SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

TREVES, Susan Nella
 Distribuzione geografica
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Continente #
NA - Nord America 10.334
AS - Asia 4.727
EU - Europa 2.303
SA - Sud America 855
Continente sconosciuto - Info sul continente non disponibili 211
AF - Africa 97
OC - Oceania 9
Totale 18.536
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Nazione #
US - Stati Uniti d'America 10.103
SG - Singapore 1.775
CN - Cina 1.057
BR - Brasile 675
VN - Vietnam 527
UA - Ucraina 458
HK - Hong Kong 442
DE - Germania 356
IT - Italia 313
TR - Turchia 286
GB - Regno Unito 256
PL - Polonia 241
FI - Finlandia 153
BD - Bangladesh 140
FR - Francia 137
JP - Giappone 122
SE - Svezia 118
CA - Canada 117
RU - Federazione Russa 114
IN - India 98
ID - Indonesia 67
MX - Messico 62
AR - Argentina 58
IQ - Iraq 44
NL - Olanda 41
ZA - Sudafrica 40
EC - Ecuador 34
ES - Italia 23
PK - Pakistan 23
CH - Svizzera 21
CO - Colombia 20
BE - Belgio 19
CL - Cile 19
JM - Giamaica 19
PY - Paraguay 18
PH - Filippine 15
UZ - Uzbekistan 15
SA - Arabia Saudita 13
VE - Venezuela 13
MA - Marocco 12
PE - Perù 12
AT - Austria 11
MY - Malesia 11
KR - Corea 10
KE - Kenya 9
TW - Taiwan 9
AZ - Azerbaigian 8
JO - Giordania 8
TN - Tunisia 8
AU - Australia 7
KZ - Kazakistan 7
LT - Lituania 7
CR - Costa Rica 6
GT - Guatemala 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
TH - Thailandia 4
AL - Albania 3
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
CY - Cipro 3
CZ - Repubblica Ceca 3
ET - Etiopia 3
IR - Iran 3
KG - Kirghizistan 3
MD - Moldavia 3
PT - Portogallo 3
SN - Senegal 3
SY - Repubblica araba siriana 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AO - Angola 2
BB - Barbados 2
BN - Brunei Darussalam 2
BO - Bolivia 2
BZ - Belize 2
LB - Libano 2
NG - Nigeria 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
RO - Romania 2
RS - Serbia 2
SV - El Salvador 2
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
BS - Bahamas 1
CD - Congo 1
GA - Gabon 1
GD - Grenada 1
GE - Georgia 1
Totale 18.311
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Città #
Ashburn 1.104
Fairfield 1.093
Singapore 1.067
Woodbridge 878
Houston 605
Santa Clara 536
Ann Arbor 524
San Jose 520
Jacksonville 514
Seattle 453
Hong Kong 432
Wilmington 358
Chandler 356
Cambridge 325
Beijing 274
Warsaw 239
Council Bluffs 208
Izmir 183
Ho Chi Minh City 168
Nanjing 137
Hanoi 121
Princeton 119
Tokyo 117
Los Angeles 113
New York 112
San Diego 101
Lauterbourg 98
Boardman 97
Dallas 88
Ferrara 83
São Paulo 64
Munich 54
Milan 46
Jakarta 45
Hefei 41
Helsinki 40
Mexico City 40
Chicago 39
Orem 39
Nanchang 37
Shenyang 36
London 32
Tianjin 31
Buffalo 30
Rio de Janeiro 30
Toronto 30
San Francisco 29
Da Nang 27
Falkenstein 27
Falls Church 27
Redwood City 27
Montreal 26
Atlanta 25
Dong Ket 25
Johannesburg 25
Norwalk 24
Shanghai 23
Addison 21
Hebei 21
Mountain View 21
Nuremberg 21
Phoenix 21
Denver 19
Haiphong 19
Jiaxing 19
Moscow 19
The Dalles 19
Auburn Hills 18
Boston 17
Brussels 17
Chennai 17
Brasília 16
Changsha 16
Rome 16
Baghdad 15
Des Moines 15
Guangzhou 15
Hải Dương 15
Basel 14
Brooklyn 14
Stockholm 14
Columbus 13
San Mateo 13
Dhaka 12
Frankfurt am Main 12
Kingston 12
Mumbai 12
Philadelphia 12
Zhengzhou 12
Curitiba 11
Hangzhou 11
Kunming 11
Medellín 11
Tashkent 11
Turku 11
Amsterdam 10
Campinas 10
Manchester 10
Orange 10
Tappahannock 10
Totale 12.575
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Nome #
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction 301
The metabolomic profile of gammairradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect 279
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain 253
An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities 237
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity 228
Increased Ca2+ storage capacity of the skeletal muscle sarcoplasmic reticulum of transgenic mice over-expressing membrane bound calcium binding protein junctate 225
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies 224
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy 220
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A 216
Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy? 209
Calmodulin Binding Sites of the Skeletal, Cardiac, and Brain Ryanodine Receptor Ca2+ Channels: Modulation by the Catalytic Subunit of cAMP-Dependent Protein Kinase? 208
Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex 203
Apoptosis is dependent on intracellular zinc and independent of intracellular calcium in lymphocytes 199
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity 195
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutations 195
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling 192
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle 188
Gain of function in the immune system caused by a ryanodine receptor 1 mutation 188
Ryanodine receptor activation by Cav1.2 is involved in dendritic cell major histocompatibility complex class II surface expression 187
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion 187
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives 187
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle 184
Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging 183
SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase 181
Alteration of intracellular Ca2+ in COS-7 cells transfected with the cDNA encoding skeltal muscle ryanodine receptor carrying a mutation associated with malignant hyperthermia 180
Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 179
RYR1-related myopathies: A wide spectrum of phenotypes throughout life 179
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies 179
Agonist-activated Ca2+ influx occurs at stable plasma membrane and endoplasmic reticulum junctions 177
B-lymphocytes from Malignant Hyperthermia-susceptible Patients Have an Increased Sensitivity to Skeletal Muscle Ryanodine Receptor Activators 175
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene 174
Functional characterization of orbicularis oculi and extraocular muscles 172
A ryanodine receptor-like Ca2+ channel is expressed in nonexcitable cells 169
Junctate, an inositol 1,4,5-triphosphate receptor associated protein, is present in rodent sperm and binds TRPC2 and TRPC5 but not TRPC1 channels 168
Identification and characterization of a calreticulin-binding nuclear protein as histone (H1), an autoantigen in systemic lupus erythematosus 166
Atypical periodic paralysis and myalgia. A novel RYR1 phenotype 166
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies 164
Characterization of excitation-contraction coupling components in human extraocular muscles 162
Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance 160
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated muscles 160
Effect of cytochalasins on cytosolic-free calcium concentration and phosphoinositide metabolism in leukocytes 159
Inositol phosphate formation in fMet-Leu-Phe-stimulated human neutrophils does not require an increase in the cytosolic free Ca2+ concentration 158
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm 157
Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms 155
Increasing the number of diagnostic mutations in malignant hyperthermia 154
Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles 154
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization 154
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages. 152
Role of malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine Receptor) of skeletal muscle sarcoplasmic reticulum 151
Enhanced excitation coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with Central core disease 151
Identification of calreticulin isoforms in the central nervous system 151
Identification of a novel 45 kDa protein (JP-45) from rabbit sarcoplasmic-reticulum junctional-face membrane 151
Screening of the ryanodine 1 gene for malignant hyperthermia causative mutations by high resolution melt curve analysis. 150
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders 149
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle 149
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 148
Functional effects of mutations identified in patients with multiminicore disease 148
Extraocular muscle function is impaired in ryr3(-/-) mice 148
Malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine receptor) 147
Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation 147
Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow-twitch muscles in mice 147
Mapping domains and mutations on the skeletal muscle ryanodine receptor channel 146
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells 146
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis 145
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane 144
null 143
Methyl p-hydroxybenzoate (E-218) a preservative for drugs and food is an activator of the ryanodine receptor Ca2+ release channel 143
Current and future therapeutic approaches to the congenitalmyopathies 141
Functional characterization of RYR1 variants identified in malignant hyperthermia susceptible individuals 139
Genotype-phenotype comparison of the Swiss malignant hyperthermia population 139
Frequent calcium oscillations lead to NFAT activation in human immature dendritic cells 139
Remodeling of calcium handling in skeletal muscle through PGC-1 alpha: impact on force, fatigability, and fiber type 138
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy 138
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor 137
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 137
The junctional SR protein JP-45 affects the functional expression of the voltage-dependent Ca2+ channel Cav1.1 136
Frog brain expresses a 60 KDa Ca2+ binding protein similar to mammalian calreticulin 136
Interaction of lymphokine-activated killer cells with susceptible targets does not induce second messenger generation and cytolytic granule exocytosis 134
Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin 134
P1 promoter transcriptional activity of the human AbetaH-J-J locus, encoding Aspartil-beta-hydroxylase, Junctin and Junctate 130
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice 130
Calumin, a novel Ca2+-binding transmembrane protein on the endoplasmic reticulum 130
150th ENMC International Workshop: Core Myopathies, 9-11th March 2007, Naarden, The Netherlands 130
Multiple levels of control of the expression of the human AβH-J-J locus encoding aspartyl-β-hydroxylase, junctin, and junctate 129
Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin 127
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 127
Amino acid residues 4425-4621 localizied on the three diminesional structure of the skeletal muscle ryanodine receptor 126
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 125
Chlorocresol: An activator of ryanodine receptor-mediated Ca2+ release 122
Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles 122
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia 121
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 121
A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice 119
Agrin regulates CLASP2-mediated capture of microtubules at the neuromuscular junction synaptic membrane 119
Myocyte enhancer factor 2 activates promoter sequences of the human AβH-J-J locus, encoding aspartyl-β-hydroxylase, junctin, and junctate 118
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 118
null 117
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locus 116
Molecular regulation of the expression of AbetaHJ-J locus, encoding Aspartyl-beta-hydroxylase, Junctin and Junctate 115
STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility 113
Totale 16.069
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Categoria #
all - tutte 89.344
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 89.344
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.131 0 112 110 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
2025/20266.372 587 321 562 819 825 329 659 380 627 784 250 229
2026/2027474 231 243 0 0 0 0 0 0 0 0 0 0
Totale 18.536