[1] Greenberg LH, Tanaka KR, Verdes P. Congenital anomalies probably induced by cyclophosphamide[J]. JAMA, 1964,188:4. [2] 王爱平, 张清林, 王治乔. 上皮生长因子对小鼠的致畸胎作用研究[J]. 中国临床药理学与治疗学, 2003, 8(5): 534-536. [3] 栾世钦, 武玉玲, 马金龙. 叶酸、纤维素C拮抗环磷酰胺致大鼠胚胎神经管畸形的研究[J]. 山东医科大学学报, 1995, 33: 122-151. [4] 栾世钦, 马保华, 陈乃文. 凝集素受体在叶酸、维生素C拮抗环磷酰胺致大鼠胚胎神经管畸形中作用的研究[J]. 解剖学杂志, 1998, 21: 422-424. [5] 栾世钦, 陈乃文, 姜恩亭, 等. 环磷酰胺致神经管畸形与细胞凋亡的关系[J]. 卫生毒理学杂志, 2000, 14(4): 225. [6] Schneider S. Tethered cord syndrome: The neurological examination. In: Yamada S (ed) Tethered cord syndrome. The American Association of Neurological Surgeons[M]. Park Ridge, Illinois, 1996:49-54. [7] Chaube S, Kury G, Murphy ML. Teratogenic effects of cyclophosphamide(NSC-26271)in the rat[J]. Cancer Chemother Rep, 1967, 51(2):363-76. [8] 章晓玲, 项华, 袁振华. 环磷酰胺对大鼠的致畸性和染毒程序的探讨[J]. 癌变·畸变·突变, 1994, 6(6): 27-29. [9] Hengarmer MO, Ellis RE, Horvits HR. Caenorhabiditis elegans gene ced-9 protects cells from programmed cell death[J]. Nature, 1992, 356(6369): 494-499. [10] Marshall KA, Daniel SE, Caims N. Up regulation of the anti-apoptotic protein Bcl-2 may be an early event in neurodegeneration:studies on parkinson's incidental lewy body disease[J]. Bioehem Biophys Res Conunun, 1997, 240(1): 84-87. [11] Blaschke AJ, weiner JA, Chun J. Programmed cell death is a universal feature of embryonic and postnatal neuroproliferative regions throughout the central nervous system[J]. J Comp Neurol, 1998, 396: 39-50. [12] 管孝鞠,王治乔,廖明阳,等. 利用全胚胎培养研究环磷酞胺致畸作用[J]. 中国公共卫生, 2000, 16(2): 113-114. [13] Chipuk JE, Moldoveanu T, Llambi F, et al. The BCL-2 Family Reunion[J]. Molecular Cell, 2010, 37: 299-310. |