全文获取类型
收费全文 | 2644篇 |
免费 | 158篇 |
国内免费 | 2篇 |
出版年
2022年 | 7篇 |
2021年 | 29篇 |
2020年 | 11篇 |
2019年 | 18篇 |
2018年 | 18篇 |
2017年 | 27篇 |
2016年 | 53篇 |
2015年 | 70篇 |
2014年 | 93篇 |
2013年 | 259篇 |
2012年 | 142篇 |
2011年 | 159篇 |
2010年 | 105篇 |
2009年 | 106篇 |
2008年 | 158篇 |
2007年 | 175篇 |
2006年 | 175篇 |
2005年 | 184篇 |
2004年 | 180篇 |
2003年 | 156篇 |
2002年 | 166篇 |
2001年 | 27篇 |
2000年 | 46篇 |
1999年 | 49篇 |
1998年 | 22篇 |
1997年 | 29篇 |
1996年 | 14篇 |
1995年 | 19篇 |
1994年 | 14篇 |
1993年 | 17篇 |
1992年 | 19篇 |
1991年 | 23篇 |
1990年 | 20篇 |
1989年 | 26篇 |
1988年 | 13篇 |
1987年 | 14篇 |
1986年 | 14篇 |
1985年 | 9篇 |
1984年 | 14篇 |
1983年 | 17篇 |
1982年 | 20篇 |
1981年 | 10篇 |
1980年 | 10篇 |
1979年 | 10篇 |
1978年 | 12篇 |
1977年 | 9篇 |
1976年 | 7篇 |
1975年 | 6篇 |
1973年 | 4篇 |
1972年 | 4篇 |
排序方式: 共有2804条查询结果,搜索用时 15 毫秒
31.
Tatsuo Kawarasaki Tetsuya Kohsaka Masaru Sone Mitsutoshi Yoshida Kimio Bamba 《Molecular reproduction and development》1995,40(4):455-459
This study was carried out to determine whether Y-bearing porcine spermatozoa could be detected by in situ hybridization using a digoxigenin (Dig)-labelled DNA probe specific to the Y chromosome produced by polymerase chain reaction (PCR). A conventional PCR (with Dig-dUTP) was performed using a set of oligonucleotide primers (5′-AAGTGGTCAGCGTGTCCATA-3′ and 5′-TTTCTCCTGTATCCTCCTGC-3′) for 236 bp fragment of porcine male-specific DNA sequence and 1.25 × 104 template white blood cells obtained from a boar. When fluorescence in situ hybridization with the Dig-labelled DNA probe was applied to the metaphase chromosome spreads prepared from both boar and gilts, the fluorescein signal was only detected on the long arm of the Y chromosome. In addition, immunocytochemical detection with the Dig-labelled DNA probe and alkaline phosphatase-labeled anti-Dig was applied to both sperm nuclei pretreated with dithiothreitol and white blood cells; 51% of sperm nuclei and 96% of white blood cells obtained from boar were labelled, whereas none of white blood cells obtained from gilts were labelled with the Dig-labelled DNA probe. The results indicated that in situ hybridization with porcine male-specific DNA probe produced by PCR made possible the direct visualization of Y-bearing porcine spermatozoa by in situ hybridization. © 1995 Wiley-Liss, Inc. 相似文献
32.
Immortalization-susceptible elements and their binding factors mediate rejuvenation of regulation of the type I collagenase gene in simian virus 40 large T antigen-transformed immortal human fibroblasts. 总被引:3,自引:1,他引:2 下载免费PDF全文
S Imai T Fujino S Nishibayashi T Manabe T Takano 《Molecular and cellular biology》1994,14(11):7182-7194
33.
Axillary bud flowering after apical decapitation in Pharbitis in relation to photoinduction 总被引:2,自引:0,他引:2
Michiyuki Ono Kimiyo Sage Ono Koichiro Yamada Masaru Yasui Mitsuo Okazaki 《Physiologia plantarum》1993,87(1):1-6
The flowering response of axillary buds of seedlings of Pharbitis nil Choisy, cv. Violet, was examined in relation to the timing of apical bud removal (plumule including the first leaf or second leaf) before or after a flower-inductive 16-h dark period. When the apical bud was removed well before the dark period, flower buds formed on the axillary shoots that subsequently developed, but when removed just before, or after, the dark period, different results were observed depending on the timing of the apical bud removal and plant age. In the case of 8-day-old seedlings, fewer flower buds formed on the axillary shoots developing from the cotyledonary node when plumules were removed 20 to 0 h before the dark period. When the apical bud was removed after the dark period, no flower buds formed. Using 14-day-old seedlings a similar reduction of flowering response was observed on the axillary shoots developing from the first leaf node when the apical bud was removed just after the dark period. To further elucidate the relationship between apical dominance and flowering, kinetin or IAA was applied to axillary buds or the cut site where the apical bud was located. Both chemicals influenced flowering, probably by modulating apical dominance which normally forces axillary buds to be dormant. 相似文献
34.
Nakazawa Miki; Hayashi Hidenori; Yoshida Yuhji; Manabe Katsushi 《Plant & cell physiology》1993,34(1):83-91
Peptide fragments were obtained by limited proteolysis withtrypsin and Staphylococcus aureus V 8 protease from either thePR or the PFR form of 121-kDa phytochrome purified from etiolatedpea (Pisum sativum L.) shoots. Patterns of bands after polyacrylamidegel electrophoresis in the presence of SDS of the digests weredifferent, with some bands appearing preferentially when thedigestions were carried out with the PR or the PFR form. Amino-terminalsequences of the fragments were analyzed to determine the exactlocations of the amino-termini of the fragments within the aminoacid sequence of the apoprotein of pea phytochrome. The aminoacid compositions of some of the sequenced fragments were determinedin order to confirm the carboxy-terminal amino acids. Threecleavage regions were identified as kinetically favored sitesof cleavage of PFR (Arg-746 to Lys-752, around Glu-877 and aroundArg-1010), whereas only one was identified for PR (Glu-38 toArg-62). Regions of Glu-255, Arg-383, Arg-583 to Glu-620 andLys-1093 to Glu-1115 were also identified as potential sitesof proteolytic cleavage in both forms of the phytochrome. Othercleavage sites, the specificities of which have not yet beendetermined, are Glu-404, Glu-695 and Lys-1045. Surface-exposed parts of phytochrome in the PR and PFR formsare discussed. (Received June 13, 1992; Accepted October 27, 1992) 相似文献
35.
36.
A genomic fragment containing the dihydroflavonol 4-reductase B (DFR-B) gene was cloned from the sweet potato (Ipomoea batatas) and its nucleotide sequence was analyzed. The exons and flanking regions were highly homologous to those of previously reported DFR-B genes of the Japanese morning glory, whereas the introns and the intergenic region were less conserved. In addition to the sequences of three miniature inverted-repeat transposable elements (MITEs) and one direct repeat previously reported in the DFR-B gene of Japanese morning glory, two mobile element-like sequences were newly identified in the sweet potato DFR-B gene. At least four allelic sequences were found to exist by amplification of the DFR-B gene from various sweet potato cultivars. One of these allelic sequences had a 2-kb deletion in the intergenic region and was observed in the cultivars with high anthocyanin content in their storage roots. 相似文献
37.
Masaru Nakano Keizo Hosokawa Tomo Oomiya Saburo Yamamura 《Plant Cell, Tissue and Organ Culture》1995,41(3):221-227
A protoplast-to-plant system was developed in Gentiana using a gellan gum-embedding culture. Viable protoplasts could be routinely isolated from in vitro-grown plantlets, and they were embedded in 0.2% gellan gum-solidified B5 medium containing 2 mg l-1 NAA, 0.1 mg l-1 TDZ, 0.1 M sucrose and 0.4 M mannitol. Weekly addition of fresh liquid medium was essential for preventing cell browning. Colony growth was promoted by lowering mannitol concentration of the culture media after one month, and visible colonies were produced after 2 months of culture. Shoot regeneration from protoplast-derived calluses was stimulated by 1 to 10 mg l-1 TDZ in combination with 0.1 mg l-1 NAA. Protoplast-derived plants were recovered following rooting of the shoots in plant growth regulator-free medium and they were successfully transferred to soil.Abbreviations BA
benzylaminopurine
- FDA
fluorescein diacetate
- FW
fresh weight
- MES
2-N-morpholinoethane sulfonic acid
- NAA
-naphthaleneacetic acid
- TDZ
N-1,2,3-thiadiazol-5-yl-N-phenylurea (also called thidiazuron) 相似文献
38.
Y. Kobayashi Yufuko Takahashi Satoshi Chikayama Motomi Ikeda Nobuhiko Uoshima Shinya Kimura Koji Tanaka Katuya Wada Masaru Ozawa Tatuo Sugano Naoyuki Maruo Motoharu Kondo 《Histochemistry and cell biology》1997,108(2):115-120
We devised a new microfluorometric method for determining the ploidy of megakaryocytes identified immunologically in bone
marrow smears. The smears were immunostained by incubation with mouse monoclonal anti-glycoproteins (GP) IIb antibodies, followed
by fluorescein isothiocyanate-conjugated goat anti-mouse IgG antibodies. They were then stained with 4′,6-diamidino-2-phenylindole
(DAPI). Megakaryocytes were identified by their GPIIb immunofluorescence using a microfluorometer and, after the filters were
changed, their DNA content was assayed by measuring the intensity of DAPI fluorescence. This intensity was shown to be proportional
to the DNA content when the aperture of the objective lens was reduced. We compared these results with those obtained when
megakaryocytes were identified morphologically, using DAPI staining after Wright-Giemsa destaining. In all 12 normal controls,
the ploidy peaks were shown to be 16N by both methods, and the mean ploidy detected by the immunological method was only reduced
0.961 times relative to the estimate from the morphological method. In contrast, in eight myelodysplastic syndrome (MDS) patients,
the ploidy peaks were either 8N or 4N and the mean was reduced by 0.906 times (P=0.018). Thus we could immunologically identify small megakaryocytes which we could not identify morphologically. Therefore,
this method is useful for measuring megakaryocytic ploidy, especially in the pathological megakaryocytes of MDS patients.
Accepted: 29 April 1997 相似文献
39.
An electroblotting apparatus for multiple replica technique and identification of human serum proteins on micro two-dimensional gels 总被引:1,自引:0,他引:1
A new apparatus for electrophoretic transfer of proteins from micro polyacrylamide slab gels has been developed. The apparatus enabled the easy changing of nitrocellulose sheets and was suited for obtaining multiple blots from a gel. Electrophoretic conditions were determined so that all of the blots obtained sequentially from one slab gel were successfully used to visualize specific proteins irrespective of their molecular weight. Combining the transfer technique with the technique of parallel micro two-dimensional electrophoresis, 20 blots could be obtained within 1 h of electroblotting time. The locations of 28 human serum proteins were determined simultaneously on these blots using commercial specific antisera. 相似文献
40.
In Rana pipiens, mating behavior could be induced readily in intact males by several pituitary implantations, but never in castrates. Systemic testosterone injection (1 mg daily), with or without pituitary implantation, failed to restore mating behavior in castrated frogs. On the other hand, intracranial implantation of testosterone (approximately 60-μg pellets in which testosterone is mixed with cholesterol 1:1) in castrates evoked mating behavior, including mating calls and clasping. The most effective implantation site was the rostral part of the preoptic nucleus. Thus, the rostral part of the preoptic nucleus is the androgen-sensitive site which governs sexual behavior in this species. The relative ineffectiveness of systemic injection of testosterone is discussed. 相似文献