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Example text
Ous transmitter functions and identify roughly the penods when such functions can be detected (Table 1). To prepare thIS table, we have usee bott. our results and data from other authors. Most results were obtained in experiments on echinoderms and vertebrates. Obviously. this list is far from being complete. It cannot be ruled out that some transmitter functions l1sted individually 1n tr,e table, belong in fact to the same function. Perl ods of appearance and disappearance are known for non-synoptic functions.
Capasso. • and De Prisco. E. • 1983. On ~he role o~ sero~onin and 5~me~hoxyLryp~amine in ~he regula~ion o~ cell division in sea urchin eggs. Develop. • 98:37. Shaposhnikova. G. • Prokazova. N. • Zvezdina. N. • Tepli~z. N. • and Bergelson. L. • 1984. Shedding o~ gangliosides ~rom ~umor cells depends on cell densi~y. • 140:587. Vacquier. V. • and May. G. • 1980. The cyLolyLic isola~ion o~ ~he cor~ex of ~he sea urchin egg. Develop. • 77:178. Zvezdina. N. D.. Sadykova. K. A.. Mar~ynova. L. E.. Prokazova.
36 Pre-nervous biogenic monoamines are synthesized 1n yolk granules. granules represent the main site for non-receptor binding of biogenic monoomlnes and their l1pophillc cytostatic antagonists. The increase of cytoplasmic Ca2+ leyel triggered by fertilization stimulates monoamine synthesis and also releases monoamines from the yolk gremules. Monoamlnes then react. receptor binding sltes WhlCh are prObably located on the membranes of the endoplasmic reticulum. e. the microfiloments of the cortical cytoplasmic layer.
