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4篇 您的检索式:作者名="Ruiliang Ge"
    题名 作者 年代 出处 被引量
1The critical role of CD133*CD44+/high tumor cells in hematogenous metastasis of liver cancers显示文摘变形 hepatocellular 癌(HCC ) 是世界范围的最致命的癌症之一。然而,为它的转移负责的房间人口仍然保持大部分未知。这里,我们报导了那 CD133 + CD44 +/high 定义为肝癌症的造血的转移负责的肿瘤房间的亚群。人的 HCC 标本的 Immunohistochemical 调查表明 CD133 + 和 CD44 + HCC 房间的数字被增加并且与门静脉侵略被联系。净化的 CD133 + 或 CD44 HCC 细胞分别地在 clonogenic 生长和脉管的侵略是优异的。因此, CD133 和 CD44 的联合被用来定义一张新奇 HCC 亚人口。CD133 + CD44 , 然而并非 CD133 + CD44 low/− , CD133 CD44 或 CD133 CD44 low/−在裸体老鼠的 异种皮移植,生产 intrahepatic 或肺转移。由流动 cytometry 的人的 HCC 样品的进一步的分析证明 CD133 + CD44 + 肿瘤房间与门静脉转移被联系。CD133 + CD44 + 和 CD133 + 从变形 HCC 病人孤立的 CD44 肿瘤房间表明这些房间拥有不同基因表示侧面的二张不同人口包括了。我们的结果建议那 CD133 + CD44 + 肿瘤房间是为在肝癌症和那的造血的转移负责的一张特别人口这些房间可能是为 HCC 的治疗的目标转移。Ying Hou QifeiZou Ruiliang Ge Feng Shen Yizheng Wang 2012Cell Research2012,22,1:15
2Survival Outcomes and Prognostic Factors of Surgical Therapy for All Potentially Resectable Intrahepatic Cholangiocarcinoma: a Large Single-Center Cohort Study显示文摘Xianwu Luo Lei Yuan Yi Wang Ruiliang Ge Yanfu Sun Gongtian Wei 2014Journal of Gastrointestinal Surgery2014,,3:1
3Corosolic acid in- duces apoptosis through mitochondrial pathway and caspases ac- tivation in human cervix adenocarcinoma HeLa cells 显示文摘Yanfeng Xu Ruiliang Ge Juan Du 2009Canc- er Letters2009,283,:1
4Engineered Spindles of Little Molecules Around Electrospun Nanofbers for Biphasic Drug Release显示文摘Biphasic drug release is a popular advanced drug controlled release profle that has been drawing increasing attention from many felds.Electrospun nanofbers and their derivatives can be act as a strong platform for developing biphasic release dosage forms.In this study,a modifed coaxial electrospinning was implemented,in which little molecule solutions that contain a drug ibuprofen(IBU)and polyethylene glycol(PEG)were exploited as a sheath fuid to surround the core solutions composed of polymer ethyl cellulose(EC)and IBU.The prepared nanofber-based structural hybrids,i.e.,engineered spindles-on-astring(SOS)products,were successfully created and subjected to a series of characterizations.Scanning electron microscopy and transmission electron microscopy results showed the engineered SOS structures.IBU and the carriers EC and PEG had good compatibility,as suggested by X-ray difraction and Fourier transform infrared spectroscopy assessments.In vitro dissolution tests verifed that the SOS products were able to provide a typical biphasic release profle,releasing 40%of the loaded IBU within 1 h in an immediate manner in the frst phase,and the rest of the IBU in a sustained manner in the second phase.A combined mechanism of erosion and difusion is proposed for manipulating the IBU molecule release behaviors.Hua He Mian Wu Jingwen Zhu Yaoyao Yang Ruiliang Ge Deng‑Guang Yu 2022Advanced Fiber Materials2022,4,2:0
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