| P50 | author | Dilyana Filipova | Q59704564 |
| | Anna Brunn | Q63977993 |
| | Symeon Papadopoulos | Q87841101 |
| | Agapios Sachinidis | Q90241000 |
| | Martina Deckert | Q91150759 |
| | Jürgen Hescheler | Q94114332 |
| | Gabriele Pfitzer | Q114780094 |
| | Tamara Rotshteyn | Q114780098 |
| P2093 | author name string | Margit Henry | |
| | Mariana Carstov | |
| P2860 | cites work | MicroRNA transcriptome profiles during swine skeletal muscle development | Q21283739 |
| | Excitation-contraction coupling in muscular response | Q24647456 |
| | The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation | Q24650204 |
| | Distinctive patterns of microRNA expression in primary muscular disorders | Q24675407 |
| | Ca2+-dependent regulations and signaling in skeletal muscle: from electro-mechanical coupling to adaptation | Q27001582 |
| | Structural Basis for Gating and Activation of RyR1. | Q27728108 |
| | Channelopathies of skeletal muscle excitability | Q28082428 |
| | Costameres are sites of force transmission to the substratum in adult rat cardiomyocytes | Q28268876 |
| | The effects of obesity on skeletal muscle regeneration | Q28393087 |
| | Differential gene expression in skeletal muscle cells after membrane depolarization | Q28572827 |
| | DEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. II. DEVELOPMENTAL ANALYSIS | Q28584771 |
| | DEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. I. GENETIC ANALYSIS AND GROSS MORPHOLOGY | Q28585851 |
| | Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene | Q28587644 |
| | Effects of the muscular dysgenesis gene on developmental stability in the mouse mandible | Q28593869 |
| | ClustVis: a web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap | Q30950943 |
| | RyR1-mediated Ca2+ leak and Ca2+ entry determine resting intracellular Ca2+ in skeletal myotubes | Q33810099 |
| | Looking for answers to EC coupling's persistent questions | Q33950677 |
| | Calcium ion in skeletal muscle: its crucial role for muscle function, plasticity, and disease | Q33967669 |
| | Genome-wide profiling of the microRNA-mRNA regulatory network in skeletal muscle with aging | Q34128597 |
| | M3 subtype of muscarinic acetylcholine receptor promotes cardioprotection via the suppression of miR-376b-5p | Q34187234 |
| | Mir193b-365 is essential for brown fat differentiation | Q34199261 |
| | Building muscle: molecular regulation of myogenesis. | Q34251533 |
| | Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction | Q34307627 |
| | Muscle as a secretory organ | Q34360586 |
| | The sarcomeric Z-disc: a nodal point in signalling and disease | Q34485166 |
| | Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool | Q34668270 |
| | Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome | Q34739919 |
| | Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leak | Q34880821 |
| | Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor | Q35060776 |
| | TNF-α and IGF1 modify the microRNA signature in skeletal muscle cell differentiation | Q35077416 |
| | miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells | Q35618210 |
| | miR-431 promotes differentiation and regeneration of old skeletal muscle by targeting Smad4. | Q35952729 |
| | Mechanical signal transduction in skeletal muscle growth and adaptation | Q36097626 |
| | Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro. | Q36233592 |
| | MicroRNA expression patterns in post-natal mouse skeletal muscle development. | Q36243045 |
| | Fluorescence resonance energy transfer (FRET) indicates that association with the type I ryanodine receptor (RyR1) causes reorientation of multiple cytoplasmic domains of the dihydropyridine receptor (DHPR) α(1S) subunit | Q36436167 |
| | Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca(2+) release channel | Q36527573 |
| | TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy | Q36590389 |
| | miR-434-3p and DNA hypomethylation co-regulate eIF5A1 to increase AChRs and to improve plasticity in SCT rat skeletal muscle. | Q36675011 |
| | miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors | Q36797876 |
| | Cellular heterogeneity during vertebrate skeletal muscle development | Q36870830 |
| | The functional consequences of age-related changes in microRNA expression in skeletal muscle | Q36958102 |
| | MicroRNA-22 regulates cardiac hypertrophy and remodeling in response to stress | Q37038566 |
| | A CaV1.1 Ca2+ channel splice variant with high conductance and voltage-sensitivity alters EC coupling in developing skeletal muscle | Q37260318 |
| | Effects of inserting fluorescent proteins into the alpha1S II-III loop: insights into excitation-contraction coupling | Q37267658 |
| | Myotube-derived exosomal miRNAs downregulate Sirtuin1 in myoblasts during muscle cell differentiation | Q37587033 |
| | Skeletal muscle stem cells in developmental versus regenerative myogenesis | Q37599934 |
| | miR-127 enhances myogenic cell differentiation by targeting S1PR3. | Q37745404 |
| | Skeletal muscle: energy metabolism, fiber types, fatigue and adaptability | Q37767925 |
| | A new L-type calcium channel isoform required for normal patterning of the developing neuromuscular junction. | Q37945006 |
| | microRNAs in skeletal muscle differentiation and disease | Q38034250 |
| | MicroRNAs involved in skeletal muscle differentiation | Q38092278 |
| | Calcium's role in mechanotransduction during muscle development | Q38187834 |
| | Origin, evolution, and biological role of miRNA cluster in DLK-DIO3 genomic region in placental mammals | Q38514376 |
| | Myostatin inhibits osteoblastic differentiation by suppressing osteocyte-derived exosomal microRNA-218: A novel mechanism in muscle-bone communication | Q38705141 |
| | Targeting of miR-432 to myozenin1 to regulate myoblast proliferation and differentiation | Q38724976 |
| | Autoregulatory loop between TGF-β1/miR-411-5p/SPRY4 and MAPK pathway in rhabdomyosarcoma modulates proliferation and differentiation | Q38842344 |
| | Axial and limb muscle development: dialogue with the neighbourhood. | Q38877226 |
| | Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors. | Q39569719 |
| | Calcium regulation of muscle contraction | Q41480233 |
| | The Ca2+ influx through the mammalian skeletal muscle dihydropyridine receptor is irrelevant for muscle performance. | Q41536477 |
| | Myostatin-deficiency in mice increases global gene expression at the Dlk1-Dio3 locus in the skeletal muscle | Q42283360 |
| | Ca2+ release through ryanodine receptors regulates skeletal muscle L-type Ca2+ channel expression. | Q43559613 |
| | Depolarization-induced slow calcium transients activate early genes in skeletal muscle cells | Q44279055 |
| | Mapping sites of potential proximity between the dihydropyridine receptor and RyR1 in muscle using a cyan fluorescent protein-yellow fluorescent protein tandem as a fluorescence resonance energy transfer probe | Q44997701 |
| | Dyspedic mouse skeletal muscle expresses major elements of the triadic junction but lacks detectable ryanodine receptor protein and function | Q45256995 |
| | Membrane electrical activity elicits inositol 1,4,5-trisphosphate-dependent slow Ca2+ signals through a Gbetagamma/phosphatidylinositol 3-kinase gamma pathway in skeletal myotubes | Q46973000 |
| | Intra-familial variability associated with recessive RYR1 mutation diagnosed prenatally by exome sequencing. | Q51519721 |
| | The muscular dysgenesis mutation in mice leads to arrest of the genetic program for muscle differentiation. | Q52246190 |
| | Craniofacial development in the absence of muscle contraction. | Q52290331 |
| | Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor. | Q52519047 |
| | MicroRNA-431 accelerates muscle regeneration and ameliorates muscular dystrophy by targeting Pax7 in mice. | Q53436627 |
| | Mechanotransduction pathways in skeletal muscle hypertrophy. | Q54543090 |
| | Intrinsic phenotypic diversity of embryonic and fetal myoblasts is revealed by genome-wide gene expression analysis on purified cells. | Q59120502 |
| | Muscle fibers from dysgenic mouse in vivo lack a surface component of peripheral couplings | Q68247683 |
| | The origin of secondary myotubes in mammalian skeletal muscles: ultrastructural studies | Q69133653 |
| | The development of spontaneous body movement in prenatal and perinatal mice | Q71297546 |
| | Temporal differences in the induction of dihydropyridine receptor subunits and ryanodine receptors during skeletal muscle development | Q72136092 |
| | During fetal muscle development, clones of cells contribute to both primary and secondary fibers | Q72345744 |
| | Localization in the II-III loop of the dihydropyridine receptor of a sequence critical for excitation-contraction coupling | Q77300019 |
| | Serum profiling identifies novel muscle miRNA and cardiomyopathy-related miRNA biomarkers in Golden Retriever muscular dystrophy dogs and Duchenne muscular dystrophy patients | Q85261421 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | transcriptome | Q252857 |
| P304 | page(s) | e0194428 | |
| P577 | publication date | 2018-03-15 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5. | |
| P478 | volume | 13 | |