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141.
142.
Madan K. Bhattacharyya Nancy L. Paiva Richard A. Dixon Kenneth L. Korth Bruce A. Stermer 《Plant molecular biology》1995,27(1):1-15
3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) catalyzes a key step in isoprenoid metabolism leading to a range of compounds that are important for the growth, development and health of the plant. We have isolated 7 classes of genomic clones encoding HMGR from a potato genomic library. Comparison of nucleic acid sequences reveals a high degree of identity between all seven classes of clones and the potato hmg 1 gene described by Choi et al. (Plant Cell 4: 1333, 1992), indicating that all are members of the same subfamily in potato. A representative member (hmg 1.2) of the most abundant class of genomic clones was selected for further characterization. Transgenic tobacco and potato containing the -glucuronidase (GUS) reporter gene under the control of the hmg 1.2 promoter expressed GUS activity constitutively at a low level in many plant tissues. High levels of GUS activity were observed only in the pollen. GUS assays of isolated pollen, correlations of GUS activity with the HMGR activity of anthers, hmg 1.2 promoter deletion studies, and segregation analysis of the expression of hmg 1.2::GUS among the R2 pollen of R1 progeny plants demonstrated that the hmg 1.2 promoter controls pollen expression. 相似文献
143.
Intron-dependent transient expression of the maize GapA1 gene 总被引:2,自引:0,他引:2
144.
The ability of most higher plants to withstand freezing can be enhanced by cold acclimation, although the freezing tolerance of plant tissues is also affected by their developmental stage. In addition, low temperature has pleiotropic effects on many plant developmental processes such as vernalization. The interaction between plant development and low temperature implies that some genes are regulated by both environmental factors and developmental cues. Although a number of cold-inducible genes from plants have been identified, information concerning their regulation during plant development is limited. In order to understand their developmental regulation and obtain possible clues as to function, the promoters of kin1 and cor6.6, two cold- and abscisic acid (ABA)-regulated genes from Arabidopsis thaliana, were fused to the -glucuronidase (GUS)-coding sequence and the resulting constructs were used to transform tobacco and A. thaliana. Transgenic plants with either the kin1 or cor6.6 promoter showed strong GUS expression in pollen, developing seeds, trichomes and, most interestingly, in guard cells. During pollen development, maximum GUS activity was found in mature pollen. In contrast, the maximum GUS activity during seed development was during early embryogenesis. These patterns of expression distinguish kin1 and cor6.6 from related lea genes which are strongly expressed during late embryogenesis. There was no major qualitative difference in patterns of GUS expression between kin1 and cor6.6 promoters and the results were similar for transgenic tobacco and Arabidopsis. Considering the results described, as well as those in an accompanying paper Wang et al., 1995, Plant Mol Biol 28: 605–617 (this issue), we suggest that osmotic potential might be a major factor in regulating the expression of kin1 and cor6.6 during several developmental processes. The implication of the results for possible function of the gene products is discussed. 相似文献
145.
146.
We have identified two types of structural elements in genomic DNA for annexin I that provide physical evidence of genetic events leading to conserved changes in gene structure. The sequence upstream of the transcribed region in human annexin I contained a rare, Alu-like repetitive element with flanking direct repeats, probably derived from the active BC200 gene via germline retroposition. Nucleotide substitutions in this BC200 insert relative to the 7SL gene and its absence in rodent annexins I identified it as a recent primate pseudogene. Phylogenetic analysis showed that the BC200 gene represents a new clade of primate Alu evolution that branched near the time of appearance of the progenitor to the free left Alu monomer, FLAM-C. Separate analysis identified a Z-DNA motif in pigeon annexin I intron 7 that may represent the vestigial recombination site involved in primordial assembly of the annexin tetrad. These distinct structural features in annexin I genes provide insight into the evolution of Alu repeats and the mechanism of annexin tetrad formation. 相似文献
147.
Julia C. McNaughton Craig J. Marshall Judith E. Broom Gillian Hughes Wyn A. Jones Peter A. Stockwell George B. Petersen 《Journal of molecular evolution》1995,40(2):127-135
A THE-1 sequence in intron 7 of the human dystrophin gene has been found to represent a new subfamily of THE-1 elements. The sequence is closely related to the MstII family of repetitive sequences and is more like single-copy sequences found in the galago genome than any other THE-1 sequence previously reported. This new THE-1 sequence has been compared with two other complete THE-1 sequences and three related long-terminal repeat elements that we have previously found in intron 7 of the dystrophin gene, and with members of the same family from elsewhere in the primate genome. Parsimony and deletion analysis show that the cluster of THE-1 sequences in intron 7 of the dystrophin gene has arisen from at least three individual insertion events, rather than from the insertion and duplication of a single progenitor sequence.
Correspondence to: G.B. Petersen 相似文献
148.
Clare Gough Pascale Hemon Maurice Tronchet Christophe Lacomme Yves Marco Dominique Roby 《Molecular & general genetics : MGG》1995,247(3):323-337
A family of genes, the so-called msr genes (multiple stimulus response), has recently been identified on the basis of sequence homology in various plant species. Members of this gene family are thought to be regulated by a number of environmental or developmental stimuli, although it is not known whether any one member responds more specifically to one stimulus, or whether each gene member responds to various environmental stimuli. In this report, we address this question by studying the tobacco msr gene str246C. Using transgenic tobacco plants containing 2.1 kb of 5 flanking DNA sequence from the str246C gene fused to the -glucuronidase (GUS) coding region, the complex expression pattern of the str246C promoter has been characterized. Expression of the str246C promoter is strongly and rapidly induced by bacterial, fungal and viral infection and this induction is systemic. Elicitor preparations from phytopathogenic bacteria and fungi activate the str246C promoter to high levels, as do wounding, the application of auxin, auxin and cytokinin, salicylic acid or copper sulfate, indicating the absence of gene specialization within the msr gene family, at least for str246C. In addition, GUS activity was visualized. histochemically in root meristematic tissues of tobacco seedlings and is restricted to roots and sepals of mature plants. Finally, analysis of a series of 5 deletions of the str246C promoter-GUS gene fusion in transgenic tobacco plants confirms the involvement of multiple regulatory elements. A region of 83 by was found to be necessary for induction of promoter activity in response to Pseudomonas solanacearum, while auxin inducibility and root expression are apparently not controlled by this element, since its removal does not abolish either response. An element of the promoter with a negative effect on promoter activation by P. solanacearum was also identified.Joint first authors 相似文献
149.
Christian Biémont Cristina Vieira Christine Hoogland Géraldine Cizeron Catherine Lœvenbruck Claude Arnault Jean-Pierre Carante 《Genetica》1997,100(1-3):161-166
To investigate the main forces controlling the containment of transposable elements (TE) in natural populations, we analyzed
the copia, mdg1, and 412 elements in various populations of Drosophila melanogaster and D. simulans. A lower proportion of
insertion sites on the X chromosome in comparison with the autosomes suggests that selection against the detrimental effects
of TE insertions is the major force containing TE copies in populations of Drosophila. This selection effect hypothesis is
strengthened by the absence of the negative correlation between recombination rate and TE copy number along the chromosomes,
which was expected under the alternative ectopic exchange model (selection against the deleterious rearrangements promoted
by recombination between TE insertions). A cline in 412 copy number in relation to latitude was observed among the natural
populations of D. simulans, with very high numbers existing in some local populations (around 60 copies in a sample from Canberra,
Australia). An apparent absence of selection effects in this Canberra sample and a value of transposition rate equal to 1–2
× 10-3 whatever the population and its copy number agree with the idea of recent but temporarily drastic TE movements in local populations.
The high values of transposition rate in D. simulans clearly disfavor the hypothesis that the low amount of transposable elements
in this species could result from a low transposition rate.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
150.
The phylogenetic distribution of transposable families, P, gypsy, hobo, I, and mariner has been analyzed in 33 species of
11 groups of neotropical Drosophila and a Drosophilidae species Zygotrica vittimaculosa, using squash blot and dot blot. Genomic
DNA of almost all neotropical species tested hybridized with gypsy probe and some species showed a particularly strong hybridization
signal, as D. gaucha, D. virilis, and species of flavopilosa group. The hobo element was restricted to melanogaster group
and some strains of D. willistoni. Only D. simulans DNA showed hybridization to mariner probe in all species tested and D.
simulans and D. melanogaster showed hybridization with I element probe. P element homologous sequence was present in D. melanogaster
and all species and strains of the willistoni and saltans groups tested. The presence of at least one P-homologous sequence
was detected in Drosophila mediopunctata. This one was the only P-bearing species of all six tested from the tripunctata group.
Four different pairs of primers homologous to segments of the canonical sequence of D. melanogaster's P were used to amplify
specific sequences from D. mediopunctata DNA, showing the occurrence of seemingly well-conserved P-homologous sequences.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献