Hui tu hou Hong lou meng quan ji : [6 juan : 32 hui /

Mode of access: Internet.

Fen men ji zhu Du Gongbu shi : 25 juan /

Fu: Nian pu : 1 juan / Lü Dafang, Cai Xingzong, Lu Yin zhuan.

Bulletin - Far Eastern American Bar Association.

Each vol. also has distinctive title.

Li dai hua shi hui zhuan /

Mode of access: Internet.

An introduction to the history of Chinese pictorial art,

"English and Chinese index to names": p. [173]-178.

Yu shi shu hua ti ba ji.

Mode of access: Internet.

Documents diplomatiques. Chine ... [1885, 1894-1898--octobre, 1901]

1885 has title: Documents diplomatiques. Affaires de Chine.

The China Christian year book

Mode of access: Internet.

Shi yong guo yu wen fa.

Nei rong you ci lun, ju lun ji dan ju, fu ju deng.

Xiao shuo lin.

Mode of access: Internet.

Shuo wen jie zi : 15 juan /

Facsimile reproduction of Jiaqing 12 [1807] Teng hua xie cang ban ben.

Jing xuan Lu Fangweng shi ji : qian ji 10 juan, hou ji 8 juan, bie ji 1 juan /

Ju Liu shi Jia ye tang cang Hongzhi 10 nian kan ben ying yin.

Da Dai li ji : 13 juan /

Ju Wuxi Sun shi Xiao lü tian cang Ming Wujun Yuan shi Jia qu tang kan ben ying yin.

The Formation and Circulation of Early Yanzi Lore, Fourth Century B.C. - Third Century A.D.

Thesis (Ph.D.)--University of Washington, 2016-06

Inhibition of epidermal growth factor receptor expression by RNA interference in A549 cells

AIM: To investigate the biological features of A549 cells in which epidermal growth factor (EGF) receptors expression were suppressed by RNA interference (RNAi). METHODS: A549 cells were transfected using short small interfering RNAs (siRNAs) formulated with Lipofectamine 2000. The EGF receptor numbers were determined by Western blotting and flowcytometry. The antiproliferative effects of sequence specific double stranded RNA (dsRNA) were assessed using cell count, colony assay and scratch assay. The chemosensitivity of transfected cells to cisplatin was measured by MTT. RESULTS: Sequence specific dsRNA-EGFR down-regulated EGF receptor expression dramatically. Compared with the control group, dsRNA-EGFR reduced the cell number by 85.0 %, decreased the colonies by 63.3 %, inhibited the migration by 87.2 %, and increased the sensitivity of A549 to cisplatin by four-fold. CONCLUSION: Sequence specific dsRNA-EGFR were capable of suppressing EGF receptor expression, hence significantly inhibiting cellular proliferation and motility, and enhancing chemosensitivity of A549 cells to cisplatin. The successful application of dsRNA-EGFR for inhibition of proliferation in EGF receptor overexpressing cells can help extend the list of available therapeutic modalities in the treatment of non-small-cell lung carcinoma (NSCLC).