IRIS
SORRENTINO, VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 19.933
EU - Europa 12.505
AS - Asia 5.982
SA - Sud America 943
AF - Africa 105
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 39.493
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Nazione #
US - Stati Uniti d'America 19.773
GB - Regno Unito 3.278
CN - Cina 2.565
RU - Federazione Russa 2.336
SG - Singapore 1.760
IE - Irlanda 1.681
IT - Italia 1.392
UA - Ucraina 1.098
SE - Svezia 821
BR - Brasile 819
DE - Germania 686
FR - Francia 541
HK - Hong Kong 519
KR - Corea 378
FI - Finlandia 328
VN - Vietnam 269
TR - Turchia 114
CA - Canada 94
IN - India 94
ES - Italia 80
AR - Argentina 55
BD - Bangladesh 50
JP - Giappone 50
NL - Olanda 45
BE - Belgio 44
PL - Polonia 43
MX - Messico 37
ZA - Sudafrica 36
AT - Austria 29
CI - Costa d'Avorio 28
ID - Indonesia 28
EC - Ecuador 22
IQ - Iraq 20
IR - Iran 17
RO - Romania 16
AU - Australia 15
SA - Arabia Saudita 15
AE - Emirati Arabi Uniti 12
MA - Marocco 12
VE - Venezuela 12
EG - Egitto 11
LT - Lituania 11
CZ - Repubblica Ceca 10
PK - Pakistan 10
UZ - Uzbekistan 10
CL - Cile 9
CO - Colombia 9
AZ - Azerbaigian 8
SK - Slovacchia (Repubblica Slovacca) 8
CH - Svizzera 7
CR - Costa Rica 7
HU - Ungheria 7
IL - Israele 7
PY - Paraguay 7
TW - Taiwan 7
UY - Uruguay 7
GR - Grecia 6
PT - Portogallo 6
JO - Giordania 5
KE - Kenya 5
NP - Nepal 5
OM - Oman 5
RS - Serbia 5
TT - Trinidad e Tobago 5
AL - Albania 4
JM - Giamaica 4
LU - Lussemburgo 4
NG - Nigeria 4
NZ - Nuova Zelanda 4
PA - Panama 4
TH - Thailandia 4
BG - Bulgaria 3
DK - Danimarca 3
ET - Etiopia 3
EU - Europa 3
GE - Georgia 3
GT - Guatemala 3
HN - Honduras 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LB - Libano 3
LV - Lettonia 3
PS - Palestinian Territory 3
TN - Tunisia 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
HR - Croazia 2
LA - Repubblica Popolare Democratica del Laos 2
MY - Malesia 2
PE - Perù 2
SY - Repubblica araba siriana 2
AD - Andorra 1
AF - Afghanistan, Repubblica islamica di 1
BB - Barbados 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
GY - Guiana 1
Totale 39.480
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Città #
Fairfield 2.942
Southend 2.904
Dallas 2.109
Dublin 1.666
Ashburn 1.611
Woodbridge 1.368
Seattle 1.153
Chandler 1.120
Wilmington 1.094
Houston 1.040
Cambridge 1.019
Singapore 932
Jacksonville 894
Ann Arbor 683
Moscow 666
Beijing 655
Santa Clara 572
Siena 547
Hong Kong 506
Seoul 376
Hefei 337
Nanjing 327
Princeton 311
The Dalles 206
Los Angeles 170
Council Bluffs 166
Boardman 159
San Diego 147
Helsinki 126
Menlo Park 118
New York 118
Milan 114
Columbus 112
Buffalo 109
Nanchang 109
Munich 99
Shenyang 86
Florence 85
San Mateo 84
Dong Ket 82
Izmir 77
Lancaster 77
London 76
Ho Chi Minh City 74
São Paulo 71
Shanghai 69
Tianjin 66
Rome 55
Hebei 50
Changsha 49
Kunming 48
Málaga 46
Dearborn 45
San Francisco 44
Tokyo 44
Toronto 43
Washington 43
Jiaxing 40
Hangzhou 39
Zhengzhou 39
Warsaw 37
Brussels 35
Bengaluru 33
Hanoi 30
Jinan 30
Brooklyn 29
Abidjan 28
Rio de Janeiro 28
Atlanta 27
Guangzhou 27
Phoenix 27
Norwalk 25
Redondo Beach 25
Chicago 24
Venezia 24
Ningbo 23
Stockholm 23
Denver 22
Düsseldorf 22
Redwood City 22
Belo Horizonte 21
Johannesburg 21
Frankfurt am Main 20
Sovicille 19
Jakarta 17
Orem 17
Brasília 16
Changchun 16
Montreal 16
Nuremberg 16
Poplar 16
Porto Alegre 16
Padova 15
Turku 15
Vienna 14
Ankara 13
Taizhou 12
Biên Hòa 11
Campinas 11
Lanzhou 11
Totale 28.871
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Nome #
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 427
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 372
A Rett syndrome MECP2 mutation that causes mental retardation in men 345
Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers 341
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b 339
A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects 333
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 330
Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice 327
Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers 319
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q) 317
A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush 312
Not all pericytes are born equal: Pericytes from human adult tissues present different differentiation properties 310
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 296
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia 296
A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene 295
The potential of obscurin as a therapeutic target in muscle disorders 288
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 287
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles 287
Tissue-Specific Cultured Human Pericytes: Perivascular Cells from Smooth Muscle Tissue Have Restricted Mesodermal Differentiation Ability 286
Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channels 277
Constant expression of hexose-6-phosphate dehydrogenase during differentiation of human adipose-derived mesenchymal stem cells 277
Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle 274
Pluripotency regulators in human mesenchymal stem cells: expression of NANOG but not of OCT-4 and SOX-2 273
Calcium Homeostasis Is Modified in Skeletal Muscle Fibers of Small Ankyrin1 Knockout Mice 273
Human pericytes isolated from adipose tissue have better differentiation abilities than their mesenchymal stem cell counterparts 273
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres 272
Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers 272
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates 270
Multi-potent progenitors in freshly isolated and cultured human mesenchymal stem cells: a comparison between adipose and dermal tissue 267
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication 266
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 265
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy 265
Calsequestrin, a key protein in striated muscle health and disease 265
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients 262
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study 259
Identification of cancer stem cells from human glioblastomas: growth and differentiation capabilities and CD133/prominin-1 expression 258
Compound heterozygosity in the GALC gene in a late onset Iranian patient with spastic paraparesis, peripheral neuropathy and leukoencephalopathy 258
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 257
Ca2+ release induced by cyclic ADP ribose in mice lacking type 3 ryanodine receptor 257
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene 255
The sarcoplasmic reticulum: an organized patchwork of specialized domains 254
Alteration in calcium handling at the subcellular level in mdx myotubes 252
Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity 247
Functional electrical stimulation: A possible strategy to improve muscle function in central core disease? 247
Molecular interactions with obscurin are involved in the localization of muscle-specific small ankyrin1 isoforms to subcompartments of the sarcoplasmic reticulum 245
Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum 245
A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells 240
MECP2 mutation in male patients with non-specific X-linked mental retardation 239
Calcium pools in Ehrlich carcinoma cells. A major, high affinity Ca2+ pool is sensitive to both inositol 1,4,5-trisphosphate and thapsigargin 238
The 12 kDa FK506-binding protein, FKBP12, modulates the Ca(2+)-flux properties of the type-3 ryanodine receptor 238
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning 238
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 235
Putative endothelial progenitor cells predict long-term mortality in type-2 diabetes 233
Metyrapone prevents cortisone-induced preadipocyte differentiation by depleting luminal NADPH of the endoplasmic reticulum 233
Junctophilin 1 and 2 proteins interact with the L-type Ca2+ channel dihydropyridine receptors (DHPRs) in skeletal muscle 231
Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain 229
Expression of growth arrest-specific (gas) genes in senescent murine cells 227
SCN1A mutation associated with atypical Panayiotopoulos syndrome 227
C-myc gene effects on cell growth and transformation 224
Levels of circulating CXCR4-positive cells are decreased and negatively correlated with risk factors in cardiac transplant recipients 222
Mesenchymal stem cells: from the perivascular environment to clinical applications 220
Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c 220
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene 219
RYR2 proteins contribute to the formation of Ca(2+) sparks in smooth muscle 219
Generalised reduction of putative endothelial progenitors and CXCR4-positive peripheral blood cells in type 2 diabetes. 218
Ryanodine receptors are expressed and functionally active in mouse spermatogenic cells and their inhibition interferes with spermatogonial differentiation 215
Murine obscurin and Obsl1 have functionally redundant roles in sarcolemmal integrity, sarcoplasmic reticulum organization, and muscle metabolism 215
The Sarcoplasmic Reticulum of Skeletal Muscle Cells: A Labyrinth of Membrane Contact Sites 215
Properties of ryanodine receptor in rat muscles submitted to unloaded conditions 213
Ca2+ sparks and waves in canine purkinje cells: a triple layered system of Ca2+ activation 212
The KSR2-calcineurin complex regulates STIM1-ORAI1 dynamics and Store-Operated Calcium Entry (SOCE) 212
A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids 209
A human amniotic cell line yielding high titres of human fibroblast interferon 208
Induction and/or selective retention of proteins in mammalian cells exposed to cycloheximide 208
Bcl-2 binds to and inhibits ryanodine receptors 208
Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors 208
Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T 208
Expression and functional activity of ryanodine receptors (RyRs) during skeletal muscle development 206
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome) 206
Homer proteins and InsP(3) receptors co-localise in the longitudinal sarcoplasmic reticulum of skeletal muscle fibres 205
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 205
Muscle Research and Gene Ontology: New standards for improved data integration 204
Cardiac expression of ryanodine receptor subtype 3; a strategic component in the intracellular Ca2 + release system of Purkinje fibers in large mammalian heart 203
Assembly and dynamics of proteins of the longitudinal and junctional sarcoplasmic reticulum in skeletal muscle cells 203
Cell proliferation inhibited by MyoD1 independently of myogenic differentiation 202
Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia 201
The conserved sites for the FK506-binding proteins in ryanodine receptors and inositol 1,4,5-trisphosphate receptors are structurally and functionally different 199
ATP-induced activation of expressed RyR3 at low free calcium 198
Impaired Intracellular Ca2+ Dynamics, M-Band and Sarcomere Fragility in Skeletal Muscles of Obscurin KO Mice 198
A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum 198
Probing luminal negative charge in the type 3 ryanodine receptor 197
Evidence for the transport of glutathione through ryanodine receptor channel type 1 196
Functional properties of the ryanodine receptor type 3 (RyR3) Ca2+ release channel 196
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization 196
Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis 196
Dihydropyridine receptor and ryanodine receptor gene expression in long-term denervated rat muscles 191
Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing? 190
Structure and mutation analysis of the glycogen storage disease type 1b gene 188
Spontaneous and voltage-activated Ca2+ release in adult mouse skeletal muscle fibres expressing the type 3 ryanodine receptor 188
Imperatoxin a enhances Ca(2+) release in developing skeletal muscle containing ryanodine receptor type 3 187
Totale 24.626
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Categoria #
all - tutte 120.402
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 120.402
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.891 0 0 0 0 0 452 164 618 534 449 369 305
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
2025/20268.068 978 1.867 1.720 1.304 2.115 84 0 0 0 0 0 0
Totale 39.753