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Volumn 112, Issue 2, 1985, Pages 458-466
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Abnormal transverse tubule system and abnormal amount of receptors for Ca2+ channel inhibitors of the dihydropyridine family in skeletal muscle from mice with embryonic muscular dysgenesis
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Author keywords
[No Author keywords available]
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Indexed keywords
CALCIMYCIN;
DIHYDROPYRIDINE DERIVATIVE;
ISRADIPINE;
RADIOISOTOPE;
ANIMAL CELL;
ANIMAL MODEL;
CALCIUM CHANNEL;
DRUG EFFICACY;
DRUG RECEPTOR BINDING;
ELECTRON MICROSCOPY;
ISRADIPINE H 3;
MOUSE;
MUSCLE;
MUSCLE CELL;
MUSCLE DYSGENESIS;
NITRENDIPINE H 3;
NONHUMAN;
PHARMACOKINETICS;
PRIORITY JOURNAL;
SARCOPLASMIC RETICULUM;
TRANSVERSE TUBULAR SYSTEM;
ANIMAL;
CALCIUM;
CALCIUM CHANNEL BLOCKERS;
CALCIUM CHANNELS;
ION CHANNELS;
ISRADIPINE;
MICE;
MICE, MUTANT STRAINS;
MICROSCOPY, ELECTRON;
MUSCLES;
MUSCULAR DISEASES;
MYOFIBRILS;
OXADIAZOLES;
RECEPTORS, NICOTINIC;
SARCOPLASMIC RETICULUM;
SUPPORT, NON-U.S. GOV'T;
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EID: 0022312714
PISSN: 00121606
EISSN: None
Source Type: Journal
DOI: 10.1016/0012-1606(85)90418-X Document Type: Article |
Times cited : (65)
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References (41)
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