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101.
Momozawa Y Mni M Nakamura K Coppieters W Almer S Amininejad L Cleynen I Colombel JF de Rijk P Dewit O Finkel Y Gassull MA Goossens D Laukens D Lémann M Libioulle C O'Morain C Reenaers C Rutgeerts P Tysk C Zelenika D Lathrop M Del-Favero J Hugot JP de Vos M Franchimont D Vermeire S Louis E Georges M 《Nature genetics》2011,43(1):43-47
Genome-wide association studies (GWAS) have identified dozens of risk loci for many complex disorders, including Crohn's disease. However, common disease-associated SNPs explain at most ~20% of the genetic variance for Crohn's disease. Several factors may account for this unexplained heritability, including rare risk variants not adequately tagged thus far in GWAS. That rare susceptibility variants indeed contribute to variation in multifactorial phenotypes has been demonstrated for colorectal cancer, plasma high-density lipoprotein cholesterol levels, blood pressure, type 1 diabetes, hypertriglyceridemia and, in the case of Crohn's disease, for NOD2 (refs. 14,15). Here we describe the use of high-throughput resequencing of DNA pools to search for rare coding variants influencing susceptibility to Crohn's disease in 63 GWAS-identified positional candidate genes. We identify low frequency coding variants conferring protection against inflammatory bowel disease in IL23R, but we conclude that rare coding variants in positional candidates do not make a large contribution to inherited predisposition to Crohn's disease. 相似文献
102.
Ford CB Lin PL Chase MR Shah RR Iartchouk O Galagan J Mohaideen N Ioerger TR Sacchettini JC Lipsitch M Flynn JL Fortune SM 《Nature genetics》2011,43(5):482-486
Tuberculosis poses a global health emergency, which has been compounded by the emergence of drug-resistant Mycobacterium tuberculosis (Mtb) strains. We used whole-genome sequencing to compare the accumulation of mutations in Mtb isolated from cynomolgus macaques with active, latent or reactivated disease. We sequenced 33 Mtb isolates from nine macaques with an average genome coverage of 93% and an average read depth of 117×. Based on the distribution of SNPs observed, we calculated the mutation rates for these disease states. We found a similar mutation rate during latency as during active disease or in a logarithmically growing culture over the same period of time. The pattern of polymorphisms suggests that the mutational burden in vivo is because of oxidative DNA damage. We show that Mtb continues to acquire mutations during disease latency, which may explain why isoniazid monotherapy for latent tuberculosis is a risk factor for the emergence of isoniazid resistance. 相似文献
103.
Initial sequencing and comparative analysis of the mouse genome 总被引:2,自引:0,他引:2
Mouse Genome Sequencing Consortium Waterston RH Lindblad-Toh K Birney E Rogers J Abril JF Agarwal P Agarwala R Ainscough R Alexandersson M An P Antonarakis SE Attwood J Baertsch R Bailey J Barlow K Beck S Berry E Birren B Bloom T Bork P Botcherby M Bray N Brent MR Brown DG Brown SD Bult C Burton J Butler J Campbell RD Carninci P Cawley S Chiaromonte F Chinwalla AT Church DM Clamp M Clee C Collins FS Cook LL Copley RR Coulson A Couronne O Cuff J Curwen V Cutts T Daly M David R Davies J 《Nature》2002,420(6915):520-562
The sequence of the mouse genome is a key informational tool for understanding the contents of the human genome and a key experimental tool for biomedical research. Here, we report the results of an international collaboration to produce a high-quality draft sequence of the mouse genome. We also present an initial comparative analysis of the mouse and human genomes, describing some of the insights that can be gleaned from the two sequences. We discuss topics including the analysis of the evolutionary forces shaping the size, structure and sequence of the genomes; the conservation of large-scale synteny across most of the genomes; the much lower extent of sequence orthology covering less than half of the genomes; the proportions of the genomes under selection; the number of protein-coding genes; the expansion of gene families related to reproduction and immunity; the evolution of proteins; and the identification of intraspecies polymorphism. 相似文献
104.
Rentel MC Lecourieux D Ouaked F Usher SL Petersen L Okamoto H Knight H Peck SC Grierson CS Hirt H Knight MR 《Nature》2004,427(6977):858-861
Active oxygen species (AOS) generated in response to stimuli and during development can function as signalling molecules in eukaryotes, leading to specific downstream responses. In plants these include such diverse processes as coping with stress (for example pathogen attack, wounding and oxygen deprivation), abscisic-acid-induced guard-cell closure, and cellular development (for example root hair growth). Despite the importance of signalling via AOS in eukaryotes, little is known about the protein components operating downstream of AOS that mediate any of these processes. Here we show that expression of an Arabidopsis thaliana gene (OXI1) encoding a serine/threonine kinase is induced in response to a wide range of H2O2-generating stimuli. OXI1 kinase activity is itself also induced by H2O2 in vivo. OXI1 is required for full activation of the mitogen-activated protein kinases (MAPKs) MPK3 and MPK6 after treatment with AOS or elicitor and is necessary for at least two very different AOS-mediated processes: basal resistance to Peronospora parasitica infection, and root hair growth. Thus, OXI1 is an essential part of the signal transduction pathway linking oxidative burst signals to diverse downstream responses. 相似文献
105.
阳生红 《中山大学学报(自然科学版)》2007,46(6):30-33
利用可旋转四极质谱仪对氢原子束与氢化Si(100)表面作用中氢提取反应产生的氢分子角分布进行了系统的分析。发现氢原子束与氢化Si(100)表面作用中,从氢化Si(100)表面脱附的氢分子具有较宽的角分布,并可以用函数cosnθf(其中n<1)拟合氢分子角分布。脱附的氢分子角分布与Si(100)表面温度和表面重构模型无关。根据硅表面重构机制,用非活性脱氢模型对实验结果进行了合理的解释。 相似文献
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Emilsson V Thorleifsson G Zhang B Leonardson AS Zink F Zhu J Carlson S Helgason A Walters GB Gunnarsdottir S Mouy M Steinthorsdottir V Eiriksdottir GH Bjornsdottir G Reynisdottir I Gudbjartsson D Helgadottir A Jonasdottir A Jonasdottir A Styrkarsdottir U Gretarsdottir S Magnusson KP Stefansson H Fossdal R Kristjansson K Gislason HG Stefansson T Leifsson BG Thorsteinsdottir U Lamb JR Gulcher JR Reitman ML Kong A Schadt EE Stefansson K 《Nature》2008,452(7186):423-428
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