全文获取类型
收费全文 | 2761篇 |
免费 | 252篇 |
国内免费 | 1篇 |
出版年
2023年 | 19篇 |
2022年 | 12篇 |
2021年 | 85篇 |
2020年 | 61篇 |
2019年 | 51篇 |
2018年 | 87篇 |
2017年 | 64篇 |
2016年 | 139篇 |
2015年 | 161篇 |
2014年 | 172篇 |
2013年 | 225篇 |
2012年 | 250篇 |
2011年 | 229篇 |
2010年 | 143篇 |
2009年 | 111篇 |
2008年 | 174篇 |
2007年 | 172篇 |
2006年 | 129篇 |
2005年 | 131篇 |
2004年 | 112篇 |
2003年 | 106篇 |
2002年 | 79篇 |
2001年 | 22篇 |
2000年 | 13篇 |
1999年 | 21篇 |
1998年 | 20篇 |
1997年 | 16篇 |
1996年 | 12篇 |
1995年 | 17篇 |
1994年 | 10篇 |
1993年 | 12篇 |
1992年 | 14篇 |
1991年 | 7篇 |
1990年 | 15篇 |
1989年 | 10篇 |
1988年 | 7篇 |
1987年 | 6篇 |
1986年 | 14篇 |
1985年 | 7篇 |
1984年 | 5篇 |
1983年 | 4篇 |
1982年 | 7篇 |
1977年 | 4篇 |
1974年 | 3篇 |
1973年 | 6篇 |
1971年 | 4篇 |
1970年 | 6篇 |
1969年 | 3篇 |
1958年 | 3篇 |
1944年 | 3篇 |
排序方式: 共有3014条查询结果,搜索用时 375 毫秒
21.
Jonathan D. G. Jones David A. Jones Gerard J. Bishop Kate Harrison Bernard J. Carroll Steven R. Scofield 《Transgenic research》1993,2(2):63-78
Cell-autonomous genes have been used to monitor the excision of both endogenous transposons in maize andAntirrhinum, and transposons introduced into transgenic plants. In tobacco andArabidopsis, the streptomycin phosphotransferase (SPT) gene reveals somatic excision of the maize transposonActivator (Ac) as green sectors on a white background in cotyledons of seedlings germinated in the presence of streptomycin. Cotyledons of tomato seedlings germinated on streptomycin-containing medium do not bleach, suggesting that a different assay for transposon excision in tomato is desirable. We have tested the use of the spectinomycin resistance (SPEC) gene (aadA) and a Basta resistance (BAR) gene (phosphinothricin acetyltransferase, or PAT) for monitoring somatic excision ofAc in tobacco and tomato. Both genetic and molecular studies demonstrate that genotypically variegated individuals that carry clones of cells from whichAc orDs have excised from either SPEC or BAR genes, can be phenotypically completely resistant to the corresponding antibiotic. This demonstrates that these genes act non-cell-autonomously, in contrast to the SPT gene in tobacco. Possible reasons for this difference are discussed. 相似文献
22.
Anthony G. Lee Kate A. Dalton Richard C. Duggleby J. Malcolm East Anthony P. Starling 《Bioscience reports》1995,15(5):289-298
Effects of lipid structure on the function of the Ca2+-ATPase of skeletal muscle of sarcoplasmic reticulum are reviewed. Binding of phospholipids to the ATPase shows little specificity. Phosphatidylcholines with short (C14) or long (C24) fatty acyl chains have marked effects on the activity of the ATPase, including a change in the stoichiometry of Ca binding. Low ATPase activity in gel phase lipid follows from low rate of phosphorylation. Phosphatidylinositol 4-phosphate increases ATPase activity by increasing the rate of dephosphorylation of the phosphorylated ATPase. Stimulation is not seen with other anionic phospholipids; phosphatidic acid decreases ATPase activity in a Mg2+-dependent manner.Abbreviations di(C141)PC
dimyristoleoylphosphatidycholine
- di(C160)PC
dipalmitoylphosphatidylcholine
- di(C181)PC
dioleoylphosphatidylcholine
- di(Br2C180)PC
dibromostearoylphosphatidylcholine
- di(C241)PC
dinervonylphosphatidylcholine
- di(C181)PA
dioleoylphosphatidic acid
- di(C181)PE
dioleoylphosphatidylethanolamine
- Ptdlns
phosphatidylinositol
- PtdIns-4P
phos-phatidylinositol 4-phosphate 相似文献
23.
Human medulloblastoma gangliosides 总被引:2,自引:0,他引:2
To establish a model system for the study of ganglioside metabolismof the human brain tumor, medulloblastoma, we have chemicallycharacterized the gangliosides of the Daoy cell line. Thesecells contain a high concentration of gangliosides (143 ±13 nmol LBSA/108 cells). The major species have been structurallyconfirmed to be GM2 (65.9%), GM3 (13.0%), and GDla (10.3%).Isolation of individual gangliosides homogeneous in both carbohydrateand ceramide moieties by reversed-phase HPLC and analysis bynegative-ion fast atom bombardment collisionally activated dissociationtandem mass spectrometry have allowed us to unequivocally characterizeceramide structures. In the case of GM2, 10 major ceramide subspecieswere identified: d18:1-hC16:0, d18:1-C16:0, d18:0-C16:0, d18:1-C18:0,d18:1-C20:0, d18:1-C22:0, d18:2-C24:1, d18: 1-C23:1, d18:1-C24:1,and d18:1-C24:0. Taken together with previous studies, thesefindings in human medullo-blastoma cells support the view thathigh expression and marked heterogeneity of ceramide structureare general characteristics of tumor gangliosides, moleculeswhich are shed by the tumor cells and which are biologicallyactive in vivo. medulloblastoma gangliosides ceramide structure HPLC mass spectrometry 相似文献
24.
25.
Corien C. Verschuuren-Bemelmans Ewout R. P. Brunt Margaret Burton Rob G. J. Mensink Martin A. van der Meulen Nico H. Smit Irene Stolte-Dijkstra Charles H. C. M. Buys Hans Scheffer 《Human genetics》1995,96(6):691-694
The autosomal dominant cerebellar ataxias (ADCA) are clinically and genetically heterogeneous. To date, several loci (SCAI-V) have been identified for ADCA type I. We have studied two large families from the northern part of The Netherlands with ADCA type I with a broad intra-familial variation of symptoms. In both families significant linkage is shown of the disease to the markers of the SCA3 locus on chromosome 14. Through recombinations, the candidate region for SCA3 could be refined to a 13-cM range between D14S256 and D14S81. No recombinations were detected with the markers D14S291 and D14S280, which suggests that the SCA3 gene lies close to these loci. This finding will benefit the individuals at risk in these two families who are seeking predictive testing or prenatal diagnosis. 相似文献
26.
H. G. de Vries J. M. Collée W. P. Meeuwsen H. Scheffer L. P. Ten Kate 《Human genetics》1995,95(5):575-576
Number and sex of offspring were determined in a group of 7,841 randomly selected blood donors who were screened for the F508 mutation. We did not find any evidence for differences in number or sex ratio of offspring between F508 carriers and non-carriers. 相似文献
27.
28.
29.
J E De Vries F H Kornips J Wiegant P M Moerkerk N Senden B Schutte J P Geraedts F T Bosman J Ten Kate 《The journal of histochemistry and cytochemistry》1992,40(7):1053-1058
We describe the combination of hot banding with fluorescence in situ hybridization as a rapid and efficient method to identify integration sites of transfected DNA sequences in chromosomes. As a test system we used SW480 EJ2, a clonal cell line obtained after transfection of SW480 with pSV2neoEJ, a plasmid containing a point-mutated, c-Ha-RAS oncogene. Nick-translated probes were compared with random primed-labeled probes to evaluate their relative efficiency in fluorescence in situ hybridization. The fluorescence signals were quantified in interphase nuclei by confocal scanning laser microscopy. Nick-translated probes were found to yield better results. Hot banding followed by fluorescence in situ hybridization localized the integration site of pSV2neoEJ in SW480 EJ2 at the site of a translocation on a marker chromosome Xp+. The combination of fluorescence in situ hybridization and hot banding can be used to (a) rapidly and efficiently analyze integration sites in large numbers of transfectants, (b) assess the clonality of transfected cell lines, and (c) localize the site of integration of transfected genes in the recipient genome. 相似文献
30.