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Neuromuscular Disorders : NMD|November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridizationC Rosenberg, L Navajas, D F Vagenas, et al.Brain Research|June 1, 1981
Injection of alpha-bungarotoxin near the suprachiasmatic nucleus blocks the effects of light on nocturnal pineal enzyme activityM Zatz, M J BrownsteinThe American Journal of Physiology|December 1, 1991
Low salt mimics effects of dark pulses on circadian pacemaker in cultured chick pineal cellsM Zatz, H M WangJournal of the Neurological Sciences|September 1, 1980
Effect of age on the detection rate in Duchenne muscular dystrophyM Zatz, P A OttoJournal of the Neurological Sciences|September 1, 1980
The use of concomitant serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysisM Zatz, P A OttoThe Journal of Biological Chemistry|April 25, 1984
Acylation of bovine rhodopsin by [3H]palmitic acidP J O'Brien, M ZatzJournal of Cyclic Nucleotide Research|November 1, 1976
Regulation of protein kinase in rat pineal: increased Vmax in supersensitive glandsM Zatz, R F O'DeaBrain Research|October 31, 1994
Synthesis of heat shock proteins in cultured chick pineal cellsM S Wolfe, M ZatzBrain Research|October 30, 1989
Ouabain (or salt solution lacking potassium) mimics the effects of dark pulses on the circadian pacemaker in cultured chick pineal cellsM Zatz, D A MullenAmerican Journal of Medical Genetics|November 1, 1983
Creatine-kinase (CK) and pyruvate-kinase (PK) activities in cord blood of normal newborn infants: application to Duchenne muscular dystrophy screening programsM R Passos, M ZatzPageof 26