Calcium homeostasis in myogenic differentiation factor 1 (MyoD)-transformed, virally-transduced, skin-derived equine myotubes

scientific article

Calcium homeostasis in myogenic differentiation factor 1 (MyoD)-transformed, virally-transduced, skin-derived equine myotubes is …
instance of (P31):
scholarly articleQ13442814

External links are
P819ADS bibcode2014PLoSO...9j5971F
P356DOI10.1371/JOURNAL.PONE.0105971
P932PMC publication ID4141859
P698PubMed publication ID25148524
P5875ResearchGate publication ID264990177

P50authorGeorges VassauxQ39997171
Sue BrownQ43179657
P2093author name stringCesare M Terracciano
Marta Fernandez-Fuente
Richard J Piercy
Pilar Martin-Duque
P2860cites workA simplified system for generating recombinant adenovirusesQ24682328
Enhanced resistance to fatigue and altered calcium handling properties of sarcalumenin knockout miceQ28509838
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasisQ29871452
A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skippingQ33523810
Genetics and pathogenesis of malignant hyperthermiaQ33789806
RyR1-mediated Ca2+ leak and Ca2+ entry determine resting intracellular Ca2+ in skeletal myotubesQ33810099
MyoD converts primary dermal fibroblasts, chondroblasts, smooth muscle, and retinal pigmented epithelial cells into striated mononucleated myoblasts and multinucleated myotubesQ33843740
Ryanodine receptor mutations in malignant hyperthermia and central core diseaseQ33903152
Epidemiology of exertional rhabdomyolysis susceptibility in standardbred horses reveals associated risk factors and underlying enhanced performanceQ33996146
Myoblasts generated by lentiviral mediated MyoD transduction of myotonic dystrophy type 1 (DM1) fibroblasts can be used for assays of therapeutic moleculesQ34073069
Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release channel (RYR1).Q34092847
Anaesthetic deaths in a familyQ34251990
Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD.Q34290920
Use of thapsigargin to study Ca2+ homeostasis in cardiac cellsQ34399135
Identification of a Mutation in Porcine Ryanodine Receptor Associated with Malignant HyperthermiaQ34795568
Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leakQ34880821
Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptorQ35060776
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathiesQ35221453
Effects of tetracaine on voltage-activated calcium sparks in frog intact skeletal muscle fibersQ36295622
The role of Ca2+ in muscle cell damageQ36420086
Effects of perchlorate on the molecules of excitation-contraction coupling of skeletal and cardiac muscleQ36435118
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core diseaseQ36460971
Dantrolene-induced inhibition of skeletal L-type Ca2+ current requires RyR1 expressionQ36665389
The skeletal L-type Ca(2+) current is a major contributor to excitation-coupled Ca(2+) entryQ37023260
SERCA pumps and human diseases.Q37056443
A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activityQ37142856
Effects of tetracaine on sarcoplasmic calcium release in mammalian skeletal muscle fibres.Q51471892
Dual effects of tetracaine on spontaneous calcium release in rat ventricular myocytes.Q51544236
Differential effects of ryanodine and tetracaine on charge movement and calcium transients in frog skeletal muscleQ51722203
Intracellular ionized calcium concentration in muscles from humans with malignant hyperthermia.Q51825849
RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling.Q52639740
Pale, soft exudative pork, porcine stress syndrome and malignant hyperpyrexia--an identity?Q52735184
Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathiesQ57334263
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-q13.2.Q68873777
Pharmacokinetics of dantrolene sodium in horsesQ69403368
[Ca2+]i in muscles of malignant hyperthermia susceptible pigs determined in vivo with Ca2+ selective microelectrodesQ70020725
Ratio of dihydropyridine to ryanodine receptors in mammalian and frog twitch muscles in relation to the mechanical hypothesis of excitation-contraction couplingQ72704089
Epidemiologic analysis of factors influencing exertional rhabdomyolysis in ThoroughbredsQ73326857
Methods for animal satellite cell culture under a variety of conditionsQ73391179
In vitro contractile responses and contracture testing of skeletal muscle from Quarter Horses with exertional rhabdomyolysisQ77905616
Exclusion of linkage of the RYR1, CACNA1S, and ATP2A1 genes to recurrent exertional rhabdomyolysis in ThoroughbredsQ80041563
Prevalence and demographic characteristics of exertional rhabdomyolysis in horses in AustraliaQ81082626
Incidence and risk factors associated with exertional rhabdomyolysis syndrome in National Hunt racehorses in Great BritainQ81840578
Effect of feed restriction on plasma dantrolene concentrations in horsesQ82358920
High efficiency myogenic conversion of human fibroblasts by adenoviral vector-mediated MyoD gene transfer. An alternative strategy for ex vivo gene therapy of primary myopathiesQ37381930
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rodsQ37458493
Conformational activation of Ca2+ entry by depolarization of skeletal myotubesQ37595562
Core myopathiesQ37968743
Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: a review of literature and a cross-sectional clinical study in 17 patientsQ38019238
Standardization of the caffeine halothane muscle contracture test. North American Malignant Hyperthermia GroupQ38693338
Elevated resting [Ca(2+)](i) in myotubes expressing malignant hyperthermia RyR1 cDNAs is partially restored by modulation of passive calcium leak from the SR.Q40191570
Characterization of recessive RYR1 mutations in core myopathiesQ40238382
Myocyte differentiation generates nuclear invaginations traversed by myofibrils associating with sarcomeric protein mRNAsQ40486212
The effects of pentobarbital on 2,4-dinitrophenol induced malignant hyperthermia during halothane general anesthesia in dogsQ40923434
Malignant hyperthermia: excitation-contraction coupling, Ca2+ release channel, and cell Ca2+ regulation defectsQ40980921
Measurement of resting cytosolic Ca2+ concentrations and Ca2+ store size in HEK-293 cells transfected with malignant hyperthermia or central core disease mutant Ca2+ release channels.Q40984666
Adenovirus-mediated expression of myogenic differentiation factor 1 (MyoD) in equine and human dermal fibroblasts enables their conversion to caffeine-sensitive myotubesQ42248848
Store-operated Ca2+ entry modulates sarcoplasmic reticulum Ca2+ loading in neonatal rabbit cardiac ventricular myocytes.Q42678340
Assessment of the transformation of equine skin-derived fibroblasts to multinucleated skeletal myotubes following lentiviral-induced expression of equine myogenic differentiation 1.Q42805722
Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia GroupQ42908824
T-tubule depolarization-induced SR Ca2+ release is controlled by dihydropyridine receptor- and Ca(2+)-dependent mechanisms in cell homogenates from rabbit skeletal muscleQ42976969
A quantitative technique for growing human adult skeletal muscle in culture starting from mononucleated cellsQ43878653
Effect of oral administration of dantrolene sodium on serum creatine kinase activity after exercise in horses with recurrent exertional rhabdomyolysisQ44726032
Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core diseaseQ45010236
Association of a mutation in the ryanodine receptor 1 gene with equine malignant hyperthermiaQ45023074
Pharmacokinetics and metabolism of dantrolene in horsesQ45826305
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis.Q45982130
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.Q46023528
Three independent mechanisms contribute to tetracaine inhibition of cardiac calcium release channelsQ48259475
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue8
P407language of work or nameEnglishQ1860
P304page(s)e105971
P577publication date2014-01-01
P1433published inPLOS OneQ564954
P1476titleCalcium homeostasis in myogenic differentiation factor 1 (MyoD)-transformed, virally-transduced, skin-derived equine myotubes
P478volume9

Search more.