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29. High molecular weight polymers block cortical granule exocytosis in sea urchin eggs at the level of granule matrix disassembly. Chandler DE, Whitaker M, Zimmerberg J. J Cell Biol; 1989 Sep; 109(3):1269-78. PubMed ID: 2475509 [Abstract] [Full Text] [Related]
33. Non-propagated cortical reactions induced by the divalent ionophore A23187 in eggs of the sea urchin, Lytechinus variegatus. Chambers EL, Hinkley RE. Exp Cell Res; 1979 Dec; 124(2):441-6. PubMed ID: 389650 [No Abstract] [Full Text] [Related]
34. Change in the calcium-binding capacity of sea urchin egg homogenate caused by treatment with ATP and magnesium ions. Nakamura M, Yasumasu I. Exp Cell Res; 1974 Sep; 88(1):121-6. PubMed ID: 4472785 [No Abstract] [Full Text] [Related]
35. Isolated cortical granules: a model system for studying membrane fusion and calcium-mediated exocytosis. Vacquier VD. J Supramol Struct; 1976 Sep; 5(1):27-35. PubMed ID: 11368 [Abstract] [Full Text] [Related]
36. Sodium-potassium exchange in sea urchin egg. II. Ionic events stimulating the Na+-K+ pump activity at fertilization. Ciapa B, Allemand D, Payan P, Girard JP. J Cell Physiol; 1984 Oct; 121(1):243-50. PubMed ID: 6090478 [Abstract] [Full Text] [Related]
38. Intracellular calcium release and the mechanisms of parthenogenetic activation of the sea urchin egg. Zucker RS, Steinhardt RA, Winkler MM. Dev Biol; 1978 Aug; 65(2):285-95. PubMed ID: 355009 [No Abstract] [Full Text] [Related]