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61.
G. R. Newman N. Hoffner M. A. Di Berardino 《Cellular and molecular life sciences : CMLS》1977,33(4):430-432
Summary Karyotype analyses of prometaphases from medullary plate cells derived from mid-neurulae of Rana pipiens have led to the identification of the nucleolar chromosome and nucleolar organizing region, which is located on the longer arm of a small sub-metacentric chromosome (No. 10).Supported in part by research grant GB19631X from the Natioal Science Foundation. This study constituted a portion of a dissertation submitted by G. R. N. to the Medical College of Pennsylvania in partial fulfillment of requirements for a Ph. D. degree.Supported by NDEA and subsequently NSF predoctoral traineeships.To whom reprint requests should be sent. 相似文献
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64.
Maoz E Newman JA Ferrarese L Stetson PB Zepf SE Davis M Freedman WL Madore BF 《Nature》1999,401(6751):351-354
Cepheid variable stars pulsate in a way that is correlated with their intrinsic luminosity, making them useful as 'standard candles' for determining distances to galaxies; the potential systematic uncertainties in the resulting distances have been estimated to be only 8-10%. They have played a crucial role in establishing the extragalactic distance scale and hence the value of the Hubble constant. Here we report observations of Cepheids in the nearby galaxy NGC4258; the distance calculated from the Cepheids is 8.1 +/- 0.4 Mpc, where the uncertainty does not include possible systematic errors. There is an independently determined geometric distance to this galaxy of 7.2 +/- 0.5 Mpc, based on the observed proper motions of water masers orbiting the central black hole; the distances differ by 1.3sigma. If the maser-based distance is adopted and the Cepheid distance scale revised accordingly, the derived value of the Hubble constant would increase by 12 +/- 9%, while the expansion age of the Universe would decrease by the same amount. 相似文献
65.
Extracellular electron transfer 总被引:23,自引:0,他引:23
Results from several laboratories indicate that extracellular electron transfer may be a general mechanism whereby microoorganisms
generate energy for cell growth and/or maintenance. Specifically, bacteria can use redox-active organic small molecules, generated
outside or inside the cells, to shuttle electrons between reduced and oxidized compounds. Electron shuttling has now been
reported for several different bacterial species, and exchanges of shuttling compounds may even syntrophically link diverse
organisms in nature. Biofilm systems in both geological and clinical settings are likely to be important environments for
metabolisms that employ extracellular electron transfer. Both structural and functional analyses suggest that electron shuttles
and some virulence factors may be related to one another.
Received 21 March 2001; received after revision 10 May 2001; accepted 11 May 2001 相似文献
66.
Kidd JM Cooper GM Donahue WF Hayden HS Sampas N Graves T Hansen N Teague B Alkan C Antonacci F Haugen E Zerr T Yamada NA Tsang P Newman TL Tüzün E Cheng Z Ebling HM Tusneem N David R Gillett W Phelps KA Weaver M Saranga D Brand A Tao W Gustafson E McKernan K Chen L Malig M Smith JD Korn JM McCarroll SA Altshuler DA Peiffer DA Dorschner M Stamatoyannopoulos J Schwartz D Nickerson DA Mullikin JC Wilson RK Bruhn L Olson MV Kaul R Smith DR Eichler EE 《Nature》2008,453(7191):56-64
Genetic variation among individual humans occurs on many different scales, ranging from gross alterations in the human karyotype to single nucleotide changes. Here we explore variation on an intermediate scale--particularly insertions, deletions and inversions affecting from a few thousand to a few million base pairs. We employed a clone-based method to interrogate this intermediate structural variation in eight individuals of diverse geographic ancestry. Our analysis provides a comprehensive overview of the normal pattern of structural variation present in these genomes, refining the location of 1,695 structural variants. We find that 50% were seen in more than one individual and that nearly half lay outside regions of the genome previously described as structurally variant. We discover 525 new insertion sequences that are not present in the human reference genome and show that many of these are variable in copy number between individuals. Complete sequencing of 261 structural variants reveals considerable locus complexity and provides insights into the different mutational processes that have shaped the human genome. These data provide the first high-resolution sequence map of human structural variation--a standard for genotyping platforms and a prelude to future individual genome sequencing projects. 相似文献