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941.
Interest in the biology of planktonic, chain-forming Pseudonitzschia species has grown recently after the discovery of toxin production in Pseudonitzschia pungens and related taxa, following the outbreak of shellfish toxicity in Canada in 1987. As part of a broader study on the effects of enhanced ultraviolet light on the growth of bloom-forming phytoplankton, we have examined the growth rates and production of the toxin domoic acid and two additional chemicals [bacillariolides I and II] by Pseudonitzschia pungens varieties and Pseudonitzschia fraudulenta from Narragansett Bay, Rhode Island. Growth of P. fraudulenta is significantly inhibited by enhanced UV, P. pungens var. pungens shows slight inhibition, and P. pungens var. multiseries is unaffected. Production of bacillariolides I and II by P. pungens var. multiseries is similar in enhanced and deleted UV light. Tolerance of UV light by P. pungens var. multiseries appears to be acquired, and persistent. If ambient UV light continues to increase as a result of global ozone depletion, one may expect UV-resistant taxa such as P. pungens var. multiseries to become more prominent in coastal phytoplankton communities. 相似文献
942.
Guang Yi Zhang Jerry H. Wang Rajendra K. Sharma 《Molecular and cellular biochemistry》1993,122(2):159-169
Bovine brain contains two calmodulin-dependent phosphodiesterase kinases which are separated on Sephacryl S-300 column. One of these kinases has been purified to homogeneity and shown to belong to the calmodulin-dependent protein kinase II family. Phosphorylation of the 63 kDa phosphodiesterase by this purified protein kinase results in the incorporation of 1.0 mol phosphate per mol subunit and an accompanying increase in Ca2+ concentrations required for the phosphodiesterase activation by calmodulin. The protein kinase undergoes autophosphorylation to incorporate 1.0 mol phosphate per mol of subunit of the enzyme and the autophosphorylated enzyme is active, independent of the presence of Ca2+. The autophosphorylation reaction as well as the protein kinase reaction are rendered Ca2+ independent in less than 15 seconds when approximately one mol phosphate per mol protein kinase is incorporated. The result suggests that activation of phosphodiesterase phosphorylation reaction may occur prior to the activation of phosphodiesterase and phosphatase during a cell Ca2+ flux via the protein kinase autophosphorylation mechanism.Abbreviations SDS
sodium dodecyl sulfate
- EGTA
ethylene glycol bis (-aminoethyl ether)
- N,N,N,N
tetra acetic acid
- EDTA
ethylenediamine-tetraacetic acid
- cAMP
cyclic adenosine 35 monophosphate
This work is supported by grants from the Medical Research Council of Canada (JHW), the Heart and Stroke Foundation of Alberta (JHW and RKS) and the Heart and Stroke Foundation of Saskatchewan (RKS) 相似文献
943.
Murine monoclonal antibodies specific for conserved and non-conserved antigenic determinants of the human and murine Ku autoantigens 总被引:5,自引:0,他引:5
944.
Previous immunohistochemical studies have identified several regulatory peptides in the carotid body chief cells in both humans and animals. These peptides, together with amines, may be important in the modulation of the chemoreflex by the carotid body. We report the localization and distribution of calcitonin and cholecystokinin-like (CCK) immunoreactivity in chief cells of human infant carotid body by light- and electron-microscopic immunohistochemical techniques. Consecutive sections immunostained with calcitonin and/or CCK antibodies revealed positively stained chief cells, both alone and in clusters, scattered throughout the carotid body lobule. Generally more chief cells were positive for calcitonin than for CCK. This was confirmed by quantiative analysis showing that the ratio of calcitonin to CCK immunoreactive cells was consistently >2:1 in all cases studied. There was no apparent correlation between the immunoreactivity for the two peptides and the age, sex, or postmortem interval. Calcitonin-like and CCK-like immunoreactivities were localized electron-microscopically over the dense core granules of the chief cells. Calcitonin and CCK-like peptides in carotid body chief cells may act as neutransmitters or neuromodulators involved in chemoreception. 相似文献
945.
复合四倍体异育银鲫个体间遗传异质性的研究 总被引:1,自引:0,他引:1
用聚丙烯酰胺梯度凝胶电泳,分析比较了4个不同的银鲫雌核发育系,红鲤和复合四倍体异育银鲫鳍的5种不同的同工酶及蛋白表型的差异,表明复合四倍体异育银鲫表型上的差异主要是来自银鲫种内的遗传差异(不同的雌核发育系)。来源于同一个银鲫雌核发育系的复合四倍体异育银鲫,个体间的EST同工酶出现差异,并与父体红鲤的EST同工酶的多态性相关,因此,复合四倍体异育银鲫个体间的异质性也包含了来自父本的遗传影响。在所检测 相似文献
946.
947.
鱼类远缘杂交正反交杂种胚胎发育差异的细胞遗传学分析 总被引:19,自引:0,他引:19
本文报道了鲤(Cyprinus carpio)×鲢(Hypophthalmichthys molitrix)、鲫(Carassiusauratus)×鲢、白鲫(Carassius auratus cuvieri)×鲢和鲢×鲤、鲢×鲫、鲢×白鲫的正反交试验。在鲤×鲢、鲫×鲢和白鲫×鲢3个正交组中,胚胎发育基本正常,尽管孵出的鱼苗绝大多数生命力弱,但孵化率都在50%左右;而在鲢×鲤、鲢×鲫和鲢×白鲫3个反交组中,胚胎发育均为畸形,不能孵化出苗。 胚胎发育细胞遗传学分析表明,鲤×鲢、鲫×鲢和白鲫×鲢的杂种胚胎几乎都是整倍体,而鲢×鲤、鲢×鲫×鲢×白鲫的杂种胚胎基本上是非整倍体,染色体数变化较大。这些正反交杂种胚胎发育的显著差异可能与其亲本物种间的基因组大小有关。文中还分析讨论了这些正反交差异与天然多倍体物种以及胚胎发育速度的相关性,认为天然多倍体物种可能具有一些不同于普通二倍体物种协调外源基因组的能力。 相似文献
948.
949.
In Saccharomyces cerevisiae, TRK1 and TRK2 are required for high- and low-affinity K+ transport. Among suppressors of the K+ transport defect in trk1 delta trk2 delta cells, we have identified members of the sugar transporter gene superfamily. One suppressor encodes the previously identified glucose transporter HXT1, and another encodes a new member of this family, HXT3. The inferred amino acid sequence of HXT3 is 87% identical to that of HXT1, 64% identical to that of HXT2, and 32% identical to that of SNF3. Like HXT1 and HXT2, overexpression of HXT3 in snf3 delta cells confers growth on low-glucose or raffinose media. The function of another new member of the HXT superfamily, HXT4 (previously identified by its ability to suppress the snf3 delta phenotype; L. Bisson, personal communication), was revealed in experiments that deleted all possible combinations of the five members of the glucose transporter gene family. Neither SNF3, HXT1, HXT2, HXT3, nor HXT4 is essential for viability. snf3 delta hxt1 delta hxt2 delta hxt3 delta hxt4 delta cells are unable to grow on media containing high concentrations of glucose (5%) but can grow on low-glucose (0.5%) media, revealing the presence of a sixth transporter that is itself glucose repressible. This transporter may be negatively regulated by SNF3 since expression of SNF3 abolishes growth of hxt1 delta hxt2 delta hxt3 delta hxt4 delta cells on low-glucose medium. HXT1, HXT2, HXT3, and HXT4 can function independently: expression of any one of these genes is sufficient to confer growth on medium containing at least 1% glucose. A synergistic relationship between SNF3 and each of the HXT genes is suggested by the observation that SNF2 hxt1 delta hxt2 delta hxt3 delta hxt4 delta cells and snf3 delta HXT1 HXT2 HXT3 HXT4 cells are unable to grow on raffinose (low fructose) yet SNF3 in combination with any single HXT gene is sufficient for growth on raffinose. HXT1 and HXT3 are differentially regulated. HXT1::lacZ is maximally expressed during exponential growth whereas HXT3::lacZ is maximally expressed after entry into stationary phase. 相似文献
950.