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91.
野生猕猴声行为的研究 总被引:4,自引:2,他引:2
本文通过在华南四省区对四个野生种群猕猴声行为的观察和现场录音,对它们的叫声声学特性,行为模式和其它个体对其相应的行为反应进行了定量的分析研究,并得出11种不同的声行为,这些声行为有相互不同的声学特性,不同的行为模式并引起其它个体相应的行为反应,从而起着通讯的作用。叫声在猕猴的声行为通讯中,一些借助视觉提示,至少以不同的刺激度来“表示”某一类事物,并得到个体间的“共识”有些甚至无需视觉提示而单独传递 相似文献
92.
广西龙虎山猕猴种群生态特征 总被引:5,自引:1,他引:4
1988~1995年,采用定点观察法和绝对计数与相对计数结合法对龙虎山猕猴种群生态作了调查研究。1990年核心区有猕猴14群,500只左右,猴群密度1.6群/km2,种群密度55.6只/km2.猴群大小平均33.8±23.1(n=6)只。一般每隔4~5年分群一次,猴群群体年均增长率14.8%,种群年均增长率为9.7%。猴群中成年猴性比为7.6±6.5(n=12),1~3岁组的性比为0.74±0.61(n=4),群内未成年猴比例为67.7±3.1%(n=12)。发情交配期最早11月12日,最晚次年1月20日,高峰期12月上旬,持续3个月.产仔期最早4月1日,最晚8月14日,高峰期5月上旬,持续时间4个半月.繁殖率45.5%~100%,平均75.4±13.2%(n=21)。新生猴死亡率较低,新生猴性比(雌:雄)平均0.74±0.34(n=5)。 相似文献
93.
Summary Double fluorescent labeling, with fluorescein isothiocyanate (FITC)-labeled F(ab)2 specific for the heavy chain and R-phycoerythrin (R-PE)-labeled F(ab)2 specific for the light chain, was demonstrated as a convenient means for the accurate evaluation of a heterogeneous non-antibody-producing population. Furthermore, it could be used for monitoring the changes in each immunoglobulin (Ig) chain content of the cells during the batch culture, which will facilitate the study on antibody synthesis, assembly and secretion. 相似文献
94.
为克隆肺腺癌分化相关基因, 采用诱导分化与消减杂交相结合的策略, 建立了全反式维甲酸(RA)诱导前后人肺腺癌细胞系的cDNA消减文库, 得到124个cDNA消减克隆. 经加减法杂交差异筛选、DNA和RNA印迹、cDNA全序列测定和生物学功能分析, 分离到3个在人肺腺癌细胞系分化过程中由RA激活而特异表达的新的cDNA序列这一策略和技术路线适用于分离细胞中呈过量表达或表达抑制基因的cDNA克隆, 并具有反映细胞分化过程中基因表达动态变化特征和相对简便适用的特点. 相似文献
95.
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97.
建立了测定人乳腺癌胞浆cAMP结合蛋白(cAMPb.p.)方法。综合研究了其温度、保温时间、配体浓度、稳定性等条件。cAMPb.p.的K_D值为2.90×10~(-8)mol/L.并测定了60例雌激素受体(ER)Fu性乳腺癌标本的cAMPb.p.含量。此组病人术后均接受系统的内分泌治疗,ER/cAMPbp,比值范围为7.7~362×10~(-3),ER/cAMPb.p.比值≥40×10~(-3)的五年生存率明显高于比值<40×10~(-3)组,(p<0.005).表明测定ER/cAMPb.p.比值对预测患者内分泌治疗疗效,优于单独测定ER. 相似文献
98.
Hyun Koo Kim Moon Sun Ham Jong Soo Hong Jin Ha Lee Kyung Yu Park Hyeon Yong Lee 《Biotechnology and Bioprocess Engineering》1996,1(1):32-35
A moving aeration-membrane (MAM) bioreactor was employed for the production of 2 μg/mL of tissue type Plasminogen Activator (tPA) in serum free medium from normal human fibroblast cells. This system could maintain high cell density for long periods of steady state conditions in perfusion cultivation. Under normal operating conditions, shear stress was as low as 0.65 dynes/cm2 at the agitation speed of 80 rpm. Even though cell density gradually decreased with increasing agitation speed, tPA production increased linearly with increasing shear stress within a moderate range. This culture system allowed production of 2 μg tPA/mL while maintaining a high cell density of 1.0×107 viable cells/mL. 相似文献
99.
Shinichi Yoshida Saori Yonehara Shigemi Minami Hyo-cheol Ha Kenji Iwahara Takashi Watanabe Yoichi Honda Masaaki Kuwahara 《Mycoscience》1996,37(4):417-425
Manganese peroxidase (MnP) and lignin peroxidase (LiP) were produced by growing a white-rot fungusBjerkandera adusta statically, on a wood meal/wheat bran culture in flasks. MnP and LiP reached their maximum activity after 6 and 19 days of
inoculation, respectively. Both MnP and LiP are thought to be important enzymes in lignin biodegradation byB. adusta. Ion exchange chromatography showed thatB. adusta produced a single LiP and a single MnP enzyme in wood meal/wheat bran culture. These enzymes were separated and characterized.
The molecular weight of MnP was 46,500 with a pl of 3.9. The molecular weight of LiP was estimated to be 47,000 with a pl of 3.5. Spectral analysis demonstrated that both enzymes are heme proteins. Production of these enzymes was also achieved
using a rotarysolid culture fermenter. MnP, LiP and veratryl alcohol oxidase were produced byB. adusta in the fermenter. 相似文献
100.
Characterization of a Chlamydomonas reinhardtii gene encoding a protein of the DNA photolyase/blue light photoreceptor family 总被引:6,自引:0,他引:6
The organization and nucleotide sequence of a gene from Chlamydomonas reinhardtii encoding a member of the DNA photolyase/blue light photoreceptor protein family is reported. A region of over 7 kb encompassing the gene was sequenced. Northern analysis detected a single 4.2 kb mRNA. The gene consists of eight exons and seven introns, and encodes a predicted protein of 867 amino acids. The first 500 amino acids exhibit significant homology with previously sequenced DNA photolyases, showing the closest relationship to mustard (Sinapis alba) photolyase (43% identity). An even higher identity, 49%, is obtained when the Chlamydomonas gene product is compared to the putative blue-light photoreceptor (HY4) from Arabidopsis thaliana. Both the Chlamydomonas and the Arabidopsis proteins differ from the well characterized DNA photolyases in that they contain a carboxyl terminal extension of 367 and 181 amino acids, respectively. However, there is very little homology between the carboxyl terminal domains of the two proteins. A previously isolated Chlamydomonas mutant, phrl, which is deficient in DNA photolyase activity, especially in the nucleus, was shown by RFLP analysis not to be linked to the gene we have isolated. We propose this gene encodes a candidate Chlamydomonas blue light photoreceptor. 相似文献