- 基本信息
导师姓名:
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易静
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学科代码:
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100100
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性别:
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女
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学科名称:
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基础医学
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培养单位:
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基础医学院
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三级学科
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导师类型:
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博士生导师
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专业领域名称:
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联系方式:
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专业领域代码:
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邮编:
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邮箱地址:
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yijing@shsmu.edu.cn
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- 研究方向 (点击浏览详细信息)
- 社会任职
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细胞生物学学报编委
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中国细胞生物学会继续教育工作委员会主任
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中华医学会医学细胞生物学分会常务理事
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中国细胞生物学会资深理事
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- 科研项目
31471263 | 基于单个活细胞实时影像技术对B23蛋白感应核仁应激发生定位和功能改变机制的研究 | 国家自然科学基金,面上项目 |
2015-01~2018-12
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80万元
| 课题负责人 |
2013CB910902 | 赖氨酸翻译后修饰及对蛋白质功能的调控作用 课题二:肿瘤发生发展过程中细胞核蛋白的赖氨酸修饰信号调控网络 | 科技部重大科学研究计划项目子课题 |
2013-01~2017-12
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246万元
| 子课题负责人 |
31230037 | SENP3应答细胞氧化应激调控转录因子修饰的机制及其在胃炎相关胃癌中的作用 | 国家自然科学基金重点项目 |
2013-01~2017-12
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285万元
| 课题负责人 |
11JC1406900 | SENP3在氧化应激诱导上皮间质转化中的作用及其对胃炎相关胃癌的影响 | 市科委基础研究重点项目(连续支持) |
2011-12~-2014-12
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30万元
| 课题负责人 |
91013012 | 以紫草素衍生物/低氧诱导因子-1为模型,探讨抗癌醌类化合物结构与靶向作用特异性和活性氧效应普遍性的关系 | 国家自然科学基金重大研究计划培育项目 |
2011-01~-2013-12
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50万元
| 课题负责人 |
0810410704000 | 利用以脂质体模拟线粒体的无细胞系统进行靶向Bcl-2蛋白的抗癌化合物筛选和机制研究 | 市科委国际合作项目 |
2010-04~2012-03
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15万元
| 课题负责人 |
C0701 | 核仁蛋白质SENP3应答细胞氧化应激信号的机制 | 国家自然基金,面上项目 |
2010-01~2012-12
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35万元
| 课题负责人 |
08JC1413800 | 植物小分子化合物靶向抑制HIF-1治疗非雄激素依赖的前列腺癌的机制和应用研究 | 市科委基础研究重点项目 |
2008-10~2010-09
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30万元
| 课题负责人 |
30570965 | 活性氧通过低氧诱导因子-1的化学修饰影响肿瘤细胞耐药性的机制 | 国家自然基金委,面上项目 |
2006-01~2008-12
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28万元
| 课题负责人 |
08JC1413800 | 植物小分子化合物靶向抑制HIF-1治疗非雄激素依赖的前列腺癌的机制和应用研究 | 上海市科委,基础重点项目 |
~2010-09
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30万元
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- 学术论文
Wang M, Sang J, Ren Y1 Liu K, Liu X, Zhang J, Wang H, Wang J, Orian A4, Yang J, Yi J
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SENP3 regulates the global protein turnover and the Sp1 level via antagonizing SUMO2/3-targeted ubiquitination and degradation.
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Protein Cell.
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2016
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7(1):63–77
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Yang K, Wang M, Zhao Y, Sun X, Yang Y, Li X, Zhou A, Chu H, Zhou H, Xu J, Wu M, Yang J,
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A redox mechanism underlying nucleolar stress sensing by nucleophosmin.
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Nat Commun.
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2016
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Nov 25;7:13599. doi: 10.1038/ncomms13599.
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Zhou Z, Wang M, Li J, Xiao M, Chin YE, Cheng J, Yeh ET, Yang J,
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SUMOylation and SENP3 regulate STAT3 activation in head and neck cancer.
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Oncogene.
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2016
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35(45):5826–5838
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Zhao Y, Hu Q, Cheng F, Su N, Wang A, Zou Y, Hu H, Chen X, Zhou HM5, Huang X, Yang K, Zhu Q, Wang X,, Zhu L, Qian X, Chen L, Tang Y, Loscalzo J, Yang Y.
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SoNar, a highly responsive NAD(+)/NADH sensor, allows high-throughput metabolic screening of anti-tumor agents.
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Cell Metab.
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2015
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21(5):777-789
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Ren YH, Liu KJ, Wang M, Yu YN, Yang K, Chen Q, Yu B, Wang W, Li QW, Wang J, Hou ZY, Fang JY, Yeh ET, Yang J,
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De-SUMOylation of FOXC2 by SENP3 promotes the epithelial-mesenchymal transition in gastric cancer cells.
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Oncotarget
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2014
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5(16):7093-7104
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Wang Y, Yang J,
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Redox sensing by proteins: oxidative modifications on cysteines and the consequent events.
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Antioxid Redox Signal.
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2012
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16 (7):649-657
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Wang Y, Yang J, Yang K, Cang H, Huang XZ, Li H, Yi J
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The biphasic redox sensing of SENP3 accounts for the HIF-1 transcriptional activity shift by oxidative stress.
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Acta Pharmacol Sin.
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2012
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33(7):953-963
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Sang J, Yang K, Sun Y, Han Y, Cang H, Chen Y, Shi G, Wang K, Zhou J, Wang X,
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SUMO2 and SUMO3 transcription is differentially regulated by oxidative stress in an Sp1-dependent manner.
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Biochem J.
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2011
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435(2):489-498.
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Han Y, Huang C, Xiang B, Sun Y, Yeh ET, Chen Y, Hu Q, Wang J, Gao F,
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SENP3-mediated de-conjugation of SUMO2/3 from PML is correlated with accelerated cell proliferation under mild oxidative stress.
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J Biol Chem
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2010
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285(17):12906-15
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Yan S, Sun X, Xiang B, Cang C, Kang X, Chen Y, Li H, Shi G, Yeh ETH, Wang B, Wang X Yi J,
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Redox regulation of the stability of the SUMO protease SENP3 via interactions with CHIP and Hsp90.
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The EMBO Journal.
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2010
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29(22):3773-3786
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Wang R, Zou Y, Yuan Z, Wang Y, Chen Y, Mao Y, Zhu Z, Li H, Tang X, Lu J,,
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Autografts and xenografts of the skin fibroblasts delivering BMP-2 effectively promote orthotopic and ectopic osteogenesis.
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The Anatomical Record,
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2009
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292 (6):778-786
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Zuo Y, Xiang B, Yang J, Sun X, Wang Y, Cang H,
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Oxidative modification of caspase-9 facilitates its activation via disulfide-mediated interaction with Apaf-1
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Cell Research
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2009
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19(4):449-457
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Huang C, Han Y, Wang Y, Yan S, Sun XX, Yeh ET, Chen Y, Cang H, Li H, Cheng J, Tang XM,
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SUMO-specific protease 3 is responsible for HIF-1 transactivation under mild oxidative stress via P300 de-SUMOylation.
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EMBO J
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2009
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28(18):2748-2762
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Wang J.,
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Cancer cell killing via ROS: To increase or decrease, that is a question
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Cancer Biol Ther.
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2008
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7(12):1875-1884
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Cai J, Niu X, Chen Y, Hu Q, Shi G, Wu H, Wang J,
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Emodin-induced generation of reactive oxygen species inhibits RhoA activation to sensitize gastric carcinoma cells to anoikis
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Neoplasia
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2008
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10(1):41-51
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Huang XZ, Wang J, Huang C, Chen Y, Shi G, Hu Q Yi J.
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Emodin enhances cytotoxicity of chemotherapeutic drugs in prostate cancer cells: the mechanisms involve ROS-mediated suppression of multidrug resistance and hypoxia inducible factor-1.
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Cancer Biol Ther.
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2008
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7(3):468-475
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Wang J, Li L, Cang H, Shi G,
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NADPH oxidase-derived reactive oxygen species are responsible for the high susceptibility to arsenic cytotoxicity in acute promyelocytic leukemia cells.
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Leuk Res.
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2008
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32(3): 429-436
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Li L., Wang J., Ye RD, Shi G. Jin H., Tang X.,Yi J.
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PML/RARa fusion protein mediates the unique sensitivity to arsenic cytotoxicity in acute promyelocytic leukemia cells:
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Journal of Cellular Physiology.
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2008
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217(2):486-493
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Wang YM. Huang XZ. Cang H. Gao F. Ozaki T. Yamamoto T. Yi J
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The endogenous reactive oxygen species promote NF-κB activation by targeting on activation of NF-κB-inducing kinase in oral squamous carcinoma cells.
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Free Radic Res.
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2007
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41(9):963-71
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Jing Y, Yang J, Wang Y, Li H, Chen Y, Hu Q, Shi G, Tang X,
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Alteration of subcellular redox equilibrium and the consequent oxidative modification of nuclear factor kappaB are critical for anticancer cytotoxicity by emodin
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Free Radic Biol Med.
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2006
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40(12):2183-97
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, J.; Yang, J.; He, R.; Gao, F.; Sang, H.R.; Tang, X.M.; Ye, R.D
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Emodin enhances arsenic trioxide-induced apoptosis via generation of reactive oxygen species and inhibition of survival signaling
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Cancer Research
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2004
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64(1):108-116
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Yang J, Li H, Chen YY, Wang XJ, Shi GY, Hu QS, Kang XL, Lu Y, Tang XM, Guo QS,
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Anthraquinones sensitize tumor cells to arsenic cytotoxicity in vitro and in vivo via reactive oxygen species-mediated dual regulation of apoptosis
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Free Radical Biology and Medicine
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2004
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37(12):2027-2041
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The inherent cellular level of reactive oxygen species: One of the mechanisms determing apoptotic susceptibility of leukemic cells to arsenic trioxide
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Apoptosis
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2002
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7(3): 209-215
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, Wang ZW, Cang H, Chen YY, Zhao R, Yu BM, Tang XM
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p16 gene methylation in colorectal cancers is associated with Dukes’staging
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World Journal of Gastrienterology
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2001
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7(5):722-725
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, Yu DR, Chen Y, Xiong W, Li X, Shen J, Tang XM
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p16 overexpression in pituitary adenoma studied by immunohistochemistry and in situ hybridization
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Chin Med J
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2000
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113 (2):162-166
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The convergent point of the endocytotic and autophgic pathways
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Cell Research
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1999
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9(4):243-253
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Chevalier J,, Michel O, Tang XM
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Biotin and digoxigenin as labels for light and electron microscopy in situ hybridization probes: Where do we stand?
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Journal of Histochemistry and Cytochemistry
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1997
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45 (4):481-491
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, Michel O, Sassy-Prigent C, Chevalier J
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Electron Microscopic Location of mRNA in the rat kidney: improved post-embedding in situ hybridization
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Journal of Histochemistry and Cytochemistry
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1995
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43(8):801-809
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, Tang XM
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Functional Implication of Autophagy in Steroid-Secreting Cells of the Rat
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The Anatomical Record
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1995
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242(1):137-146
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