全文获取类型
收费全文 | 49812篇 |
免费 | 116篇 |
国内免费 | 206篇 |
专业分类
系统科学 | 269篇 |
丛书文集 | 1078篇 |
教育与普及 | 107篇 |
理论与方法论 | 281篇 |
现状及发展 | 22770篇 |
研究方法 | 1897篇 |
综合类 | 23039篇 |
自然研究 | 693篇 |
出版年
2013年 | 387篇 |
2012年 | 654篇 |
2011年 | 1382篇 |
2010年 | 286篇 |
2008年 | 861篇 |
2007年 | 915篇 |
2006年 | 942篇 |
2005年 | 919篇 |
2004年 | 873篇 |
2003年 | 861篇 |
2002年 | 882篇 |
2001年 | 1447篇 |
2000年 | 1336篇 |
1999年 | 915篇 |
1992年 | 884篇 |
1991年 | 704篇 |
1990年 | 760篇 |
1989年 | 780篇 |
1988年 | 751篇 |
1987年 | 806篇 |
1986年 | 776篇 |
1985年 | 944篇 |
1984年 | 744篇 |
1983年 | 637篇 |
1982年 | 568篇 |
1981年 | 580篇 |
1980年 | 744篇 |
1979年 | 1537篇 |
1978年 | 1331篇 |
1977年 | 1313篇 |
1976年 | 997篇 |
1975年 | 1065篇 |
1974年 | 1483篇 |
1973年 | 1293篇 |
1972年 | 1342篇 |
1971年 | 1576篇 |
1970年 | 2049篇 |
1969年 | 1546篇 |
1968年 | 1514篇 |
1967年 | 1540篇 |
1966年 | 1304篇 |
1965年 | 940篇 |
1964年 | 275篇 |
1959年 | 535篇 |
1958年 | 870篇 |
1957年 | 656篇 |
1956年 | 561篇 |
1955年 | 488篇 |
1954年 | 545篇 |
1948年 | 326篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
981.
Protease inhibitor domain encoded by an amyloid protein precursor mRNA associated with Alzheimer's disease 总被引:104,自引:0,他引:104
R E Tanzi A I McClatchey E D Lamperti L Villa-Komaroff J F Gusella R L Neve 《Nature》1988,331(6156):528-530
Amyloid B-protein/amyloid A4 is a peptide present in the neuritic plaques, neurofibrillary tangles and cerebrovascular deposits in patients with Alzheimer's disease and Down's syndrome (trisomy 21) and may be involved in the pathogenesis of Alzheimer's disease. Recent molecular genetic studies have indicated that amyloid protein is encoded as part of a larger protein by a gene on human chromosome 21 (refs 6-9). The amyloid protein precursor (APP) gene is expressed in brain and in several peripheral tissues, but the specific biochemical events leading to deposition of amyloid are not known. We have now screened complementary DNA libraries constructed from peripheral tissues to determine whether the messenger RNA encoding APP in these tissues is identical to that expressed in brain, and we identify a second APP mRNA that encodes an additional internal domain with a sequence characteristic of a Kunitz-type serine protease inhibitor. The alternative APP mRNA is present in both brain and peripheral tissues of normal individuals and those with Alzheimer's disease, but its pattern of expression differs from that of the previously reported APP mRNA. 相似文献
982.
983.
984.
Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphisms 总被引:85,自引:0,他引:85
A H Paterson E S Lander J D Hewitt S Peterson S E Lincoln S D Tanksley 《Nature》1988,335(6192):721-726
The conflict between the Mendelian theory of particulate inheritance and the observation of continuous variation for most traits in nature was resolved in the early 1900s by the concept that quantitative traits can result from segregation of multiple genes, modified by environmental effects. Although pioneering experiments showed that linkage could occasionally be detected to such quantitative trait loci (QTLs), accurate and systematic mapping of QTLs has not been possible because the inheritance of an entire genome could not be studied with genetic markers. The use of restriction fragment length polymorphisms (RFLPs) has made such investigations possible, at least in principle. Here, we report the first use of a complete RFLP linkage map to resolve quantitative traits into discrete Mendelian factors, in an interspecific back-cross of tomato. Applying new analytical methods, we mapped at least six QTLs controlling fruit mass, four QTLs for the concentration of soluble solids and five QTLs for fruit pH. This approach is broadly applicable to the genetic dissection of quantitative inheritance of physiological, morphological and behavioural traits in any higher plant or animal. 相似文献
985.
Type I phosphatidylinositol kinase makes a novel inositol phospholipid, phosphatidylinositol-3-phosphate 总被引:87,自引:0,他引:87
The generation of second messengers from the hydrolysis of phosphatidylinositol-4,5-bisphosphate (PtdInsP2) by phosphoinositidase C has been implicated in the mediation of cellular responses to a variety of growth factors and oncogene products. The first step in the production of PtdInsP2 from phosphatidylinositol (PtdIns) is catalysed by PtdIns kinase. A PtdIns kinase activity has been found to associate specifically with several oncogene products, as well as with the platelet-derived growth factor (PDGF) receptor. We have previously identified two biochemically distinct PtdIns kinases in fibroblasts, and have found that only one of these, designated type I, specifically associates with activated tyrosine kinases. We have now characterized the site on the inositol ring phosphorylated by type I PtdIns kinase, and find that this kinase specifically phosphorylates the D-3 ring position to generate a novel phospholipid, phosphatidylinositol-3-phosphate (PtdIns(3)P). In contrast, the main PtdIns kinase in fibroblasts, designated type II, specifically phosphorylates the D-4 position to produce phosphatidylinositol-4-phosphate (PtdIns(4)P), previously considered to be the only form of PtdInsP. We have also tentatively identified PtdIns(3)P as a minor component of total PtdInsP in intact fibroblasts. We propose that type I PtdIns kinase is responsible for the generation of PtdIns(3)P in intact cells, and that this novel phosphoinositide could be important in the transduction of mitogenic and oncogenic signals. 相似文献
986.
Myeloid leukaemia inhibitory factor maintains the developmental potential of embryonic stem cells 总被引:102,自引:0,他引:102
R L Williams D J Hilton S Pease T A Willson C L Stewart D P Gearing E F Wagner D Metcalf N A Nicola N M Gough 《Nature》1988,336(6200):684-687
Embryonic stem (ES) cells, the totipotent outgrowths of blastocysts, can be cultured and manipulated in vitro and then returned to the embryonic environment where they develop normally and can contribute to all cell lineages. Maintenance of the stem-cell phenotype in vitro requires the presence of a feeder layer of fibroblasts or of a soluble factor, differentiation inhibitory activity (DIA) produced by a number of sources; in the absence of DIA the ES cells differentiate into a wide variety of cell types. We recently noted several similarities between partially purified DIA and a haemopoietic regulator, myeloid leukaemia inhibitory factor (LIF), a molecule which induces differentiation in M1 myeloid leukaemic cells and which we have recently purified, cloned and characterized. We demonstrate here that purified, recombinant LIF can substitute for DIA in the maintenance of totipotent ES cell lines that retain the potential to form chimaeric mice. 相似文献
987.
Inositol 1,4,5-trisphosphate activates a channel from smooth muscle sarcoplasmic reticulum 总被引:35,自引:0,他引:35
Inositol 1,4,5-trisphosphate (InsP3) can initiate calcium release into the cytoplasm in a variety of cells. From experiments using permeabilized cells, membrane vesicles, and patch-clamp techniques, it has been suggested that InsP3 acts by directly opening calcium channels. Here, we show that InsP3 induced openings of channels in planar lipid bilayers into which vesicles made from aortic muscle sarcoplasmic reticulum (SR) were incorporated. Activation of channels by InsP3 was not observed when vesicles made from SR of cardiac or skeletal muscle were incorporated into planar lipid bilayers. The present study demonstrates for the first time unique properties of an InsP3-gated calcium channel in sarcoplasmic reticulum vesicles from vascular smooth muscle. This InsP3-activated channel from aortic SR differs strikingly from the calcium-gated calcium channel of striated muscle SR in single-channel conductance and pharmacology. 相似文献
988.
Multiple liquid crystal phases of DNA at high concentrations 总被引:3,自引:0,他引:3
DNA packaging in vivo is very tight, with volume concentrations approaching 70% w/v in sperm heads, virus capsids and bacterial nucleoids. The packaging mechanisms adopted may be related to the natural tendency of semi-rigid polymers to form liquid crystalline phases in concentrated solutions. We find that DNA forms at least three distinct liquid crystalline phases at concentrations comparable to those in vivo, with phase transitions occurring over relatively narrow ranges of DNA concentration. A weakly birefringent, dynamic, 'precholesteric' mesophase with microscopic textures intermediate between those of a nematic and a true cholesteric phase forms at the lowest concentrations required for phase separation. At slightly higher DNA concentrations, a second mesophase forms which is a strongly birefringent, well-ordered cholesteric phase with a concentration-dependent pitch varying from 2 to 10 micron. At the highest DNA concentrations, a phase forms which is two-dimensionally ordered and resembles smectic phases of thermotropic liquid crystals observed with small molecules. 相似文献
989.
Self-tolerance eliminates T cells specific for Mls-modified products of the major histocompatibility complex 总被引:83,自引:0,他引:83
In mice the product of the Mlsa locus is an unusual antigen capable of interaction with certain products of the major histocompatibility locus (MHC) to form a ligand for a large portion of the T-cell alpha/beta receptor repertoire, including nearly all receptors that use V beta 8.1. The presence of Mlsa/MHC during T-cell development results in the deletion of T cells that express V beta 8.1, documenting the importance of clonal deletion in establishing tolerance to self antigens. 相似文献
990.
Brain-derived neurotrophic factor prevents neuronal death in vivo 总被引:32,自引:0,他引:32
Developing vertebrate neurons are thought to depend for their survival on specific neurotrophic proteins present in their target fields. The limited availability of these proteins does not allow the survival of all neurons initially innervating a target, resulting in the widely observed phenomenon of naturally occurring neuronal death. Although a variety of proteins have been reported to promote the survival of neurons in tissue culture, the demonstration that these proteins increase neuronal numbers and/or decrease neuronal death in vivo has only been possible with nerve growth factor (NGF). The generalization of the concept that neurotrophic proteins regulate neuronal survival during normal development critically depends on the demonstration that the survival of neurons in vivo can be increased by the administration of a neurotrophic protein different from NGF. We report here that this is the case with brain-derived neurotrophic factor, a protein of extremely low abundance purified from the central nervous system. 相似文献