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11.
Pei Huang Huan Huang Xueqiang Lin Pan Liu Lun Zhao Wen-Feng Nie Jian-Kang Zhu Zhaobo Lang 《The Plant journal : for cell and molecular biology》2021,108(2):347-357
DNA methylation is an important epigenetic mark. In plants, de novo DNA methylation occurs mainly through the RNA-directed DNA methylation (RdDM) pathway. Researchers have previously inferred that a flowering regulator, MULTICOPY SUPPRESSOR OF IRA1 4 (MSI4)/FVE, is involved in non-CG methylation at several RdDM targets, suggesting a role of FVE in RdDM. However, whether and how FVE affects RdDM genome-wide is not known. Here, we report that FVE is required for DNA methylation at thousands of RdDM target regions. In addition, dysfunction of FVE significantly reduces 24-nucleotide siRNA accumulation that is dependent on factors downstream in the RdDM pathway. By using chromatin immunoprecipitation and sequencing (ChIP-seq), we show that FVE directly binds to FVE-dependent 24-nucleotide siRNA cluster regions. Our results also indicate that FVE may function in RdDM by physically interacting with RDM15, a downstream factor in the RdDM pathway. Our study has therefore revealed that FVE, by associating with RDM15, directly regulates DNA methylation and siRNA accumulation at a subset of RdDM targets. 相似文献
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Huiting Ho Harmeet Singh Sophea Heng Tracy L. Nero Sarah Paule Michael W. Parker Alan T. Johnson Guan-Sheng Jiao Guiying Nie 《PloS one》2013,8(12)
Uterine proprotein convertase (PC) 6 plays a critical role in embryo implantation and is pivotal for pregnancy establishment. Inhibition of PC6 may provide a novel approach for the development of non-hormonal and female-controlled contraceptives. We investigated a class of five synthetic non-peptidic small molecule compounds that were previously reported as potent inhibitors of furin, another PC member. We examined (i) the potency of these compounds in inhibiting PC6 activity in vitro; (ii) their binding modes in the PC6 active site in silico; (iii) their efficacy in inhibiting PC6-dependent cellular processes essential for embryo implantation using human cell-based models. All five compounds showed potent inhibition of PC6 activity in vitro, and in silico docking demonstrated that these inhibitors could adopt a similar binding mode in the PC6 active site. However, when these compounds were tested for their inhibition of decidualization of primary human endometrial stromal cells, a PC6-dependent cellular process critical for embryo implantation, only one (compound 1o) showed potent inhibition. The lack of activity in the cell-based assay may reflect the inability of the compounds to penetrate the cell membrane. Because compound''s lipophilicity is linked to cell penetration, a measurement of lipophilicity (logP) was calculated for each compound. Compound 1o is unique as it appears the most lipophilic among the five compounds. Compound 1o also inhibited another crucial PC6-dependent process, the attachment of human trophoblast spheroids to endometrial epithelial cells (a model for human embryo attachment). We thus identified compound 1o as a potent small molecule PC6 inhibitor with pharmaceutical potential to inhibit embryo implantation. Our findings also highlight that human cell-based functional models are vital to complement the biochemical and in silico analyses in the selection of promising drug candidates. Further investigations for compound 1o are warranted in animal models to test its utility as an implantation-inhibiting contraceptive drug. 相似文献
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Distributed hash tables (DHTs) are usually used in the open networking environment, where they are vulnerable to Sybil attacks. Pebble-Rotating Game (PRG) mixes the nodes of the honest and the adversarial randomly, and can resist the Sybil attack efficiently. However, the adversary may have some tricks to corrupt the rule of PRG. This paper proposes a set of mechanisms to make the rule of PRG be obliged to obey. A new joining node must ask the Certificate Authority (CA) for its signature and certificate, which records the complete process on how a node joins the network and obtains the legitimacy of the node. Then, to prevent the adversary from accumulating identifiers, any node can make use of the latest certificate to judge whether one identifier is expired with the help of the replacement property of RPG. This paper analyzes in details the number of expired certificates which are needed to store in every node, and gives asymptotic solution of this problem. The analysis and simulations show that the mean number of the certificates stored in each node are , where n is the size of the network. 相似文献
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草果组织培养快速繁殖育苗研究 总被引:2,自引:0,他引:2
以草果(Amomum tsao-ko Crevost et Lemaire)茎尖为外植体,MS为基本培养基,探讨不同浓度的培养基因子,对草果不定芽的诱导、增殖分化、生根情况和试管苗移栽成活率的影响.结果表明:①以MS+6-BA 6 mg/L+NAA 0.1 mg/L+TDZ 0.05 mg/L的培养基对不定芽增殖分化效果较好,增殖倍数达到2.34,不定芽叶色绿,苗粗壮,整体感最好.②糖浓度对草果不定芽分化增殖有一定影响,以糖浓度为30~35g/L增殖分化效果较好.③在草果不定芽生根中,以1/2MS+IBA 0.2 mg/L、1/2MS+NAA 0.2 mg/L效果较好.出根率较高,须根最多,平均根数最多,移栽成活率为100%. 相似文献
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Svetlana A. Romanenko Polina L. Perelman Natalya A. Serdukova Vladimir A. Trifonov Larisa S. Biltueva Jinhuan Wang Tangliang Li Wenhui Nie Patricia C.M. O’Brien Vitaly T. Volobouev Roscoe Stanyon Malcolm A. Ferguson-Smith Fengtang Yang Alexander S. Graphodatsky 《Mammalian genome》2006,17(12):1183-1192
The laboratory mouse (Mus musculus, 2n = 40), the Chinese hamster (Cricetulus griseus, 2n = 22), and the golden (Syrian) hamster (Mesocricetus auratus, 2n = 44) are common laboratory animals, extensively used in biomedical research. In contrast with the mouse genome, which was
sequenced and well characterized, the hamster species has been set aside. We constructed a chromosome paint set for the golden
hamster, which for the first time allowed us to perform multidirectional chromosome painting between the golden hamster and
the mouse and between the two species of hamster. From these data we constructed a detailed comparative chromosome map of
the laboratory mouse and the two hamster species. The golden hamster painting probes revealed 25 autosomal segments in the
Chinese hamster and 43 in the mouse. Using the Chinese hamster probes, 23 conserved segments were found in the golden hamster
karyotype. The mouse probes revealed 42 conserved autosomal segments in the golden hamster karyotype. The two largest chromosomes
of the Chinese hamster (1 and 2) are homologous to seven and five chromosomes of the golden hamster, respectively. The golden
hamster karyotype can be transformed into the Chinese hamster karyotype by 15 fusions and 3 fissions. Previous reconstructions
of the ancestral murid karyotype proposed diploid numbers from 2n = 52 to 2n = 54. By integrating the new multidirectional chromosome painting data presented here with previous comparative genomics
data, we can propose that syntenies to mouse Chrs 6 and 16 were both present and to hypothesize a diploid number of 2n = 48 for the ancestral Murinae/Cricetinae karyotype. 相似文献