[Pathogenic mechanisms of Leber hereditary optic neuropathy caused by m.3472T>C mutation]. [PDF]
Zhang H, Shan W, Yasheng M, Guan M.
europepmc +1 more source
[Clinical application value of detecting the mutation load of the FLT3-ITD gene before allogeneic hematopoietic stem cell transplantation using PCR-NGS technology]. [PDF]
Shao YC +11 more
europepmc +1 more source
[Targeting Regulatory T Cells to Remodel Peripheral Immune Tolerance: Research Advances and Future Directions]. [PDF]
Zhang W +4 more
europepmc +1 more source
将α-心钠素(α-hANF)基因克隆到PUC18载体上,经菌落原位杂交筛选鉴定出有α-hANF基因的克隆株。用BamⅡ和BamH Ⅰ消化并分离纯化得到含5′端部分α-hANF基因及PUC18载体的F1片段。用DNA合成仪合成3′端部分α-hANF基因的F2接头,在基因3′端加入谷氨酸的密码子GAA,作为表达产物用内肽酶Glu-C专一裂解的位置,并去掉基因3′端的终止信号TGA,将原BamH Ⅰ接头改为EcoR Ⅰ接头。最后,将F1和F2片段与α-hANF基因酶促连接后进行转化 ...
doaj
[Overexpression of lncRNA SNHG12 promotes docetaxel resistance of prostate cancer cells by activating PI3K/AKT signaling <i>via</i> interacting with ELAVL1]. [PDF]
Zhao C +5 more
europepmc +1 more source
[Chronic myelomonocytic leukemia complicated with T-lymphoblastic lymphoma: a case report and literature review]. [PDF]
Yang YZ, Xu WY, Jiao YJ, Guo ZX.
europepmc +1 more source
【目的】 分析预测申克孢子丝菌cDNA中编号为Locus_168_Contig_1序列编码的基因及蛋白质结构、功能特征,并进行分子克隆。 【方法】 利用NCBI及Expasy网站提供的BLASTx、SignalIP、InterPro Scan等生物信息学软件分析其序列,判断其是否为全长编码序列、同源序列名称,并分析其结构、定位及功能等;将其中的全长编码区利用PCR方法进行扩增后克隆到pET-30a(+)载体,测序验证。 【结果】 该序列是亚精胺合成酶(SPDS)的同源基因,全长序列为1062 bp ...
doaj
[High expression of MPP6 predicts poor patient prognosis and promotes malignant biological behaviors of hepatocellular carcinoma cells]. [PDF]
Yu H +5 more
europepmc +1 more source
[Myelodysplastic neoplasms with acute myeloid leukemia-like mutations: clinical features, molecular profiles, and prognosis]. [PDF]
Bao ZF +13 more
europepmc +1 more source
[Antitumor component-Ι in <i>Agkistrodon halys</i> venom inhibits proliferation and migration of cisplatin-resistant gastric cancer cells by downregulating RAI14]. [PDF]
Li Y +7 more
europepmc +1 more source

