TREVES, Susan Nella
 Distribuzione geografica
Continente #
NA - Nord America 8.678
AS - Asia 3.429
EU - Europa 1.982
SA - Sud America 722
AF - Africa 57
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 2
Totale 14.878
Nazione #
US - Stati Uniti d'America 8.538
SG - Singapore 1.441
CN - Cina 858
BR - Brasile 606
UA - Ucraina 457
HK - Hong Kong 389
DE - Germania 346
TR - Turchia 267
PL - Polonia 241
VN - Vietnam 240
GB - Regno Unito 238
IT - Italia 199
FI - Finlandia 131
SE - Svezia 112
RU - Federazione Russa 110
CA - Canada 65
MX - Messico 54
ID - Indonesia 53
AR - Argentina 43
IN - India 38
ZA - Sudafrica 30
NL - Olanda 28
BD - Bangladesh 26
FR - Francia 25
EC - Ecuador 24
JP - Giappone 24
CH - Svizzera 21
IQ - Iraq 20
ES - Italia 19
BE - Belgio 16
PY - Paraguay 14
AT - Austria 11
CL - Cile 10
CO - Colombia 9
KR - Corea 9
TW - Taiwan 9
PE - Perù 8
LT - Lituania 7
MA - Marocco 7
PK - Pakistan 7
UZ - Uzbekistan 7
AU - Australia 6
JM - Giamaica 6
KE - Kenya 6
VE - Venezuela 5
AZ - Azerbaigian 4
DK - Danimarca 4
DO - Repubblica Dominicana 4
KZ - Kazakistan 4
TT - Trinidad e Tobago 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
EG - Egitto 3
IL - Israele 3
IR - Iran 3
JO - Giordania 3
KG - Kirghizistan 3
PH - Filippine 3
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
CI - Costa d'Avorio 2
CR - Costa Rica 2
CY - Cipro 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
GT - Guatemala 2
IE - Irlanda 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 2
RO - Romania 2
RS - Serbia 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BO - Bolivia 1
ET - Etiopia 1
GA - Gabon 1
GY - Guiana 1
KH - Cambogia 1
LV - Lettonia 1
MD - Moldavia 1
ME - Montenegro 1
MM - Myanmar 1
MY - Malesia 1
NG - Nigeria 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
TN - Tunisia 1
UY - Uruguay 1
Totale 14.878
Città #
Fairfield 1.093
Woodbridge 878
Ashburn 796
Singapore 783
Houston 599
Ann Arbor 524
Jacksonville 513
Santa Clara 492
Seattle 452
Hong Kong 389
Wilmington 357
Chandler 356
Cambridge 325
Beijing 243
Warsaw 239
Izmir 182
Nanjing 137
Princeton 119
San Diego 101
Boardman 96
Los Angeles 91
Ferrara 83
Ho Chi Minh City 79
Dallas 70
New York 65
São Paulo 63
Munich 53
Jakarta 44
Hanoi 43
Hefei 41
Nanchang 37
Milan 36
Shenyang 36
Mexico City 34
Chicago 32
London 31
Tianjin 30
Falkenstein 27
Falls Church 27
Redwood City 27
Dong Ket 25
Norwalk 24
Rio de Janeiro 24
Buffalo 23
Montreal 23
San Francisco 23
Addison 21
Hebei 21
Johannesburg 21
Mountain View 21
Nuremberg 21
Shanghai 21
Tokyo 20
Jiaxing 19
Auburn Hills 18
Helsinki 18
Moscow 18
Phoenix 17
Changsha 16
Brasília 15
Brussels 15
Denver 15
Atlanta 14
Basel 14
The Dalles 14
Toronto 14
Boston 13
Des Moines 13
Guangzhou 13
San Mateo 13
Stockholm 13
Brooklyn 12
Zhengzhou 12
Da Nang 11
Kunming 11
Orem 11
Turku 11
Columbus 10
Tappahannock 10
Campinas 9
Curitiba 9
Haiphong 9
Hangzhou 9
Orange 9
Salt Lake City 9
Chennai 8
Council Bluffs 8
Guarulhos 8
Amsterdam 7
Belo Horizonte 7
Frankfurt am Main 7
Indiana 7
Ningbo 7
Philadelphia 7
Poplar 7
Rome 7
Changchun 6
Guayaquil 6
Jinan 6
Kingston 6
Totale 10.429
Nome #
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction 248
The metabolomic profile of gammairradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect 237
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain 215
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity 199
An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities 194
Increased Ca2+ storage capacity of the skeletal muscle sarcoplasmic reticulum of transgenic mice over-expressing membrane bound calcium binding protein junctate 189
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies 184
Calmodulin Binding Sites of the Skeletal, Cardiac, and Brain Ryanodine Receptor Ca2+ Channels: Modulation by the Catalytic Subunit of cAMP-Dependent Protein Kinase? 181
Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex 177
Gain of function in the immune system caused by a ryanodine receptor 1 mutation 175
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A 172
Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy? 172
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity 170
Apoptosis is dependent on intracellular zinc and independent of intracellular calcium in lymphocytes 166
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutations 166
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion 164
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle 160
Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging 159
Alteration of intracellular Ca2+ in COS-7 cells transfected with the cDNA encoding skeltal muscle ryanodine receptor carrying a mutation associated with malignant hyperthermia 152
Ryanodine receptor activation by Cav1.2 is involved in dendritic cell major histocompatibility complex class II surface expression 152
SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase 150
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives 149
B-lymphocytes from Malignant Hyperthermia-susceptible Patients Have an Increased Sensitivity to Skeletal Muscle Ryanodine Receptor Activators 146
Functional characterization of orbicularis oculi and extraocular muscles 146
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle 146
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy 146
Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 144
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm 143
null 143
A ryanodine receptor-like Ca2+ channel is expressed in nonexcitable cells 143
Identification and characterization of a calreticulin-binding nuclear protein as histone (H1), an autoantigen in systemic lupus erythematosus 140
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling 139
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene 138
Increasing the number of diagnostic mutations in malignant hyperthermia 136
Junctate, an inositol 1,4,5-triphosphate receptor associated protein, is present in rodent sperm and binds TRPC2 and TRPC5 but not TRPC1 channels 135
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages. 135
Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance 135
Effect of cytochalasins on cytosolic-free calcium concentration and phosphoinositide metabolism in leukocytes 134
Screening of the ryanodine 1 gene for malignant hyperthermia causative mutations by high resolution melt curve analysis. 134
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated muscles 134
Inositol phosphate formation in fMet-Leu-Phe-stimulated human neutrophils does not require an increase in the cytosolic free Ca2+ concentration 133
Characterization of excitation-contraction coupling components in human extraocular muscles 133
Malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine receptor) 132
Identification of a novel 45 kDa protein (JP-45) from rabbit sarcoplasmic-reticulum junctional-face membrane 132
RYR1-related myopathies: A wide spectrum of phenotypes throughout life 132
Atypical periodic paralysis and myalgia. A novel RYR1 phenotype 131
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies 131
Agonist-activated Ca2+ influx occurs at stable plasma membrane and endoplasmic reticulum junctions 130
Enhanced excitation coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with Central core disease 130
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization 130
Identification of calreticulin isoforms in the central nervous system 129
Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation 129
Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles 129
Functional properties of EGFP-tagged skeletal muscle calcium-release channel (ryanodine receptor) expressed in COS-7 cells: sensitivity to caffeine and 4-chloro-m-cresol 128
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies 127
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders 127
Methyl p-hydroxybenzoate (E-218) a preservative for drugs and food is an activator of the ryanodine receptor Ca2+ release channel 127
Role of malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine Receptor) of skeletal muscle sarcoplasmic reticulum 126
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells 126
Mapping domains and mutations on the skeletal muscle ryanodine receptor channel 125
Functional effects of mutations identified in patients with multiminicore disease 124
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane 123
Frequent calcium oscillations lead to NFAT activation in human immature dendritic cells 122
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle 120
Genotype-phenotype comparison of the Swiss malignant hyperthermia population 119
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor 119
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis 119
Extraocular muscle function is impaired in ryr3(-/-) mice 118
Frog brain expresses a 60 KDa Ca2+ binding protein similar to mammalian calreticulin 118
null 117
Interaction of lymphokine-activated killer cells with susceptible targets does not induce second messenger generation and cytolytic granule exocytosis 115
Current and future therapeutic approaches to the congenitalmyopathies 114
Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms 113
Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin 113
The junctional SR protein JP-45 affects the functional expression of the voltage-dependent Ca2+ channel Cav1.1 112
Remodeling of calcium handling in skeletal muscle through PGC-1 alpha: impact on force, fatigability, and fiber type 112
P1 promoter transcriptional activity of the human AbetaH-J-J locus, encoding Aspartil-beta-hydroxylase, Junctin and Junctate 107
Functional properties of ryanodine receptors carrying three amino acid substitutions identified in patients affected by multi-minicore disease and central core disease, expressed in immortalized lymphocytes 107
Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin 106
Chlorocresol: An activator of ryanodine receptor-mediated Ca2+ release 105
Multiple levels of control of the expression of the human AβH-J-J locus encoding aspartyl-β-hydroxylase, junctin, and junctate 105
Calumin, a novel Ca2+-binding transmembrane protein on the endoplasmic reticulum 105
null 103
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice 102
Amino acid residues 4425-4621 localizied on the three diminesional structure of the skeletal muscle ryanodine receptor 100
Intracellular calcium homeostatis in human primary muscle cells from malignant hyperthermia-susceptible and normal individuals. Effect of overexpression of recombinant wild type and Arg163Cys mutated ryanodine receptors 99
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 98
null 97
Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow-twitch muscles in mice 97
150th ENMC International Workshop: Core Myopathies, 9-11th March 2007, Naarden, The Netherlands 97
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy 96
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locus 95
Myocyte enhancer factor 2 activates promoter sequences of the human AβH-J-J locus, encoding aspartyl-β-hydroxylase, junctin, and junctate 94
Molecular regulation of the expression of AbetaHJ-J locus, encoding Aspartyl-beta-hydroxylase, Junctin and Junctate 94
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia 94
Effect of ryanodine receptor mutations on IL-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia susceptible individuals and patients affected by central core disease 93
Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles 92
Identification of the domain recognized by anti-(ryanodine receptor) antibodies which affect Ca2+-induced Ca2+ release 91
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 90
null 89
Totale 13.269
Categoria #
all - tutte 75.696
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 75.696


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.086 0 0 0 0 0 149 130 188 69 265 185 100
2021/20221.178 47 112 110 56 89 59 61 68 54 80 90 352
2022/2023938 107 26 31 97 187 143 33 86 101 5 81 41
2023/2024498 68 63 29 21 49 50 9 65 4 5 10 125
2024/20252.207 50 63 178 19 307 283 52 172 323 254 296 210
2025/20263.396 587 321 562 819 825 282 0 0 0 0 0 0
Totale 15.086