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CSF-1R激酶突变子的构建及其突变体在真核细胞的表达
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作者 李敏 《高技术通讯》 CAS CSCD 1996年第6期52-56,共5页
通过PCR二步法,构建了mCSF-1R激酶负性突变子,以及野生型和突变型CSF-1R的送病毒表达载体pCEN/MPSV。进行了125I-CSF-1受体结合分析:检测了激酶负性突变子,删除了CSF-1RC-末端氨基酸9... 通过PCR二步法,构建了mCSF-1R激酶负性突变子,以及野生型和突变型CSF-1R的送病毒表达载体pCEN/MPSV。进行了125I-CSF-1受体结合分析:检测了激酶负性突变子,删除了CSF-1RC-末端氨基酸925以后部分的突变体(CTRUNC925)和删除了激酶插入区的突变体(△KI)在32D髓细胞表达。表达水平可达1~2×104受体/细胞。初步测定了通过CSF-1R所介导的促细胞分裂效应。 展开更多
关键词 突变 细胞表达 激酶突变子
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Identification of EGFR kinase domain mutations among lung cancer patients in China:implication for targeted cancer therapy 被引量:66
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作者 BaoMingQIN XiaoCHEN +1 位作者 JingDeZHU DuanQingPEI 《Cell Research》 SCIE CAS CSCD 2005年第3期212-217,共6页
Lung cancer is one of the leading causes of death with one of the lowest survival rates. However, a subset of lung cancer patients who are of Asian origin and carry somatic mutations in epidermal growth factor recepto... Lung cancer is one of the leading causes of death with one of the lowest survival rates. However, a subset of lung cancer patients who are of Asian origin and carry somatic mutations in epidermal growth factor receptor or EGFR have responded remarkable well to two tyrosine kinase inhibitors, gefitinib and erlotinib. While EGFR mutation profiles have been reported from Japan, South Korea, and Taiwan, there is no such report from mainland of China where the largest pool of patients reside. In this report, we identified ten somatic mutations from a total of 41 lung cancer patients in China. Among them, seven mutations were found in 17 adenocarcinomas. In contrast to previous reports, eight of these mutations are deletions in exon 19 and two of these deletions are homozygous. These results suggest that a large portion of Chinese adenocarcinoma patients could benefit from gefitinib or erlotinib. This unique mutation profile provides a rationale to develop the next generation of EGFR inhibitors more suitable for the Chinese population. 展开更多
关键词 lung cancer epidermal growth factor receptor (EGFR) somatic mutation.
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Generation of obese rat model by transcription activator-like effector nucleases targeting the leptin receptor gene 被引量:4
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作者 Yuting Chen Wenqing Lu +8 位作者 Na Gao Yi Long Yanjiao Shao Meizhen Liu Huaqing Chen Shixin Ye Xueyun Ma Mingyao Liu Dali Li 《Science China(Life Sciences)》 SCIE CAS CSCD 2017年第2期152-157,共6页
The laboratory rat is a valuable mammalian model organism for basic research and drug discovery. Here we demonstrate an efficient methodology by applying transcription activator-like effector nucleases(TALENs) technol... The laboratory rat is a valuable mammalian model organism for basic research and drug discovery. Here we demonstrate an efficient methodology by applying transcription activator-like effector nucleases(TALENs) technology to generate Leptin receptor(Lepr) knockout rats on the Sprague Dawley(SD) genetic background. Through direct injection of in vitro transcribed m RNA of TALEN pairs into SD rat zygotes, somatic mutations were induced in two of three resulting pups. One of the founders carrying bi-allelic mutation exhibited early onset of obesity and infertility. The other founder carried a chimeric mutation which was efficiently transmitted to the progenies. Through phenotyping of the resulting three lines of rats bearing distinct mutations in the Lepr locus, we found that the strains with a frame-shifted or premature stop codon mutation led to obesity and metabolic disorders. However, no obvious defect was observed in a strain with an in-frame 57 bp deletion in the extracellular domain of Lepr. This suggests the deleted amino acids do not significantly affect Lepr structure and function. This is the first report of generating the Lepr mutant obese rat model in SD strain through a reverse genetic approach. This suggests that TALEN is an efficient and powerful gene editing technology for the generation of disease models. 展开更多
关键词 TALENs Lepr knockout rat germ-line transmission
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