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Wei Wang Mei Zhang Weimin Sun Shanmin Yang Ying Su Hengshan Zhang Chaomei Liu Xinfeng Li Ling Lin Sunghee Kim Paul Okunieff Zhenhuan Zhang Lurong Zhang 《PloS one》2013,8(10)
Most human pancreatic cancer cells are resistant to tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis. However, the mechanisms by which pancreatic cancer cells utilize their extracellular molecules to counteract the proapoptotic signaling mediated by the TNF family are largely unknown. In this study, we demonstrate for the first time that DcR3, a secreted decoy receptor that malignant pancreatic cancer cells express at a high level, acts as an extracellular antiapoptotic molecule by binding to TRAIL and counteracting its death-promoting function. The reduction of DcR3 with siRNA unmasked TRAIL and greatly enhanced TRAIL-induced apoptosis. Gemcitabine, a first-line drug for pancreatic cancer, also reduced the level of DcR3. The addition of DcR3 siRNA further enhanced gemcitabine-induced apoptosis. Notably, our in vivo study demonstrated that the therapeutic effect of gemcitabine could be enhanced via further reduction of DcR3, suggesting that downregulation of DcR3 in tumor cells could tip the balance of pancreatic cells towards apoptosis and potentially serve as a new strategy for pancreatic cancer therapy. 相似文献
44.
Huiyun Li Ye Liu Sumei Chen Jiafu Jiang Aiping Song Weimin Fang Fadi Chen 《Phyton》2020,89(4):851-859
Black spot disease, caused by the necrotrophic fungus Alternaria
tenuissima (Fr.) Wiltsh (A. tenuissima), is considered a highly destructive disease
of Chrysanthemum (Chrysanthemum morifolium Ramat.). A set of 17 accessions
of commercial chrysanthemum cultivars were evaluated for resistance to A.
tenuissima by seedling artificial inoculation. It was found that the reaction of
the accessions to artificial inoculation ranged from resistant to highly susceptible.
Five varieties of chrysanthemum (‘Zhongshan Taogui’, ‘Jinba’, ‘Zhongshan Jinguan’, ‘Jinling Wanhuang’ and ‘Jinling Yangguang’) were resistant; two varieties
of chrysanthemum (‘Zhongshan Xinggui’ and ‘Zhongshan Jinkui’) were moderately resistant; and others were susceptible to various degrees, four varieties of
chrysanthemum (‘Zhongshan Zihe’, ‘Zhongshan Jiuhong’, ‘Zaoyihong’ and ‘Jinling Jiaohuang’) were highly susceptible, especially. Some leaf morphological features of two resistant and two highly susceptible cultivars were further researched.
Trichome density, length, height, gland size and stomata density were found to be
associated with plant passive resistance. Resistant varieties that were identified in
present study will be promising germplasm for exploitation of breeding programmes aimed at developing A. tenuissima-resistant cultivars and increasing
genetic diversity. 相似文献
45.
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
46.
Le Wang Xiaodong She Guixia Lv Yongnian Shen Qing Cai Rong Zeng Caixia Li Yiping Ge Shuwen Deng G. S. de Hoog Min Li Weida Liu 《Mycopathologia》2013,175(3-4):331-338
We report a case of mucocutaneous phaeohyphomycosis caused by Exophiala spinifera. Crusty plaques and nodules were major clinical features. Histological examination revealed brown yeast-like cells and hyphae. Mycological and molecular data identified E. spinifera as etiologic agent. Oral itraconazole was effective, which was in accordance with the results of in vitro susceptibility testing. We speculated that her pregnancy may play a role of risk factor in the infection by E. spinifera. 相似文献
47.
Wang Xinhong Liu Weimin Wu Yue Liu Xiaojun Liang Xiao Wan Zhaofei Wang Nanping Yuan Zuyi 《Molecular and cellular biochemistry》2013,377(1-2):131-141
Glycodelin A (GdA) is a dimeric glycoprotein synthesized by the human endometrium under progesterone regulation. Based on the high sequence similarity with β-lactoglobulin, it is placed under the lipocalin superfamily. The protein is one of the local immunomodulators present at the feto-maternal interface which affects both the innate as well as the acquired arms of the immune system, thereby bringing about successful establishment and progression of pregnancy. Our previous studies revealed that the domain responsible for the immunosuppressive activity of glycodelin lies on its protein backbone and the glycans modulate the same. This study attempts to further delineate the apoptosis inducing region of GdA. Our results demonstrate that the stretch of amino acid sequence between Met24 to Leu105 is necessary and sufficient to inhibit proliferation of T cells and induce apoptosis in them. Further, within this region the key residues involved in harboring the activity were shown to be present between Asp52 and Ser65. 相似文献
48.
Yuqi Wang Weimin Dai Xiangyang Chu Bo Yang Ming Zhao Yu’e Sun 《Biotechnology letters》2013,35(12):2013-2019
Metformin, which is commonly used as an oral anti-hyperglycemic agent of the biguanide family, may reduce cancer risk and improve prognosis. However, the mechanism by which metformin affects various cancers, including lung cancer, remains unknown. MiR-222 induces cell growth and cell cycle progression via direct targeting of p27, p57 and PTEN in cancer cells. In the present study, we used A549 and NCI-H358 human lung cancer cell lines to study the effects and mechanisms of metformin. Metformin treatment reduced expression of miR-222 in these cells (p < 0.05). As a result, protein abundance of p27, p57 and PTEN were increased in cells exposed to metformin. Therefore, these data provide novel evidence for a mechanism that may contribute to the anti-neoplastic effects of metformin suggested by recent population studies and justifying further work to explore potential roles for it in lung cancer treatment. 相似文献
49.
Can Chen Yi Wang Sally S. L. Goh Jing Yang Dang Hoang Lam Yukti Choudhury Felix Chang Tay Shouhui Du Wee Kiat Tan Yovita Ida Purwanti Weimin Fan Shu Wang 《Journal of neurochemistry》2013,126(3):318-330
The breakthrough in derivation of human‐induced pluripotent stem cells (hiPSCs) provides an approach that may help overcome ethical and allergenic challenges posed in numerous medical applications involving human cells, including neural stem/progenitor cells (NSCs). Considering the great potential of NSCs in targeted cancer gene therapy, we investigated in this study the tumor tropism of hiPSC‐derived NSCs and attempted to enhance the tropism by manipulation of biological activities of proteins that are involved in regulating the migration of NSCs toward cancer cells. We first demonstrated that hiPSC‐NSCs displayed tropism for both glioblastoma cells and breast cancer cells in vitro and in vivo. We then compared gene expression profiles between migratory and non‐migratory hiPSC‐NSCs toward these cancer cells and observed that the gene encoding neuronal nitric oxide synthase (nNOS) was down‐regulated in migratory hiPSC‐NSCs. Using nNOS inhibitors and nNOS siRNAs, we demonstrated that this protein is a relevant regulator in controlling migration of hiPSC‐NSCs toward cancer cells, and that inhibition of its activity or down‐regulation of its expression can sensitize poorly migratory NSCs and be used to improve their tumor tropism. These findings suggest a novel application of nNOS inhibitors in neural stem cell‐mediated cancer therapy. 相似文献
50.
Tracey M. Doyle Changgui Li Doris J. Bucher Anwar M. Hashem Gary Van Domselaar Junzhi Wang Aaron Farnsworth Yi-Min She Terry Cyr Runtao He Earl G. Brown Aeron C. Hurt Xuguang Li 《Biochemical and biophysical research communications》2013
All influenza viral neuraminidases (NA) of both type A and B viruses have only one universally conserved sequence located between amino acids 222–230. A monoclonal antibody against this region has been previously reported to provide broad inhibition against all nine subtypes of influenza A NA; yet its inhibitory effect against influenza B viral NA remained unknown. Here, we report that the monoclonal antibody provides a broad inhibition against various strains of influenza B viruses of both Victoria and Yamagata genetic lineage. Moreover, the growth and NA enzymatic activity of two drug resistant influenza B strains (E117D and D197E) are also inhibited by the antibody even though these two mutations are conformationally proximal to the universal epitope. Collectively, these data suggest that this unique, highly-conserved linear sequence in viral NA is exposed sufficiently to allow access by inhibitory antibody during the course of infection; it could represent a potential target for antiviral agents and vaccine-induced immune responses against diverse strains of type B influenza virus. 相似文献