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61.
62.
OsHUS1 Facilitates Accurate Meiotic Recombination in Rice   总被引:1,自引:0,他引:1  
Meiotic recombination normally takes place between allelic sequences on homologs. This process can also occur between non-allelic homologous sequences. Such ectopic interaction events can lead to chromosome rearrangements and are normally avoided. However, much remains unknown about how these ectopic interaction events are sensed and eliminated. In this study, using a screen in rice, we characterized a homolog of HUS1 and explored its function in meiotic recombination. In Oshus1 mutants, in conjunction with nearly normal homologous pairing and synapsis, vigorous, aberrant ectopic interactions occurred between nonhomologous chromosomes, leading to multivalent formation and subsequent chromosome fragmentation. These ectopic interactions relied on programed meiotic double strand breaks and were formed in a manner independent of the OsMER3-mediated interference-sensitive crossover pathway. Although early homologous recombination events occurred normally, the number of interference-sensitive crossovers was reduced in the absence of OsHUS1. Together, our results indicate that OsHUS1 might be involved in regulating ectopic interactions during meiosis, probably by forming the canonical RAD9-RAD1-HUS1 (9-1-1) complex.  相似文献   
63.
Male moths can accurately perceive the sex pheromone emitted from conspecific females by their highly accurate and specific olfactory sensory system. Pheromone receptors are of special importance in moth pheromone reception because of their central role in chemosensory signal transduction processes that occur in olfactory receptor neurons in the male antennae. There are a number of pheromone receptor genes have been cloned, however, only a few have been functionally characterized. Here we cloned six full-length pheromone receptor genes from Helicoverpa armigera male antennae. Real-time PCR showing all genes exhibited male-biased expression in adult antennae. Functional analyses of the six pheromone receptor genes were then conducted in the heterologous expression system of Xenopus oocytes. HarmOR13 was found to be a specific receptor for the major sex pheromone component Z11-16:Ald. HarmOR6 was equally tuned to both of Z9-16: Ald and Z9-14: Ald. HarmOR16 was sensitively tuned to Z11-16: OH. HarmOR11, HarmOR14 and HarmOR15 failed to respond to the tested candidate pheromone compounds. Our experiments elucidated the functions of some pheromone receptor genes of H. armigera. These advances may provide remarkable evidence for intraspecific mating choice and speciation extension in moths at molecular level.  相似文献   
64.

Background and Objective

Vascular endothelial growth factor (VEGF) is one of the key initiators and regulators of angiogenesis and it plays a vital role in the onset and development of malignancy. The association between VEGF gene polymorphisms and lung cancer risk has been extensively studied in recent years, but currently available results remain controversial or ambiguous. The aim of this meta-analysis is to investigate the associations between four common VEGF polymorphisms (i.e., −2578C>A, −460C>T, +936C>T and +405C>G) and lung cancer risk.

Methods

A comprehensive search was conducted to identify all eligible studies to estimate the association between VEGF polymorphisms and lung cancer risk. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were used to evaluate the strength of this association.

Results

A total of 14 published case-control studies with 4,664 cases and 4,571 control subjects were identified. Our meta-analysis provides strong evidence that VEGF −2578C>A polymorphism is capable of increasing lung cancer susceptibility, especially among smokers and lung squamous cell carcinoma (SCC) patients. Additionally, for +936C>T polymorphism, increased lung cancer susceptibility was only observed among lung adenocarcinoma patients. In contrast, VEGF −460C>T polymorphism may be a protective factor among nonsmokers and SCC patients. Nevertheless, we did not find any association between +405C>G polymorphism and lung cancer risk, even when the groups were stratified by ethnicity, smoking status or histological type.

Conclusion

This meta-analysis recommends more investigations into the relationship between −2578C>A and −460C>T lung cancer risks. More detailed and well-designed studies should be conducted to identify the causal variants and the underlying mechanisms of the possible associations.  相似文献   
65.
66.
人为干扰下的亚高山草甸功能多样性和功能冗余 人为干扰程度的加剧会引起植物群落物种多样性和功能多样性的改变,并降低生态系统的稳定性。较高水平的功能冗余对于物种损失引起的生态系统功能和稳定性的改变起到了重要的缓冲作用。然而,关于亚高山草甸植物群落功能冗余对干扰的响应的研究相对较少。本研究的目的是,确定人为干扰下不同退化程度的亚高山草甸,其植物群落功能多样性和功能冗余对干扰的响应特征,及不同物种对功能冗余的贡献程度及其在干扰梯度上的变化规律。研究区位于青藏高原东南缘玉龙雪山上的亚高山草甸。本研究识别出4类干扰强度(无干扰、弱干扰、中度干扰和重度干扰),测定了干扰梯度上的植物物种组成、土壤性质和5个关键的植物功能性状等指标,进一步计算了Simpson多样性指数、功能多样性指数(RaoQ)、功能冗余度、群落的植物功能性状加权平均值(CWM)以及物种水平的功能冗余等指数。研究结果表明,功能多样性和功能冗余在干扰梯度上呈现单峰变化规律,即二者分别在中度干扰、弱干扰下达到最大值。物种多样性在干扰梯度上整体呈下降趋势。随着干扰程度的增加,采取保守生长策略并具有相关性状特征(如较低比叶面积和较高的干物质含量)的物种的丰富度降低,采取资源获取策略并具有相关性状(如低矮植株、较高的比叶面积和较低的干物质含量)的物种增加。不同物种的功能冗余程度存在差异。值得注意的是,一些物种在群落中扮演着独特的功能角色,如无干扰梯度下的网脉橐吾(Ligularia dictyoneura)以及中度和重度干扰梯度下的滇西委陵菜(Potentilla delavayi)。  相似文献   
67.

Aims

This study sought to evaluate the prognostic significance of postoperative complications for colon cancer patients undergoing laparoscopic surgery.

Methods

From May 2006 to May 2009, a total 224 patients who underwent laparoscopic curative resection (R0) for colon cancer were included in our retrospective study. Postoperative complications were evaluated according to a standardized grading system. The main outcome measurements of our study were overall survival (OS) and relapse-free survival (RFS), which were then compared between the no complication and complication groups. Univariate and multivariate analysis were used to assess the correlation between complications and prognosis.

Results

Fifty-nine postoperative complications occurred in 43 patients. The overall morbidity rate was 26.3%. The 5-year OS in the complication group was 41.4% compared with 78.5% in the no complication group (P<0.001). The cumulative incidence of relapse was also more aggressive in patients with complications (5-year RFS: complication group 40.9% vs. no complication group 82.1%, P<0.001). Multivariate analysis identified complications as a significant factor increasing the risk for both OS (RR 2.737; 95% CI 1.512–4.952; P = 0.001) and RFS (RR 4.247; 95% CI 2.291–7.876; P<0.001).

Conclusion

Postoperative complications could pose a significant adverse impact not only on OS but also on RFS in patients with colon cancer even when laparoscopic R0 resection is available.  相似文献   
68.
During meiosis, the paired homologous chromosomes are tightly held together by the synaptonemal complex (SC). This complex consists of two parallel axial/lateral elements (AEs/LEs) and one central element. Here, we observed that PAIR3 localized to the chromosome core during prophase I and associated with both unsynapsed AEs and synapsed LEs. Analyses of the severe pair3 mutant demonstrated that PAIR3 was essential for bouquet formation, homologous pairing and normal recombination, and SC assembly. In addition, we showed that although PAIR3 was not required for the initial recruitment of PAIR2, it was required for the proper association of PAIR2 with chromosomes. Dual immunostaining revealed that PAIR3 highly colocalized with REC8. Moreover, studies using a rec8 mutant indicated that PAIR3 localized to chromosomes in a REC8-dependent manner.  相似文献   
69.
药物递送载体的应用使得小分子药物、蛋白质药物,以及基因药物能够通过多种给药方式用于癌症的治疗。聚乳酸-羟基乙酸共聚物因其具有良好的生物相容性及生物可降解性,成为广泛采用的抗癌药物载体之一,可以通过静脉、皮下、口服等多种给药途径用于化疗、基因治疗、蛋白治疗给药及接种免疫等诸多方面,显示了良好的应用前景。  相似文献   
70.
Targeted mutagenesis in rice using CRISPR-Cpf1 system   总被引:2,自引:0,他引:2  
正Cpfl is a class 2/type V CRISPR effector that has been recently harnessed for genome editing(Zetsche et al.,2015;Hur et al.,2016;Kim et al.,2016).Cpfl recognizes thymidine-rich sequence as the protospacer-adjacent motif(PAM)at the 5'end of target sequences.In addition,Cpfl requires only a single shorter crRNA and  相似文献   
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