[1] |
MICHALOPOULOS GK, BHUSHAN B. Liver regeneration: biological and pathological mechanisms and implications[J]. Nat Rev Gastroenterol Hepatol, 2021, 18( 1): 40- 55. DOI: 10.1038/s41575-020-0342-4.
|
[2] |
LIN S, NASCIMENTO EM, GAJERA CR, et al. Distributed hepatocytes expressing telomerase repopulate the liver in homeostasis and injury[J]. Nature, 2018, 556( 7700): 244- 248. DOI: 10.1038/s41586-018-0004-7.
|
[3] |
CHEN HX, HUANG SJ, CHEN JY, et al. Role of complement in liver injury and regeneration[J]. Central South Pharm, 2021, 19( 10): 2123- 2127. DOI: 10.7539/j.issn.1672-2981.2021.10.023.
陈海霞, 黄少杰, 陈锦仪, 等. 补体在肝脏损伤与再生中的作用[J]. 中南药学, 2021, 19( 10): 2123- 2127. DOI: 10.7539/j.issn.1672-2981.2021.10.023.
|
[4] |
WANG Q, QU X. New insights into the roles of RGC32[J]. Cell Mol Immunol, 2018, 15( 8): 803- 804. DOI: 10.1038/cmi.2017.154.
|
[5] |
LI JX, LI MY. Research progress in animal models of regeneration[J]. Med Recapitulate, 2021, 27( 23): 4629- 4633. DOI: 10.3969/j.issn.1006-2084.2021.23.011.
李嘉兴, 李明意. 肝脏再生动物模型研究进展[J]. 医学综述, 2021, 27( 23): 4629- 4633. DOI: 10.3969/j.issn.1006-2084.2021.23.011.
|
[6] |
NEVZOROVA YA, TOLBA R, TRAUTWEIN C, et al. Partial hepatectomy in mice[J]. Lab Anim, 2015, 49( Suppl 1): 81- 88. DOI: 10.1177/0023677215572000.
|
[7] |
LÓPEZ-LUQUE J, FABREGAT I. Revisiting the liver: from development to regeneration-what we ought to know![J]. Int J Dev Biol, 2018, 62( 6- 7- 8): 441- 451. DOI: 10.1387/ijdb.170264JL.
|
[8] |
van HAELE M, SNOECK J, ROSKAMS T. Human liver regeneration: an etiology dependent process[J]. Int J Mol Sci, 2019, 20( 9): 2332. DOI: 10.3390/ijms20092332.
|
[9] |
YAGI S, HIRATA M, MIYACHI Y, et al. Liver regeneration after hepatectomy and partial liver transplantation[J]. Int J Mol Sci, 2020, 21( 21): 8414. DOI: 10.3390/ijms21218414.
|
[10] |
YU ZY, LIN X, HAN Y, et al. Role of liver sinusoidal endothelial cells in liver regeneration and the development of liver fibrosis[J]. J Clin Hepatol, 2019, 35( 9): 2072- 2074. DOI: 10.3969/j.issn.1001-5256.2019.09.041.
于子越, 蔺鑫, 韩英, 等. 肝血窦内皮细胞在肝再生和肝纤维化发生中的作用[J]. 临床肝胆病杂志, 2019, 35( 9): 2072- 2074. DOI: 10.3969/j.issn.1001-5256.2019.09.041.
|
[11] |
LI N, LIU C, MA G, et al. Asparaginyl endopeptidase may promote liver sinusoidal endothelial cell angiogenesis via PI3K/Akt pathway[J]. Rev Esp Enferm Dig, 2019, 111( 3): 214- 222. DOI: 10.17235/reed.2018.5709/2018.
|
[12] |
VLAICU SI, TATOMIR A, ANSELMO F, et al. RGC32 and diseases: the first 20 years[J]. Immunol Res, 2019, 67( 2- 3): 267- 279. DOI: 10.1007/s12026-019-09080-0.
|
[13] |
YU L, YU YH. Research of RGC32 in tumor[J]. Mil Med J Southeast China, 2020, 22( 1): 71- 75. DOI: 10.3969/j.issn.1672-271X.2020.01.016.
禹乐, 余英豪. RGC32在肿瘤中的研究进展[J]. 东南国防医药, 2020, 22( 1): 71- 75. DOI: 10.3969/j.issn.1672-271X.2020.01.016.
|
[14] |
VLAICU SI, TATOMIR A, BOODHOO D, et al. RGC32 is expressed in the human atherosclerotic arterial wall: Role in C5b-9-induced cell proliferation and migration[J]. Exp Mol Pathol, 2016, 101( 2): 221- 230. DOI: 10.1016/j.yexmp.2016.09.004.
|
[15] |
CUI XB, GUO X, CHEN SY. Response gene to complement 32 deficiency causes impaired placental angiogenesis in mice[J]. Cardiovasc Res, 2013, 99( 4): 632- 639. DOI: 10.1093/cvr/cvt121.
|
[16] |
CUI XB, LUAN JN, DONG K, et al. RGC32(response gene to complement 32) deficiency protects endothelial cells from inflammation and attenuates atherosclerosis[J]. Arterioscler Thromb Vasc Biol, 2018, 38( 4): e36-e47. DOI: 10.1161/ATVBAHA.117.310656.
|
[17] |
HU C, WU Z, LI L. Mesenchymal stromal cells promote liver regeneration through regulation of immune cells[J]. Int J Biol Sci, 2020, 16( 5): 893- 903. DOI: 10.7150/ijbs.39725.
|
[18] |
ZHENG J, LI JT, JIN J, et al. Characteristics of incision bacterial infection and changes of immune cytokines in patients with hepatocellular carcinoma after hepatectomy[J]. Chin J Microecol, 2022, 34( 7): 819- 823, 845. DOI: 10.13381/j.cnki.cjm.202207014.
郑杰, 李江涛, 金晶, 等. 肝癌患者肝切除术后切口细菌感染特征及免疫细胞因子水平变化[J]. 中国微生态学杂志, 2022, 34( 7): 819- 823, 845. DOI: 10.13381/j.cnki.cjm.202207014.
|
[19] |
SAIGUSA K, IMOTO I, TANIKAWA C, et al. RGC32, a novel p53-inducible gene, is located on centrosomes during mitosis and results in G2/M arrest[J]. Oncogene, 2007, 26( 8): 1110- 1121. DOI: 10.1038/sj.onc.1210148.
|