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961.
HGPRT~-人早幼粒白血病细胞突变株(HL-60-AR)与RA保温一定时间后,洗去药物继续培养,细胞分化性状(NBT还原能力、细胞膜C_3补体受体及形态变化)不但继续存在,而且能持续表达。撤去RA后连续传代培养,至少在传三代后细胞分化性状仍高度表达。然而,DMSO对HL-60-AR细胞的作用特点明显不同于RA。HL-60-AR细胞分化伴随增殖能力的降低。核酸分子杂交结果表明,细胞c-myc癌基因表达受抑先于细胞分化性状的获得和增殖能力的下降。 相似文献
962.
J. C. Afele L. W. Kannenberg R. Keats S. Sohota E. B. Swanson 《Plant Cell, Tissue and Organ Culture》1992,28(1):87-90
Microspore cultures were initiated from the North American sweet corn hybrid, Seneca 60. Donor plants were grown under two environments. One treatment comprised plants that matured completely in the greenhouse (GH) (28°C/23°C: day/night), while in a second treatment donor plants were isolated and divided into two treatment sets: cultured directly at 25°C, or given a heat treatment of 32°C for 10 days.Greenhouse-grown plants produced fewer embryo-like structures (ELS) than growth chambertreated plants regardless of the culture temperature treatment. If the microspores isolated from GC plants were subsequently provided with the initial high culture temperature, the number of ELS that could be recovered was more than doubled compared to the cultures incubated at 25°C continuously. The high culture temperature treatment also resulted in a higher quality of ELS (more compact), which led to a higher frequency of ELS that survived and were subsequently transferred to regeneration medium. However, while plant regeneration and subsequent selfed seeds were obtained, the frequency was very low and further research is required in this area. 相似文献
963.
Postnatal Age and Protein Tyrosine Phosphorylation at Synapses in the Developing Rat Brain 总被引:8,自引:3,他引:5
The relationship between postnatal age and protein tyrosine kinase activity in synaptosomes prepared from the rat forebrain was studied. Synaptosomal particulate and soluble fractions, as well as total homogenates, the cell soluble fraction, and P3, were prepared from rats ranging in postnatal age from 5 to 60 days and analyzed for (a) tyrosine kinase activity using polyglutamyltyrosine (4:1) as the substrate, (b) the presence of endogenous substrates for tyrosine phosphorylation using polyclonal antibodies specific for phosphotyrosine, and (c) levels of pp60src. Enzyme activity, expressed per milligram of protein, in the total homogenate, P3, and both the cell and synaptosomal soluble fractions was highest in the brains of young animals (postnatal days 5-10) and decreased thereafter to adult levels. In contrast, tyrosine kinase activity in the synaptosomal particulate fraction exhibited a unique biphasic developmental profile, increasing to maxima at postnatal days 10 and 20 before decreasing to adult values. Endogenous substrates for tyrosine phosphorylation were identified by incubating subcellular fractions with 2 mM ATP in the presence of sodium orthovanadate and probing nitrocellulose blots of proteins separated by gel electrophoresis with antiphosphotyrosine antibodies. Several phosphotyrosine-containing proteins were detected in the synaptosomal particulate and P3 fractions, including proteins of Mr 180K, 145K, 120K, 100K, 77K, 68K, 62K, 54K, 52K, and 42K. In the cell soluble fraction a protein doublet of Mr 54/52K and a 120K protein were the major phosphotyrosine-containing proteins. The 54/52K doublet was the major protein tyrosine kinase substrate in the synaptosomal soluble fraction.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
964.
以人早幼粒白血病细胞株(HL-60)为材料,对维甲酸与星状孢子素联合诱导HL-60细胞过程中胞浆和膜部分的蛋白质酪氨酸磷酸化水平变化进行了研究.结果表明,诱导后2~24h范围内,TPK活力出现波动,随时间延长(24~27h),胞浆部分TPK活力下降,膜溶脱部分TPK活力上升;PTPP活力明显升高且上升幅度比TPK大得多.利用抗P-tyr-BSA抗体分析底物含量变化的结果与相应时相的TPK和PTPP活力变化趋势一致. 相似文献
965.
Molecular Mechanisms of Apoptosis in HL-60 Cells Induced by a Nitric Oxide-Releasing Compound 总被引:3,自引:0,他引:3
Munehisa Yabuki A. Shwji Yoko Inni Keisuke Hamazaki Tamotsu Yoshioka Tatsuji Yasuda Alan A. Horton Kozo Utsumi 《Free radical research》1997,27(3):325-335
Nitric oxide (NO) generated from 1-hydroxy-2-0×0-3, 3-bis(2-aminoethyl)-l-triazene (NOC 18), an NO-releasing compound, induced monocytic differentiation of human promyelocytic leukemia HL-60 cells as assessed by expression of nonspecific esterases and morphologic maturation. Simultaneously, DNA fragmentation and morphological alterations typical of apoptosis were also induced. To investigate the mechanisms of apoptosis during differentiation of HL-60 cells induced by NO, the endogenous levels of Bcl-2 and Bax were assessed by immunoblotting. Treatment of cells with NOC 18 slightly reduced the level of Bcl-2 followed by Bax. These changes might be involved in the induction of apoptosis. The involvement of the activation of the interleukin-lβ converting enzyme (ICE) family of proteases (caspases), such as ICE and CPP32, in the pathways was also investigated. CPP32, but not ICE, was strongly activated in response to NOC 18 stimulation, thereby implicating CPP32-like activity in the induction of apoptosis. Moreover, the possible involvement of tyrosine phosphorylation in apoptosis was investigated. Pretreatment of cells with herbimycin A, an inhibitor of tyrosine kinases, suppressed DNA fragmentation and CPP32-like activity, whereas pretreatment with vanadate, an inhibitor of tyrosine phosphatases, enhanced both parameters, suggesting that tyrosine phosphorylation might be involved in the pathways of apoptosis in HL-60 cells induced by NO. 相似文献
966.
967.
968.
Inhibition of lipid peroxidation 总被引:1,自引:0,他引:1
Enjie Sun Huibi Xu Dijiang Wen Ping Zuo Jingyan Zhou Jünjian Wang 《Biological trace element research》1997,59(1-3):87-92
Lipid peroxy radicals (ROO-) were detected by electron spin resonance (ESR) at low temperature after formation by addition
of H2O2 into a suspension of mice lymphocites. If lymphocytes were treated with selenomethionine (Se-Met) prior to addition of H2O2, ROO-formation was inhibited in a fashion that was dependent on Se-Met concentration. Formation of ROO- in the spleen of
mice was induced by60Co irradiation. Animals that were supplemented with Na2SeO3 prior to irradiation exhibited a lower ROO-concentration than that of nontreated animals. Based on our experiments, we have
concluded that Se has an oxygen-free radical scavenging effect. This should be a protective effect against lipid peroxy radical
cellular attack. 相似文献
969.
Plasma Membrane Ubiquinone Controls Ceramide Production and Prevents Cell Death Induced by Serum Withdrawal 总被引:2,自引:0,他引:2
María P. Barroso Consuelo Gómez-Díaz José M. Villalba María I. Burón Guillermo López-Lluch Plácido Navas 《Journal of bioenergetics and biomembranes》1997,29(3):259-267
Serum provides cultured cells with survival factors required to maintain growth. Its withdrawal induces the development of programmed cell death. HL-60 cells were sensitive to serum removal, and an increase of lipid peroxidation and apoptosis was observed. Long-term treatment with ethidium bromide induced the mitochondria-deficient °HL-60 cell line. These cells were surprisingly more resistant to serum removal, displaying fewer apoptotic cells and lower lipid peroxidation. HL-60 cells contained less ubiquinone at the plasma membrane than °HL-60 cells. Both cell types increased plasma membrane ubiquinone in response to serum removal, although this increase was much higher in ° cells. Addition of ubiquinone to both cell cultures in the absence of serum improved cell survival with decreasing lipid peroxidation and apoptosis. Ceramide was accumulated after serum removal in HL-60 but not in °HL-60 cells, and exogenous ubiquinone reduced this accumulation. These results demonstrate a relationship between ubiquinone levels in the plasma membrane and the induction of serum withdrawal induced apoptosis, and ceramide accumulation. Thus, ubiquinone, which is a central component of the plasma membrane electron transport system, can represent a first level of protection against oxidative damage caused by serum withdrawal. 相似文献
970.
Nandini V. L. Hayes Gareth W. Phillips Martin J. Carden Anthony J. Baines 《Journal of neurochemistry》1997,68(4):1686-1695
Abstract: Spectrin isotypes segregate in neurons and are differentially distributed between axons and somatodendritic compartments. Their functions in those compartments are likely to be mediated by proteins that interact selectively with one or other isotype. Fodaxin (an axon-specific protein previously termed A60) colocalizes in CNS neurons with axonal spectrin and in vitro binds brain spectrin (a mixture of αI, βI, αII, and βII polypeptides) but not erythrocyte spectrin (αI and βI). Because αII and βII spectrin polypeptides are enriched in axons, we investigated a possible binding of fodaxin to the types of spectrin found in axons. Fodaxin did not bind to isolated brain α chains. Bacterially expressed C-terminal segments 18–19 of βII spectrin bound to fodaxin and inhibited the binding of fodaxin to whole brain spectrin. By contrast, recombinant segments 18–19 of the somatodendritic βIΣ2 spectrin showed no interaction with fodaxin. Within βII, fodaxin binding activity was localized to residues 2,087–2,198, which are unique to βII and link between the end of segment 18 and the pleckstrin homology domain in segment 19. The divergent regions of sequence in segments 19 of βII and βIΣ2 are candidates to mediate the isotype-specific functions of spectrin. Fodaxin is the first protein to be described that discriminates between the unique regions of β spectrin isoforms. 相似文献