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51.
Rebecca Cohen REGAN Robert Michael GOGAL Jr James Perry BARBER Richard Cary TUCKFIELD Elizabeth Wynne HOWERTH Jessica Ann LAWRENCE 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2014,76(12):1563-1568
Loperamide is a peripheral
opiate agonist that can cause apoptosis and G2/M arrest in human cancer cell lines and may
sensitize cells to chemotherapy. The objectives of this study were to investigate the
effects of loperamide on viability, apoptosis and cell cycle kinetics in canine cancer
cells and to establish whether the drug sensitizes cells to doxorubicin. Cell viability
was assessed using Alamar Blue. Cell death and cell cycle were studied using flow
cytometry with 7-Aminoactinomycin-D (7-AAD) and propidium iodide (PI), respectively.
Loperamide decreased cell viability in a dose-dependent fashion and was most effective
against canine osteosarcoma cells. In all cell lines, it induced a dose and time dependent
apoptosis and resulted in accumulation in G0/G1. When co-incubated with doxorubicin,
loperamide induced a synergistic cell kill in canine carcinoma cells. Investigation is
warranted into the role of loperamide in the treatment of canine cancer. 相似文献
52.
53.
A. Valencakova‐Agyagosova Z. Frischova Z. Sevcikova J. Hajurka J. Lepej I. Szakallova G. Kredatusova V. Nagy V. Ledecky 《Veterinary and comparative oncology》2014,12(3):205-214
The aim of this work was to determine levels of carcinoembryonic antigen (CEA) and cancer antigen (CA 15‐3) in the blood serum of 45 bitches. A modified procedure was used to determine the CEA and CA 15‐3 markers with the human kits using the radioimmunoassay method. Samples collected from extirpated tumour of mammary glands were histologically processed and classified as per WHO guidelines. The average age of animals with tumour was 10.00 ± 2.2 years; for healthy bitches average age was 4.2 ± 3.2 years. Values of CEA and CA 15‐3 were considered positive, if they exceeded 0.23 ng mL?1 and 7 IU mL?1, respectively. Average levels of CEA in the tumour group were 0.25 ± 0.06 versus 0.20 ± 0.03 in healthy bitches (P = 0.0001). The average CA 15‐3 value in bitches with tumour was 8.58 ± 1.27 versus 5.14 ± 1.34 in healthy animals (P < 0.0001). 相似文献
54.
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56.
Jin-Kyu Rhee Ok Kyu Park Aeju Lee Dae Hyeok Yang Kyeongsoon Park 《Marine drugs》2014,12(12):6038-6057
Theranostics is an integrated nanosystem that combines therapeutics with diagnostics in attempt to develop new personalized treatments with enhanced therapeutic efficacy and safety. As a promising therapeutic paradigm with cutting-edge technologies, theranostic agents are able to simultaneously deliver therapeutic drugs and diagnostic imaging agents and also monitor the response to therapy. Polymeric nanosystems have been intensively explored for biomedical applications to diagnose and treat various cancers. In recent years, glycol chitosan-based nanoagents have been developed as dual-purpose materials for simultaneous diagnosis and therapy. They have shown great potential in cancer therapies, such as chemotherapeutics and nucleic acid and photodynamic therapies. In this review, we summarize the recent progress and potential applications of glycol chitosan-based fluorescent theranostic nanoagents for cancer treatments and discuss their possible underlying mechanisms. 相似文献
57.
Shuo-Chueh Chen Yi-Chung Chien Chun-Hsu Pan Jyh-Horng Sheu Chih-Yi Chen Chieh-Hsi Wu 《Marine drugs》2014,12(1):196-213
There are many major causes of cancer death, including metastasis of cancer. Dihydroaustrasulfone alcohol, which is isolated from marine coral, has shown antioxidant activity, but has not been reported to have an anti-cancer effect. We first discovered that dihydroaustrasulfone alcohol provided a concentration-dependent inhibitory effect on the migration and motility of human non-small cell lung carcinoma (NSCLC) A549 cells by trans-well and wound healing assays. The results of a zymography assay and Western blot showed that dihydroaustrasulfone alcohol suppressed the activities and protein expression of matrix metalloproteinase (MMP)-2 and MMP-9. Further investigation revealed that dihydroaustrasulfone alcohol suppressed the phosphorylation of ERK1/2, p38, and JNK1/2. Dihydroaustrasulfone alcohol also suppressed the expression of PI3K and the phosphorylation of Akt. Furthermore, dihydroaustrasulfone alcohol markedly inhibited tumor growth in Lewis lung cancer (LLC)-bearing mice. We concluded that dihydroaustrasulfone alcohol is a new pure compound with anti-migration and anti-tumor growth activity in lung cancer and might be applied to clinical treatment in the future. 相似文献
58.
Due to taxonomic positions and special living environments, marine organisms produce secondary metabolites that possess unique structures and biological activities. This review is devoted to recently isolated and/or earlier described marine compounds with potential or established cancer preventive activities, their biological sources, molecular mechanisms of their action, and their associations with human health and nutrition. The review covers literature published in 2003–2013 years and focuses on findings of the last 2 years. 相似文献
59.
Xiao-Cong Huang Xue Xiao Yun-Kai Zhang Tanaji T. Talele Angela A. Salim Zhe-Sheng Chen Robert J. Capon 《Marine drugs》2014,12(7):3818-3837
ATP binding cassette (ABC) transporters, such as P-gp, BCRP and MRP1, can increase efflux of clinical chemotherapeutic agents and lead to multi-drug resistance (MDR) in cancer cells. While the discovery and development of clinically useful inhibitors has proved elusive to date, this molecular target nevertheless remains a promising strategy for addressing and potentially overcoming MDR. In a search for new classes of inhibitor, we used fluorescent accumulation and efflux assays supported by cell flow cytometry and MDR reversal assays, against a panel of sensitive and MDR human cancer cell lines, to evaluate the marine sponge co-metabolites 1–12 as inhibitors of P-gp, BCRP or MRP1 initiated MDR. These studies identified and characterized lamellarin O (11) as a selective inhibitor of BCRP mediated drug efflux. A structure–activity relationship analysis inclusive of the natural products 1–12 and the synthetic analogues 13–19, supported by in silico docking studies, revealed key structural requirements for the lamellarin O (11) BCRP inhibitory pharmacophore. 相似文献
60.
Michael W. Mullowney Eoghainín ó hAinmhire Anam Shaikh Xiaomei Wei Urszula Tanouye Bernard D. Santarsiero Joanna E. Burdette Brian T. Murphy 《Marine drugs》2014,12(6):3574-3586
As part of our program to identify novel secondary metabolites that target drug-resistant ovarian cancers, a screening of our aquatic-derived actinomycete fraction library against a cisplatin-resistant ovarian cancer cell line (OVCAR5) led to the isolation of novel diaza-anthracene antibiotic diazaquinomycin E (DAQE; 1), the isomeric mixture of diazaquinomycin F (DAQF; 2) and diazaquinomycin G (DAQG; 3), and known analog diazaquinomycin A (DAQA; 4). The structures of DAQF and DAQG were solved through deconvolution of X-Ray diffraction data of their corresponding co-crystal. DAQE and DAQA exhibited moderate LC50 values against OVCAR5 of 9.0 and 8.8 μM, respectively. At lethal concentrations of DAQA, evidence of DNA damage was observed via induction of apoptosis through cleaved-PARP. Herein, we will discuss the isolation, structure elucidation, and biological activity of these secondary metabolites. 相似文献