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131.
紫竹梅雄蕊毛细胞发育过程中胞间连丝超微结构的变化 总被引:6,自引:0,他引:6
紫竹梅(Setcreasea purpurea)雄蕊毛细胞间的胞间连丝随着细胞的生长、发育、衰老而呈现动态变化的过程.花蕾和开放花的雄蕊毛细胞间的胞间连丝,具备胞间连丝的一般结构,直径约50 nm .衰老花雄蕊毛细胞间的胞间连丝拓宽,内部结构逐步降解、撤离,呈开放式通道,直径约100 nm . 在胞间连丝的动态开放过程中,细胞内的细胞器也发生相应变化. 对胞间连丝形成开放性通道及其机理进行了讨论 相似文献
132.
Proteolytic disruption of laminin-integrin complexes on muscle cells during synapse formation.
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To explore whether a neural modulation of muscle integrins' extracellular ligand interactions contributes to synapse induction, we compared the distributions of beta1-integrins and basal lamina proteins on Xenopus myotomal myocytes developing in culture. beta1-Integrins formed numerous organized aggregates scattered over the entire muscle surface, with particularly dense accumulations at specialized sites resembling myotendinous and neuromuscular junctions. Integrin aggregates on muscle cells differed from those on surrounding fibroblasts and epithelial cells, both in their lack of response to cross-linking by multivalent ligands and in their consistent association with the cells' own extracellular matrices. Muscle integrin clusters were usually associated with congruent basal lamina accumulations containing laminin and a heparan sulfate proteoglycan (HSPG), sometimes including fibronectin and vitronectin acquired from the surrounding medium. Immediately prior to synaptic differentiation, any existing laminin and HSPG accumulations along the path of cell contact were eliminated, disrupting otherwise stable laminin-integrin complexes. This apparently proteolytic modulation of integrins' extracellular ligand interactions was soon followed by the accumulation of new congruent accumulations of laminin and HSPG in the developing synaptic basal lamina. Combining these results with earlier findings, we consider the possibility that postsynaptic differentiation is induced, at least in part, by the proteolytic disruption of integrin-ligand complexes at sites of nerve-muscle contact. 相似文献
133.
Two thioredoxin cDNAs from soybean were isolated by screening an expression library using an anti-(plasma membrane) serum. The nucleotide sequences of the two cDNAs were found to be 89% identical. The polypeptides encoded by the two cDNAs, designated TRX1 and TRX2, contain a disulfide active site, as found in other thioredoxins. TRX1 was expressed as a fusion protein in Escherichia coli and shown to possess thiol-disufide interchange activity. Unlike other eukaryotic thioredoxins, these two soybean thioredoxins contain a putative transmembrane domain in their N-terminal regions. To determine subcellular location, the TRX1 was fused with a reporter epitope at its C-terminus and expressed in transgenic tobacco plants. The fusion protein was co-purified with plasma membrane markers 1,3-glucan synthase and vanadate-sensitive ATPase, indicating the plasma membrane location of TRX1. When the reporter epitope was inserted between the start codon and the transmembrane domain in the N-terminus, the fusion protein was found in the soluble fraction, possibly due to disruption of the transmembrane domain by the highly hydrophilic epitope sequence. Taken together, our results demonstrate that soybean TRX1 is a plasma membrane-bound thioredoxin, which is most likely anchored to the membrane through the N-terminal transmembrane domain. It is known that plant plasma membranes contain various proteins with thiol-disulfide interchange activity. The soybean thioredoxins reported here are the first group of such proteins to be characterized at the molecular level. However, the biological function of the plasma membrane-bound thioredoxin remains to be determined. 相似文献
134.
Utilization of individual cellodextrins by three predominant ruminal cellulolytic bacteria. 总被引:5,自引:3,他引:2
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Growth of the ruminal bacteria Fibrobacter succinogenes S85, Ruminococcus flavefaciens FD-1, and R. albus 7 followed Monod kinetics with respect to concentrations of individual pure cellodextrins (cellobiose, cellotriose, cellotetraose, cellopentaose, and cellohexaose). Under the conditions tested, R. flavefaciens FD-1 possesses the greatest capacity to compete for low concentrations of these cellodextrins. 相似文献
135.
Relationship between the levels of wheat-rye metaphase I chromosomal pairing and recombination revealed by GISH 总被引:3,自引:0,他引:3
The metaphase I and anaphase I stages of meiosis of wheat×rye hybrids carrying the ph1b mutation were analyzed by genomic in situ hybridization. This technique allows distinction between three different types of
wheat-rye associations in metaphase I configurations as well as detection of wheat-rye recombinant chromosomes in anaphase
I cells. The frequency of associations between wheat and rye chromosomes greatly exceeded the level of wheat-rye recombination
found in the three hybrids examined. Extremely distal associations, which account for about 50% of the total wheat-rye metaphase
I chromosomal pairing, can explain such a discrepancy between metaphase I and anaphase I data. It is further discussed whether
these associations reflect very distally located chiasmata or nonchiasmatic pairing. The sizes of the segments exchanged in
wheat-rye recombinant chromosomes provide cytological evidence that wheat-rye recombination is restricted to the distal chromosomal
regions.
Received: 24 August 1995; in revised form: 27 February 1996 / Accepted: 28 March 1996 相似文献
136.
Akihiro Ohira Eugene de Juan Jr Yasuo Tano Charles A. Wilson 《The Histochemical journal》1996,28(9):607-611
Summary It has been proposed that basic fibroblast growth factor (basic FGF) mediates the neovascular response in a variety of conditions,
including diabetic retinopathy and branch retinal vein occlusion. To test the hypothesis that basic FGF was released from
retinal stores as a result of retinal ischaemia, transient retinal ischaemia was induced, followed by 48 h of reperfusion,
in the rat by combined central retinal vasculature and optic nerve ligation. The immunolocalization of basic FGF was studied
in the retina. We found that basic FGF in the normal retina is present around the deeper retinal vessels and in the neuronal
tissue of the outer plexiform layer. In the eyes that had ischaemia followed by reperfusion, there was moderate cellular oedema
with retinal swelling, and mitoses in the inner nuclear and plexiform layers. There were no changes evident at the immunohistochemical
level either in the intensity or distribution of stores of basic FGF. We conclude from these data that stores of basic FGF
are not altered dramatically under the conditions of transient experimental ischaemia and reperfusion in the rat, despite
the presence of cellular proliferation. 相似文献
137.
Thehigh growth(hg) locus in mice produces a 30–50% increase in weight gain of homozygous individuals. Here we report that the microsatellite markerD10Mit69is deleted in high growth mice. The deletion ofD10Mit69was uncovered in a screen of the high growth mouse and its progenitor strains for available markers in thehgregion. We demonstrate thathgandD10Mit69cosegregate in a cross of congenic strains C57BL/6J-hghg× C57BL/6J. These results suggest that deletion of a region aroundD10Mit69is responsible for the high growth effect. MarkerD10Mit69will be utilized as an entry point to physical cloning of thehg-containing segment. A dense map of markers aroundhgconstructed here should allow identification of markers in homologous regions in domestic animals and humans, which may be utilized to assess the role of thehglocus in these other species. 相似文献
138.
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140.
汉滩病毒核壳蛋白(NP)在杆状病毒系统的表达及其免疫原性研究 总被引:11,自引:0,他引:11
应用杆状病毒表达载体成功地表达了汉滩病毒76-118株(HTNV)核壳蛋白,将HTNVS基因插入杆状病毒转染质粒pAcYMIB的多角体基因启动子下游附近,与经Bsu361酶切线性化的杆状病毒(AcVEPA)DNA共同转染S19细胞,经空斑筛选获得了高效表达NP的重组杆状病毒(AcVHanS)。经SDS-PAGE和Western blot证实,表达产物与HTNV毒粒NP分子量均为50KD左右,紫外扫 相似文献