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61.
Taati M Moghadasi M Dezfoulian O Asadian P Kheradmand A Abbasi M Zendehdel M 《Journal of physiology and biochemistry》2012,68(1):91-97
Ghrelin, the endogenous ligand for growth hormone secretagogue receptor, has been reported to prevent ischemia/reperfusion
(I/R) injury in various tissues by its antioxidant activity. Therefore, this study was aimed to investigate the effect of
ghrelin on sperm quality and antioxidant enzyme activity in a rat testicular ischemia/reperfusion injury model. Forty-two
male Wistar rats were divided into groups control, I/R, and I/R plus ghrelin. The right testes were rotated 720° for 1 h and
were allowed to reperfuse for 4 h and 30 days thereafter. Ghrelin (40 nmol/kg IP) or vehicle (physiological saline) was administrated
15 min before reperfusion. After 4 h of reperfusion, a right orchiectomy was performed to measure the biochemical parameters.
In addition, the sperm was collected from the epididymis after 30 days of reperfusion, and sperm characteristics were examined.
The malondialdehyde levels of the testis tissues were significantly increased, but a statistically significant decrease was
found in the superoxide dismutase, glutathione peroxidase, and catalase activities in the I/R group as compared with the control,
indicating I/R injury. The sperm evaluation showed a significant reduction in all characteristics resulted from I/R compared
with the control. In the ghrelin-treated group, the malondialdehyde values were significantly lowered, and only enzyme activity
of glutathione peroxidase showed significant increases compared with the I/R group. Ghrelin significantly enhanced sperm motility,
movement, and concentration but did not prevent I/R-induced reduction in membrane integrity in the testes of rats compared
to the I/R group. Our results suggest that ghrelin treatment has a protective role on IR-induced testicular injury, and this
effect may be due to its antioxidant properties. 相似文献
62.
Using first principle calculations, we investigated cation-π interactions between alkali cations (Li(+), Na(+), and K(+)) and pristine C(24) or doped fullerenes of BC(23), and NC(23). The most suitable adsorption site is found to be atop the center of a six-membered ring of the exterior surface of C(24) molecule. Interaction energies of these cations decreased in the order: Li(+)?>?Na(+)?>?K(+), with values of -31.82, -22.36, and -15.68 kcal mol(-1), respectively. It was shown that the interaction energies are increased and decreased by impurity doping of B and N atoms in adjacent wall of adsorption site, depending on electron donating or receptivity of the doping atoms. 相似文献
63.
Fooladi AA Sattari M Hassan ZM Mahdavi M Azizi T Horii A 《Biotechnology letters》2008,30(12):2061-2059
The bacterial superantigen staphylococcal enterotoxin B (SEB) is a potent inducer of cytotoxic T-cell activity and cytokine
production in vivo. We investigated the possibility of the therapeutic application of SEB in patients with fibrosarcoma. The
anti-tumor effect of SEB in mice with inoculated fibrosarcoma (WEHI-164) was examined by intravenous (IV) and intratumoral
(IT) injection and the sizes of the inoculated tumors, IFN-γ production, and CD4+/CD8+ T cell infiltration were determined.
The inoculated tumors were also examined histologically. In the mice in the IV-injected group, a significant reduction (P < 0.02) of tumor size was observed in comparison with mice in the IT-injected and control groups. Furthermore, the mice in
the IV-injected group showed significantly higher levels of IFN-γ (P < 0.009) and CD4+/CD8+ T cell infiltration when compared with the other groups (P < 0.02). A significantly higher frequency of necrosis in tumor tissues was also observed in mice in the IV-injected group
(P < 0.05). Our present findings suggest that tumor cell death is caused by increased cytotoxic T-cell activity and cytokine
levels in response to the IV injection of SEB and that SEB may be a good option for use as a novel therapy in patients with
fibrosarcoma.
An erratum to this article can be found at 相似文献
64.
65.
Elena Marinova Sandy P. Harrison Fran Bragg Simon Connor Veronique de Laet Suzanne A.G. Leroy Petra Mudie Juliana Atanassova Elissaveta Bozilova Hülya Caner Carlos Cordova Morteza Djamali Mariana Filipova‐Marinova Natalia Gerasimenko Susanne Jahns Katerina Kouli Ulrich Kotthoff Eliso Kvavadze Maria Lazarova Elena Novenko Elias Ramezani Astrid Röpke Lyudmila Shumilovskikh Ioan Tanţǎu Spassimir Tonkov 《Journal of Biogeography》2018,45(2):484-499
66.
Hélio Nitta Matsuura Sonia Malik Fernanda de Costa Morteza Yousefzadi Mohammad Hossein Mirjalili Randolph Arroo Avninder S. Bhambra Miroslav Strnad Mercedes Bonfill Arthur Germano Fett-Neto 《Molecular biotechnology》2018,60(2):169-183
Plant secondary metabolism evolved in the context of highly organized and differentiated cells and tissues, featuring massive chemical complexity operating under tight environmental, developmental and genetic control. Biotechnological demand for natural products has been continuously increasing because of their significant value and new applications, mainly as pharmaceuticals. Aseptic production systems of plant secondary metabolites have improved considerably, constituting an attractive tool for increased, stable and large-scale supply of valuable molecules. Surprisingly, to date, only a few examples including taxol, shikonin, berberine and artemisinin have emerged as success cases of commercial production using this strategy. The present review focuses on the main characteristics of plant specialized metabolism and their implications for current strategies used to produce secondary compounds in axenic cultivation systems. The search for consonance between plant secondary metabolism unique features and various in vitro culture systems, including cell, tissue, organ, and engineered cultures, as well as heterologous expression in microbial platforms, is discussed. Data to date strongly suggest that attaining full potential of these biotechnology production strategies requires being able to take advantage of plant specialized metabolism singularities for improved target molecule yields and for bypassing inherent difficulties in its rational manipulation. 相似文献
67.
68.
Length‐weight relationships of three gobiid species (Perciformes: Gobiidae) along the Iranian intertidal coast of the Persian Gulf and Makran Sea 下载免费PDF全文
Length weight relationships (LWRs) were estimated for three gobiid species, Bathygobius meggitti(Hora & Mukerji, 1936), Acentrogobius dayi Koumans, 1941 and Cryptocentroides arabicus(Gmelin, 1789) (Perciformes: Gobiidae) collected from 13 localities of the Iranian intertidal coast of the Persian Gulf and Makran Sea in seven times from November 2015 to September 2017 using a hand net with mesh size 1.30 mm. The b values showed significant differences between males and females of all species except the C. arabicus. Bailey's t test revealed that b value significantly deviated from the expected cube value of 3 in three species. 相似文献
69.
Afsaneh Sadremomtaz Kamran Mansouri Golnaz Alemzadeh Majid Safa Ahmadreza Esmaeili Rastaghi S. Mohsen Asghari 《Biochimica et Biophysica Acta (BBA)/General Subjects》2018,1862(12):2688-2700
Background
Neutralization of vascular endothelial growth factor receptor 1 (VEGFR1) and/or VEGFR2 is a widely used means of inhibiting tumor angiogenesis.Methods
Based on the complex X-ray structures of VEGFA/VEGFR1, VEGFA/VEGFR2, and VEGFB/VEGFR1, a peptide (referred to as VGB) was designed to simultaneously bind to VEGFR1 and VEGFR2, and binding, antiangiogenic and antitumor properties of the peptide was investigated in vitro.Results
VGB bound to both VEGFR1 and VEGFR2 in human umbilical vein endothelial cells (HUVECs) and 4?T1 mammary carcinoma tumor (MCT) cells, and inhibited the proliferation of HUVE, 4?T1 MCT, and U87 glioblastoma cells. Through abrogation of AKT and ERK1/2 phosphorylation, VEGFA-stimulated proliferation, migration, and two- and three-dimensional tube formation in HUVECs were inhibited more potently by VGB than by bevacizumab. In a murine 4?T1 MCT model, VGB strongly inhibited tumor growth without causing weight loss, accompanied by inhibition of AKT and ERK1/2 phosphorylation, a significant decrease in tumor cell proliferation (Ki-67 expression), angiogenesis (CD31 and CD34 expression), an increase in apoptosis index (increased TUNEL staining and p53 expression and decreased Bcl-2 expression), and the suppression of systematic spreading of the tumor (reduced NF-κB and MMP-9 and increased E-cadherin expression).Conclusion
The dual specificity of VGB for VEGFR1 and VEGFR2, through which the PI3K/AKT and MAPK/ERK1/2 signaling pathways can be abrogated and, subsequently, angiogenesis, tumor growth, and metastasis are inhibited.General significance
This study demonstrated that simultaneous blockade of VEGFR1 and VEGFR2 downstream cascades is an effective means for treatment of various angiogenic disorders, especially cancer. 相似文献70.
Darvizheh Hakimeh Zahedi Morteza Abaszadeh Bohloul Razmjoo Jamshid 《Journal of Plant Growth Regulation》2018,37(4):1267-1285
Journal of Plant Growth Regulation - This study investigated the effect of irrigation regimes and the foliar application of salicylic acid (SA) and spermine (SPM) on the content of essential oil... 相似文献