全文获取类型
收费全文 | 502篇 |
免费 | 53篇 |
专业分类
555篇 |
出版年
2024年 | 3篇 |
2023年 | 4篇 |
2021年 | 11篇 |
2020年 | 3篇 |
2019年 | 7篇 |
2018年 | 11篇 |
2017年 | 6篇 |
2016年 | 14篇 |
2015年 | 17篇 |
2014年 | 23篇 |
2013年 | 27篇 |
2012年 | 27篇 |
2011年 | 30篇 |
2010年 | 25篇 |
2009年 | 27篇 |
2008年 | 32篇 |
2007年 | 30篇 |
2006年 | 36篇 |
2005年 | 19篇 |
2004年 | 24篇 |
2003年 | 9篇 |
2002年 | 17篇 |
2001年 | 10篇 |
2000年 | 9篇 |
1999年 | 11篇 |
1998年 | 5篇 |
1997年 | 8篇 |
1996年 | 9篇 |
1995年 | 6篇 |
1994年 | 4篇 |
1993年 | 8篇 |
1992年 | 8篇 |
1991年 | 7篇 |
1990年 | 3篇 |
1989年 | 7篇 |
1988年 | 5篇 |
1987年 | 2篇 |
1986年 | 5篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 4篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1980年 | 5篇 |
1977年 | 4篇 |
1975年 | 3篇 |
1974年 | 3篇 |
1972年 | 3篇 |
1966年 | 2篇 |
1953年 | 1篇 |
排序方式: 共有555条查询结果,搜索用时 0 毫秒
1.
The measurement of the ATP content of fresh semen is as accurate as the estimation of sperm motility by conventional methods in discriminating between semen of fertile versus subfertile men. The ATP content of frozen thawed donor semen is correlated with the probability of conception per cycle of insemination. Exact quantification of cytotoxic sperm antibodies in serum is possible with the adenosine-triphosphate-release-cytotoxicity test, since measurement is free of the bias of microscopic examination. The procedure has been simplified by testing only one serum dilution and calculating the ‘sperm toxicity index’. 相似文献
2.
3.
Crude extracts from human cells were microinjected into the cytoplasm of cultured fibroblasts from 9 excision-deficient xeroderma pigmentosum (XP) complementation groups. The level of UV-induced unscheduled DNA synthesis (UDS) was measured to determine the effect of the extract on the repair capacity of the injected cells. With a sensitive UDS assay procedure a (transient) increase in UV-induced UDS level was found in fibroblasts from all complementation groups after injection of extracts from repair-proficient (HeLa) or complementing XP cells (except in the case of XP-G), but not after introduction of extracts from cells belonging to the same complementation group. This indicates that the phenotypic correction is exerted by complementation-group-specific factors in the extract, a conclusion that is in agreement with the observation that different levels of correction are found for different complementation groups. The XP-G-correcting factor was shown to be sensitive to proteolytic degradation, suggesting that it is a protein like the XP-A factor. 相似文献
4.
Microinjection of human cell extracts corrects xeroderma pigmentosum defect 总被引:8,自引:0,他引:8 下载免费PDF全文
Cultured fibroblasts of patients with the DNA repair syndrome xeroderma pigmentosum (XP) were injected with crude cell extracts from various human cells. Injected fibroblasts were then assayed for unscheduled DNA synthesis (UDS) to see whether the injected extract could complement their deficiency in the removal of u.v.-induced thymidine dimers from their DNA. Microinjection of extracts from repair-proficient cells (such as HeLa, placenta) and from cells belonging to XP complementation group C resulted in a temporary correction of the DNA repair defect in XP-A cells but not in cells from complementation groups C, D or F. Extracts prepared from XP-A cells were unable to correct the XP-A repair defect. The UDS of phenotypically corrected XP-A cells is u.v.-specific and can reach the level of normal cells. The XP-A correcting factor was found to be sensitive to the action of proteinase K, suggesting that it is a protein. It is present in normal cells in high amounts, it is stable on storage and can still be detected in the injected cells 8 h after injection. The microinjection assay described in this paper provides a useful tool for the purification of the XP-A (and possibly other) factor(s) involved in DNA repair. 相似文献
5.
6.
Rospars Jean-Pierre Lánský Petr Tuckwell Henry C. Vermeulen Arthur 《Journal of computational neuroscience》1996,3(1):51-72
The coding of odor intensity by an olfactory receptor neuron model was studied under steady-state stimulation. Our model neuron is an elongated cylinder consisting of the following three components: a sensory dendritic region bearing odorant receptors, a passive region consisting of proximal dendrite and cell body, and an axon. First, analytical solutions are given for the three main physiological responses: (1) odorant-dependent conductance change at the sensory dendrite based on the Michaelis-Menten model, (2) generation and spreading of the receptor potential based on a new solution of the cable equation, and (3) firing frequency based on a Lapicque model. Second, the magnitudes of these responses are analyzed as a function of odorant concentration. Their dependence on chemical, electrical, and geometrical parameters is examined. The only evident gain in magnitude results from the activation-to-conductance conversion. An optimal encoder neuron is presented that suggests that increasing the length of the sensory dendrite beyond about 0.3 space constant does not increase the magnitude of the receptor potential. Third, the sensivities of the responses are examined as functions of (1) the concentration at half-maximum response, (2) the lower and upper concentrations actually discriminated, and (3) the width of the dynamic range. The overall gain in sensitivity results entirely from the conductance-to-voltage conversion. The maximum conductance at the sensory dendrite appears to be the main tuning constant of the neuron because it determines the shift toward low concentrations and the increase in dynamic range. The dynamic range of the model cannot exceed 5.7 log units, for a sensitivity increase at low odor concentration is compensated by a sensitivity decrease at high odor concentration. 相似文献
7.
B. C. Broughton A. F. Thompson S. A. Harcourt W. Vermeulen J. H. J. Hoeijmakers E. Botta M. Stefanini M. D. King C. A. Weber J. Cole C. F. Arlett A. R. Lehmann 《American journal of human genetics》1995,56(1):167-174
Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are quite distinct genetic disorders that are associated with defects in excision repair of UV-induced DNA damage. A few patients have been described previously with the clinical features of both disorders. In this paper we describe an individual in this category who has unusual cellular responses to UV light. We show that his cultured fibroblasts and lymphocytes are extremely sensitive to irradiation with UV-C, despite a level of nucleotide excision repair that is 30%–40% that of normal cells. The deficiency is assigned to the XP-D complementation group, and we have identified two causative mutations in the XPD gene: a gly→arg change at amino acid 675 in the allele inherited from the patient's mother and a −1 frameshift at amino acid 669 in the allele inherited from his father. These mutations are in the C-terminal 20% of the 760-amino-acid XPD protein, in a region where we have recently identified several mutations in patients with trichothiodystrophy. 相似文献
8.
9.
Evidence for a lipid dependence of membrane-associated chitin synthase inSchizophyllum commune is based on the following observations: Arrhenius plots of the temperature dependence of this enzyme showed deflections from linearity that are characteristic for lipid-affected membrane-bound enzymes. The activity of chitin synthase dissociated by digitonin decreased at increasing digitonin/protein ratios and could be restored by addition of egg lecithin. After further delipification by sucrose gradient centrifugation, enzyme activity progressively decreased, banded at higher densities, and was less effectively restored by lecithin. The activity of dissociated chitin synthase was also restored by soybean phosphatidylcholine and low concentrations of phosphatidylinositol and phosphatidylserine. At higher concentrations, phosphatidylinositol and phosphatidylserine were inhibitory. Lysophosphatidylcholine and phosphatidylethanolamine were slightly stimulatory, whereas no effect resulting from ergosterol was observed. 相似文献
10.