全文获取类型
收费全文 | 318篇 |
免费 | 1篇 |
国内免费 | 4篇 |
专业分类
系统科学 | 6篇 |
教育与普及 | 3篇 |
理论与方法论 | 1篇 |
现状及发展 | 30篇 |
研究方法 | 47篇 |
综合类 | 234篇 |
自然研究 | 2篇 |
出版年
2022年 | 1篇 |
2021年 | 1篇 |
2018年 | 1篇 |
2017年 | 3篇 |
2016年 | 1篇 |
2014年 | 1篇 |
2013年 | 2篇 |
2012年 | 24篇 |
2011年 | 23篇 |
2010年 | 8篇 |
2009年 | 5篇 |
2008年 | 31篇 |
2007年 | 23篇 |
2006年 | 44篇 |
2005年 | 24篇 |
2004年 | 43篇 |
2003年 | 30篇 |
2002年 | 13篇 |
2001年 | 6篇 |
2000年 | 1篇 |
1999年 | 2篇 |
1997年 | 1篇 |
1993年 | 1篇 |
1990年 | 2篇 |
1986年 | 3篇 |
1984年 | 1篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1979年 | 2篇 |
1974年 | 1篇 |
1973年 | 2篇 |
1972年 | 4篇 |
1971年 | 3篇 |
1970年 | 5篇 |
1969年 | 2篇 |
1968年 | 2篇 |
1967年 | 1篇 |
1966年 | 2篇 |
1948年 | 1篇 |
1945年 | 1篇 |
排序方式: 共有323条查询结果,搜索用时 31 毫秒
1.
滨南油田低渗欠注井酸化增注技术研究与应用 总被引:1,自引:0,他引:1
提出了一种针对滨南低渗油田欠注井酸化增注的系统实验研究方法。根据储层特征分析了注污水和重复酸化对地层的损害及对酸化液的选取原则。根据长岩心酸化流动模拟实验进行了酸化工艺参数优选及其评估分析。现场施工证明该酸化液体系适应性较好 ,工艺参数合理 ,能够较好地解除地层中有机物和无机物堵塞 ,提高注水量 ,降低泵注压力 ,在低渗油田注水井中具有推广价值。 相似文献
2.
3.
4.
It is important that migration is measured accurately, for example to inform population estimates and projections. However, current sources of information present challenges in producing robust estimates of emigration from Great Britain. This article reports on work carried out by the Office for National Statistics to investigate the potential for using administrative data sources to contribute to the measurement of emigration. 相似文献
5.
Romeo S Pennacchio LA Fu Y Boerwinkle E Tybjaerg-Hansen A Hobbs HH Cohen JC 《Nature genetics》2007,39(4):513-516
Resequencing genes provides the opportunity to assess the full spectrum of variants that influence complex traits. Here we report the first application of resequencing to a large population (n = 3,551) to examine the role of the adipokine ANGPTL4 in lipid metabolism. Nonsynonymous variants in ANGPTL4 were more prevalent in individuals with triglyceride levels in the lowest quartile than in individuals with levels in the highest quartile (P = 0.016). One variant (E40K), present in approximately 3% of European Americans, was associated with significantly lower plasma levels of triglyceride and higher levels of high-density lipoprotein cholesterol in European Americans from the Atherosclerosis Risk in Communities Study and in Danes from the Copenhagen City Heart Study. The ratio of nonsynonymous to synonymous variants was higher in European Americans than in African Americans (4:1 versus 1.3:1), suggesting population-specific relaxation of purifying selection. Thus, resequencing of ANGPTL4 in a multiethnic population allowed analysis of the phenotypic effects of both rare and common variants while taking advantage of genetic variation arising from ethnic differences in population history. 相似文献
6.
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy 总被引:4,自引:0,他引:4
Nicot AS Toussaint A Tosch V Kretz C Wallgren-Pettersson C Iwarsson E Kingston H Garnier JM Biancalana V Oldfors A Mandel JL Laporte J 《Nature genetics》2007,39(9):1134-1139
Centronuclear myopathies are characterized by muscle weakness and abnormal centralization of nuclei in muscle fibers not secondary to regeneration. The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases. By direct sequencing of functional candidate genes, we identified homozygous mutations in amphiphysin 2 (BIN1) in three families with autosomal recessive inheritance. Two missense mutations affecting the BAR (Bin1/amphiphysin/RVS167) domain disrupt its membrane tubulation properties in transfected cells, and a partial truncation of the C-terminal SH3 domain abrogates the interaction with DNM2 and its recruitment to the membrane tubules. Our results suggest that mutations in BIN1 cause centronuclear myopathy by interfering with remodeling of T tubules and/or endocytic membranes, and that the functional interaction between BIN1 and DNM2 is necessary for normal muscle function and positioning of nuclei. 相似文献
7.
8.
Oleksiewicz U Liloglou T Field JK Xinarianos G 《Cellular and molecular life sciences : CMLS》2011,68(23):3869-3883
Since the discovery of cytoglobin (Cygb) a decade ago, growing amounts of data have been gathered to characterise Cygb biochemistry,
functioning and implication in human pathologies. Its molecular roles remain under investigation, but nitric oxide dioxygenase
and lipid peroxidase activities have been demonstrated. Cygb expression increases in response to various stress conditions
including hypoxia, oxidative stress and fibrotic stimulation. When exogenously overexpressed, Cygb revealed cytoprotection
against these factors. Cygb was shown to be upregulated in fibrosis and neurodegenerative disorders and downregulated in multiple
cancer types. CYGB was also found within the minimal region of a hereditary tylosis with oesophageal cancer syndrome, and its expression was
reduced in tylotic samples. Recently, Cygb has been shown to inhibit cancer cell growth in vitro, thus confirming its suggested
tumour suppressor role. This article aims to review the biochemical and functional aspects of Cygb, its involvement in various
pathological conditions and potential clinical utility. 相似文献
9.
Macgregor S Montgomery GW Liu JZ Zhao ZZ Henders AK Stark M Schmid H Holland EA Duffy DL Zhang M Painter JN Nyholt DR Maskiell JA Jetann J Ferguson M Cust AE Jenkins MA Whiteman DC Olsson H Puig S Bianchi-Scarrà G Hansson J Demenais F Landi MT Dębniak T Mackie R Azizi E Bressac-de Paillerets B Goldstein AM Kanetsky PA Gruis NA Elder DE Newton-Bishop JA Bishop DT Iles MM Helsing P Amos CI Wei Q Wang LE Lee JE Qureshi AA Kefford RF Giles GG Armstrong BK Aitken JF Han J Hopper JL Trent JM Brown KM 《Nature genetics》2011,43(11):1114-1118
We performed a genome-wide association study of melanoma in a discovery cohort of 2,168 Australian individuals with melanoma and 4,387 control individuals. In this discovery phase, we confirm several previously characterized melanoma-associated loci at MC1R, ASIP and MTAP-CDKN2A. We selected variants at nine loci for replication in three independent case-control studies (Europe: 2,804 subjects with melanoma, 7,618 control subjects; United States 1: 1,804 subjects with melanoma, 1,026 control subjects; United States 2: 585 subjects with melanoma, 6,500 control subjects). The combined meta-analysis of all case-control studies identified a new susceptibility locus at 1q21.3 (rs7412746, P = 9.0 × 10(-11), OR in combined replication cohorts of 0.89 (95% CI 0.85-0.95)). We also show evidence suggesting that melanoma associates with 1q42.12 (rs3219090, P = 9.3 × 10(-8)). The associated variants at the 1q21.3 locus span a region with ten genes, and plausible candidate genes for melanoma susceptibility include ARNT and SETDB1. Variants at the 1q21.3 locus do not seem to be associated with human pigmentation or measures of nevus density. 相似文献
10.
This paper describes the design of a unified framework for a multilingual text-to-speech (TTS) synthesis engine – Crystal. The unified framework defines the common TTS modules for different languages and/or dialects. The interfaces between consecutive modules conform to the speech synthesis markup language (SSML) specification for standardization, interoperability, multilinguality, and extensibility. Detailed module divisions and implementation technologies for the unified framework are introduced, together with possible extensions for the algorithm research and evaluation of the TTS synthesis. Implementation of a mixed-language TTS system for Chinese Putonghua, Chinese Cantonese, and English demonstrates the feasibility of the proposed unified framework. 相似文献