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31.
32.
以淀粉珠为载体的亲和层析法分离纯化高温α淀粉酶张学忠,宋伦,王群,吴晓霞,唐锌进(吉林大学酶工程国家重点实验室,长春130023;南京师范大学生物系,南京210024)金凤燮等人从酒曲中筛选出高产热稳定α淀粉酶的菌株,命名为Bacillussp-JF... 相似文献
33.
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酶电泳资料和系统与进化植物学研究综述 总被引:39,自引:0,他引:39
酶电泳资料和系统与进化植物学研究综述葛颂(中国科学院植物研究所系统与进化植物学开放研究实验室北京100093)关键词同工酶,电泳,植物系统学,进化ELECTROPHORETICDATAANDSTUDIESOFPLANTSYSTEMATICSANDEV... 相似文献
35.
36.
福州地区桑白蚧发生动态和药剂防治试验 总被引:1,自引:0,他引:1
桑白蚧在福州地区一年发生4代.以雌成虫在寄主枝干上越冬.越冬代(第4代)一雌虫产卵量多的达278粒.少的36粒,平均171粒,比第2代产卵量多2.6倍.比第3代多4.5倍.药剂防治试验结果,在2龄幼蚧高峰期,用25%扑虱灵可温性粉剂1500倍液,40%氧化乐果乳油800-1000倍液和95%机油乳剂50—100倍液喷雾.防治效果可达90%左右.用25%扑虱是可湿性粉剂1000-1500倍液.喷酒幼蚕触杀试验和喷洒桑叶喂蚕胃毒试验结果.对幼蚕安全.用扑虱灵防治桑树上的桑白蚧,对养蚕业无不良影响。 相似文献
37.
Yun Li Yunhong Song Yulian Liang 《Journal of biochemical and molecular toxicology》2023,37(10):e23439
Abnormal apoptosis of vascular endothelial cells is an important feature of arteriosclerosis (AS). Here, we induced apoptosis in human umbilical vein endothelial cells (HUVECs) using transforming growth factor-β (TGF-β), and investigated the role of antiapoptotic E3 ubiquitin ligase (AREL1) in the apoptosis of vascular endothelial cells. We proved that AREL1 is downregulated in TGF-β treated HUVECs. The overexpression of AREL1 inhibits the activation of Caspase-3 and Caspase-9 and attenuates cell apoptosis induced by TGF-β. According to the result of coimmunoprecipitation, AREL1 interacts with the proapoptotic proteins the second mitochondria-derived activator of caspases (SMAC) in TGF-β treated HUVECs. In addition, miR-320b inhibits the expression of AREL1, and the overexpression of AREL1 attenuates the apoptosis induced by miR-320b mimics in HUVECs. In conclusion, AREL1 is downregulated by miR-320b. AREL1 overexpression inhibits TGF-β induced apoptosis through downregulating SMAC in vascular endothelial cells. Our study explores pathogenesis regulation mechanism and new biological therapeutic targets for vascular disease. 相似文献
38.
Haoran Xu Shuai Chen Xue Song Jingying Wang 《Molecular & cellular biomechanics : MCB》2023,20(1):15-22
Clinically, it is common for Class III patients with maxillary skeletal deficiency, which may result in a variety of
adverse consequences. Protraction headgear and rapid maxillary expansion (PE) is an effective treatment, but its
effect on upper airway hydrodynamics has not been reported. The main purpose of this study was to evaluate the
changes of the flow in the upper airway after PE by computational fluid dynamics (CFD). The sample includes
fifteen patients (6 males, 9 females, age 11.00 ± 1.00) and the paired T-test was used to analyze the differences
between the measured data before and after treatment. The maximum flow velocity decreased from 8.42 ±
0.16 m/s to 6.98 ± 0.36 m/s (p < 0.05), and the maximum shear force decreased from 3.72 ± 1.48 Pa to 2.13 ±
0.18 Pa. The maximum negative pressure decreased from −101.78 ± 33.60 Pa to 58.15 ± 9.16 Pa, only the changes
of velopharynx and glossopharynx were statistically significant; while the maximum resistance decreased from
140.88 ± 68.68 Pa/mL/s to 45.95 ± 22.96 Pa/mL/s. PE can effectively reduce the airflow resistance of the upper
airway and the probability of airway collapse, thus improving the patient’s ventilation function. 相似文献
39.
X. Weng H. Luecke I. S. Song D. S. Kang S. H. Kim R. Huber 《Protein science : a publication of the Protein Society》1993,2(3):448-458
cDNA coding for N-terminally truncated human annexin I, a member of the family of Ca(2+)-dependent phospholipid binding proteins, has been cloned and expressed in Escherichia coli. The expressed protein is biologically active, and has been purified and crystallized in space group P2(1)2(1)2(1) with cell dimensions a = 139.36 A, b = 67.50 A, and c = 42.11 A. The crystal structure has been determined by molecular replacement at 3.0 A resolution using the annexin V core structure as the search model. The average backbone deviation between these two structures is 2.34 A. The structure has been refined to an R-factor of 17.7% at 2.5 A resolution. Six calcium sites have been identified in the annexin I structure. Each is located in the loop region of the helix-loop-helix motif. Two of the six calcium sites in annexin I are not occupied in the annexin V structure. The superpositions of the corresponding loop regions in the four domains show that the calcium binding loops in annexin I can be divided into two classes: type II and type III. Both classes are different from the well-known EF-hand motif (type I). 相似文献
40.
Ying-Ying Li Xi Chen Jin-Xian Yang Qiang Chen Tie-Ying Song Jun-Qing Ge 《Journal of fish biology》2023,102(1):141-154
Eels are important aquaculture species for which an increasing number of reference genes are being identified and applied. In this study, five housekeeping genes [RPL7 (ribosomal protein L7), 18 S (18 S ribosomal RNA), EF1A (elongation factor 1α), ACTB (β-actin) and GAPDH (glyceraldehyde-3-phosphate dehydrogenase)] were chosen to evaluate their reliability as reference genes for quantitative real-time PCR (qPCR) for the study of Anguilla anguilla. The expression of the selected genes in different eel tissues was determined using qPCR at different growth stages or upon challenge by Anguillid herpesvirus (AngHV), and the expression levels of these genes were then compared and evaluated using the geNorm and NormFinder algorithms. Then, RefFinder was used to comprehensively rank the examined housekeeping genes. Interestingly, the expression of the evaluated housekeeping genes exhibited tissue-dependent and treatment-dependent variations. In different growth periods A. anguilla tissues, the most stable genes were the following: ACTB in mucus; 18 S in skin and kidney; RPL7 in muscle, gill, intestine and brain; EF1A in heart and liver; and GAPDH in spleen. In contrast, in AngHV-challenged A. anguilla tissues, the most stable genes were the following: 18 S in mucus; RPL7 in skin, gill, heart, spleen, kidney and intestine; EF1A in muscle and liver; and ACTB in brain. Further comparison analysis indicated that the expression of RPL7 and EF1A was stable in multiple A. anguilla tissues in different growth periods and in eels challenged by AngHV. Nonetheless, the expression level of GAPDH in eel tissues was lower, and it was unstable in several tissues. These results indicated that the selection of reference genes for qPCR analysis in A. anguilla should be made in accordance with experimental parameters, and both RPL7 and EF1A could be used as reference genes for qPCR study of A. anguilla at different growth stages or upon challenge by AngHV. The reference genes identified in this study could improve the accuracy of qPCR data and facilitate further studies aimed at understanding the biology of eels. 相似文献