全文获取类型
收费全文 | 146篇 |
免费 | 1篇 |
专业分类
系统科学 | 3篇 |
理论与方法论 | 1篇 |
现状及发展 | 38篇 |
研究方法 | 29篇 |
综合类 | 65篇 |
自然研究 | 11篇 |
出版年
2022年 | 1篇 |
2019年 | 1篇 |
2018年 | 2篇 |
2017年 | 3篇 |
2016年 | 4篇 |
2015年 | 2篇 |
2013年 | 2篇 |
2012年 | 11篇 |
2011年 | 24篇 |
2010年 | 1篇 |
2008年 | 8篇 |
2007年 | 13篇 |
2006年 | 11篇 |
2005年 | 7篇 |
2004年 | 11篇 |
2003年 | 12篇 |
2002年 | 12篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1997年 | 1篇 |
1982年 | 1篇 |
1981年 | 3篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1971年 | 1篇 |
1970年 | 2篇 |
1968年 | 3篇 |
1967年 | 1篇 |
排序方式: 共有147条查询结果,搜索用时 15 毫秒
71.
Friedrich R Panizzi P Fuentes-Prior P Richter K Verhamme I Anderson PJ Kawabata S Huber R Bode W Bock PE 《Nature》2003,425(6957):535-539
Many bacterial pathogens secrete proteins that activate host trypsinogen-like enzyme precursors, most notably the proenzymes of the blood coagulation and fibrinolysis systems. Staphylococcus aureus, an important human pathogen implicated in sepsis and endocarditis, secretes the cofactor staphylocoagulase, which activates prothrombin, without the usual proteolytic cleavages, to directly initiate blood clotting. Here we present the 2.2 A crystal structures of human alpha-thrombin and prethrombin-2 bound to a fully active staphylocoagulase variant. The cofactor consists of two domains, each with three-helix bundles; this is a novel fold that is distinct from known serine proteinase activators, particularly the streptococcal plasminogen activator streptokinase. The staphylocoagulase fold is conserved in other bacterial plasma-protein-binding factors and extracellular-matrix-binding factors. Kinetic studies confirm the importance of isoleucine 1 and valine 2 at the amino terminus of staphylocoagulase for zymogen activation. In addition to making contacts with the 148 loop and (pro)exosite I of prethrombin-2, staphylocoagulase inserts its N-terminal peptide into the activation pocket of bound prethrombin-2, allosterically inducing functional catalytic machinery. These investigations demonstrate unambiguously the validity of the zymogen-activation mechanism known as 'molecular sexuality'. 相似文献
72.
73.
Patricia Fara 《Studies in history and philosophy of science》2004,35(3):549-571
Although many historians of science acknowledge the extent to which Greek and Roman ideals framed eighteenth-century thought, many classical references in the texts they study remain obscure. Poems played an important role not only in spreading ideas about natural philosophy, but also in changing people’s perceptions of its value; they contributed to Newton’s swelling reputation as an English hero. By writing about Latin poetry, we focus on the intersection of two literary genres that were significant for eighteenth-century natural philosophy, but seem alien to modern science. We classify Augustan Latinate scientific poetry by considering the audiences for whom the poems were intended. We distinguish three broad categories. One type of poetry was circulated amongst gentlemanly scholars (we look particularly at Tripos verses, and laments for Queen Caroline). A second group comprised poetry written specifically to promote or criticise Newton and his books, particularly the Principia (we look at versions of Pope’s epitaph, and Halley’s Lucretian poem). After Newton’s death, a third type of poetry became increasingly significant, included in collections of poems rather than in texts of natural philosophy. Overall, we show how the classical past was vital for creating the scientific future. 相似文献
74.
Patricia L. Chang Jennifer M. Sturgess Dr M. A. Moscarello 《Cellular and molecular life sciences : CMLS》1977,33(9):1136-1137
Summary A Golgi-rich fraction from rat liver has been shown to synthesize phosphatidylethanolamine from CDP-ethanolamine in vitro. The implications of the existence of such a pathway for the membrane flow hypothesis are discussed.Acknowledgments. This study was supported by the Medical Research Council of Canada. 相似文献
75.
Grützner F Rens W Tsend-Ayush E El-Mogharbel N O'Brien PC Jones RC Ferguson-Smith MA Marshall Graves JA 《Nature》2004,432(7019):913-917
Two centuries after the duck-billed platypus was discovered, monotreme chromosome systems remain deeply puzzling. Karyotypes of males, or of both sexes, were claimed to contain several unpaired chromosomes (including the X chromosome) that form a multi-chromosomal chain at meiosis. Such meiotic chains exist in plants and insects but are rare in vertebrates. How the platypus chromosome system works to determine sex and produce balanced gametes has been controversial for decades. Here we demonstrate that platypus have five male-specific chromosomes (Y chromosomes) and five chromosomes present in one copy in males and two copies in females (X chromosomes). These ten chromosomes form a multivalent chain at male meiosis, adopting an alternating pattern to segregate into XXXXX-bearing and YYYYY-bearing sperm. Which, if any, of these sex chromosomes bears one or more sex-determining genes remains unknown. The largest X chromosome, with homology to the human X chromosome, lies at one end of the chain, and a chromosome with homology to the bird Z chromosome lies near the other end. This suggests an evolutionary link between mammal and bird sex chromosome systems, which were previously thought to have evolved independently. 相似文献
76.
77.
Xironogiton, a genus of crayfish worm (order Branchiobdellida), is historically endemic to North America. To date, six species of Xironogiton have been described, including five and one from areas west and east of the Continental Divide, respectively. Recent collections of the crayfishes Pacifastacus connectens and Pacifastacus leniusculus from the endorheic Harney Basin in south-eastern Oregon, USA, revealed the presence of two previously unknown Xironogiton species, which we describe herein. Discovery and characterisation of Xironogiton bibendumi sp. nov. and Xironogiton malheurensis sp. nov. suggests that much work remains to understand branchiobdellidan diversity in western North America, and additional targeted sampling is needed to determine intra- and interspecific variation, and thus define species limits.http://www.zoobank.org/urn:lsid:zoobank.org:pub:B24AA844-4A73-48F2-B269-7CD08DC8389A http://www.zoobank.org/urn:lsid:zoobank.org:pub:F1787846-BF04-44A6-949B-551EE3453F26 相似文献
78.
Tarttelin EE Fransen MP Edwards PC Hankins MW Schertler GF Vogel R Lucas RJ Bellingham J 《Cellular and molecular life sciences : CMLS》2011,68(22):3713-3723
Photoreception by vertebrates enables both image-forming vision and non-image-forming responses such as circadian photoentrainment.
Over the recent years, distinct non-rod non-cone photopigments have been found to support circadian photoreception in diverse
species. By allowing specialization to this sensory task a selective advantage is implied, but the nature of that specialization
remains elusive. We have used the presence of distinct rod opsin genes specialized to either image-forming (retinal rod opsin)
or non-image-forming (pineal exo-rod opsin) photoreception in ray-finned fish (Actinopterygii) to gain a unique insight into this problem. A comparison of biochemical features for these paralogous opsins in two model
teleosts, Fugu pufferfish (Takifugu rubripes) and zebrafish (Danio rerio), reveals striking differences. While spectral sensitivity is largely unaltered by specialization to the pineal environment,
in other aspects exo-rod opsins exhibit a behavior that is quite distinct from the cardinal features of the rod opsin family.
While they display a similar thermal stability, they show a greater than tenfold reduction in the lifetime of the signaling
active Meta II photoproduct. We show that these features reflect structural changes in retinal association domains of helices
3 and 5 but, interestingly, not at either of the two residues known to define these characteristics in cone opsins. Our findings
suggest that the requirements of non-image-forming photoreception have lead exo-rod opsin to adopt a characteristic that seemingly
favors efficient bleach recovery but not at the expense of absolute sensitivity. 相似文献
79.
Bicknell LS Walker S Klingseisen A Stiff T Leitch A Kerzendorfer C Martin CA Yeyati P Al Sanna N Bober M Johnson D Wise C Jackson AP O'Driscoll M Jeggo PA 《Nature genetics》2011,43(4):350-355
Studies into disorders of extreme growth failure (for example, Seckel syndrome and Majewski osteodysplastic primordial dwarfism type II) have implicated fundamental cellular processes of DNA damage response signaling and centrosome function in the regulation of human growth. Here we report that mutations in ORC1, encoding a subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome. We establish that these mutations disrupt known ORC1 functions including pre-replicative complex formation and origin activation. ORC1 deficiency perturbs S-phase entry and S-phase progression. Additionally, we show that Orc1 depletion in zebrafish is sufficient to markedly reduce body size during rapid embryonic growth. Our data suggest a model in which ORC1 mutations impair replication licensing, slowing cell cycle progression and consequently impeding growth during development, particularly at times of rapid proliferation. These findings establish a novel mechanism for the pathogenesis of microcephalic dwarfism and show a surprising but important developmental impact of impaired origin licensing. 相似文献
80.
During the past two decades of research in T cell biology, an increasing number of distinct T cell subsets arising during the transition from naïve to antigen-experienced T cells have been identified. Recently, it has been appreciated that, in different experimental settings, distinct T cell subsets can be generated in parallel within the same immune response. While signals driving a single “lineage” path of T cell differentiation are becoming increasingly clear, it remains largely enigmatic how the phenotypic and functional diversification creating a multi-faceted T cell response is achieved. Here, we review current literature indicating that diversification is a stable trait of CD8+ T cell responses. We showcase novel technologies providing deeper insights into the process of diversification among the descendants of individual T cells, and introduce two models that emphasize either intrinsic noise or extrinsic signals as driving forces behind the diversification of single cell-derived T cell progeny populations in vivo. 相似文献