SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

TREVES, Susan Nella
 Distribuzione geografica
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Continente #
NA - Nord America 9.545
AS - Asia 4.583
EU - Europa 2.196
SA - Sud America 845
AF - Africa 97
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 3
Totale 17.277
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Nazione #
US - Stati Uniti d'America 9.378
SG - Singapore 1.745
CN - Cina 1.035
BR - Brasile 670
VN - Vietnam 525
UA - Ucraina 458
HK - Hong Kong 433
DE - Germania 356
TR - Turchia 286
GB - Regno Unito 255
PL - Polonia 241
IT - Italia 227
FI - Finlandia 153
FR - Francia 136
JP - Giappone 122
SE - Svezia 113
RU - Federazione Russa 112
IN - India 97
CA - Canada 77
ID - Indonesia 67
BD - Bangladesh 65
MX - Messico 60
AR - Argentina 55
IQ - Iraq 44
ZA - Sudafrica 40
EC - Ecuador 34
NL - Olanda 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
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
GT - Guatemala 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
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
BB - Barbados 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 17.264
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Città #
Fairfield 1.093
Singapore 1.057
Ashburn 1.052
Woodbridge 878
Houston 601
Ann Arbor 524
Jacksonville 513
Santa Clara 498
Seattle 452
Hong Kong 423
San Jose 403
Wilmington 358
Chandler 356
Cambridge 325
Beijing 263
Warsaw 239
Izmir 183
Ho Chi Minh City 166
Nanjing 137
Hanoi 121
Princeton 119
Tokyo 117
San Diego 101
Lauterbourg 98
Boardman 96
Los Angeles 96
Ferrara 83
Dallas 78
New York 71
São Paulo 64
Munich 54
Council Bluffs 46
Jakarta 45
Hefei 41
Helsinki 40
Milan 39
Mexico City 38
Nanchang 37
Orem 37
Shenyang 36
Chicago 34
London 32
Tianjin 31
Rio de Janeiro 29
Da Nang 27
Falkenstein 27
Falls Church 27
Redwood City 27
Dong Ket 25
Johannesburg 25
San Francisco 25
Norwalk 24
Buffalo 23
Montreal 23
Shanghai 23
Atlanta 22
Addison 21
Hebei 21
Mountain View 21
Nuremberg 21
Haiphong 19
Jiaxing 19
Moscow 19
Auburn Hills 18
Chennai 17
Denver 17
Phoenix 17
Brasília 16
Brussels 16
Changsha 16
Baghdad 15
Boston 15
Guangzhou 15
Hải Dương 15
The Dalles 15
Basel 14
Des Moines 14
Stockholm 14
Toronto 14
San Mateo 13
Brooklyn 12
Dhaka 12
Frankfurt am Main 12
Mumbai 12
Zhengzhou 12
Kunming 11
Medellín 11
Tashkent 11
Turku 11
Amsterdam 10
Campinas 10
Columbus 10
Curitiba 10
Hangzhou 10
Manchester 10
Tappahannock 10
Vancouver 10
Belo Horizonte 9
Guarulhos 9
Kingston 9
Totale 12.015
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Nome #
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction 283
The metabolomic profile of gammairradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect 275
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain 240
An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities 231
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity 219
Increased Ca2+ storage capacity of the skeletal muscle sarcoplasmic reticulum of transgenic mice over-expressing membrane bound calcium binding protein junctate 214
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies 211
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A 200
Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy? 197
Calmodulin Binding Sites of the Skeletal, Cardiac, and Brain Ryanodine Receptor Ca2+ Channels: Modulation by the Catalytic Subunit of cAMP-Dependent Protein Kinase? 196
Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex 193
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity 189
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutations 189
Apoptosis is dependent on intracellular zinc and independent of intracellular calcium in lymphocytes 188
Gain of function in the immune system caused by a ryanodine receptor 1 mutation 187
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy 186
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle 185
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion 180
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives 178
Ryanodine receptor activation by Cav1.2 is involved in dendritic cell major histocompatibility complex class II surface expression 177
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle 177
Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging 176
Alteration of intracellular Ca2+ in COS-7 cells transfected with the cDNA encoding skeltal muscle ryanodine receptor carrying a mutation associated with malignant hyperthermia 175
Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 173
SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase 172
B-lymphocytes from Malignant Hyperthermia-susceptible Patients Have an Increased Sensitivity to Skeletal Muscle Ryanodine Receptor Activators 170
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene 167
Functional characterization of orbicularis oculi and extraocular muscles 167
Agonist-activated Ca2+ influx occurs at stable plasma membrane and endoplasmic reticulum junctions 162
A ryanodine receptor-like Ca2+ channel is expressed in nonexcitable cells 160
Identification and characterization of a calreticulin-binding nuclear protein as histone (H1), an autoantigen in systemic lupus erythematosus 159
Junctate, an inositol 1,4,5-triphosphate receptor associated protein, is present in rodent sperm and binds TRPC2 and TRPC5 but not TRPC1 channels 158
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies 158
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated muscles 157
RYR1-related myopathies: A wide spectrum of phenotypes throughout life 155
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm 154
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling 154
Inositol phosphate formation in fMet-Leu-Phe-stimulated human neutrophils does not require an increase in the cytosolic free Ca2+ concentration 153
Characterization of excitation-contraction coupling components in human extraocular muscles 153
Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance 153
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization 153
Effect of cytochalasins on cytosolic-free calcium concentration and phosphoinositide metabolism in leukocytes 152
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages. 152
Atypical periodic paralysis and myalgia. A novel RYR1 phenotype 152
Increasing the number of diagnostic mutations in malignant hyperthermia 151
Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles 150
Screening of the ryanodine 1 gene for malignant hyperthermia causative mutations by high resolution melt curve analysis. 148
Role of malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine Receptor) of skeletal muscle sarcoplasmic reticulum 147
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies 147
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
Identification of a novel 45 kDa protein (JP-45) from rabbit sarcoplasmic-reticulum junctional-face membrane 145
Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation 144
Functional effects of mutations identified in patients with multiminicore disease 144
Identification of calreticulin isoforms in the central nervous system 143
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders 143
null 143
Mapping domains and mutations on the skeletal muscle ryanodine receptor channel 142
Extraocular muscle function is impaired in ryr3(-/-) mice 142
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 141
Malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine receptor) 140
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 137
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle 137
Current and future therapeutic approaches to the congenitalmyopathies 137
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells 137
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane 136
Genotype-phenotype comparison of the Swiss malignant hyperthermia population 135
Frequent calcium oscillations lead to NFAT activation in human immature dendritic cells 135
Remodeling of calcium handling in skeletal muscle through PGC-1 alpha: impact on force, fatigability, and fiber type 133
Frog brain expresses a 60 KDa Ca2+ binding protein similar to mammalian calreticulin 133
Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms 132
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor 130
The junctional SR protein JP-45 affects the functional expression of the voltage-dependent Ca2+ channel Cav1.1 130
Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin 130
Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow-twitch muscles in mice 130
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 129
Multiple levels of control of the expression of the human AβH-J-J locus encoding aspartyl-β-hydroxylase, junctin, and junctate 126
Interaction of lymphokine-activated killer cells with susceptible targets does not induce second messenger generation and cytolytic granule exocytosis 126
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy 125
P1 promoter transcriptional activity of the human AbetaH-J-J locus, encoding Aspartil-beta-hydroxylase, Junctin and Junctate 124
Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin 124
150th ENMC International Workshop: Core Myopathies, 9-11th March 2007, Naarden, The Netherlands 124
Amino acid residues 4425-4621 localizied on the three diminesional structure of the skeletal muscle ryanodine receptor 123
Calumin, a novel Ca2+-binding transmembrane protein on the endoplasmic reticulum 123
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 120
Chlorocresol: An activator of ryanodine receptor-mediated Ca2+ release 119
null 117
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia 115
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice 115
Agrin regulates CLASP2-mediated capture of microtubules at the neuromuscular junction synaptic membrane 114
Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles 113
Myocyte enhancer factor 2 activates promoter sequences of the human AβH-J-J locus, encoding aspartyl-β-hydroxylase, junctin, and junctate 112
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 112
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
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locus 110
Molecular regulation of the expression of AbetaHJ-J locus, encoding Aspartyl-beta-hydroxylase, Junctin and Junctate 109
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 106
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 105
null 103
STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility 102
Totale 15.214
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Categoria #
all - tutte 79.928
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 79.928
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021550 0 0 0 0 0 0 0 0 0 265 185 100
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
2025/20265.795 587 321 562 819 825 329 659 380 627 686 0 0
Totale 17.485