全文获取类型
收费全文 | 858篇 |
免费 | 184篇 |
专业分类
1042篇 |
出版年
2021年 | 9篇 |
2019年 | 5篇 |
2018年 | 7篇 |
2017年 | 5篇 |
2016年 | 10篇 |
2015年 | 12篇 |
2014年 | 21篇 |
2013年 | 32篇 |
2012年 | 41篇 |
2011年 | 44篇 |
2010年 | 62篇 |
2009年 | 54篇 |
2008年 | 20篇 |
2007年 | 21篇 |
2006年 | 21篇 |
2005年 | 28篇 |
2004年 | 26篇 |
2003年 | 19篇 |
2002年 | 25篇 |
2001年 | 43篇 |
2000年 | 50篇 |
1999年 | 51篇 |
1998年 | 20篇 |
1997年 | 22篇 |
1996年 | 30篇 |
1995年 | 20篇 |
1994年 | 24篇 |
1993年 | 11篇 |
1992年 | 42篇 |
1991年 | 30篇 |
1990年 | 27篇 |
1989年 | 26篇 |
1988年 | 19篇 |
1987年 | 9篇 |
1986年 | 17篇 |
1985年 | 13篇 |
1984年 | 10篇 |
1983年 | 8篇 |
1982年 | 7篇 |
1981年 | 7篇 |
1980年 | 8篇 |
1979年 | 6篇 |
1977年 | 4篇 |
1976年 | 4篇 |
1975年 | 6篇 |
1974年 | 5篇 |
1973年 | 4篇 |
1972年 | 5篇 |
1971年 | 10篇 |
1969年 | 5篇 |
排序方式: 共有1042条查询结果,搜索用时 15 毫秒
31.
Sap1, a protein that binds to sequences required for mating-type switching, is essential for viability in Schizosaccharomyces pombe. 总被引:2,自引:1,他引:1 下载免费PDF全文
The pattern of mating-type switching in cell pedigrees of the fission yeast Schizosaccharomyces pombe is dictated by the inheritance of specific DNA chains at the mating-type locus (mat1). The recombination event essential for switching is initiated by a site-specific double-strand break at mat1. The switch-activating protein, Sap1, binds in vitro to a mat1 cis-acting site that was shown earlier to be essential for efficient mating-type switching. We isolated the sap1 gene by using oligonucleotides corresponding to the amino acid sequence of purified Sap1 protein. The sequence of that gene predicted a 30-kDa protein with no significant homology to other canonical DNA-binding protein motifs. To facilitate its biochemical characterization, Sap1 was expressed in Escherichia coli. The protein expressed in bacteria displayed the same DNA-binding specificities as the protein purified from S. pombe. Interestingly, analysis of a sap1 null mutation showed that the gene is essential for growth even in a strain in which mating-type switching is prohibited because of a defect in generation of the double-strand break. Thus, the sap1 gene product implicated in mating-type switching is shown to be essential for cell viability. 相似文献
32.
Mapping of Murine Fibroblast Growth Factor Receptors Refines Regions of Homology between Mouse and Human Chromosomes 总被引:1,自引:0,他引:1
Karen B. Avraham David Givol Aaron Avivi Avner Yayon Neal G. Copeland Nancy A. Jenkins 《Genomics》1994,21(3)
The genes for the fibroblast growth factor receptors Fgfr2, Fgfr3, and Fgfr4 have been mapped in the mouse using an interspecific backcross mapping panel. The Fgfr loci map to previously defined regions of homology between human and mouse chromosomes and provide additional information regarding human/mouse comparative mapping. 相似文献
33.
Leslie F. Lock Debra J. Gilbert Valerie A. Street Mary B. Migeon Nancy A. Jenkins Neal G. Copeland Bruce L Tempel 《Genomics》1994,20(3)
Cloning of the Drosophila Shaker gene established that a neurological phenotype including locomotor dysfunction can be caused by a mutation in a voltage-gated potassium (K) channel gene. Shaker sequences have been used to isolate a large family of related K channel genes from both flies and mammals. Toward elucidating the evolutionary relationship between loci and the potential causal connection that K channels may have to mammalian genetic disorders, we report here the genetic mapping of 12-16 different murine, voltage-gated K channel genes. We find that multiple genes, in some cases from distantly related K channel subfamilies, occur in clusters in the mouse genome. These mapping results suggest that the K channel gene subfamilies arose through ancient localized gene duplication events, followed by chromosomal duplications and rearrangements as well as further gene duplication. We also note that several neurologic disorders of both mouse and human are associated with the chromosomal regions containing K channel genes. 相似文献
34.
Robert A. Copeland 《Journal of bioenergetics and biomembranes》1993,25(2):93-102
The electronic transitions of the two heme groups of cytochromec oxidase have been resolved by application of second-derivative and cryogenic absorption spectroscopy. Both methods reveal a splitting of the ferrocytochromea Soret transition into two features at 443 and 450 nm. The relative intensity of the 450 nm feature appears to depend on the ligation state of cytochromea
3, the solution pH, and complex formation with cytochromec. The structural origin and mechanistic significance of this second Soret transition of cytochromea are discussed in terms of the electron transfer and proton translocation activities of the enzyme.Dedicated to the memory of James Carl Copeland. 相似文献
35.
Kim IK Copeland RL Lee JH Kim HS Asafo-Adjei E Brown ND Estrada JS Gordon RK Garcia GE Chiang PK 《Journal of biomedical science》1994,1(3):154-157
High concentrations of adenosine (Ado), when added to L1210 lymphocytic leukemia cells, resulted in apoptosis or programmed cell death. The apoptotic process was accompanied by distinct morphological changes including chromatin condensation and blebbing of plasma membranes. Extensive DNA fragmentation was correlated with Ado concentrations. Furthermore, apoptosis in these cells was preceded by an early but transient expression of c-myc proto-oncogene, and was not influenced by homocysteine thiolactone added to the cells. Since severe combined immunodeficiency (SCID) is associated with a deficiency of adenosine deaminase, leading to defects in both cellular and humoral immunity, Ado-induced apoptosis may thus be a contributing factor in the pathology of SCID. 相似文献
36.
37.
38.
Stefania Francesconi William C. Copeland Teresa S.-F. Wang 《Molecular genetics and genomics : MGG》1993,241(3-4):457-466
The DNA polymerase a enzymes from human, and budding (Saccharomyces cerevisiae) and fission yeast (Schizosaccharomyces pombe) are homologous proteins involved in initiation and replication of chromosomal DNA. Sequence comparision of human DNA polymerase α with that of S. cerevisiae and S. pombe shows overall levels of amino acid sequence identity of 32% and 34%, respectively. We report here that, despite the sequence conservation among these three enzymes, functionally active human DNA polymerase a fails to rescue several different conditional lethal alleles of the budding yeast POL1 gene at nonpermissive temperature. Furthermore, human DNA polymerase α cannot complement a null allele of budding yeast POL1 either in germinating spores or in vegetatively growing cells. In fission yeast, functionally active human DNA polymerase α is also unable to complement the disrupted polα::ura4 + allele in germinating spores. Thus, in vivo, DNA polymerase α has stringent species specificity for initiation and replication of chromosomal DNA. 相似文献
39.
Florence W. L. Tsui Hing-Wo Tsui Samuel Mok Irena Mlinaric Neal G. Copeland Debra J. Gilbert Nancy A. Jenkins Katherine A. Siminovitch 《Genomics》1993,15(3)
Stefins or Type 1 cystatins belong to a large, evolutionarily conserved protein superfamily, the members of which inhibit the papain-like cysteine proteinases. We report here on the molecular cloning and chromosomal localization of three newly identified members of the murine stefin gene family. These genes, designated herein as mouse stefins 1, 2, and 3, were isolated on the basis of their relatively increased expression in moth-eaten viable compared to normal congenic mouse bone marrow cells. The open reading frames of the stefin cDNAs encode proteins of approximately 11.5 kDa that show between 50 and 92% identity to sequences of stefins isolated from various other species. Data from Southern analysis suggest that the murine stefin gene family encompasses at least 6 and possibly 10-20 members, all of which appear to be clustered in the genome. Analysis of interspecific backcross mice indicates that the genes encoding the three mouse stefins all map to mouse chromosome 16, a localization that is consistent with the recent assignment of the human stefin A gene to a region of conserved homology between human chromosome 3q and the proximal region of mouse chromosome 16. 相似文献
40.
P J Hurlin C Quéva P J Koskinen E Steingrímsson D E Ayer N G Copeland N A Jenkins R N Eisenman 《The EMBO journal》1995,14(22):5646-5659