scholarly article | Q13442814 |
P356 | DOI | 10.1002/JCP.1040820104 |
P953 | full work available at URL | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjcp.1040820104 |
https://onlinelibrary.wiley.com/doi/full/10.1002/jcp.1040820104 | ||
P698 | PubMed publication ID | 4738109 |
P2093 | author name string | D. M. Fambrough | |
J. A. Powell | |||
P2860 | cites work | LETHAL GENES AND ANALYSIS OF DIFFERENTIATION | Q28155892 |
Hydrogen Ion Buffers for Biological Research* | Q28257659 | ||
Fine structure of mutant (muscular dysgenesis) embryonic mouse muscle | Q28513981 | ||
DEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. I. GENETIC ANALYSIS AND GROSS MORPHOLOGY | Q28585851 | ||
The influence of collagen on the development of muscle clones | Q33802327 | ||
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Electrical properties and acetylcholine sensitivity of singly and multiply innervated avian muscle fibers | Q36387218 | ||
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Retention of differentiation potentialities during prolonged cultivation of myogenic cells | Q36475611 | ||
Acetylcholine receptors: number and distribution at neuromuscular junctions in rat diaphragm | Q44769899 | ||
Induction of thymidine-3H incorporation in multinucleated myotubes by Rous sarcoma virus | Q45823813 | ||
Acetycholine receptor production and incorporation into membranes of developing muscle fibers | Q47968068 | ||
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Fast and slow mammalian muscles after denervation. | Q53764603 | ||
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An in vitro study of normal and mutant myogenesis in the mouse | Q70354301 | ||
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A Comparative Study of Membrane Properties of Innervated and Chronically Denervated Fast and Slow Skeletal Muscles of the Rat | Q72183643 | ||
Anomalous rectification in cat spinal motoneurons and effect of polarizing currents on excitatory postsynaptic potential | Q72300752 | ||
Resting potential and electrical properties of frog slow muscle fibres. Effect of different external solutions | Q72416133 | ||
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P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | physiology | Q521 |
мембраны бололцоо | Q389844 | ||
cell biology | Q7141 | ||
Calcium channel, voltage-dependent, L type, alpha 1S subunit | Q21497155 | ||
electrical properties | Q110583288 | ||
P304 | page(s) | 21–38 | |
P577 | publication date | 1973-08-01 | |
P1433 | published in | Journal of Cellular Physiology | Q1524270 |
P1476 | title | Electrical properties of normal and dysgenic mouse skeletal muscle in culture | |
Electrical properties of normal and dysgenib mouse skeletal muscle in culture | |||
P478 | volume | 82 |
Q28586651 | A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells |
Q39882341 | A maturational defect in passive membrane properties of dystrophic mouse muscle |
Q42667282 | A probable role of dihydropyridine receptors in repression of Ca2+ sparks demonstrated in cultured mammalian muscle |
Q67450956 | A voltage clamp study of the sodium, calcium and chloride spikes of chick skeletal muscle cells grown in tissue culture |
Q68938069 | Acetylcholine receptors of skeletal muscle cells in cultures of rat thymus glands |
Q36510485 | Alpha2delta1 dihydropyridine receptor subunit is a critical element for excitation-coupled calcium entry but not for formation of tetrads in skeletal myotubes |
Q69242863 | An electrophysiological study of skeletal muscle fibres in the 'muscular dysgenesis' mutation of the mouse |
Q69106165 | Appearance of the slow Ca conductance in myotubes from mutant mice with "muscular dysgenesis" |
Q52227796 | Ca2+ levels in myotubes grown from the skeletal muscle of dystrophic (mdx) and normal mice. |
Q70760894 | Calcium-dependent slow potassium conductance in rat skeletal myotubes |
Q53839183 | Calcium-induced release of calcium in muscle: 50 years of work and the emerging consensus. |
Q52422236 | Charge movement and Ca2+ release in normal and dysgenic foetal myotubes |
Q52529385 | Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors. |
Q36410817 | Contractions of dysgenic skeletal muscle triggered by a potentiated, endogenous calcium current |
Q43438664 | Cultured myotubes from skeletal muscle of adult rats. Characterization and action of Anemonia sulcata toxin II. |
Q52710087 | Development of spike potentials in skeletal muscle cells differentiated in vitro from chick embryo |
Q43799376 | Developmental changes of membrane electrical properties in a rat skeletal muscle cell line |
Q36530667 | Dihydropyridine receptor alpha subunits in normal and dysgenic muscle in vitro: expression of alpha 1 is required for proper targeting and distribution of alpha 2 |
Q39716157 | Diseased muscle cells in culture |
Q40858579 | Diseases and disorders of muscle |
Q36412914 | Effect of postnatal development on calcium currents and slow charge movement in mammalian skeletal muscle |
Q67268738 | Effects of thyroxine on transmembrane resting potentials of skeletal muscle cells in culture |
Q39645377 | Electrophysiological and Pharmacological Properties of Skeletal Muscle in Culture |
Q36429103 | Electrophysiological properties of the membrane and acetylcholine receptor in developing rat and chick myotubes |
Q36237030 | Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle |
Q70171925 | Fura-2 imaging of spontaneous and electrically induced oscillations of intracellular free Ca2+ in rat myotubes |
Q35228568 | Heterologous expression of calcium channels |
Q52415118 | Intramembrane charge movement in developing skeletal muscle cells from fetal mice. |
Q57816998 | Long-Term High-Density Extracellular Recordings Enable Studies of Muscle Cell Physiology |
Q71502165 | Measurement of membrane potential and myoplasmic [Ca2+] in developing rat myotubes at rest and in response to stimulation |
Q59467667 | Membrane ionic conductances in normal and denervated skeletal muscle of the rat during development |
Q41460062 | Molecular diversity of voltage-dependent calcium channel |
Q28512350 | Muscle and nerve in muscular dysgenesis in the mouse at birth: Sprouting and multiple innervation |
Q68247683 | Muscle fibers from dysgenic mouse in vivo lack a surface component of peripheral couplings |
Q41376673 | Myofibrillogenesis in rodent skeletal muscle in vitro: two pathways involving thick filament aggregates |
Q67450952 | Physiological and structural properties of colchicine-treated chick skeletal muscle cells grown in tissue culture |
Q91718358 | Postsynaptic CaV1.1-driven calcium signaling coordinates presynaptic differentiation at the developing neuromuscular junction |
Q51728761 | Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling. |
Q42976855 | Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors |
Q34560693 | Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. |
Q59046950 | Restoration of normal function in genetically defective myotubes by spontaneous fusion with fibroblasts |
Q41460054 | Structure and function of voltage-dependent calcium channels from muscle |
Q38275832 | Structure, function, and regulation of the skeletal muscle dihydropyridine receptor |
Q34968538 | Synapse Formation Between Two Clonal Cell Lines |
Q32123389 | Tagging with green fluorescent protein reveals a distinct subcellular distribution of L-type and non-L-type Ca2+ channels expressed in dysgenic myotubes |
Q28584920 | Tissue culture study of murine muscular dysgenesis: role of spontaneous action potential generation in the regulation of muscle maturation |
Q36233592 | Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro. |
Q69352894 | Trophic functions of the neuron. I. Development of neural connections. Receptor properties of developing muscle |
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