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981.
Zhu Jiangxiong Chen Ziyan Zhou Hui Yu Chuang Han Zi Shao Shengrong Hu Xincheng Wei Xinlin Wang Yuanfeng 《Glycoconjugate journal》2020,37(2):241-250
Glycoconjugate Journal - Coarse tea is made of mature tea plant (Camellia sinensis L.) shoots and is generally discarded as a worthless crop product, but has been proved an excellent material for... 相似文献
982.
Kumar P. S. Ling C. Y. Zhou Z. B. Dong Y. L. Sun C. L. Song Y. X. Wong N. K. Ju J. H. 《Microbiology》2020,89(4):483-492
Microbiology - Marine actinobacteria particularly from marine environments are believed to be inexhaustible sources of biologically active molecules for biomedical and industrial applications. We... 相似文献
983.
Wang Y. Tian T. Li X. Tang L. Li Y. Wang H. Zhang J. Zhang L. Zhang X. 《Microbiology》2020,89(1):122-128
Microbiology - An aerobic, gram-negative-staining, motile and rod-shaped bacterium, designated strain 3-BNT, was isolated from sewage sediment collected from Baiyangdian, located in Xiongan New... 相似文献
984.
Yang Z. T. Lu D. X. Hong E.-K. Zhang B. Y. Jiang M. C. Yang Y. J. Zhang D. J. 《Molecular Biology》2020,54(6):911-918
Molecular Biology - Brassica campestris L. is the important oil-bearing crop in China. Rapeseed cake is the main byproduct of rapeseed oil extraction. As the main active ingredient in rapeseed... 相似文献
985.
Shan Pan Jun Leng Xinzhou Deng Honggang Ruan Lu Zhou Muhammad Jamal Ruijing Xiao Jie Xiong Qian Yin Yingjie Wu Meng Wang Wen Yuan Liang Shao Qiuping Zhang 《Journal of cellular biochemistry》2020,121(1):574-586
The NAD-dependent deacetylase Sirtuin 1 (SIRT1) plays a vital role in leukemogenesis. Nicotinamide (NAM) is the principal NAD+ precursor and a noncompetitive inhibitor of SIRT1. In our study, we showed that NAM enhanced the sensitivity of chronic myeloid leukemia (CML) to doxorubicin (DOX) via SIRT1. We found that SIRT1 high expression in CML patients was associated with disease progression and drug resistance. Exogenous NAM efficiently repressed the deacetylation activity of SIRT1 and induced the apoptosis of DOX-resistant K562 cells (K562R) in a dose-dependent manner. Notably, the combination of NAM and DOX significantly inhibited tumor cell proliferation and induced cell apoptosis. The knockdown of SIRT1 in K562R cells enhanced NAM+DOX-induced apoptosis. SIRT1 rescue in K562R reduced the NAM+DOX-induced apoptosis. Mechanistically, the combinatory treatment significantly increased the cleavage of caspase-3 and PARP in K562R in vitro and in vivo. These results suggest the potential role of NAM in increasing the sensitivity of CML to DOX via the inhibition of SIRT1. 相似文献
986.
Kaur Parampreet Jindal Suruchi Yadav Bharat Yadav Inderjit Mahato Ajay Sharma Priti Kaur Satinder Gupta O. P. Vrána Jan Šimková Hana Doležel Jaroslav Gill Bikram Singh Meyer Klaus F. X. Khurana J. P. Singh N. K. Chhuneja Parveen Singh Kuldeep 《Molecular biology reports》2020,47(3):1991-2003
Molecular Biology Reports - Diploid A genome wheat species harbor immense genetic variability which has been targeted and proven useful in wheat improvement. Development and deployment of... 相似文献
987.
Li Qifa Zhang Yue Ge Bi-Ying Li Na Sun Hai- Lun Ntim Michael Sun Yi-Ping Wu Xue-Fei Yang Jin-Yi Li Shao 《Neurochemical research》2020,45(10):2312-2323
Neurochemical Research - G protein-coupled receptor 50 (GPR50) belongs to the G protein-coupled receptor which is highly homologous with the sequence of melatonin receptor MT1 and MT2. GPR50... 相似文献
988.
989.
Chengdi Wang Wenliang Qiao Yuting Jiang Min Zhu Jun Shao Tao Wang Dan Liu Weimin Li 《Journal of cellular physiology》2020,235(5):4913-4927
990.
Breast carcinoma is one of the most commonly diagnosed tumors and also one of the deadliest cancers in the female. Long noncoding RNAs (lncRNAs) are emerging as novel targets and biomarkers for breast cancer diagnosis and treatment. In this study, we aimed to study the lncRNAs associated with the outcomes in patients using the breast invasive carcinoma datasets from The Cancer Genome Atlas. The Cox proportional hazards regression model was fitted to each lncRNA. Hierarchy clustering was carried out using these survival-related lncRNAs and the log-rank test was carried out for the clustered groups. DNA methylation status was utilized to identify the lncRNAs regulated by epigenetics. Finally, the coexpressed messenger RNA with the potential lncRNAs were utilized to study the possible functions and mechanisms of lncRNAs. In total, 182 lncRNAs had an impact on the survival time of the patients with a cutoff <0.01. The patients were clustered into three groups using these survival-related genes, which performed significantly different prognosis. Two lncRNAs, which were significantly correlated with the outcomes of breast cancer and were regulated by methylation status, were obtained. These two lncRNAs were TP53TG1 and RP5-1061H20.4. We proposed that TP53TG1 was activated by the wild-type TP53 and performed an impact on the PI3Ks family by binding YBX2 in breast cancer. 相似文献