全文获取类型
收费全文 | 28727篇 |
免费 | 99篇 |
国内免费 | 119篇 |
专业分类
系统科学 | 195篇 |
丛书文集 | 454篇 |
教育与普及 | 43篇 |
理论与方法论 | 114篇 |
现状及发展 | 12270篇 |
研究方法 | 1387篇 |
综合类 | 13920篇 |
自然研究 | 562篇 |
出版年
2013年 | 247篇 |
2012年 | 490篇 |
2011年 | 1062篇 |
2010年 | 200篇 |
2008年 | 561篇 |
2007年 | 698篇 |
2006年 | 623篇 |
2005年 | 647篇 |
2004年 | 700篇 |
2003年 | 594篇 |
2002年 | 640篇 |
2001年 | 869篇 |
2000年 | 836篇 |
1999年 | 592篇 |
1992年 | 565篇 |
1991年 | 392篇 |
1990年 | 431篇 |
1989年 | 412篇 |
1988年 | 406篇 |
1987年 | 414篇 |
1986年 | 455篇 |
1985年 | 583篇 |
1984年 | 406篇 |
1983年 | 338篇 |
1982年 | 298篇 |
1981年 | 319篇 |
1980年 | 371篇 |
1979年 | 872篇 |
1978年 | 681篇 |
1977年 | 654篇 |
1976年 | 522篇 |
1975年 | 516篇 |
1974年 | 773篇 |
1973年 | 643篇 |
1972年 | 705篇 |
1971年 | 767篇 |
1970年 | 1073篇 |
1969年 | 840篇 |
1968年 | 724篇 |
1967年 | 748篇 |
1966年 | 710篇 |
1965年 | 530篇 |
1964年 | 180篇 |
1959年 | 267篇 |
1958年 | 526篇 |
1957年 | 361篇 |
1956年 | 280篇 |
1955年 | 255篇 |
1954年 | 297篇 |
1948年 | 186篇 |
排序方式: 共有10000条查询结果,搜索用时 78 毫秒
861.
Mutations of the BRAF gene in human cancer 总被引:2,自引:0,他引:2
Davies H Bignell GR Cox C Stephens P Edkins S Clegg S Teague J Woffendin H Garnett MJ Bottomley W Davis N Dicks E Ewing R Floyd Y Gray K Hall S Hawes R Hughes J Kosmidou V Menzies A Mould C Parker A Stevens C Watt S Hooper S Wilson R Jayatilake H Gusterson BA Cooper C Shipley J Hargrave D Pritchard-Jones K Maitland N Chenevix-Trench G Riggins GJ Bigner DD Palmieri G Cossu A Flanagan A Nicholson A Ho JW Leung SY Yuen ST Weber BL Seigler HF Darrow TL Paterson H Marais R Marshall CJ Wooster R 《Nature》2002,417(6892):949-954
Cancers arise owing to the accumulation of mutations in critical genes that alter normal programmes of cell proliferation, differentiation and death. As the first stage of a systematic genome-wide screen for these genes, we have prioritized for analysis signalling pathways in which at least one gene is mutated in human cancer. The RAS RAF MEK ERK MAP kinase pathway mediates cellular responses to growth signals. RAS is mutated to an oncogenic form in about 15% of human cancer. The three RAF genes code for cytoplasmic serine/threonine kinases that are regulated by binding RAS. Here we report BRAF somatic missense mutations in 66% of malignant melanomas and at lower frequency in a wide range of human cancers. All mutations are within the kinase domain, with a single substitution (V599E) accounting for 80%. Mutated BRAF proteins have elevated kinase activity and are transforming in NIH3T3 cells. Furthermore, RAS function is not required for the growth of cancer cell lines with the V599E mutation. As BRAF is a serine/threonine kinase that is commonly activated by somatic point mutation in human cancer, it may provide new therapeutic opportunities in malignant melanoma. 相似文献
862.
863.
864.
865.
866.
867.
A. Iserles 《国外科技新书评介》2005,12(6):4-5
本书是由英国剑桥大学出版、发行的不定期专题论文集,每年出版一卷,登载数值分析、计算方法及其应用等方面的高水平创造性研究论文或综述报告,论文作者多为当代相关领域的国际性学术带头人。 相似文献
868.
本文根据衡量非物质文化遗产的四条标准:具有突出的历史、文化和科学价值;具有展现中华民族文化创造力的典型性和代表性;具有在一定群体中世代传承、活态存在的特点;具有鲜明特色,在当地有较大影响。结合南涧彝族“跳菜”的实际情况进行比照分析,得出了南涧彝族“跳菜”是一种非物质文化遗产的结论。 相似文献
869.
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice. 总被引:11,自引:0,他引:11
Michael G Anderson Richard S Smith Norman L Hawes Adriana Zabaleta Bo Chang Janey L Wiggs Simon W M John 《Nature genetics》2002,30(1):81-85
Pigmentary glaucoma is a significant cause of human blindness. Abnormally liberated iris pigment and cell debris enter the ocular drainage structures, leading to increased intraocular pressure (IOP) and glaucoma. DBA/2J (D2) mice develop a form of pigmentary glaucoma involving iris pigment dispersion (IPD) and iris stromal atrophy (ISA). Using high-resolution mapping techniques, sequencing and functional genetic tests, we show that IPD and ISA result from mutations in related genes encoding melanosomal proteins. IPD is caused by a premature stop codon mutation in the Gpnmb (GpnmbR150X) gene, as proved by the occurrence of IPD only in D2 mice that are homozygous with respect to GpnmbR150X; otherwise, similar D2 mice that are not homozygous for GpnmbR150X do not develop IPD. ISA is caused by the recessive Tyrp1b mutant allele and rescued by the transgenic introduction of wildtype Tyrp1. We hypothesize that IPD and ISA alter melanosomes, allowing toxic intermediates of pigment production to leak from melanosomes, causing iris disease and subsequent pigmentary glaucoma. This is supported by the rescue of IPD and ISA in D2 eyes with substantially decreased pigment production. These data indicate that pigment production and mutant melanosomal protein genes may contribute to human pigmentary glaucoma. The fact that hypopigmentation profoundly alleviates the D2 disease indicates that therapeutic strategies designed to decrease pigment production may be beneficial in human pigmentary glaucoma. 相似文献
870.
The extent of linkage disequilibrium in Arabidopsis thaliana. 总被引:20,自引:0,他引:20
Magnus Nordborg Justin O Borevitz Joy Bergelson Charles C Berry Joanne Chory Jenny Hagenblad Martin Kreitman Julin N Maloof Tina Noyes Peter J Oefner Eli A Stahl Detlef Weigel 《Nature genetics》2002,30(2):190-193
Linkage disequilibrium (LD), the nonrandom occurrence of alleles in haplotypes, has long been of interest to population geneticists. Recently, the rapidly increasing availability of genomic polymorphism data has fueled interest in LD as a tool for fine-scale mapping, in particular for human disease loci. The chromosomal extent of LD is crucial in this context, because it determines how dense a map must be for associations to be detected and, conversely, limits how finely loci may be mapped. Arabidopsis thaliana is expected to harbor unusually extensive LD because of its high degree of selfing. Several polymorphism studies have found very strong LD within individual loci, but also evidence of some recombination. Here we investigate the pattern of LD on a genomic scale and show that in global samples, LD decays within approximately 1 cM, or 250 kb. We also show that LD in local populations may be much stronger than that of global populations, presumably as a result of founder events. The combination of a relatively high level of polymorphism and extensive haplotype structure bodes well for developing a genome-wide LD map in A. thaliana. 相似文献