IRIS
SORRENTINO, VINCENZO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 20.811
EU - Europa 13.022
AS - Asia 7.310
SA - Sud America 1.054
AF - Africa 267
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 42.499
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 20.607
GB - Regno Unito 3.320
CN - Cina 2.778
RU - Federazione Russa 2.342
SG - Singapore 2.212
IE - Irlanda 1.682
IT - Italia 1.536
UA - Ucraina 1.103
BR - Brasile 875
SE - Svezia 822
FR - Francia 735
DE - Germania 724
VN - Vietnam 664
HK - Hong Kong 578
KR - Corea 378
FI - Finlandia 353
IN - India 145
TR - Turchia 130
ZA - Sudafrica 114
CA - Canada 109
ES - Italia 89
BD - Bangladesh 81
AR - Argentina 70
NL - Olanda 66
JP - Giappone 61
PL - Polonia 53
MX - Messico 51
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
IR - Iran 17
MA - Marocco 17
CO - Colombia 16
CL - Cile 14
NP - Nepal 14
AE - Emirati Arabi Uniti 13
CH - Svizzera 13
EG - Egitto 13
LT - Lituania 13
UZ - Uzbekistan 13
AZ - Azerbaigian 12
CZ - Repubblica Ceca 11
JO - Giordania 10
PY - Paraguay 10
SK - Slovacchia (Repubblica Slovacca) 10
UY - Uruguay 10
CR - Costa Rica 8
IL - Israele 8
SY - Repubblica araba siriana 8
TN - Tunisia 8
TW - Taiwan 8
GR - Grecia 7
HU - Ungheria 7
JM - Giamaica 7
RS - Serbia 7
SN - Senegal 7
ET - Etiopia 6
MY - Malesia 6
OM - Oman 6
PA - Panama 6
PT - Portogallo 6
AL - Albania 5
LV - Lettonia 5
TT - Trinidad e Tobago 5
DK - Danimarca 4
DO - Repubblica Dominicana 4
GT - Guatemala 4
HN - Honduras 4
KG - Kirghizistan 4
KZ - Kazakistan 4
LU - Lussemburgo 4
NZ - Nuova Zelanda 4
PH - Filippine 4
PS - Palestinian Territory 4
TH - Thailandia 4
AM - Armenia 3
BG - Bulgaria 3
EU - Europa 3
GE - Georgia 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
NI - Nicaragua 3
PE - Perù 3
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
BO - Bolivia 2
GD - Grenada 2
HR - Croazia 2
KW - Kuwait 2
Totale 42.476
Salva come PNG Salva come JPEG
Città #
Fairfield 2.942
Southend 2.904
Dallas 2.116
Ashburn 1.682
Dublin 1.667
Woodbridge 1.368
Singapore 1.193
Seattle 1.153
Chandler 1.120
Wilmington 1.094
Houston 1.041
Cambridge 1.019
Jacksonville 897
Ann Arbor 683
Moscow 667
Beijing 655
Santa Clara 583
Hong Kong 551
Siena 549
Hefei 414
Seoul 376
The Dalles 364
San Jose 348
Nanjing 327
Princeton 311
Council Bluffs 249
Ho Chi Minh City 199
Los Angeles 197
Lauterbourg 178
Boardman 162
San Diego 147
Helsinki 145
Milan 137
New York 127
Hanoi 122
Menlo Park 118
Columbus 112
Buffalo 110
Nanchang 109
Florence 107
Munich 100
Johannesburg 94
Shenyang 86
San Mateo 84
Dong Ket 82
London 81
Izmir 80
Lancaster 77
São Paulo 75
Shanghai 70
Tianjin 66
Rome 62
Tokyo 55
Hebei 50
Changsha 49
Orem 49
Kunming 48
Málaga 46
San Francisco 46
Toronto 46
Dearborn 45
Washington 45
Frankfurt am Main 43
Warsaw 43
Abuja 41
Jiaxing 40
Hangzhou 39
Zhengzhou 39
Haiphong 38
Brussels 36
Bengaluru 34
Jinan 30
Rio de Janeiro 30
Brooklyn 29
Guangzhou 29
Phoenix 29
Abidjan 28
Atlanta 28
Chicago 27
Da Nang 27
Chennai 26
Norwalk 25
Redondo Beach 25
Stockholm 24
Venezia 24
Denver 23
Düsseldorf 23
Ningbo 23
Redwood City 22
Belo Horizonte 21
Jakarta 21
Montreal 20
Nuremberg 20
Sovicille 19
Amsterdam 18
Brasília 17
Manchester 17
Ankara 16
Changchun 16
Poplar 16
Totale 30.705
Salva come PNG Salva come JPEG
Nome #
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 467
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 394
A Rett syndrome MECP2 mutation that causes mental retardation in men 365
Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers 365
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 359
A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects 356
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b 349
Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice 344
Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers 341
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q) 335
A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush 334
Not all pericytes are born equal: Pericytes from human adult tissues present different differentiation properties 327
The potential of obscurin as a therapeutic target in muscle disorders 310
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia 307
A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene 307
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 306
Tissue-Specific Cultured Human Pericytes: Perivascular Cells from Smooth Muscle Tissue Have Restricted Mesodermal Differentiation Ability 302
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 300
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles 300
Calsequestrin, a key protein in striated muscle health and disease 300
Multi-potent progenitors in freshly isolated and cultured human mesenchymal stem cells: a comparison between adipose and dermal tissue 297
Calcium Homeostasis Is Modified in Skeletal Muscle Fibers of Small Ankyrin1 Knockout Mice 295
Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers 294
Constant expression of hexose-6-phosphate dehydrogenase during differentiation of human adipose-derived mesenchymal stem cells 293
Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channels 290
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy 290
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates 289
Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle 288
Human pericytes isolated from adipose tissue have better differentiation abilities than their mesenchymal stem cell counterparts 288
Pluripotency regulators in human mesenchymal stem cells: expression of NANOG but not of OCT-4 and SOX-2 287
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres 285
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 280
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients 279
Identification of cancer stem cells from human glioblastomas: growth and differentiation capabilities and CD133/prominin-1 expression 276
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication 275
Alteration in calcium handling at the subcellular level in mdx myotubes 274
Ca2+ release induced by cyclic ADP ribose in mice lacking type 3 ryanodine receptor 274
Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity 270
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study 269
Functional electrical stimulation: A possible strategy to improve muscle function in central core disease? 267
Compound heterozygosity in the GALC gene in a late onset Iranian patient with spastic paraparesis, peripheral neuropathy and leukoencephalopathy 266
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 266
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene 266
Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum 264
The sarcoplasmic reticulum: an organized patchwork of specialized domains 264
Molecular interactions with obscurin are involved in the localization of muscle-specific small ankyrin1 isoforms to subcompartments of the sarcoplasmic reticulum 258
A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells 256
MECP2 mutation in male patients with non-specific X-linked mental retardation 254
The Sarcoplasmic Reticulum of Skeletal Muscle Cells: A Labyrinth of Membrane Contact Sites 254
Calcium pools in Ehrlich carcinoma cells. A major, high affinity Ca2+ pool is sensitive to both inositol 1,4,5-trisphosphate and thapsigargin 253
The 12 kDa FK506-binding protein, FKBP12, modulates the Ca(2+)-flux properties of the type-3 ryanodine receptor 253
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning 252
C-myc gene effects on cell growth and transformation 250
Putative endothelial progenitor cells predict long-term mortality in type-2 diabetes 249
Metyrapone prevents cortisone-induced preadipocyte differentiation by depleting luminal NADPH of the endoplasmic reticulum 247
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 243
Junctophilin 1 and 2 proteins interact with the L-type Ca2+ channel dihydropyridine receptors (DHPRs) in skeletal muscle 241
Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain 240
SCN1A mutation associated with atypical Panayiotopoulos syndrome 238
Levels of circulating CXCR4-positive cells are decreased and negatively correlated with risk factors in cardiac transplant recipients 237
Mesenchymal stem cells: from the perivascular environment to clinical applications 237
Expression of growth arrest-specific (gas) genes in senescent murine cells 235
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c 234
Impaired Intracellular Ca2+ Dynamics, M-Band and Sarcomere Fragility in Skeletal Muscles of Obscurin KO Mice 233
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene 232
Induction and/or selective retention of proteins in mammalian cells exposed to cycloheximide 232
The KSR2-calcineurin complex regulates STIM1-ORAI1 dynamics and Store-Operated Calcium Entry (SOCE) 231
Generalised reduction of putative endothelial progenitors and CXCR4-positive peripheral blood cells in type 2 diabetes. 229
Murine obscurin and Obsl1 have functionally redundant roles in sarcolemmal integrity, sarcoplasmic reticulum organization, and muscle metabolism 226
Ca2+ sparks and waves in canine purkinje cells: a triple layered system of Ca2+ activation 224
Properties of ryanodine receptor in rat muscles submitted to unloaded conditions 224
A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids 224
RYR2 proteins contribute to the formation of Ca(2+) sparks in smooth muscle 224
Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors 224
Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T 224
Ryanodine receptors are expressed and functionally active in mouse spermatogenic cells and their inhibition interferes with spermatogonial differentiation 223
Bcl-2 binds to and inhibits ryanodine receptors 223
A human amniotic cell line yielding high titres of human fibroblast interferon 222
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome) 222
Expression and functional activity of ryanodine receptors (RyRs) during skeletal muscle development 221
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 220
Cardiac expression of ryanodine receptor subtype 3; a strategic component in the intracellular Ca2 + release system of Purkinje fibers in large mammalian heart 220
Muscle Research and Gene Ontology: New standards for improved data integration 219
Assembly and dynamics of proteins of the longitudinal and junctional sarcoplasmic reticulum in skeletal muscle cells 216
Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis 214
Cell proliferation inhibited by MyoD1 independently of myogenic differentiation 213
Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia 212
Homer proteins and InsP(3) receptors co-localise in the longitudinal sarcoplasmic reticulum of skeletal muscle fibres 211
A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum 211
ATP-induced activation of expressed RyR3 at low free calcium 210
From growth arrest to growth suppression 210
The conserved sites for the FK506-binding proteins in ryanodine receptors and inositol 1,4,5-trisphosphate receptors are structurally and functionally different 210
Functional properties of the ryanodine receptor type 3 (RyR3) Ca2+ release channel 209
Evidence for the transport of glutathione through ryanodine receptor channel type 1 205
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization 205
Probing luminal negative charge in the type 3 ryanodine receptor 204
Structure and mutation analysis of the glycogen storage disease type 1b gene 204
The gas 5 gene shows four alternative splicing patterns without coding for a protein 204
Sarcoplasmic reticulum: structural determinants and protein dynamics 202
cDNA cloning reveales a tissue specific expression of alternatively spliced transcripts of the ryanodine receptor type 3 calcium release channel 199
Totale 26.221
Salva come PNG Salva come JPEG
Categoria #
all - tutte 126.922
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 126.922
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.123 0 0 0 0 0 0 0 0 0 449 369 305
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
2025/202611.083 978 1.867 1.720 1.304 2.115 526 1.197 350 513 513 0 0
Totale 42.768