2016
Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3
Linsley JW, Hsu IU, Groom L, Yarotskyy V, Lavorato M, Horstick EJ, Linsley D, Wang W, Franzini-Armstrong C, Dirksen RT, Kuwada JY. Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. Proceedings Of The National Academy Of Sciences Of The United States Of America 2016, 114: e228-e236. PMID: 28003463, PMCID: PMC5240691, DOI: 10.1073/pnas.1619238114.Peer-Reviewed Original ResearchConceptsEC couplingDihydropyridine receptorNative American myopathySarcoplasmic reticulumExcitation-contraction couplingSkeletal muscle contractionVoltage-sensing dihydropyridine receptorCaffeine-induced CaRyanodine receptor 1Receptor 1Muscle contractionInternal storesMuscle Ca2Muscle fibersSTAC3Luminal CaMyopathyTransverse tubule membranesTubule membranesCaffeine sensitivityHuman myopathiesCoupling apparatusHuman diseasesDynamic imagingCritical role
2014
Epigenetic patterns in successful weight loss maintainers: a pilot study
Huang Y, Maccani J, Hawley N, Wing R, Kelsey K, McCaffery J. Epigenetic patterns in successful weight loss maintainers: a pilot study. International Journal Of Obesity 2014, 39: 865-868. PMID: 25520250, PMCID: PMC4422763, DOI: 10.1038/ijo.2014.213.Peer-Reviewed Original ResearchConceptsOB individualsSuccessful weight loss maintainersBrain-derived neurotrophic factorBehavioral weight loss interventionWeight loss maintainersWeight loss interventionMyelin protein zeroLoss interventionNormal weightNeurotrophic factorObese individualsRyanodine receptor 1Weight statusAnimal modelsCalorie restrictionReceptor 1NW individualsPilot studyWeight lossProtein zeroMethylation patternsEpigenome-wide analysisHuman subjectsEpigenetic patternsDNA methylation changes
This site is protected by hCaptcha and its Privacy Policy and Terms of Service apply