SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

TREVES, Susan Nella
 Distribuzione geografica
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Continente #
NA - Nord America 6.916
EU - Europa 1.456
AS - Asia 767
SA - Sud America 9
OC - Oceania 5
AF - Africa 1
Totale 9.154
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Nazione #
US - Stati Uniti d'America 6.901
CN - Cina 438
UA - Ucraina 432
TR - Turchia 251
PL - Polonia 218
DE - Germania 210
GB - Regno Unito 190
IT - Italia 134
FI - Finlandia 104
SE - Svezia 99
HK - Hong Kong 26
VN - Vietnam 25
FR - Francia 16
BE - Belgio 15
CA - Canada 13
CH - Svizzera 10
NL - Olanda 10
KR - Corea 7
RU - Federazione Russa 7
AU - Australia 5
BR - Brasile 5
IN - India 4
JP - Giappone 4
SG - Singapore 3
CL - Cile 2
DK - Danimarca 2
ES - Italia 2
IR - Iran 2
RO - Romania 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
CO - Colombia 1
CR - Costa Rica 1
IE - Irlanda 1
IL - Israele 1
IQ - Iraq 1
KZ - Kazakistan 1
MD - Moldavia 1
ME - Montenegro 1
MX - Messico 1
NG - Nigeria 1
PE - Perù 1
PH - Filippine 1
RS - Serbia 1
TW - Taiwan 1
Totale 9.154
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Città #
Fairfield 1.093
Woodbridge 878
Houston 593
Ann Arbor 524
Jacksonville 512
Ashburn 499
Seattle 449
Chandler 356
Wilmington 355
Cambridge 325
Warsaw 216
Izmir 180
Nanjing 137
Princeton 119
San Diego 101
Boardman 90
Ferrara 75
Beijing 53
Nanchang 37
Shenyang 36
New York 33
Milan 28
Falls Church 27
Redwood City 27
Tianjin 27
Hong Kong 26
Dong Ket 25
Norwalk 24
Addison 21
Hebei 21
Mountain View 21
Auburn Hills 18
Jiaxing 18
London 18
Changsha 15
Brussels 14
Des Moines 13
San Mateo 13
Shanghai 13
Zhengzhou 11
Kunming 10
Tappahannock 10
Guangzhou 9
Los Angeles 9
Orange 9
Basel 8
Chicago 7
Indiana 7
Ningbo 7
Changchun 6
Helsinki 6
Jinan 6
Philadelphia 6
Dearborn 5
Hangzhou 5
Taizhou 5
Toronto 5
Bologna 4
Haikou 4
Kilburn 4
Lanzhou 4
Redmond 4
San Francisco 4
Acton 3
Barrie 3
Baton Rouge 3
Bremen 3
Hounslow 3
Lethbridge 3
New Bedfont 3
Verona 3
Walnut 3
Augusta 2
Bari 2
Changshahsien 2
Chiswick 2
Clifton 2
Copenhagen 2
Edinburgh 2
Ferrara di Monte Baldo 2
Fuzhou 2
Las Vegas 2
Madrid 2
Mount Vernon 2
Mumbai 2
Occhiobello 2
Oyster Bay 2
Phoenix 2
Savignano sul Rubicone 2
Seongnam 2
Seoul 2
Shaoxing 2
Washington 2
Almaty 1
Andover 1
Austin 1
Bandar Seri Begawan 1
Basildon 1
Bayville 1
Belgrade 1
Totale 7.261
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Nome #
The metabolomic profile of gammairradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect 203
null 143
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutations 137
Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy? 136
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain 133
Increased Ca2+ storage capacity of the skeletal muscle sarcoplasmic reticulum of transgenic mice over-expressing membrane bound calcium binding protein junctate 132
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction 131
Gain of function in the immune system caused by a ryanodine receptor 1 mutation 130
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity 123
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion 122
Epigenetic changes as a common trigger of muscle weakness in congenital myopathies 121
Calcium and inositolphosphates in the activation of T cell-mediated cytotoxicity 120
null 117
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives 113
Calmodulin Binding Sites of the Skeletal, Cardiac, and Brain Ryanodine Receptor Ca2+ Channels: Modulation by the Catalytic Subunit of cAMP-Dependent Protein Kinase? 110
Functional characterization of orbicularis oculi and extraocular muscles 110
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A 109
Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 108
Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex 106
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm. 103
null 103
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. 102
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling 102
Effect of cytochalasins on cytosolic-free calcium concentration and phosphoinositide metabolism in leukocytes 100
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages. 99
Apoptosis is dependent on intracellular zinc and independent of intracellular calcium in lymphocytes 99
null 97
Ryanodine receptor activation by Cav1.2 is involved in dendritic cell major histocompatibility complex class II surface expression 96
Role of malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine Receptor) of skeletal muscle sarcoplasmic reticulum 96
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization 96
Identification and characterization of a calreticulin-binding nuclear protein as histone (H1), an autoantigen in systemic lupus erythematosus 95
Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging 95
Inositol phosphate formation in fMet-Leu-Phe-stimulated human neutrophils does not require an increase in the cytosolic free Ca2+ concentration. 95
Identification of a novel 45 kDa protein (JP-45) from rabbit sarcoplasmic-reticulum junctional-face membrane 95
An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities 95
Increasing the number of diagnostic mutations in malignant hyperthermia 94
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 94
Screening of the ryanodine 1 gene for malignant hyperthermia causative mutations by high resolution melt curve analysis. 94
Variable myopathic presentation in a single family with novel skeletal RYR1 mutation. 94
Characterization of excitation-contraction coupling components in human extraocular muscles 93
Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles 93
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor 92
Junctate, an inositol 1,4,5-triphosphate receptor associated protein, is present in rodent sperm and binds TRPC2 and TRPC5 but not TRPC1 channels. 92
Mapping domains and mutations on the skeletal muscle ryanodine receptor channel 92
Over-expression of a retinol dehydrogenase (SRP35/DHRS7C) in skeletal muscle activates mTORC2, enhances glucose metabolism and muscle performance 92
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells 92
Methyl p-hydroxybenzoate (E218) a preservative for drugs and food is an activator of the ryanodine receptor Ca2+ release channel. 92
Malignant hyperthermia domain in the regulation of Ca2+ release channel (Ryanodine receptor) 91
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis. 91
Genotype-phenotype comparison of the Swiss malignant hyperthermia population. 90
Enhanced excitation coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with Central core disease 90
Interaction of lymphokine-activated killer cells with susceptible targets does not induce second messenger generation and cytolytic granule exocytosis 89
null 89
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders. 89
Frequent calcium oscillations lead to NFAT activation in human immature dendritic cells. 88
RYR1-related myopathies: A wide spectrum of phenotypes throughout life 88
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. 87
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy 87
Functional effects of mutations identified in patients with multiminicore disease. 86
Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms 85
Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin 84
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane 84
Frog brain expresses a 60 KDa Ca2+ binding protein similar to mammalian calreticulin 84
The junctional SR protein JP-45 affects the functional expression of the voltage-dependent Ca2+ channel Cav1.1. 83
SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase 83
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle. 82
Identification of calreticulin isoforms in the central nervous system 82
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle 82
Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin 81
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 76
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle 76
Extraocular muscle function is impaired in ryr3(-/-) mice 76
Chlorocresol: an activator of ryanodine receptor mediated Ca2+ release. 75
Agonist-activated Ca2+ influx occurs at stable plasma membrane and endoplasmic reticulum junctions 73
P1 promoter transcriptional activity of the human AbetaH-J-J locus, encoding Aspartil-beta-hydroxylase, Junctin and Junctate 72
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated muscles 71
Alteration of intracellular Ca2+ in COS-7 cells transfected with the cDNA encoding skeltal muscle ryanodine receptor carrying a mutation associated with malignant hyperthermia 70
B-lymphocytes from Malignant Hyperthermia-susceptible Patients Have an Increased Sensitivity to Skeletal Muscle Ryanodine Receptor Activators 69
Current and future therapeutic approaches to the congenitalmyopathies 68
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy 68
Calumin, a novel Ca2+-binding transmembrane protein on the endoplasmic reticulum 68
A ryanodine receptor-like Ca2+ channel is expressed in nonexcitable cells 66
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locus 64
null 63
Identification of the domain recognized by anti-(ryanodine receptor) antibodies which affect Ca2+-induced Ca2+ release 60
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 59
Multiple levels of control of the expression of the human AβH-J-J locus encoding aspartyl-β-hydroxylase, junctin, and junctate 58
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 58
Quantitative reduction of RyR1 protein caused by a single-Allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres 58
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia 57
Atypical periodic paralysis and myalgia. A novel RYR1 phenotype 57
Myocyte enhancer factor 2 activates promoter sequences of the human AβH-J-J locus, encoding aspartyl-β-hydroxylase, junctin, and junctate 55
Remodeling of calcium handling in skeletal muscle through PGC-1 alpha: impact on force, fatigability, and fiber type 55
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice 55
Molecular regulation of the expression of AbetaHJ-J locus, encoding Aspartyl-beta-hydroxylase, Junctin and Junctate 54
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies 54
null 53
Chlorocresol, an additive to commercial succinylcholine, induces contracture of malignant hyperthermic muscles via activation of the ryanodine receptor Ca2+ Channel 52
Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength 50
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 49
Totale 8.920
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Categoria #
all - tutte 35.796
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 35.796
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019895 0 0 0 0 0 0 0 0 0 0 347 548
2019/20202.243 357 90 93 350 174 253 204 234 181 175 83 49
2020/20211.682 128 108 81 218 61 149 130 188 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
2023/2024366 68 63 29 21 49 50 9 65 4 5 3 0
Totale 9.351