SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

TREVES, Susan Nella
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 9.930
AS - Asia 4.683
EU - Europa 2.256
SA - Sud America 845
AF - Africa 97
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 3
Totale 17.822
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 9.747
SG - Singapore 1.762
CN - Cina 1.044
BR - Brasile 670
VN - Vietnam 525
UA - Ucraina 458
HK - Hong Kong 436
DE - Germania 356
TR - Turchia 286
IT - Italia 284
GB - Regno Unito 256
PL - Polonia 241
FI - Finlandia 153
BD - Bangladesh 136
FR - Francia 136
JP - Giappone 122
SE - Svezia 113
RU - Federazione Russa 112
IN - India 97
CA - Canada 91
ID - Indonesia 67
MX - Messico 60
AR - Argentina 55
IQ - Iraq 44
ZA - Sudafrica 40
NL - Olanda 36
EC - Ecuador 34
PK - Pakistan 22
CH - Svizzera 21
ES - Italia 21
CO - Colombia 20
BE - Belgio 18
CL - Cile 18
PY - Paraguay 18
PH - Filippine 15
UZ - Uzbekistan 15
SA - Arabia Saudita 13
VE - Venezuela 13
MA - Marocco 12
AT - Austria 11
PE - Perù 11
JM - Giamaica 10
KR - Corea 10
KE - Kenya 9
MY - Malesia 9
TW - Taiwan 9
AZ - Azerbaigian 8
JO - Giordania 8
TN - Tunisia 8
KZ - Kazakistan 7
LT - Lituania 7
AU - Australia 6
PS - Palestinian Territory 6
DK - Danimarca 5
DZ - Algeria 5
EG - Egitto 5
IE - Irlanda 5
NP - Nepal 5
TT - Trinidad e Tobago 5
AE - Emirati Arabi Uniti 4
DO - Repubblica Dominicana 4
GT - Guatemala 4
IL - Israele 4
AL - Albania 3
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
ET - Etiopia 3
IR - Iran 3
KG - Kirghizistan 3
MD - Moldavia 3
SN - Senegal 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AO - Angola 2
BB - Barbados 2
BN - Brunei Darussalam 2
BO - Bolivia 2
CY - Cipro 2
LB - Libano 2
NG - Nigeria 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
RO - Romania 2
RS - Serbia 2
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
CD - Congo 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
HU - Ungheria 1
KH - Cambogia 1
KW - Kuwait 1
Totale 17.809
Salva come PNG Salva come JPEG
Città #
Fairfield 1.093
Ashburn 1.074
Singapore 1.060
Woodbridge 878
Houston 604
Ann Arbor 524
Santa Clara 515
Jacksonville 514
San Jose 500
Seattle 453
Hong Kong 426
Wilmington 358
Chandler 356
Cambridge 325
Beijing 266
Warsaw 239
Izmir 183
Ho Chi Minh City 166
Nanjing 137
Hanoi 121
Princeton 119
Tokyo 117
Los Angeles 109
New York 105
San Diego 101
Lauterbourg 98
Boardman 96
Dallas 88
Ferrara 83
São Paulo 64
Munich 54
Council Bluffs 48
Jakarta 45
Hefei 41
Helsinki 40
Milan 40
Orem 39
Chicago 38
Mexico City 38
Nanchang 37
Shenyang 36
London 32
Tianjin 31
Buffalo 30
Rio de Janeiro 29
San Francisco 28
Da Nang 27
Falkenstein 27
Falls Church 27
Redwood City 27
Dong Ket 25
Johannesburg 25
Montreal 24
Norwalk 24
Atlanta 23
Shanghai 23
Addison 21
Hebei 21
Mountain View 21
Nuremberg 21
Phoenix 20
Haiphong 19
Jiaxing 19
Moscow 19
Toronto 19
Auburn Hills 18
Denver 18
The Dalles 18
Boston 17
Chennai 17
Brasília 16
Brussels 16
Changsha 16
Baghdad 15
Des Moines 15
Guangzhou 15
Hải Dương 15
Basel 14
Brooklyn 14
Stockholm 14
Rome 13
San Mateo 13
Columbus 12
Dhaka 12
Frankfurt am Main 12
Mumbai 12
Zhengzhou 12
Hangzhou 11
Kunming 11
Medellín 11
Philadelphia 11
Tashkent 11
Turku 11
Amsterdam 10
Campinas 10
Curitiba 10
Kingston 10
Manchester 10
Tappahannock 10
Vancouver 10
Totale 12.270
Salva come PNG Salva come JPEG
Nome #
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction 290
The metabolomic profile of gammairradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect 276
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain 246
An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities 233
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity 223
Increased Ca2+ storage capacity of the skeletal muscle sarcoplasmic reticulum of transgenic mice over-expressing membrane bound calcium binding protein junctate 221
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies 221
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy 212
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A 209
Calmodulin Binding Sites of the Skeletal, Cardiac, and Brain Ryanodine Receptor Ca2+ Channels: Modulation by the Catalytic Subunit of cAMP-Dependent Protein Kinase? 205
Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy? 203
Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex 200
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity 192
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutations 192
Apoptosis is dependent on intracellular zinc and independent of intracellular calcium in lymphocytes 190
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling 188
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle 187
Gain of function in the immune system caused by a ryanodine receptor 1 mutation 187
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives 182
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion 180
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle 180
Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging 179
Ryanodine receptor activation by Cav1.2 is involved in dendritic cell major histocompatibility complex class II surface expression 177
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies 177
Alteration of intracellular Ca2+ in COS-7 cells transfected with the cDNA encoding skeltal muscle ryanodine receptor carrying a mutation associated with malignant hyperthermia 176
Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 176
SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase 176
B-lymphocytes from Malignant Hyperthermia-susceptible Patients Have an Increased Sensitivity to Skeletal Muscle Ryanodine Receptor Activators 174
Agonist-activated Ca2+ influx occurs at stable plasma membrane and endoplasmic reticulum junctions 172
RYR1-related myopathies: A wide spectrum of phenotypes throughout life 172
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene 170
Functional characterization of orbicularis oculi and extraocular muscles 170
A ryanodine receptor-like Ca2+ channel is expressed in nonexcitable cells 166
Junctate, an inositol 1,4,5-triphosphate receptor associated protein, is present in rodent sperm and binds TRPC2 and TRPC5 but not TRPC1 channels 161
Identification and characterization of a calreticulin-binding nuclear protein as histone (H1), an autoantigen in systemic lupus erythematosus 160
Atypical periodic paralysis and myalgia. A novel RYR1 phenotype 158
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated muscles 158
Inositol phosphate formation in fMet-Leu-Phe-stimulated human neutrophils does not require an increase in the cytosolic free Ca2+ concentration 157
Characterization of excitation-contraction coupling components in human extraocular muscles 156
Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance 156
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm 154
Effect of cytochalasins on cytosolic-free calcium concentration and phosphoinositide metabolism in leukocytes 154
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies 153
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization 153
Increasing the number of diagnostic mutations in malignant hyperthermia 152
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages. 152
Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms 151
Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles 151
Screening of the ryanodine 1 gene for malignant hyperthermia causative mutations by high resolution melt curve analysis. 149
Role of malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine Receptor) of skeletal muscle sarcoplasmic reticulum 148
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 147
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle 147
Identification of a novel 45 kDa protein (JP-45) from rabbit sarcoplasmic-reticulum junctional-face membrane 147
Identification of calreticulin isoforms in the central nervous system 146
Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation 146
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders 146
Functional effects of mutations identified in patients with multiminicore disease 146
Enhanced excitation coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with Central core disease 145
Mapping domains and mutations on the skeletal muscle ryanodine receptor channel 145
null 143
Extraocular muscle function is impaired in ryr3(-/-) mice 143
Malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine receptor) 142
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells 141
Methyl p-hydroxybenzoate (E-218) a preservative for drugs and food is an activator of the ryanodine receptor Ca2+ release channel 140
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis 139
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane 139
Current and future therapeutic approaches to the congenitalmyopathies 138
Frequent calcium oscillations lead to NFAT activation in human immature dendritic cells 137
Genotype-phenotype comparison of the Swiss malignant hyperthermia population 136
Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow-twitch muscles in mice 135
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 135
Remodeling of calcium handling in skeletal muscle through PGC-1 alpha: impact on force, fatigability, and fiber type 134
Frog brain expresses a 60 KDa Ca2+ binding protein similar to mammalian calreticulin 134
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy 134
The junctional SR protein JP-45 affects the functional expression of the voltage-dependent Ca2+ channel Cav1.1 133
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor 131
Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin 130
Multiple levels of control of the expression of the human AβH-J-J locus encoding aspartyl-β-hydroxylase, junctin, and junctate 129
Interaction of lymphokine-activated killer cells with susceptible targets does not induce second messenger generation and cytolytic granule exocytosis 129
P1 promoter transcriptional activity of the human AbetaH-J-J locus, encoding Aspartil-beta-hydroxylase, Junctin and Junctate 127
150th ENMC International Workshop: Core Myopathies, 9-11th March 2007, Naarden, The Netherlands 127
Amino acid residues 4425-4621 localizied on the three diminesional structure of the skeletal muscle ryanodine receptor 124
Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin 124
Calumin, a novel Ca2+-binding transmembrane protein on the endoplasmic reticulum 124
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 122
Functional characterization of RYR1 variants identified in malignant hyperthermia susceptible individuals 121
Chlorocresol: An activator of ryanodine receptor-mediated Ca2+ release 121
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 121
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 118
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice 118
null 117
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia 116
Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles 116
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locus 115
Agrin regulates CLASP2-mediated capture of microtubules at the neuromuscular junction synaptic membrane 115
A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice 113
Myocyte enhancer factor 2 activates promoter sequences of the human AβH-J-J locus, encoding aspartyl-β-hydroxylase, junctin, and junctate 113
Identification of 4 novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis 111
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 111
Molecular regulation of the expression of AbetaHJ-J locus, encoding Aspartyl-beta-hydroxylase, Junctin and Junctate 110
Totale 15.646
Salva come PNG Salva come JPEG
Categoria #
all - tutte 85.010
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 85.010
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021100 0 0 0 0 0 0 0 0 0 0 0 100
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
2025/20266.340 587 321 562 819 825 329 659 380 627 784 250 197
Totale 18.030