参考文献/References:
[1] 王江涛.Notch信号通路在神经干细胞分化过程中的调节作用研究\[D\]. 山西医科大学,2009.
[2] 李鹏飞,李月华,王春芳.干扰miR31表达初期Notch和Hedgehog信号通路相关基因在神经干细胞中的表达变化[J]. 解剖学杂志, 2017,40(4):408411.
\[3\] 〖JP3〗张文贤,王昱军,王小燕,等.神经干细胞信号转导通路的研究进展[J].中国修复重建外科杂志,2008,22(4):492495.〖JP〗
\[4\] 〖JP3〗王 珏,邓宇斌,万 勇.Notch信号通路对神经干细胞增殖分化的作用[J].中国细胞生物学学报,2014,36 (5):708712.〖JP〗
\[5\] 陈兴书,姚忠祥.神经分化发育相关基因Mash1的研究进展[J].生理科学进展,2006,37(1):6164.
[6] 王 菲. Hes1和Mash1基因在脊髓源神经干细胞诱导分化为胆碱能神经元过程中表达的研究\[D\].山西医科大学,2009.
[7] 王剑博,刘卫平,章 翔,等.神经干细胞分化过程中bHLH基因表达[J].中华神经外科疾病研究杂志,2007,7(3):199202.
[8] 李灵玲,周达岸.脊髓损伤后Notch信号对神经再生的研究现状[J].中国康复医学杂志,2016,31(4):485488.
[9] 张 瑞. 重组Mash1慢病毒表达载体的构建及表达\[D\]. 郑州大学, 2006.
[10] 张君度,龙大宏,陈 艳,等.神经干细胞定向分化为多巴胺能神经元过程中Mash1及Hes1基因的表达[J].解剖学研究,2015,37(3):167171.
[11] Park C H, Kang J S, Kim J S, et al. Differential actions of the proneural genes encoding Mash1 and neurogenins in Nurr1induced dopamine neuron differentiation[J]. Journal of Cell Science, 2006,119(11):23102320.
[12] 赵 斌,汉 华,白登彦,等.信号转导通路在神经干细胞分化及其修复脊髓损伤过程中的作用[J].中国组织工程研究与临床康复,2008,12(51):1015910162.
[13] Roybon L, Mastracci TL, Ribeiro D, et al. GABAergic differentiation induced by Mash1 is compromised by the bHLH proteins neurogenin2, neuroD1, and neuroD2[J]. Cerebral Cortex, 2010, 20(5):12341244.
[14] Arai M D, Zhan B, Maruyama A, et al. Enriched environment and Mash1 transfection affect neural stem cell differentiation after transplantation into the adult somatosensory cortex[J]. Journal of the Neurological Sciences, 2017, 373:73.
[15] Jessberger S, Toni N, Jr CG, et al. Directed differentiation of hippocampal stem/progenitor cells in the adult brain[J]. Nature Neuroscience, 2008, 11(8):88893.
[16] Bond AM, Peng CY, Meyers EA, et al. BMP signaling regulates the tempo of adult hippocampal progenitor maturation at multiple stages of the lineage[J]. Stem Cells, 2014, 32(8):22012214.
[17] Serre A, Snyder EY, Mallet J, et al. Overexpression of basic helixloophelix transcription factors enhances neuronal differentiation of fetal human neural progenitor cells in various ways[J]. Stem Cells & Development, 2012, 21(4):539553.
[18] Horton S, Meredith A, Richardson JA, et al. Correct coordination of neuronal differentiation events in ventral forebrain requires the bHLH factor MASH1 [J].Molecular & Cellular Neuroscience, 1999, 14(45):355369.
[19] Kageyama R, Ishibashi M, Takebayashi K, et al. bHLH transcription factors and mammalian neuronal differentiation[J]. International Journal of Biochemistry & Cell Biology, 1997, 29(12):13891399.
[20] Ichimiya S, Nimura Y, Seki N, et al. Downregulation of hASH1, is associated with the retinoic acidinduced differentiation of human neuroblastoma cell lines[J]. Pediatric Blood & Cancer, 2015, 36(1):132134.
[21] 庞希宁,徐国彤,付小兵.现代干细胞与再生医学\[M\].北京:人民卫生出版社,2017:259262.
[22] 〖JP3〗LeQin XU, XiaoFeng LI, Shi Q, et al. Effects of transfection of mash1 gene on neural differentiation of embryonic stem cell in spinal cord injury mice[J]. Chinese Journal of Rehabilitation Theory & Practice, 2016,22(1):4652.〖JP〗
[23] 夏计划,邹国耀. 脊髓损伤的治疗现状及进展[J]. 中国医药科学, 2013, 3(9): 4647, 79.
[24] Meredith A, Johnson JE. Negative autoregulation of Mash1 expression in CNS development[J]. Developmental Biology, 2000, 222(2):336346.
[25] Lee JH, Kim DK. Molecular genetics of congenital central hypoventilation syndrome and Haddad syndrome[J]. Journal of Genetic Medicine, 2014, 11(1):11.
[26] Dauger S, Renolleau S, Vardon G, et al. Ventilatory responses to hypercapnia and hypoxia in Mash1 heterozygous newborn and adult mice[J]. Pediatric Research, 1999, 46(5):535.
[27] De PL, Nepote V, AttieBitach T, et al. Noradrenergic neuronal development is impaired by mutation of the proneural HASH1 gene in congenital central hypoventilation syndrome (Ondine's curse)[J]. Human Molecular Genetics, 2003, 12(23):31733180.
[28] Tang BL. The Potential of targeting brain pathology with Ascl1/Mash1[J]. Cells, 2017, 6(3):26.
[29] 刘 冰, 卞晶晶, 李晓琎,等. NeuroD1在ALS转基因鼠脊髓的表达[J]. 济宁医学院学报, 2017, 40(4):286290.