,5-trisphosphate receptors are structurally and functionally different 214
Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia 213
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization 211
Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing? 210
Functional properties of the ryanodine receptor type 3 (RyR3) Ca2+ release channel 210
Structure and mutation analysis of the glycogen storage disease type 1b gene 209
Sarcoplasmic reticulum: structural determinants and protein dynamics 209
Totale 26.991
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Categoria #
all - tutte 133.255
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 133.255
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021305 0 0 0 0 0 0 0 0 0 0 0 305
2021/20222.784 206 358 139 153 120 77 234 240 217 240 239 561
2022/20233.831 223 289 528 519 415 732 84 298 462 88 103 90
2023/20242.399 109 53 195 112 91 737 851 40 16 37 14 144
2024/20255.001 108 272 422 296 557 232 159 383 410 185 646 1.331
2025/202612.626 978 1.867 1.720 1.304 2.115 526 1.197 350 513 580 338 1.138
Totale 44.311