LETHAL GENES AND ANALYSIS OF DIFFERENTIATION

scientific article (publication date: 6 December 1963)

LETHAL GENES AND ANALYSIS OF DIFFERENTIATION is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1126/SCIENCE.142.3597.1269
P698PubMed publication ID14074837

P2093author name stringS GLUECKSOHN-WAELSCH
P433issue3597
P407language of work or nameEnglishQ1860
P304page(s)1269-76
P577publication date1963-12-06
P1433published inScienceQ192864
P1476titleLETHAL GENES AND ANALYSIS OF DIFFERENTIATION
P478volume142

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cites work (P2860)
Q4713491114-3-3ζ loss leads to neonatal lethality by microRNA-126 downregulation-mediated developmental defects in lung vasculature
Q66924653A lethal mutation (cab) affecting heart function in the mouse
Q28586651A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells
Q69242863An electrophysiological study of skeletal muscle fibres in the 'muscular dysgenesis' mutation of the mouse
Q70354301An in vitro study of normal and mutant myogenesis in the mouse
Q69106165Appearance of the slow Ca conductance in myotubes from mutant mice with "muscular dysgenesis"
Q66977344Biochemical and electrophoretic studies of cholinesterases in the muscular dysgenesis (mdg) mutant mouse
Q43107664Biogenesis of transverse tubules and triads: immunolocalization of the 1,4-dihydropyridine receptor, TS28, and the ryanodine receptor in rabbit skeletal muscle developing in situ
Q41655875Conditional immortalization of normal and dysgenic mouse muscle cells by the SV40 large T antigen under the vimentin promoter control
Q52341467Developmental genetics of a recessive allele at the complex T-locus in the mouse
Q39716157Diseased muscle cells in culture
Q28508591Electrical properties of normal and dysgenib mouse skeletal muscle in culture
Q39805359Embryology of two murine muscle diseases: muscular dystrophy and muscular dysgenesis
Q28588243Endogenous cardiac Ca2+ channels do not overcome the E‐C coupling defect in immortalized dysgenic muscle cells: evidence for a missing link
Q28587644Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene
Q28513981Fine structure of mutant (muscular dysgenesis) embryonic mouse muscle
Q39256104Genetic control of morphogenetic and biochemical differentiation: Lethal albino deletions in the mouse
Q68457439Induction of normal ultrastructure by CGRP treatment in dysgenic myotubes
Q40608398Inherited muscle and nerve diseases in mice: a tabulation with commentary
Q59051250Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle
Q54023197Metabolic Availability of Vitamin C in the Guinea-pig
Q41460062Molecular diversity of voltage-dependent calcium channel
Q28512350Muscle and nerve in muscular dysgenesis in the mouse at birth: Sprouting and multiple innervation
Q68247683Muscle fibers from dysgenic mouse in vivo lack a surface component of peripheral couplings
Q24517877Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis
Q52307095Neuromuscular interactions--tendencies toward a biochemical-genetic analysis
Q34242858On the genetic etiology of scurvy
Q51728761Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling.
Q42976855Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors
Q54075376Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics.
Q34560693Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA.
Q28513694Restoration of normal ultrastructure after expression of the alpha 1 subunit of the L-type Ca2+ channel in dysgenic myotubes
Q67585118Spermatogenesis revisited. III. The course of spermatogenesis in a male-sterile pink-eyed mutant type in the mouse
Q34244575The Genetic Disease, Hypoascorbemia: A Fresh Approach to an Ancient Disease and Some of its Medical Implications
Q39987720The Migration and Differentiation of Neural Crest Cells
Q28250118The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32
Q36762503Towards a compendium of essential genes - From model organisms to synthetic lethality in cancer cells
Q35401537Vitamin C deficiency: more than just a nutritional disorder

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