Borrelli M J, Mackey M A, Dewey W C
Exp Cell Res. 1987 Jun;170(2):363-8. doi: 10.1016/0014-4827(87)90313-2.
A modification of the protocol developed by Kawamoto, J C & Barrett, J N, Brain res (1986), in press for freezing primary neuron cultures in a solution containing low sodium and high lactate and potassium concentrations was used to freeze synchronous mitotic and G1 CHO cells. After thawing, the cells behaved as if they had never been frozen with respect to cell growth, cell division, plating efficiency, and hyperthermic sensitivity.
采用了由川本（Kawamoto, J C）和巴雷特（Barrett, J N）开发的方案的一种改进方法（《脑研究》（Brain res），1986年，即将发表），该方案用于在含有低钠、高乳酸和高钾浓度的溶液中冷冻原代神经元培养物，以此来冷冻同步有丝分裂期和G1期的中国仓鼠卵巢（CHO）细胞。解冻后，这些细胞在细胞生长、细胞分裂、接种效率和热敏感性方面的表现就如同从未被冷冻过一样。
