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111.
cDNA芯片技术和病毒感染的基因表达 总被引:9,自引:0,他引:9
论述了最近发展的cDNA芯片技术及其在基因的发现和表达以及在疾病诊断上的应用。该技术是把cDNA的阵列由高速自动控制仪器置于玻璃片上,用标记的探针测定互补结合的情况,可同时进行大量基因的表达和基因的发现研究。这是一个高效率和大规模的基因组分析和表达的研究技术。使用这一新技术,发现了HIV感染期间hsp70基因表达发生的变化,传统的Northern分析证实了芯片的测定结果。综述中还包括了作者未作发表 相似文献
112.
p53 and Pten control neural and glioma stem/progenitor cell renewal and differentiation 总被引:1,自引:0,他引:1
113.
The genome of the model beetle and pest Tribolium castaneum 总被引:6,自引:0,他引:6
Tribolium Genome Sequencing Consortium Richards S Gibbs RA Weinstock GM Brown SJ Denell R Beeman RW Gibbs R Beeman RW Brown SJ Bucher G Friedrich M Grimmelikhuijzen CJ Klingler M Lorenzen M Richards S Roth S Schröder R Tautz D Zdobnov EM Muzny D Gibbs RA Weinstock GM Attaway T Bell S Buhay CJ Chandrabose MN Chavez D Clerk-Blankenburg KP Cree A Dao M Davis C Chacko J Dinh H Dugan-Rocha S Fowler G Garner TT Garnes J Gnirke A Hawes A Hernandez J Hines S Holder M Hume J Jhangiani SN Joshi V Khan ZM 《Nature》2008,452(7190):949-955
Tribolium castaneum is a member of the most species-rich eukaryotic order, a powerful model organism for the study of generalized insect development, and an important pest of stored agricultural products. We describe its genome sequence here. This omnivorous beetle has evolved the ability to interact with a diverse chemical environment, as shown by large expansions in odorant and gustatory receptors, as well as P450 and other detoxification enzymes. Development in Tribolium is more representative of other insects than is Drosophila, a fact reflected in gene content and function. For example, Tribolium has retained more ancestral genes involved in cell-cell communication than Drosophila, some being expressed in the growth zone crucial for axial elongation in short-germ development. Systemic RNA interference in T. castaneum functions differently from that in Caenorhabditis elegans, but nevertheless offers similar power for the elucidation of gene function and identification of targets for selective insect control. 相似文献
114.
115.
Gerald Midgley 《Systemic Practice and Action Research》1992,5(2):147-172
The central message of this paper is that methodological pluralism is essential for the continued legitimation of systems science. This statement is supported by a critique of our notion of complexity. Our traditional view of complexity focuses upon the natural world of object relations and thereby excludes complexities of moral decision making and subjectivity. However, we are now beginning to realize that these realms of complexity are not independent of one another. Indeed, our ability to cope adequately with many of the problems we are currently facing, especially global problems, depends on being able to understand the systemic relationships between all three. Interestingly, we find that different methods have evolved to handle the different forms of complexity. Therefore, if our inquiries are going to have any legitimacy in tackling some of the major issues of today, we must indeed embrace methodological pluralism. 相似文献
116.
H A Lubs W J Kinberling F Hecht S R Patil J Brown P Gerald R L Summitt 《Nature》1977,268(5621):631-633
117.
M Krauthammer Y Kong BH Ha P Evans A Bacchiocchi JP McCusker E Cheng MJ Davis G Goh M Choi S Ariyan D Narayan K Dutton-Regester A Capatana EC Holman M Bosenberg M Sznol HM Kluger DE Brash DF Stern MA Materin RS Lo S Mane S Ma KK Kidd NK Hayward RP Lifton J Schlessinger TJ Boggon R Halaban 《Nature genetics》2012,44(9):1006-1014
We characterized the mutational landscape of melanoma, the form of skin cancer with the highest mortality rate, by sequencing the exomes of 147 melanomas. Sun-exposed melanomas had markedly more ultraviolet (UV)-like C>T somatic mutations compared to sun-shielded acral, mucosal and uveal melanomas. Among the newly identified cancer genes was PPP6C, encoding a serine/threonine phosphatase, which harbored mutations that clustered in the active site in 12% of sun-exposed melanomas, exclusively in tumors with mutations in BRAF or NRAS. Notably, we identified a recurrent UV-signature, an activating mutation in RAC1 in 9.2% of sun-exposed melanomas. This activating mutation, the third most frequent in our cohort of sun-exposed melanoma after those of BRAF and NRAS, changes Pro29 to serine (RAC1(P29S)) in the highly conserved switch I domain. Crystal structures, and biochemical and functional studies of RAC1(P29S) showed that the alteration releases the conformational restraint conferred by the conserved proline, causes an increased binding of the protein to downstream effectors, and promotes melanocyte proliferation and migration. These findings raise the possibility that pharmacological inhibition of downstream effectors of RAC1 signaling could be of therapeutic benefit. 相似文献
118.
Kote-Jarai Z Olama AA Giles GG Severi G Schleutker J Weischer M Campa D Riboli E Key T Gronberg H Hunter DJ Kraft P Thun MJ Ingles S Chanock S Albanes D Hayes RB Neal DE Hamdy FC Donovan JL Pharoah P Schumacher F Henderson BE Stanford JL Ostrander EA Sorensen KD Dörk T Andriole G Dickinson JL Cybulski C Lubinski J Spurdle A Clements JA Chambers S Aitken J Gardiner RA Thibodeau SN Schaid D John EM Maier C Vogel W Cooney KA Park JY Cannon-Albright L Brenner H Habuchi T Zhang HW Lu YJ Kaneva R 《Nature genetics》2011,43(8):785-791
Prostate cancer (PrCa) is the most frequently diagnosed male cancer in developed countries. We conducted a multi-stage genome-wide association study for PrCa and previously reported the results of the first two stages, which identified 16 PrCa susceptibility loci. We report here the results of stage 3, in which we evaluated 1,536 SNPs in 4,574 individuals with prostate cancer (cases) and 4,164 controls. We followed up ten new association signals through genotyping in 51,311 samples in 30 studies from the Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) consortium. In addition to replicating previously reported loci, we identified seven new prostate cancer susceptibility loci on chromosomes 2p11, 3q23, 3q26, 5p12, 6p21, 12q13 and Xq12 (P = 4.0 × 10(-8) to P = 2.7 × 10(-24)). We also identified a SNP in TERT more strongly associated with PrCa than that previously reported. More than 40 PrCa susceptibility loci, explaining ~25% of the familial risk in this disease, have now been identified. 相似文献
119.
Yeager M Orr N Hayes RB Jacobs KB Kraft P Wacholder S Minichiello MJ Fearnhead P Yu K Chatterjee N Wang Z Welch R Staats BJ Calle EE Feigelson HS Thun MJ Rodriguez C Albanes D Virtamo J Weinstein S Schumacher FR Giovannucci E Willett WC Cancel-Tassin G Cussenot O Valeri A Andriole GL Gelmann EP Tucker M Gerhard DS Fraumeni JF Hoover R Hunter DJ Chanock SJ Thomas G 《Nature genetics》2007,39(5):645-649
Recently, common variants on human chromosome 8q24 were found to be associated with prostate cancer risk. While conducting a genome-wide association study in the Cancer Genetic Markers of Susceptibility project with 550,000 SNPs in a nested case-control study (1,172 cases and 1,157 controls of European origin), we identified a new association at 8q24 with an independent effect on prostate cancer susceptibility. The most significant signal is 70 kb centromeric to the previously reported SNP, rs1447295, but shows little evidence of linkage disequilibrium with it. A combined analysis with four additional studies (total: 4,296 cases and 4,299 controls) confirms association with prostate cancer for rs6983267 in the centromeric locus (P = 9.42 x 10(-13); heterozygote odds ratio (OR): 1.26, 95% confidence interval (c.i.): 1.13-1.41; homozygote OR: 1.58, 95% c.i.: 1.40-1.78). Each SNP remained significant in a joint analysis after adjusting for the other (rs1447295 P = 1.41 x 10(-11); rs6983267 P = 6.62 x 10(-10)). These observations, combined with compelling evidence for a recombination hotspot between the two markers, indicate the presence of at least two independent loci within 8q24 that contribute to prostate cancer in men of European ancestry. We estimate that the population attributable risk of the new locus, marked by rs6983267, is higher than the locus marked by rs1447295 (21% versus 9%). 相似文献
120.
This paper compares some key concepts from Buddhism with ideas from different traditions of systems thinking. There appear
to be many similarities, suggesting that there is significant potential for dialogue and mutual learning. The similarities
also indicate that it may be possible to develop a Buddhist systems methodology to help guide exploration and change within
Buddhist organisations.
相似文献
Chao Ying ShenEmail: |