IRIS
SORRENTINO, VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 23.220
EU - Europa 14.239
AS - Asia 7.527
SA - Sud America 1.172
Continente sconosciuto - Info sul continente non disponibili 277
AF - Africa 270
OC - Oceania 31
AN - Antartide 1
Totale 46.737
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Nazione #
US - Stati Uniti d'America 22.927
GB - Regno Unito 3.369
CN - Cina 2.806
IT - Italia 2.665
RU - Federazione Russa 2.342
SG - Singapore 2.258
IE - Irlanda 1.683
UA - Ucraina 1.105
BR - Brasile 914
SE - Svezia 824
FR - Francia 738
DE - Germania 724
VN - Vietnam 670
HK - Hong Kong 590
KR - Corea 380
FI - Finlandia 353
BD - Bangladesh 158
CA - Canada 156
IN - India 148
TR - Turchia 131
ZA - Sudafrica 114
ES - Italia 92
AR - Argentina 82
NL - Olanda 72
JP - Giappone 64
MX - Messico 57
EC - Ecuador 54
PL - Polonia 53
CO - Colombia 49
NG - Nigeria 47
BE - Belgio 46
IQ - Iraq 43
ID - Indonesia 40
VE - Venezuela 30
AT - Austria 29
CI - Costa d'Avorio 28
SA - Arabia Saudita 25
AU - Australia 24
PK - Pakistan 23
KE - Kenya 22
RO - Romania 20
AE - Emirati Arabi Uniti 18
NP - Nepal 18
IR - Iran 17
MA - Marocco 17
CH - Svizzera 16
CL - Cile 16
CR - Costa Rica 15
UZ - Uzbekistan 14
EG - Egitto 13
JM - Giamaica 13
LT - Lituania 13
MY - Malesia 13
AZ - Azerbaigian 12
CZ - Repubblica Ceca 12
EE - Estonia 11
PY - Paraguay 11
TH - Thailandia 11
JO - Giordania 10
SK - Slovacchia (Repubblica Slovacca) 10
UY - Uruguay 10
HN - Honduras 9
IL - Israele 9
TT - Trinidad e Tobago 9
TW - Taiwan 9
GT - Guatemala 8
HU - Ungheria 8
PH - Filippine 8
RS - Serbia 8
SY - Repubblica araba siriana 8
TN - Tunisia 8
GR - Grecia 7
SN - Senegal 7
ET - Etiopia 6
OM - Oman 6
PA - Panama 6
PT - Portogallo 6
AL - Albania 5
DO - Repubblica Dominicana 5
KG - Kirghizistan 5
LV - Lettonia 5
NI - Nicaragua 5
AM - Armenia 4
BG - Bulgaria 4
DK - Danimarca 4
KZ - Kazakistan 4
LU - Lussemburgo 4
NZ - Nuova Zelanda 4
PS - Palestinian Territory 4
EU - Europa 3
GE - Georgia 3
HR - Croazia 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
MM - Myanmar 3
PE - Perù 3
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BH - Bahrain 2
Totale 46.430
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Città #
Fairfield 2.942
Southend 2.904
Dallas 2.140
Ashburn 2.067
Dublin 1.669
Woodbridge 1.372
Singapore 1.213
Seattle 1.160
Chandler 1.120
Wilmington 1.097
Houston 1.054
Cambridge 1.020
Jacksonville 899
Milan 705
San Jose 697
Santa Clara 691
Ann Arbor 683
Moscow 667
Beijing 664
Hong Kong 561
Siena 549
Council Bluffs 499
Hefei 414
Seoul 377
The Dalles 368
Nanjing 327
Princeton 311
Rome 235
Los Angeles 228
Ho Chi Minh City 201
Lauterbourg 178
Boardman 174
New York 169
San Diego 151
Columbus 149
Florence 146
Helsinki 145
Buffalo 124
Hanoi 123
Menlo Park 118
Nanchang 109
Munich 100
Johannesburg 94
Shenyang 86
London 85
San Mateo 84
Dong Ket 82
Lancaster 81
Izmir 80
São Paulo 80
Shanghai 73
Tianjin 66
Tokyo 56
Figino 55
Toronto 55
Hebei 50
Orem 50
Changsha 49
Washington 49
Kunming 48
San Francisco 48
Málaga 46
Dearborn 45
Atlanta 43
Chicago 43
Frankfurt am Main 43
Phoenix 43
Warsaw 43
Brooklyn 42
Abuja 41
Jiaxing 40
Haiphong 39
Hangzhou 39
Zhengzhou 39
Brussels 37
Turin 35
Bengaluru 34
Rio de Janeiro 31
Jinan 30
Guangzhou 29
Abidjan 28
Da Nang 27
Chennai 26
Denver 26
Montreal 26
Norwalk 26
Redondo Beach 25
Brasília 24
Stockholm 24
Venezia 24
Düsseldorf 23
Ningbo 23
Redwood City 23
Belo Horizonte 22
Boston 22
Jakarta 21
Las Vegas 20
Newark 20
Nuremberg 20
Sovicille 19
Totale 33.002
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Nome #
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 493
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 417
Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers 410
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 387
A Rett syndrome MECP2 mutation that causes mental retardation in men 385
A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects 377
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b 365
Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers 359
Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice 359
A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush 354
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q) 345
Not all pericytes are born equal: Pericytes from human adult tissues present different differentiation properties 342
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia 336
Calsequestrin, a key protein in striated muscle health and disease 335
A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene 322
Multi-potent progenitors in freshly isolated and cultured human mesenchymal stem cells: a comparison between adipose and dermal tissue 319
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 318
The potential of obscurin as a therapeutic target in muscle disorders 318
Tissue-Specific Cultured Human Pericytes: Perivascular Cells from Smooth Muscle Tissue Have Restricted Mesodermal Differentiation Ability 316
Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers 316
Calcium Homeostasis Is Modified in Skeletal Muscle Fibers of Small Ankyrin1 Knockout Mice 315
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 314
Constant expression of hexose-6-phosphate dehydrogenase during differentiation of human adipose-derived mesenchymal stem cells 314
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles 314
Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle 309
Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channels 309
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates 306
Pluripotency regulators in human mesenchymal stem cells: expression of NANOG but not of OCT-4 and SOX-2 304
Impaired Intracellular Ca2+ Dynamics, M-Band and Sarcomere Fragility in Skeletal Muscles of Obscurin KO Mice 304
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres 302
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy 301
Functional electrical stimulation: A possible strategy to improve muscle function in central core disease? 301
Human pericytes isolated from adipose tissue have better differentiation abilities than their mesenchymal stem cell counterparts 301
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication 300
Identification of cancer stem cells from human glioblastomas: growth and differentiation capabilities and CD133/prominin-1 expression 298
The sarcoplasmic reticulum: an organized patchwork of specialized domains 295
Ca2+ release induced by cyclic ADP ribose in mice lacking type 3 ryanodine receptor 293
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients 292
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 292
Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity 286
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome) 285
Alteration in calcium handling at the subcellular level in mdx myotubes 285
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene 285
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 281
Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum 280
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study 279
The Sarcoplasmic Reticulum of Skeletal Muscle Cells: A Labyrinth of Membrane Contact Sites 279
MECP2 mutation in male patients with non-specific X-linked mental retardation 274
Compound heterozygosity in the GALC gene in a late onset Iranian patient with spastic paraparesis, peripheral neuropathy and leukoencephalopathy 274
Calcium pools in Ehrlich carcinoma cells. A major, high affinity Ca2+ pool is sensitive to both inositol 1,4,5-trisphosphate and thapsigargin 274
C-myc gene effects on cell growth and transformation 274
The 12 kDa FK506-binding protein, FKBP12, modulates the Ca(2+)-flux properties of the type-3 ryanodine receptor 271
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning 271
Molecular interactions with obscurin are involved in the localization of muscle-specific small ankyrin1 isoforms to subcompartments of the sarcoplasmic reticulum 267
A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells 265
Junctophilin 1 and 2 proteins interact with the L-type Ca2+ channel dihydropyridine receptors (DHPRs) in skeletal muscle 264
Putative endothelial progenitor cells predict long-term mortality in type-2 diabetes 262
Metyrapone prevents cortisone-induced preadipocyte differentiation by depleting luminal NADPH of the endoplasmic reticulum 260
Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain 258
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 257
SCN1A mutation associated with atypical Panayiotopoulos syndrome 256
Generalised reduction of putative endothelial progenitors and CXCR4-positive peripheral blood cells in type 2 diabetes. 255
Levels of circulating CXCR4-positive cells are decreased and negatively correlated with risk factors in cardiac transplant recipients 253
CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy 252
Induction and/or selective retention of proteins in mammalian cells exposed to cycloheximide 251
The KSR2-calcineurin complex regulates STIM1-ORAI1 dynamics and Store-Operated Calcium Entry (SOCE) 251
Mesenchymal stem cells: from the perivascular environment to clinical applications 251
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c 250
Expression of growth arrest-specific (gas) genes in senescent murine cells 248
A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids 248
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene 248
Ca2+ sparks and waves in canine purkinje cells: a triple layered system of Ca2+ activation 244
Bcl-2 binds to and inhibits ryanodine receptors 242
Properties of ryanodine receptor in rat muscles submitted to unloaded conditions 241
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 241
Murine obscurin and Obsl1 have functionally redundant roles in sarcolemmal integrity, sarcoplasmic reticulum organization, and muscle metabolism 241
A human amniotic cell line yielding high titres of human fibroblast interferon 240
Muscle Research and Gene Ontology: New standards for improved data integration 239
Expression and functional activity of ryanodine receptors (RyRs) during skeletal muscle development 239
Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors 239
Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T 239
Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis 238
Cardiac expression of ryanodine receptor subtype 3; a strategic component in the intracellular Ca2 + release system of Purkinje fibers in large mammalian heart 237
Homer proteins and InsP(3) receptors co-localise in the longitudinal sarcoplasmic reticulum of skeletal muscle fibres 235
RYR2 proteins contribute to the formation of Ca(2+) sparks in smooth muscle 235
Assembly and dynamics of proteins of the longitudinal and junctional sarcoplasmic reticulum in skeletal muscle cells 232
Ryanodine receptors are expressed and functionally active in mouse spermatogenic cells and their inhibition interferes with spermatogonial differentiation 231
From growth arrest to growth suppression 230
Intracellular membrane contact sites in skeletal muscle cells 230
Cell proliferation inhibited by MyoD1 independently of myogenic differentiation 227
The ryanodine receptor family of intracellular calcium release channels 227
ATP-induced activation of expressed RyR3 at low free calcium 226
A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum 226
Evidence for the transport of glutathione through ryanodine receptor channel type 1 224
Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia 224
The conserved sites for the FK506-binding proteins in ryanodine receptors and inositol 1,4,5-trisphosphate receptors are structurally and functionally different 224
Structure and mutation analysis of the glycogen storage disease type 1b gene 223
Sarcoplasmic reticulum: structural determinants and protein dynamics 223
Functional properties of the ryanodine receptor type 3 (RyR3) Ca2+ release channel 220
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization 219
Totale 28.167
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Categoria #
all - tutte 142.211
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 142.211
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.081 0 0 0 153 120 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
2026/20272.426 697 476 1.240 13 0 0 0 0 0 0 0 0
Totale 46.737