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排序方式: 共有63条查询结果,搜索用时 15 毫秒
41.
Prüfer K Munch K Hellmann I Akagi K Miller JR Walenz B Koren S Sutton G Kodira C Winer R Knight JR Mullikin JC Meader SJ Ponting CP Lunter G Higashino S Hobolth A Dutheil J Karakoç E Alkan C Sajjadian S Catacchio CR Ventura M Marques-Bonet T Eichler EE André C Atencia R Mugisha L Junhold J Patterson N Siebauer M Good JM Fischer A Ptak SE Lachmann M Symer DE Mailund T Schierup MH Andrés AM Kelso J Pääbo S 《Nature》2012,486(7404):527-531
Two African apes are the closest living relatives of humans: the chimpanzee (Pan troglodytes) and the bonobo (Pan paniscus). Although they are similar in many respects, bonobos and chimpanzees differ strikingly in key social and sexual behaviours, and for some of these traits they show more similarity with humans than with each other. Here we report the sequencing and assembly of the bonobo genome to study its evolutionary relationship with the chimpanzee and human genomes. We find that more than three per cent of the human genome is more closely related to either the bonobo or the chimpanzee genome than these are to each other. These regions allow various aspects of the ancestry of the two ape species to be reconstructed. In addition, many of the regions that overlap genes may eventually help us understand the genetic basis of phenotypes that humans share with one of the two apes to the exclusion of the other. 相似文献
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It has been thought that the capture of irregular moons--with non-circular orbits--by giant planets occurs by a process in which they are first temporarily trapped by gravity inside the planet's Hill sphere (the region where planetary gravity dominates over solar tides). The capture of the moons is then made permanent by dissipative energy loss (for example, gas drag) or planetary growth. But the observed distributions of orbital inclinations, which now include numerous newly discovered moons, cannot be explained using current models. Here we show that irregular satellites are captured in a thin spatial region where orbits are chaotic, and that the resulting orbit is either prograde or retrograde depending on the initial energy. Dissipation then switches these long-lived chaotic orbits into nearby regular (non-chaotic) zones from which escape is impossible. The chaotic layer therefore dictates the final inclinations of the captured moons. We confirm this with three-dimensional Monte Carlo simulations that include nebular drag, and find good agreement with the observed inclination distributions of irregular moons at Jupiter and Saturn. In particular, Saturn has more prograde irregular moons than Jupiter, which we can explain as a result of the chaotic prograde progenitors being more efficiently swept away from Jupiter by its galilean moons. 相似文献
45.
Borisenko SV Kordyuk AA Koitzsch A Knupfer M Fink J Berger H Lin CT 《Nature》2004,431(7004):1 p following 39
One of the mysteries of modern condensed-matter physics is the nature of the pseudogap state of the superconducting cuprates. Kaminski et al. claim to have observed signatures of time-reversal symmetry breaking in the pseudogap regime in underdoped Bi2Sr2CaCu2O8+delta (Bi2212). Here we argue that the observed circular dichroism is due to the 51 superstructure replica of the electronic bands and therefore cannot be considered as evidence for spontaneous time-reversal symmetry breaking in cuprates. 相似文献
46.
陈明 娄厦 刘曙光 RADNAEVA Larisa Dorzhievn NIKITINA Elen CHALOV Sergey Romanovich 《同济大学学报(自然科学版)》2022,50(6):861-870
由于植物引起的紊动作用,含刚性植物床面中悬浮泥沙浓度与无植物裸床相比显著增加,而通过平均流速计算底床切应力的传统泥沙模型无法模拟出该现象。因此,在含植物水流水沙运动物理模型试验的基础上,构建了基于Flow–3D的含刚性沉水植物条件下波浪传播的三维数学模型,模拟了植物影响下波浪动力特征和泥沙悬浮过程,同时从紊动能角度修正希尔兹数,对泥沙模块进行了改进。与实测数据相比,该模型可较精确地模拟出植物引起的整体水流流速减小和局部冠层顶部处的流速增大、水体紊动增强以及紊动能在波周期内出现两个峰值的现象。与原始泥沙模块相比,改进的模型考虑了植物尾流紊动对泥沙运动的影响,可提高含植物床面泥沙悬浮模拟的精度。 相似文献
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Nejentsev S Thye T Szeszko JS Stevens H Balabanova Y Chinbuah AM Hibberd M van de Vosse E Alisjahbana B van Crevel R Ottenhoff TH Png E Drobniewski F Todd JA Seielstad M Horstmann RD 《Nature genetics》2008,40(3):261-2; author reply 262-3
48.
Sergey Kazantsev 《Journal of Natural History》2020,54(17-18):1073-1080
ABSTRACT A second Baltic amber taxon, Retromalisus damzeni, gen. et sp. nov., is discovered in the previously monotypic extinct family Berendtimiridae. The morphological portrait of Berendtimiridae is complemented with the data on the structure of prosternum and abdomen. 相似文献
49.
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma 总被引:2,自引:0,他引:2
Nikolaev SI Rimoldi D Iseli C Valsesia A Robyr D Gehrig C Harshman K Guipponi M Bukach O Zoete V Michielin O Muehlethaler K Speiser D Beckmann JS Xenarios I Halazonetis TD Jongeneel CV Stevenson BJ Antonarakis SE 《Nature genetics》2012,44(2):133-139
We performed exome sequencing to detect somatic mutations in protein-coding regions in seven melanoma cell lines and donor-matched germline cells. All melanoma samples had high numbers of somatic mutations, which showed the hallmark of UV-induced DNA repair. Such a hallmark was absent in tumor sample-specific mutations in two metastases derived from the same individual. Two melanomas with non-canonical BRAF mutations harbored gain-of-function MAP2K1 and MAP2K2 (MEK1 and MEK2, respectively) mutations, resulting in constitutive ERK phosphorylation and higher resistance to MEK inhibitors. Screening a larger cohort of individuals with melanoma revealed the presence of recurring somatic MAP2K1 and MAP2K2 mutations, which occurred at an overall frequency of 8%. Furthermore, missense and nonsense somatic mutations were frequently found in three candidate melanoma genes, FAT4, LRP1B and DSC1. 相似文献
50.
Scheper GC van der Klok T van Andel RJ van Berkel CG Sissler M Smet J Muravina TI Serkov SV Uziel G Bugiani M Schiffmann R Krägeloh-Mann I Smeitink JA Florentz C Van Coster R Pronk JC van der Knaap MS 《Nature genetics》2007,39(4):534-539
Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation (LBSL) has recently been defined based on a highly characteristic constellation of abnormalities observed by magnetic resonance imaging and spectroscopy. LBSL is an autosomal recessive disease, most often manifesting in early childhood. Affected individuals develop slowly progressive cerebellar ataxia, spasticity and dorsal column dysfunction, sometimes with a mild cognitive deficit or decline. We performed linkage mapping with microsatellite markers in LBSL families and found a candidate region on chromosome 1, which we narrowed by means of shared haplotypes. Sequencing of genes in this candidate region uncovered mutations in DARS2, which encodes mitochondrial aspartyl-tRNA synthetase, in affected individuals from all 30 families. Enzyme activities of mutant proteins were decreased. We were surprised to find that activities of mitochondrial complexes from fibroblasts and lymphoblasts derived from affected individuals were normal, as determined by different assays. 相似文献