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排序方式: 共有622条查询结果,搜索用时 46 毫秒
1.
R. Chakraborty 《International Journal of Anthropology》1990,5(1):33-42
Simple heritability estimators of continuous as well as discrete traits from twin data are known to overestimate the degree
of genetic determination of the measured traits for several reasons. Errors of zygosity determination will, however, underestimate
the true heritability. The bias due to wrong assignment of dizygous twin pairs into monozygous type is evaluated here, and
the results indicate that this negative bias has a compensatory effect on the estimate of the degree of genetic determination
when other factors of similarity between twin pairs are taken into account. It is shown that when an estimate of zygosity
error is available, the bias due to this factor can be evaluated quantitatively, and hence the adjustment for zygosity error
can be incorporated in the estimation of the degree of genetic determination of a trait.
Although this theory is explicitly developed here for twin studies, the general principle also applies for other types of
errors of determining the degree of biological relationships for estimation of heritability, in which case this type of error
may be more important than the simple zygosity error. 相似文献
2.
Summary Heat induces a number of premutational lesions (for example, the deamination of cytosine to uracil) in DNA and RNA. These kinds of errors occur in resting as well as replicating polynucleotides. However, an increase in temperature also raises the probability of copying error occurring in nucleic acids because of increased thermal noise in the replicative machinery. In most modern genetic systems, the majority of heat-induced lesions are efficiently repaired. It follows that the importance of heat-induced error increases as the effectiveness of repair declines. We show in this paper that the error rate of enzymatic polynucleotide copying is expected to increase monotonically with temperature. We also explore the effects of temperature variations on the early evolution of biological information transmission mechanisms. 相似文献
3.
Ruben Kaufman 《Primates; journal of primatology》1996,37(4):335-350
Agonistic behaviour was studied in three groups each of free-ranging and semi-free-ranging brown lemurs (Eulemur fulvus) at Berenty, Madagascar and the Duke University Primate Center (DUPC) respectively. The purpose of the study was to answer
questions arising from the work of other researchers regarding the frequency and intensity of agonism in this species. Authors
of field studies generally concluded that agonism was rare and mild, whereas those who had studied semi-free-ranging or captive
animals at the DUPC reported intense agonism during the peaks of the mating and birth seasons, with sometimes fatal wounding
occurring among captive animals.
I recorded 30 agonistic behaviours or “signals” which I grouped into seven general categories — cuffs, other physical contact,
threats, chases, third party intervention, unprovoked submissive signals, and reciprocal aggression. The seven categories
represent the types of signals which initiated or otherwise defined agonistic interactions, regardless of whether or not there
was a submissive response to aggression. The relative percentages of all agonism constituted by the seven categories were
not found to be significantly different between study sites.
Agonistic signals were also classified as either subtle or obvious, a classification which crosscut the seven categories.
At both study sites, the majority of agonistic signals initiating or defining interactions were subtle.
Rates of agonism for the Berenty groups, studied during the birth season only, were significantly lower than those for the
DUPC groups during the birth season, possibly due to (1) easier observation conditions at the DUPC, and (2) the impossibility
of successful emigration at the DUPC, which might have resulted in social stresses translating into higher rates of agonism.
In only one DUPC group was there significant variation in rates of agonism between seasons.
I found agonistic behaviour to be mild, at both study sites, in the senses of subtlety of both aggressive and submissive signals,
unlikelihood of response to aggression, and virtual absence of wounding; and I noted that serious wounding during other studies
at the DUPC involved animals captive in caged runs. Comparing rates of the study groups with rates reported in other research
for brown lemurs, other lemuriform species, and some New and Old World anthropoid species, I concluded thatE. fulvus agonism was in fact not rare except in comparison to baboons and macaques. 相似文献
4.
报道了缢蛏碱性磷酸酶(简称ALP)经不同浓度盐酸胍处理时酶的分子构象所发生的变化以及酶变化和失活的动力学过程。在胍中酶荧光发射峰强度下降,紫外差光谱在246nm和285nm处出现2个负峰,CD谱中酶的α螺旋度下降,且随浓度增大,变化程度也加大。动力学研究表明,酶在0.5mol/L、1.0mol/L、2.0mol/L3.0mol/L、4.0mol/L盐酸胍中的变性速度常数分别为3.21×10~(-4)s~(-1)、6.38×10~(-4)s~(-1)、2.17×10~(-3)s~(-1)、2.33×10~(-3)s~9-1)、5.17×10~(-3)s~(-1);而酶在相应盐酸胍中的失活速度常数分别为2.33×10~(-4)s~(-1)、3.57×10~(-4)s~(-1)、5.86×10~(-4)s~(-1)、1.14×10~(-3)s~(-1)、3.45×10~(-3)s~(-1);表现为失活与构象伸展变化基本平行。 相似文献
5.
This work studies the structure-function relationships of Asn135, a residue situated in the GTP binding pocket of elongation factor Tu (EF-Tu). For this purpose we constructed EF-TuN135D/D138N and assayed its reactivity towards various purine nucleotides. We found that EF-TuN135D/D138N had no functional effect with GTP, ATP, XTP and isoGTP. The lack of a productive interaction with isoGTP shows that the Asn135 side-chain does not recognize the exocyclic keto group of the guanine base. However, EF-TuN 135D/D 138N, whose native conformation is stabilized by either elongation factor Ts or kirromycin, was able to support the enzymatic binding of aa-tRNA to the ribosome in the absence of any nucleotide, when in complex with the antibiotic. Taken together, these results show that Asn135 is important for the correct folding of the nucleotide binding site and that EF-Tu·kirromycin can mediate the binding of aa-tRNA to the mRNA-programmed ribosomes independently of the native conformation of this site. 相似文献
6.
Kunihiro Kuwajima Naoki Okayama Kaori Yamamoto Tsuyoshi Ishihara Shintaro Sugai 《FEBS letters》1991,290(1-2)
Kinetics of unfolding and refolding of a staphylococcal nuclease mutant, in which Pro117 is replaced by glycine, have been investigated by stopped-flow circular dichroism, and the results are compared with those for the wild-type protein. In contrast to the biphasic unfolding of the wild-type nuclease, the unfolding of the mutant is represented by a single-phase reaction, indicating that the biphasic unfolding for the wild-type protein is caused by cis-trans isomerization about the prolyl peptide bond in the native state. The proline mutation also simplifies the kinetic refolding. Importance of the results in elucidating the folding mechanism is discussed. 相似文献
7.
E. C. Holmes 《Journal of molecular evolution》1991,33(3):209-215
Summary In an attempt to resolve some points of branching order in the phylogeny of the eutherian mammals, a phylogenetic analysis of 26 nuclear and 6 mitochondrial genes was undertaken using a maximum likelihood method on a constant rate stochastic model of molecular evolution. Seventeen of the nuclear genes gave a primates/artiodactyls grouping highest support whereas three of the mitochondrial genes found a rodents/artiodactyls grouping to be best supported. The primates/rodents grouping was never the best supported. On the assumption that rodents are indeed an outgroup to primates and artiodactyls and that the latter taxa diverged 70 million years ago, an estimation was made, for each gene, of the time of divergence of the rodent lineage. In most cases such estimates were beyond the limits set by present interpretations of the paleontological record as were many estimates of the divergence time of mouse and rat. These results suggest that, although there is locus variation, the divergent position of the rodent lineage may be an artifact of an elevated rate of nucleotide substitution in this order. 相似文献
8.
In order to elucidate the protein folding problem, we performed molecular dynamics simulations for small- and middle-sized two unfolding and six refolding proteins in an explicit solvent. Histidine-containing phosphocarrier protein and small designed protein were chosen for the simulations. We found that the protein folding process of these proteins was divided into three phases: an α -helix formation phase, a packing phase and a β -sheet formation phase. In the α -helix formation phase, an α -helix was developed from a β -turn structure through a 310-helix state. In the packing phase, proteins became compact, and tertiary structures (α / α or pre- β / β packing) were formed. Formation of a hydrophobic nucleus occurred concomitant with the α -helix formation and packing phase. Finally, in the β -sheet formation phase, a β -sheet was developed owing to the sequential formation of hydrogen bonds between two neighbouring strands, just like a "closing zipper". 相似文献
9.
Zhaomin Li Hui Peng Li Qin Jing Qi Xiaobing Zuo Jing-Yuan Liu Jian-Ting Zhang 《The Journal of biological chemistry》2013,288(44):31447-31457
Many proteins exist and function as homodimers. Understanding the detailed mechanism driving the homodimerization is important and will impact future studies targeting the “undruggable” oncogenic protein dimers. In this study, we used 14-3-3σ as a model homodimeric protein and performed a systematic investigation of the potential roles of amino acid residues in the interface for homodimerization. Unlike other members of the conserved 14-3-3 protein family, 14-3-3σ prefers to form a homodimer with two subareas in the dimeric interface that has 180° symmetry. We found that both subareas of the dimeric interface are required to maintain full dimerization activity. Although the interfacial hydrophobic core residues Leu12 and Tyr84 play important roles in 14-3-3σ dimerization, the non-core residue Phe25 appears to be more important in controlling 14-3-3σ dimerization activity. Interestingly, a similar non-core residue (Val81) is less important than Phe25 in contributing to 14-3-3σ dimerization. Furthermore, dissociating dimeric 14-3-3σ into monomers by mutating the Leu12, Phe25, or Tyr84 dimerization residue individually diminished the function of 14-3-3σ in resisting drug-induced apoptosis and in arresting cells at G2/M phase in response to DNA-damaging treatment. Thus, dimerization appears to be required for the function of 14-3-3σ. 相似文献
10.
Xinmiao Fu Xiaodong Shi Linxuan Yan Hanlin Zhang Zengyi Chang 《The Journal of biological chemistry》2013,288(44):31646-31654
Small heat shock proteins (sHSPs), as ubiquitous molecular chaperones found in all forms of life, are known to be able to protect cells against stresses and suppress the aggregation of a variety of model substrate proteins under in vitro conditions. Nevertheless, it is poorly understood what natural substrate proteins are protected by sHSPs in living cells. Here, by using a genetically incorporated photo-cross-linker (p-benzoyl-l-phenylalanine), we identified a total of 95 and 54 natural substrate proteins of IbpB (an sHSP from Escherichia coli) in living cells with and without heat shock, respectively. Functional profiling of these proteins (110 in total) suggests that IbpB, although binding to a wide range of cellular proteins, has a remarkable substrate preference for translation-related proteins (e.g. ribosomal proteins and amino-acyl tRNA synthetases) and moderate preference for metabolic enzymes. Furthermore, these two classes of proteins were found to be more prone to aggregation and/or inactivation in cells lacking IbpB under stress conditions (e.g. heat shock). Together, our in vivo data offer novel insights into the chaperone function of IbpB, or sHSPs in general, and suggest that the preferential protection on the protein synthesis machine and metabolic enzymes may dominantly contribute to the well known protective effect of sHSPs on cell survival against stresses. 相似文献