Results 61 to 70 of about 5,211 (108)

[Advances in application of cell imprinting technology in biomedical field]. [PDF]

Se Pu
Zhao XM, Zhang ZY, Sun WJ, Qing GY.
europepmc   +1 more source

[Long noncoding RNA HClnc1 promotes proliferation and migration of liver cancer cells by targeting RBBP5/KAT2B complex to enhance ODC1 transcription]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao
Feng Z, Li W, Zhang M, Wang P, Shuai Y, Zhang H.   +5 more
europepmc   +1 more source

[Silencing DDX17 inhibits proliferation and migration of pulmonary arterial smooth muscle cells <i>in vitro</i> by decreasing mTORC1 activity]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao
Deng X, Wang J, Xiong M, Wang T, Yang Y, Li, Sun X.   +6 more
europepmc   +1 more source

[Progress in clinical research related to viral hepatitis in 2025]. [PDF]

Zhonghua Gan Zang Bing Za Zhi
Ding Y, Li Y, Dou XG.
europepmc   +1 more source

[Research progress on the pretreatment and analysis of prohibited components of glucocorticoids in cosmetics]. [PDF]

Se Pu
Liu L, Xiao XH, Fang JH, Li GK.
europepmc   +1 more source

丙型肝炎患者尿液特异标志物的检测及其临床意义

Zhongshan Daxue xuebao. Yixue kexue ban, 1994
对５４例丙型肝炎患者尿液特异指标检测，结果：抗－ＨＣＶ阳性５／５４例（９．２％）。ＨＣＶＲＮＡ阳性９／５４例（１６．７％）。急性ＨＣＶ感染者，尿中抗－ＨＣＶ检出率为２／６例（３３％），较慢性者３／３８例（７．９％）为高（Ｐ＜０．０５）。尿液ＨＣＶＲＮＡ全部出现在未经α－干扰素治疗的慢性患者中，故可用作判断干扰素疗效的指标之一。本文在尿中检出ＨＣＶＲＮＡ，提示ＨＣＶ可经尿液污染环境。
doaj  

[Study on the role and mechanism of quercetin promoting autophagy in HCCLM3 cells via STING signaling]. [PDF]

Zhonghua Gan Zang Bing Za Zhi
Chen L, Wu GZ, Zhu Y, Zhang TT.
europepmc   +1 more source

[Treatment with interferon α-1b, interleukin-2, and thalidomide for persistent RUNX1::RUNX1T1 in a patient with KIT-mutated acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation: a case report and literature review]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Mi RH, Chen L, Wang L, Ma YX, Fu YW, Wei XD.   +5 more
europepmc   +1 more source

siRNAs干扰EBNA1下调EBV阳性鼻咽癌细胞内ALOX12的表达

Zhongshan Daxue xuebao. Yixue kexue ban, 2010
【目的】 利用RNA干扰技术抑制C666-1细胞中EB病毒核抗原1(EBNA1)的表达,探索氧化应激与抗氧化相关基因的表达变化65377; 【方法】 采用蛋白质印迹证实了能有效抑制EBNA1表达的干扰序列,使用甲基噻唑基四唑(MTT)方法检测C666-1细胞的存活率,利用实时定量PCR芯片技术探索了氧化应激与抗氧化相关基因的转录谱变化,并通过反转录聚合酶链反应(RT-PCR)和蛋白质印迹进行了验证65377;【结果】 EBNA1-1414和EBNA1-1437干扰序列转染C666-1细胞48 h后 ...
doaj  

[Analysis of stimulating factors for serum copeptin based on liquid chromatography-tandem mass spectrometry]. [PDF]

Se Pu
Mu DN, Qi ZH, Ma YC, Gao YM, Li YM, Zhang Q, Yu SL, Qiu L, Cheng XQ.   +8 more
europepmc   +1 more source