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1.
The human adenovirus type 5 E1A, a tumor- suppressor gene[1], codes for two major related proteins of 243 amino acids (12S) and 289 amino acids (13S) by al-ternative splicing in two exons[2]. Studies have been shown that E1A can regulate expression of many genes and cell cycle[3]. Both in vitro and in vivo experiments indicated that E1A could induce tumor cells differentia-tion, convert tumor cells into an epithelial phenotype, in-hibit tumor cell growth and metastasis and strongly en-ha…  相似文献   
2.
Adenovirus 5 type E1A as a tumor suppressor gene can inhibit tumor growth and enhance the censitivity of chemotherapy and radiotherapy.E1A have the ability to integrate into the host genome,resulting in long-time expres-sion that induces Rb gene inactivation and animal cells im-mortalization.This prompted us to select the E1A protein for treatment of cancer in order to overcome the limitations of E1A gene therapy.Thus,we firstly comstructed E1A eu-caryotic expression vector (pPIC9/E1A),transformated the pichia pastoris yeast cells(GS115) and screened the high-expressing recombinant strains.The positive yeast strains were cultured in the shake flask,and induced for 3d.The crude E1A protein was purified using two steps of col-umu chromatography on HiTrap Q and HiTrap SP.The pu-rified E1A protein was identified by SDS-PAGE and Western blot.E1A protein was mostly located at cellular unclear when Cheriot delivered E1A protein into cells.The analysis in vitro indicated that the E1A protein arrested LN686 cell cycle at G2/M phase,and significantly inhibited the growth of LN686 tumor cells.The current studies firstly provided an experimental basis to further develop E1A protein for tumor treatment.  相似文献   
3.
 健康中国已上升为国家战略。介绍了《"健康中国2030"规划纲要》的主要内容,剖析了影响健康中国建设的主要问题,并提出了相应的应对措施。指出健康中国的建设关键在落实,在于政府主导、多部门合作、全社会参与的合作机制的建立。  相似文献   
4.
杨薇  刘若水 《河南科学》2014,(9):1830-1836
详细介绍了如何用Matlab实现基因算法生成两个不同的具有最小峰值的测试信号,并且把这两个不同的测试信号输入到一个识别工具箱里,通过检验输出的结果来确定这两个测试信号是否适合用作特殊系统的识别.本文所用基因算法产生的测试信号如预期的一样具有最小峰值,但当把这两个测试信号输入到识别工具箱之后,估计系统的矩阵特征值与原始系统的矩阵特征值有很大的差距.产生这种差异的原因主要有两个,一个可能是产生这两个测试信号的长度不够,另一个可能是这两个测试信号非正交.  相似文献   
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6.
Aminopeptidase N (APN) promoter region was cloned and sequenced from peripheral blood mononuclear cells. The recombinant reporter construct containing the promoter and luciferase gene, designated pXP1-APNLuc, was introduced into myeloblastic cell line, T lymphocyte cell line and various tumor cell lines. Luciferase assay showed that APN upstream promoter is myeloid-specific for high expression in myeloblastic cell line and much lower expression in T lymphocyte cell line. The promoter activity was relatively high in lung adenoma cell line compared with other tumor cell lines including hepatoma cell line, tong cancer cell line and esophageal cancer cell line in which the promoter activity significantly diminished or was almost undetectable. The characteristics of APN promoter may provide a new strategy for specific myeloprotection while tumor patients are being treated with chemotherapy and/or radiotherapy.  相似文献   
7.
Esophageal squamous cell carcinoma (ESCC) is one of the most lethal cancers worldwide. In this study, we aimed to investigate the underlying mechanisms of metastasis inhibition by miR-205 in ESCC. In microRNA (miRNA) array and quantitative RT-PCR analyses, we found that the expression level of miR-205 was significantly lower in patients with lymph node metastasis compared with that in patients without lymph node metastasis. After transfection of miR-205 mimics or inhibitors into ESCC cell lines, a significant negative correlation was observed between the expression level of miR-205 and Smad 1. In luciferase reporter assays, we revealed that miR- 205 inhibited the expression of SMAD1 by targeting the 3' untranslated region (3'-UTR) of SMAD1 mRNA in ESCC cells. Furthermore, our results showed that miR-205 sup- pressed the invasion and migration of ESCC cells, whereas Smadl increased their invasion and migration. Taken together, our study demonstrates that miR-205 functions as a suppressor of tumor metastasis by regulating SMAD1 expression through targeting the 3'-UTR of SMAD1 mRNAin ESCC. Therefore, miR-205 may be a potential therapeutic target for miRNA-based therapy of ESCC.  相似文献   
8.
Leptomeningeal metastasis (LM) is caused by the spread of malignant tumor cells into the subarachnoid space.However,classification and staging of LM in the spinal canal is rare in the literature.The authors reviewed the records of 58 Chinese patients with LM for clinical features,neuroimaging,and treatments.Gadolinium-enhanced magnetic resonance imaging (MRI) of brain and spinal cord were performed in all patients.Removal of intracranial tumors was performed in all patients and diagnoses were confirmed by histology.The study group consisted of 58 patients,with 29 cases presenting with intraspinal symptoms.Of the 58,8 patients underwent intraspinal tumor removal,8 received radiotherapy alone,9 received chemotherapy alone,and 34 patients received combined radiochemotherapy.We classified LM into 3 types:type L or leptomeninges LM,is subdivided into 2 subtypes (subtype LI and LII (a,b)),type N or nerve root LM is subdivided into 2 subtypes (subtype NI and NII (a,b)),and type M or mixed-type LM.We also divided LM into stages of I-IV according to the symptoms and the volume of the tumor based on spinal axial MRI.Type LI LM often occurs in patients with intracranial and intraspinal tumors found simultaneously.Patients who receive surgery for intracranial tumors may present with type N LM.Surgery is suitable for patients with NI LM and LIIb LM in stages III-IV,presenting with severe spinal symptoms.The prognosis is better for type N LM than type L LM.  相似文献   
9.
基于燃油消耗的工程机械排放因子研究   总被引:2,自引:0,他引:2  
为获得工程机械的实际排放因子,利用车载排放测试系统(PEMS)对45辆典型工程机械进行实际工况排放测试. 测试工况包括怠速、行走和作业工况. 结果显示:行走和作业工况下排放速率波动明显,较大的排放峰值主要分布在作业工况下. 怠速工况下CO和HC排放因子相对较高,而作业工况下基于油耗的NOx和PM排放因子高于怠速和行走工况. 推土机CO、HC和PM在3种工况下基于油耗的排放因子明显高于其他机械. 比较国1标准机械与国2标准机械发现,国2标准机械CO,HC,NOx和PM在各个测试工况下的排放因子均有不同程度的降低.   相似文献   
10.
贝叶斯网络适用于表达和分析不确定性和概率性的事物,由于具有能够对不完全、不精确或不确定的知识或信息作出有效的推理等特性,而成为目前不确定知识表达和推理领域最有效的模型之一。  相似文献   
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