全文获取类型
收费全文 | 55601篇 |
免费 | 255篇 |
国内免费 | 544篇 |
专业分类
系统科学 | 1229篇 |
丛书文集 | 335篇 |
教育与普及 | 285篇 |
理论与方法论 | 536篇 |
现状及发展 | 32415篇 |
研究方法 | 695篇 |
综合类 | 18714篇 |
自然研究 | 2191篇 |
出版年
2013年 | 802篇 |
2012年 | 541篇 |
2011年 | 2579篇 |
2009年 | 611篇 |
2008年 | 756篇 |
2007年 | 822篇 |
2006年 | 967篇 |
2005年 | 1097篇 |
2004年 | 2345篇 |
2003年 | 1864篇 |
2002年 | 1536篇 |
2001年 | 1336篇 |
2000年 | 842篇 |
1999年 | 935篇 |
1998年 | 644篇 |
1997年 | 774篇 |
1996年 | 531篇 |
1994年 | 687篇 |
1993年 | 690篇 |
1992年 | 876篇 |
1991年 | 741篇 |
1990年 | 828篇 |
1989年 | 642篇 |
1988年 | 594篇 |
1987年 | 632篇 |
1986年 | 730篇 |
1985年 | 875篇 |
1984年 | 743篇 |
1983年 | 651篇 |
1982年 | 797篇 |
1981年 | 840篇 |
1980年 | 904篇 |
1979年 | 1411篇 |
1978年 | 1302篇 |
1977年 | 1264篇 |
1976年 | 1122篇 |
1975年 | 1109篇 |
1974年 | 1029篇 |
1973年 | 1228篇 |
1972年 | 1293篇 |
1971年 | 1334篇 |
1970年 | 1446篇 |
1969年 | 1300篇 |
1968年 | 1255篇 |
1967年 | 1127篇 |
1966年 | 929篇 |
1965年 | 779篇 |
1964年 | 499篇 |
1958年 | 605篇 |
1957年 | 516篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
921.
Saenz HL Engel P Stoeckli MC Lanz C Raddatz G Vayssier-Taussat M Birtles R Schuster SC Dehio C 《Nature genetics》2007,39(12):1469-1476
The bacterial genus Bartonella comprises 21 pathogens causing characteristic intraerythrocytic infections. Bartonella bacilliformis is a severe pathogen representing an ancestral lineage, whereas the other species are benign pathogens that evolved by radial speciation. Here, we have used comparative and functional genomics to infer pathogenicity genes specific to the radiating lineage, and we suggest that these genes may have facilitated adaptation to the host environment. We determined the complete genome sequence of Bartonella tribocorum by shotgun sequencing and functionally identified 97 pathogenicity genes by signature-tagged mutagenesis. Eighty-one pathogenicity genes belong to the core genome (1,097 genes) of the radiating lineage inferred from genome comparison of B. tribocorum, Bartonella henselae and Bartonella quintana. Sixty-six pathogenicity genes are present in B. bacilliformis, and one has been lost by deletion. The 14 pathogenicity genes specific for the radiating lineage encode two laterally acquired type IV secretion systems, suggesting that these systems have a role in host adaptability. 相似文献
922.
MacArthur DG Seto JT Raftery JM Quinlan KG Huttley GA Hook JW Lemckert FA Kee AJ Edwards MR Berman Y Hardeman EC Gunning PW Easteal S Yang N North KN 《Nature genetics》2007,39(10):1261-1265
More than a billion humans worldwide are predicted to be completely deficient in the fast skeletal muscle fiber protein alpha-actinin-3 owing to homozygosity for a premature stop codon polymorphism, R577X, in the ACTN3 gene. The R577X polymorphism is associated with elite athlete status and human muscle performance, suggesting that alpha-actinin-3 deficiency influences the function of fast muscle fibers. Here we show that loss of alpha-actinin-3 expression in a knockout mouse model results in a shift in muscle metabolism toward the more efficient aerobic pathway and an increase in intrinsic endurance performance. In addition, we demonstrate that the genomic region surrounding the 577X null allele shows low levels of genetic variation and recombination in individuals of European and East Asian descent, consistent with strong, recent positive selection. We propose that the 577X allele has been positively selected in some human populations owing to its effect on skeletal muscle metabolism. 相似文献
923.
Peutz-Jeghers syndrome (PJS, OMIM 175200) is an unusual inherited intestinal polyposis syndrome associated with distinct peri-oral
blue/black freckling [1–9]. Variable penetrance and clinical heterogeneity make it difficult to determine the exact frequency
of PJS [4]. PJS is a cancer predisposition syndrome. Affected individuals are at high risk for intestinal and extra-intestinal
cancers. In 1997, linkage studies mapped PJS to chromosome 19p [10, 11], and subsequently a serine/threonine kinase gene defect
(LKB1) was noted in a majority of PJS cases [12, 13]. A phenotypically similar syndrome has been produced in an LKB1 mouse
knockout model [14–18]. Several PJS kindred without LKB1 mutations have been described, suggesting other PJS loci [19–22].
The management of PJS is complex and evolving. New endoscopic technologies may improve management of intestinal polyposis.
Identification of specific genetic mutations and their targets will more accurately assess the clinical course, and help gage
the magnitude of cancer risk for affected individuals.
Received 20 February 2006; received after revision 5 May 2006; accepted 15 June 2006 相似文献
924.
Site- and state-specific lysine methylation of histones is catalyzed by a family of proteins that contain the evolutionarily
conserved SET domain and plays a fundamental role in epigenetic regulation of gene activation and silencing in all eukaryotes.
The recently determined three-dimensional structures of the SET domains from chromosomal proteins reveal that the core SET
domain structure contains a two-domain architecture, consisting of a conserved anti-parallel β-barrel and a structurally variable
insert that surround a unusual knot-like structure that comprises the enzyme active site. These structures of the SET domains,
either in the free state or when bound to cofactor S-adenosyl-L-homocysteine and/or histone peptide, mimicking an enzyme/cofactor/substrate complex, further yield the structural insights
into the molecular basis of the substrate specificity, methylation multiplicity and the catalytic mechanism of histone lysine
methylation.
Received 10 June 2006; accepted 22 August 2006 相似文献
925.
The macromolecular peptide-loading complex in MHC class I-dependent antigen presentation 总被引:5,自引:1,他引:4
A challenging task for the adaptive immune system of vertebrates is to identify and eliminate intracellular antigens. Therefore
a highly specialized antigen presentation machinery has evolved to display fragments of newly synthesized proteins to effector
cells of the immune system at the cell surface. After proteasomal degradation of unwanted proteins or defective ribosome products,
resulting peptides are translocated into the endoplasmic reticulum by the transporter associated with antigen processing and
loaded onto major histocompatibility complex (MHC) class I molecules. Peptide-MHC I complexes are transported via the secretory
pathway to the cell surface where they are then inspected by cytotoxic T lymphocytes, which can trigger an immune response.
This review summarizes the current view of the intracellular machinery of antigen processing and of viral immune escape mechanisms
to circumvent destruction by the host.
Received 4 October 2005; received after revision 19 November 2005; accepted 24 November 2005 相似文献
926.
The mammalian olfactory system is not uniformly organized but consists of several subsystems each of which probably serves
distinct functions. Not only are the two major nasal chemosensory systems, the vomeronasal organ and the main olfactory epithelium,
structurally and functionally separate entities, but the latter is further subcompartimentalized into overlapping expression
zones and projection-related subzones. Moreover, the populations of ‘OR37’ neurons not only express a unique type of olfactory
receptors but also are segregated in a cluster-like manner and generally project to only one receptor-specific glomerulus.
The septal organ is an island of sensory epithelium on the nasal septum positioned at the nasoplatine duct; it is considered
as a ‘mini-nose’ with dual function. A specific chemosensory function of the most recently discovered subsystem, the so-called
Grueneberg ganglion, is based on the expression of olfactory marker protein and the axonal projections to defined glomeruli
within the olfactory bulb. This complexity of distinct olfactory subsystems may be one of the features determining the enormous
chemosensory capacity of the sense of smell. 相似文献
927.
Blasig IE Winkler L Lassowski B Mueller SL Zuleger N Krause E Krause G Gast K Kolbe M Piontek J 《Cellular and molecular life sciences : CMLS》2006,63(4):505-514
Tight junctions seal intercellular clefts via membrane-related strands, hence, maintaining important organ functions. We investigated
the self-association of strand-forming transmembrane tight junction proteins. The regulatory tight junction protein occludin
was differently tagged and cotransfected in eucaryotic cells. These occludins colocalized within the plasma membrane of the
same cell, coprecipitated and exhibited fluorescence resonance energy transfer. Differently tagged strand-forming claudin-5
also colocalized in the plasma membrane of the same cell and showed fluorescence resonance energy transfer. This demonstrates
self-association in intact cells both of occludin and claudin-5 in one plasma membrane. In search of dimerizing regions of
occludin, dimerization of its cytosolic C-terminal coiledcoil domain was identified. In claudin-5, the second extracellular
loop was detected as a dimer. Since the transmembrane junctional adhesion molecule also is known to dimerize, the assumption
that homodimerization of transmembrane tight junction proteins may serve as a common structural feature in tight junction
assembly is supported.
Received 6 October 2005; received after revision 14 December 2005; accepted 27 December 2005
†These authors contributed equally to this work. 相似文献
928.
Huntington’s disease: from huntingtin function and dysfunction to therapeutic strategies 总被引:3,自引:0,他引:3
Borrell-Pagès M Zala D Humbert S Saudou F 《Cellular and molecular life sciences : CMLS》2006,63(22):2642-2660
Huntington’s disease (HD) is a neurodegenerative disorder that usually starts in middle age and is characterized by involuntary
movements (chorea), personality changes and dementia, leading to death within 10–20 years. The defective gene in HD contains
a trinucleotide CAG repeat expansion within its coding region that expresses a polyglutamine repeat in the protein huntingtin.
Together with the characteristic formation of aggregates in HD, aberrant protein interactions and several post-translational
modifications affect huntingtin during disease progression and lead to the dysfunction and death of selective neurons in the
brains of patients. The exact molecular mechanisms by which mutant huntingtin induces cell death are not completely understood
but may involve the gain of new toxic functions and the loss of the beneficial properties of huntingtin. This review focuses
on the cellular functions in which huntingtin is involved and how a better understanding of pathogenic pathways can lead to
new therapeutic approaches.
Received 24 May 2006; received after revision 5 July 2006; accepted 23 August 2006 相似文献
929.
The serine/threonine protein phosphatase 2A (PP2A) represents a large family of highly conserved heterotrimeric enzymes. Their
critical importance in cell homeostasis is underlined by the fact that they are targets of natural toxins like the tumor promoter
okadaic acid, and of simian virus 40 small tumor antigen (SV40 small t), a viral protein known to promote cell transformation.
Furthermore, mutated or lower expression levels of PP2A subunits have been found in certain cancers. One major known event
in PP2A-dependent cell transformation is the alteration of key signaling pathways that control cell growth and survival. In
this review, we focus on how PP2A enzymes also affect cell adhesion and cytoskeletal dynamics, the disruption of which is
linked to loss of cell polarity, increased cell motility and invasiveness. We also examine how those various pathways participate
in the transforming activity of SV40 small t.
Received 29 June 2006; received after revision 3 August 2006; accepted 20 September 2006 相似文献
930.
Human β-defensins 总被引:1,自引:0,他引:1
Pazgier M Hoover DM Yang D Lu W Lubkowski J 《Cellular and molecular life sciences : CMLS》2006,63(11):1294-1313