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101.
牛生长激素释放因子的融合表达及其产物的化学加工 总被引:2,自引:0,他引:2
通过寡核苷酸引导的定位突变,在人工全合成的第27位为Ile的牛生长激素释放因子[Ile27]bGRF(1-44)OH基因的5'端ATG后插入Trp密码子序列,并分别了构建了Pl promoter控制下、以β-半乳糖苷酶和protein A结合IgG domainB、C为载体蛋白的融合型基因表达质粒pBLE310和pBLPAE2D,在大肠杆菌中得到高效表达。经SDS-PAGE分析,表达产物β-Gal 相似文献
102.
103.
104.
槟榔(Areca catechu L.)的民族植物学 总被引:3,自引:0,他引:3
本文从民族植物学的观点介绍了我国南方各省嚼槟榔的习俗、历史及演变,分析了这个习俗的形成原因及槟榔的药用价值。作者认为咀嚼槟榔有成瘾性,但是否对人的中枢神经系统有损害,必须进一步研究。作者对这种习俗提出了几点看法和建议,对槟榔的开发利用有重要参考价值。 相似文献
105.
不同钾水平对钾饥饿墨兰碳水化合物和蛋白质含量的影响 总被引:5,自引:1,他引:4
墨兰(Cymbidiumsinense(Andr.)Willd)植株经过钾饥饿后,无上栽培于不同钾浓度的培养液中.随着钾浓度的升高(5mmol/L),体内可溶性糖、淀粉、纤维素和蛋白质含量比对照分别增加125、117、127和41%,而还原糖和游离氨基酸含量则比对照分别下降44%和24%.假球茎是贮藏还原糖、可溶性糖、淀粉、游离氨基酸和蛋白质的主要器官,叶片是纤维素最多的器官.钾供应充足时,叶片丙酮酸激酶活性明显加强(比对照强15倍),而硝酸还原酶活性也加强(比对照强0.8倍).本文对钾促进墨兰生长发育和抗病等原因加以讨论.并初步提出诊断墨兰体内钾状况的三种生理指标. 相似文献
106.
从对照和用DEHP处理的大鼠肝脏提取核蛋白,以含酰基CoA氧化酶(AOX)基因表达调控部位的DNA片段和该基因的不同蛋白结合位点的DNA片段作为核蛋白结合反应的探针,通过凝胶电泳迁移率改变实验和Southwestern印迹分析检查了DEHP对AOX基因反式作用因子的影响。结果表明,降血脂药物DEHP可显著增加AOX基因反式作用因子的含量和(或)与基因的结合活性,在转录水平上促进基因的表达。 相似文献
107.
Inhibition of thyrotropin-stimulated DNA synthesis by microinjection of inhibitors of cellular Ras and cyclic AMP-dependent protein kinase. 总被引:2,自引:1,他引:1 下载免费PDF全文
Microinjection of a dominant interfering mutant of Ras (N17 Ras) caused a significant reduction in thyrotropin (thyroid-stimulating hormone [TSH])-stimulated DNA synthesis in rat thyroid cells. A similar reduction was observed following injection of the heat-stable protein kinase inhibitor of the cyclic AMP-dependent protein kinase. Coinjection of both inhibitors almost completely abolished TSH-induced DNA synthesis. In contrast to TSH, overexpression of cellular Ras protein did not stimulate the expression of a cyclic AMP response element-regulated reporter gene. Similarly, injection of N17 Ras had no effect on TSH-stimulated reporter gene expression. Moreover, overexpression of cellular Ras protein stimulated similar levels of DNA synthesis in the presence or absence of the heat-stable protein kinase inhibitor. Together, these results suggest that in Wistar rat thyroid cells, a full mitogenic response to TSH requires both Ras and cyclic APK-dependent protein kinase. 相似文献
108.
本文报道在我国广西隆林壮族中发现一个罕見的HbQ复合α,β地中海贫血家系。先证者女,18岁,贫血面容,肝脾肿大。化学结构分析确证本Hb变异体为HbQ Thailand[α74(EF3)Asp→His]。血红蛋白组成以及α和β珠蛋白基因分析结果表明,先证者的珠蛋白基因型为-α~Q/-α~T复合β°/β°(IVSI-1G→T/Codon17A→T);先证者父的基因型为-‘α~Q/-复合β~O/β~A(IVSI-1G→T/β~A);先证母的基因型为-α~T/αα复合β~O/β~A(Codon17A→T/β~A)。 相似文献
109.
Wen Gao Ying Xu Jianxiang Liu Xiaolei Wang Xinhong Dong Guigen Teng Binbin Liu Jinpei Dong Chaoyi Ge Hui Ye Xuezhi Zhang Hong Cheng 《Helicobacter》2023,28(2):e12947
Background
The treatment of Helicobacter pylori (H. pylori) infection is a challenge for those who cannot use amoxicillin.Objective
To evaluate the eradication rate and adverse effects of vonoprazan and tetracycline dual therapy as first-line and rescue treatment regimens used in special populations with penicillin allergy or failed in previous amoxicillin-containing therapies.Design
Patients enrolled were those who were H. pylori-positive with selected conditions: (1) allergic to penicillin, either naïve to treatment or had failed before; or (2) failed in previous amoxicillin-containing therapies. All enrolled patients accepted 14-day vonoprazan and tetracycline dual therapy (VT dual therapy) as follows: vonoprazan (20 mg b.i.d.) and tetracycline (500 mg t.i.d. [body weight < 70 kg] or 500 mg q.i.d. [body weight ≥ 70 kg]). H. pylori status was evaluated by 13C-urease breath test 6 weeks after treatment. All adverse effects were recorded. Some patients underwent bacterial culture and antibiotic susceptibility testing.Results
A total of 62 patients were enrolled; 18 of them received VT dual therapy as first-line treatment, 44 patients received VT dual therapy as rescue treatment. Overall, 58 of 62 patients achieved successful eradication (93.5%), while all involved (100%,18/18) succeeded in the first-line treatment group and 40 cases (90.9%, 40/44) succeeded in the rescue treatment group. Sixty-one (61/62, 98.4%) patients completed the whole course of treatment. Adverse events occurred in 6 patients (6/62, 9.7%), while one patient quit because of skin rash. All adverse effects were mild and relieved spontaneously after H. pylori treatment. Five patients achieved successful H. pylori culture, and all strains isolated were sensitive to tetracycline.Conclusions
For the treatment of H. pylori infection in special populations with penicillin allergy or failed in previous amoxicillin-containing therapies, a 14-day vonoprazan and tetracycline dual therapy was effective and safe as first-line and rescue treatment in our study. Further study is warranted to verify its efficacy, especially for those who cannot use amoxicillin. 相似文献110.
Intratumoral interleukin-2 immunotherapy: Activation of tumor-infiltrating and splenic lymphocytes in vivo 总被引:5,自引:1,他引:4
Steven M. Dubinett Lisa Patrone Jeffery Tobias Alistair J. Cochran Duan-Ren Wen William H. McBride 《Cancer immunology, immunotherapy : CII》1993,36(3):156-162
Direct intratumoral injection of interleukin-2 (IL-2) was evaluated in a murine model. Balb/c mice received 5 × 104 Line 1 alveolar carcinoma cells (L1C2) by subcutaneous injection. On the third day following tumor implantation, mice received injections of IL-2 (5 × 103–5 × 104 units) or diluent twice daily, either by i. p. or intratumoral injection, 5 days/week for 3 weeks. Intratumoral injection of 5 × 104 units IL-2 significantly reduced tumor volume (P <0.05 versus control), increased median survival time (P = 0.0001), and resulted in a 23.5% cure rate (P = 0.008). There were no long-term survivors in the other treatment groups. Both tumor-infiltrating lymphocytes (TIL) and splenic lymphocytes isolated directly from IL-2-treated mice demonstrated enhanced cytolytic activity compared to diluent-treated controls. To determine whether non-T-cell-mediated antitumor responses were active in our model, intratumoral immunotherapy was evaluated in athymic Balb/cnu/nu mice. In order to decrease the recruitment of lymphocyte precursors, nude mice were splenectomized and received cyclophosphamide prior to tumor injection and IL-2 therapy. Intratumoral IL-2 immunotherapy also significantly decreased tumor volume in these immunodeficient mice (P <0.02), but did not lead to long-term survival. We conclude that both TIL and splenic lymphocytes are activated in vivo in response to intratumoral IL-2 immunotherapy, suggesting that intratumoral therapy with IL-2 activates both local and systemic antitumor responses.Supported by the Tobacco-Related Disease Research Program of the University of California, the Cancer Research Coordinating Committee, the Jonsson Cancer Center Foundation, and Veterans Administration Medical Research Funds 相似文献