全文获取类型
收费全文 | 3552篇 |
免费 | 185篇 |
国内免费 | 1篇 |
出版年
2023年 | 13篇 |
2022年 | 23篇 |
2021年 | 60篇 |
2020年 | 45篇 |
2019年 | 37篇 |
2018年 | 66篇 |
2017年 | 57篇 |
2016年 | 78篇 |
2015年 | 132篇 |
2014年 | 167篇 |
2013年 | 233篇 |
2012年 | 264篇 |
2011年 | 268篇 |
2010年 | 137篇 |
2009年 | 154篇 |
2008年 | 242篇 |
2007年 | 235篇 |
2006年 | 222篇 |
2005年 | 207篇 |
2004年 | 245篇 |
2003年 | 190篇 |
2002年 | 182篇 |
2001年 | 41篇 |
2000年 | 26篇 |
1999年 | 30篇 |
1998年 | 39篇 |
1997年 | 33篇 |
1996年 | 25篇 |
1995年 | 34篇 |
1994年 | 36篇 |
1993年 | 24篇 |
1992年 | 15篇 |
1991年 | 20篇 |
1990年 | 8篇 |
1989年 | 20篇 |
1988年 | 10篇 |
1987年 | 7篇 |
1986年 | 9篇 |
1985年 | 10篇 |
1984年 | 8篇 |
1983年 | 11篇 |
1982年 | 13篇 |
1981年 | 9篇 |
1980年 | 7篇 |
1979年 | 10篇 |
1978年 | 6篇 |
1977年 | 6篇 |
1975年 | 5篇 |
1974年 | 3篇 |
1973年 | 4篇 |
排序方式: 共有3738条查询结果,搜索用时 93 毫秒
51.
Polycelis (Seidlia) auriculata is endemic to mountain districts of Japan, from the central part of Honshû to the area of the Daisetsu Mts of Hokkaidô. In northern Japan, it sometimes occurs in cold-water biotopes of lowland areas. The progenitor of P. auriculata appears to have been the oldest immigrant into northern Japan among the Japanese Polycelis species, entering through a northern route as a preglacial faunal element. P. auriculata now shows a discontinious distribution in northern Japan. By virtue of its geographical and vertical distribution, ecological niche, variation in anatomy of the copulatory apparatus, and cytodemes, this species appears to be in the process of transformation. 相似文献
52.
Naoki Koyama Yukio Takahata Michael A. Huffman Koshi Norikoshi Hisayo Suzuki 《Primates; journal of primatology》1992,33(1):33-47
Over a 30-year period from 1954 to 1983, 975 live births were recorded for Japanese macaque females at the Iwatayama Monkey
Park, Arashiyama, Japan. Excluding unknown birth dates, primiparous mothers gave birth to 185 infants (182 cases with age
of mother known) and multiparous mothers gave birth to 723 infants (603 cases with age of mother known). The peak month of
birth was May with 52.3% of the total births occurring during the period. Multiparous females who had not given birth the
previous year did so earlier than multiparous females who had given birth the previous year and also earlier than primiparous
females. Among the females who had given birth the previous year, females whose infant had died gave birth earlier than females
who had reared an infant the previous year. The offspring sex ratio (1:0.97) was not significantly different from 1:1, and
revealed no consistent association with mother's age. Age-fecundity exhibited a humped curve. The annual birth rate was low
at the age of 4 years but increased thereafter, ranging between 46.7% and 69.0%, at between 5 and 19 years of age, but again
decreased for females between 20 and 25 years of age. Some old females displayed clear reproductive senescence. The infant
mortality within the first year of age was quite low (10.3%) and the neonatal (less than 1 month old) mortality rate accounted
for 49.0% of all infant deaths. There was no significant difference between the mortality rates of male and female infants.
A female's rank-class had no apparent effect on the annual birth rate, infant mortality, and offspring sex ratio. These long-term
data are compared with those from other primate populations. 相似文献
53.
The complete nucleotide sequence of a 16S ribosomal RNA gene from tobacco chloroplasts has been determined. This nucleotide sequence has 96% homology with that of maize chloroplast 16S rRNA gene and 74% homology with that of Escherichia coli16S gene.The 3′ terminal region of this gene contains the sequence ACCTCC which is complementary to sequences found at the 5′ termini of prokaryotic mRNAs.The large stem and loop structure can be constructed from the sequences surrounding the 5′ and 3′ ends of the 16S gene. These observations demonstrate the prokaryotic nature of chloroplast 16S rRNA. 相似文献
54.
Kunie Yoshikawa Takehiko Nohmi Rumiko Miyata Motoi Ishidate Jr. Naoki Ozawa Masakazu Isobe Tadashi Watabe Tuneo Kada Takashi Kawachi 《Mutation research》1982,96(2-3)
Comparison studies for detecting differences between liver microsome and S9 preparations from 4 strains (Donryu, Fischer, Sprague-Dawley, Wistar) of young male rats were carried out with pretreatment of the animals by inducers such as PCBs and PB plus 5,6-BF. Each microsome fraction was assayed for the enzymic activity of metabolism of model substrates such as aniline, benzophetamine, BP, DMN and 7-ethoxycoumarin. The hepatic S9 sample was also compared, as regards its metabolizing ability to activate 9 pre-mutagens (2AA, AAF, o-AAT, BP, DAB, DMBA, DMN, m-PDA, quinoline) to directly acting mutagens in the Salmonella/hepatic S9 activation test by using TA98, TA100 and TA1537 strains with or without cytochrome P450 inhibitors (SKF-525A, metyrapone, 7,8-benzoflavone).In the enzymic assay with PCBs-induced microsomes, BP hydroxylation revealed a strain-specific difference: the microsomes from Fischer and Wistar rats were more effective for metabolizing BP than those from the other strains of rat. The effect of induction by PB plus 5,6-BF for Fischer rats showed relatively higher enzymic activity in the same induction group. Other microsomes prepared from rats with and without induction by PB plus 5,6-BF did not show a clear-cut strain dependency in the enzymic activities assayed.In the mutation experiments with hepatic S9 samples, the examination of DAB and quinoline revealed a marked strain difference when S9 samples prepared from PCBs-pretreated and PB-plus-5,6-BF-induced rats were used: the S9 sample from Fischer rats was available for activating the two pre-mutagens to directly acting mutagens. No marked difference in the metabolic activation of the remaining 7-pre-mutagens was observed on other S9 preparations.In examinations of mutagenicity activities with the use of three inhibitors, the two S9 preparations made with the two induction methods showed inhibition profiles closely similar to each other. However, there were minor differences in the profiles by these inhibitors.From these findings it was concluded that Fischer rat-liver S9 is useful for detecting mutagens in the metabolic activation test, when induction by PB plus 5,6-BF was used in the Ames Salmonella test. 相似文献
55.
Dissociability of the monomer ribosomes prepared from dry and imbibed pine (Pinus thunbergii) seed embryos was analyzed in sucrose density gradient containing a high salt buffer. Abnormal dissociation into the subunits
was observed with the ribosome preparation from dry seed embryos when compared with that from imbibed seed embryos, i.e. each
subunit peak was broader and localized at a lower site in sucrose density gradient. This indicates some change(s) in ribosomes
during imbibition of seeds. These ribosomal changes also progressedin vitro. That is, after incubation of ribosome preparation from dry seed embryos in a high salt buffer for 5 min at 30 C or in a
low salt buffer for 15 hr at 0 C, complete dissociation into the normal subunits was observed. No difference was found between
polyacrylamide gel electrophoresis patterns of ribosomal RNA from dry and imbibed seed embryos. These results suggest some
alteration in the protein components of ribosome during imbibition of pine seeds.
This paper is dedicated to Prof. Shyogo Sawamura, Utsunomiya University on his retirement in March, 1979. 相似文献
56.
The mechanism by which dihydroconiferyl alcohol (DCA) stimulatesindole-3-acetic acid (IAA)-induced elongation of cucumber hypocotylsections was studied. Although DCA did not affect the uptakeof IAA-5-3H by hypocotyl sections, the endogenous level of IAA-5-3Hin DCA-treated sections was much higher than in DCA untreatedones. IAA-5-3H in the incubation medium was degraded in thepresence of hypocotyl sections, and this degradation of IAAwas inhibited by DCA. An in vitro experiment with horseradishperoxidase revealed that DCA inhibited the IAA degrading activityof the oxidase, as did caffeic acid and ferulic acid. Theseresults suggested that DCA enhances IAA-induced cucumber hypocotylelongation by acting as an antioxidant of IAA. (Received June 4, 1975; ) 相似文献
57.
58.
A versatile, two-step chromatographic method using DEAE-Toyopearl(Toyo Soda, Japan) is described for purifying photosystem IIreaction center complex from digitonin extracts of spinach thylakoidmembranes. The method is very simple and brings about an approximatefour-fold increase in the specific activity, on a chlorophyllbasis, of 2,4-dichlorophenol-indophenol photoreduction with1,5-diphenylcarbazide (to about 2,000 µ electron equivalentsper mg chlorophyll per h), with an approximate 40 percent recoveryin chlorophyll. The SDS-polyacrylamide gel electrophoresis performedin the presence of 4 M urea in the analyzing gel shows fourpolypeptide bands of the photosystem II reaction center of about47, 43, 30 and 9 kilodaltons. The absorption and fluorescence properties, as well as the pigmentand chemical compositions and the above mentioned polypeptideprofile of the purified complex are essentially identical withthose of the preparations isolated by the previously describedmethod (Satoh 1982). The digitonin solubilization of thylakoid membranes destroysthe water splitting machinery, so that the purified complexshows no oxygen evolving activity, even although 0.60.7atoms of manganese per 50 chlorophyll molecules still remain. (Received March 19, 1985; Accepted July 19, 1985) 相似文献
59.
60.
Satsuki Tsuji Naoki Shibata Hayato Sawada Masayuki Ushio 《Molecular ecology resources》2020,20(5):1323-1332
Recent advances in environmental DNA (eDNA) analysis using high‐throughput sequencing (HTS) enable evaluation of intraspecific genetic diversity in a population. As the intraspecific genetic diversity provides invaluable information for wildlife conservation and management, there is an increasing demand to apply eDNA analysis to population genetics and the phylogeography by quantitative evaluation of intraspecific diversity. However, quantitative evaluations of intraspecific genetic diversity using eDNA is not straightforward because the number of eDNA sequence reads obtained by HTS may not be an index of the quantity of eDNA. In this study, to quantitatively evaluate genetic diversity using eDNA analysis, we applied a quantitative eDNA metabarcoding method using the internal standard DNAs. We targeted Ayu (Plecoglossus altivelis altivelis) and added internal standard DNAs with known copy numbers to each eDNA sample obtained from three rivers during the library preparation process. The sequence reads of each Ayu haplotype were successfully converted to DNA copy numbers based on the relationship between the copy numbers and sequence reads of the internal standard DNAs. In all rivers, the calculated copy number of each haplotype showed a significant positive correlation with the haplotype frequency estimated by a capture‐based survey. Furthermore, estimates of genetic indicators such as nucleotide diversity based on the eDNA copy numbers were comparable with those estimated based on a capture‐based study. Our results demonstrate that eDNA analysis with internal standard DNAs enables reasonable quantification of intraspecific genetic diversity, and this method could thus be a promising tool in the field of population genetics and phylogeography. 相似文献