全文获取类型
收费全文 | 14014篇 |
免费 | 724篇 |
国内免费 | 8篇 |
出版年
2022年 | 70篇 |
2021年 | 114篇 |
2020年 | 59篇 |
2019年 | 86篇 |
2018年 | 140篇 |
2017年 | 148篇 |
2016年 | 250篇 |
2015年 | 383篇 |
2014年 | 439篇 |
2013年 | 1157篇 |
2012年 | 778篇 |
2011年 | 849篇 |
2010年 | 492篇 |
2009年 | 476篇 |
2008年 | 788篇 |
2007年 | 878篇 |
2006年 | 865篇 |
2005年 | 913篇 |
2004年 | 989篇 |
2003年 | 916篇 |
2002年 | 865篇 |
2001年 | 148篇 |
2000年 | 112篇 |
1999年 | 149篇 |
1998年 | 220篇 |
1997年 | 208篇 |
1996年 | 171篇 |
1995年 | 149篇 |
1994年 | 117篇 |
1993年 | 155篇 |
1992年 | 134篇 |
1991年 | 99篇 |
1990年 | 97篇 |
1989年 | 91篇 |
1988年 | 91篇 |
1987年 | 69篇 |
1986年 | 76篇 |
1985年 | 93篇 |
1984年 | 107篇 |
1983年 | 88篇 |
1982年 | 106篇 |
1981年 | 96篇 |
1980年 | 83篇 |
1979年 | 43篇 |
1978年 | 48篇 |
1977年 | 44篇 |
1976年 | 51篇 |
1975年 | 27篇 |
1974年 | 39篇 |
1973年 | 33篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
31.
Hiroshi Ihobe 《Primates; journal of primatology》1989,30(1):17-25
When the individual Japanese macaques of the Koshima troop feed on natural food, they usually feed alone. In situations where
animals usually feed without other animals, there is a possibility that subordinate animals may avoid feeding sites at which
dominant animals are feeding. This paper examines whether social relationships such as kinship or dominance exert any influence
on an animal's choice of feeding sites, by analyzing episodes in which an animal approached and climbed into a tree where
other animals were. As a result, it was found that social relationships did not influence whether an animal climbed into a
tree where other animals were feeding, and that no particular age-sex pair co-fed. Agonistic interactions frequently occurred
when the inter-individual distance was less than 1 m. From these findings, the feeding sites were divided into two spaces:
(1) a tolerance feeding space, and (2) an intolerance feeding space. It is presumed that animals can feed without entering
others' intolerance feeding spaces when food is abundant, as it was in the present study period. Thus social relationships
do not influence an animal's choice of feeding sites in such a situation. 相似文献
32.
Fusae Shimizu Mari Ogata Tatsuhiko Yagi Sadao Wakabayashi Hiroshi Matsubara 《Biochimie》1989,71(11-12)
Rubredoxin was purified from Desulfovibrio vulgaris Miyazaki. It was sequenced and some of its properties determined. Rubredoxin is composed of 52 amino acids. It is highly homologous to that from D. vulgaris Hildenborough. Its N-methionyl residue is partially formalated. The millimolar absorption coefficients of the rubredoxin at 489 nm and 280 are 8.1 and 18.5, respectively, and the standard redox potential is +5 mB, which is slightly higher than those of other rubredoxins. Rubredoxin, as well as cytochrome c-553, was reduced with lactate by the action of lactate dehydrogenase of this organism, and the rection was stimulated with 2-methyl-1, 4-naphthoquinone. It is suggested that rubredoxin, in collaboration with membraous quinone, functions as natural electron carrier for cytoplasmic lactate dehydrogenase of this organism, whereas cytochrome c-553 plays the same role for periplasmic lactate dehydrogenase. 相似文献
33.
Takeshi Tsunetoshi Atsuhiro Otsuka Hiroshi Mikami Katsuhiko Kohara Katsutoshi Katahira Toshio Ogihara 《European journal of applied physiology and occupational physiology》1989,58(7):705-709
We have previously demonstrated that blood pressure elevation by acute blood volume expansion is volume-dependent during the infusion period and resistance-dependent in the post-infusion period in normal anesthetized dogs, and that such an increase in blood pressure is associated with a potentiation of the pressor response to norepinephrine. To evaluate the possible renal contribution to these hemodynamic changes, blood volume expansion was performed for 1 h with dextran dissolved in lactated Ringer's solution (20 ml/kg) in 15 nephrectomized dogs. The mean blood pressure, cardiac output and total peripheral resistance at the end of infusion were 126%, 225% and 60%, respectively; 3 h after volume expansion they were 126%, 151%, and 92% respectively. However, in 4 dogs, there was an increase in mean blood pressure (138%) 3 h after volume expansion. This was thought to result from an increase in the total peripheral resistance (133%) associated with the recovery of cardiac output (106%). The pressor response to norepinephrine (0.5 microgram/kg) was potentiated after volume expansion. These results indicate that the handling of volume by the kidney contributed to the maintenance of an elevated level of cardiac output. However, nephrectomy did not seem to interfere with the hemodynamic switching of the causative factor for blood pressure elevation from increased cardiac output to increased total peripheral resistance. Neither was the potentiation of pressor response to norepinephrine affected. 相似文献
34.
Hiroshi Ishii Osamu Nadaoka Yoshimasa Mimura Yoshio Inoue Riichir Chûj 《International journal of biological macromolecules》1989,11(6)
A tetrapetide containing an Aib residue, Boc-Asn-Aib-Thr-Aib-OMe, was synthesized as a peptide model for the N-glycosylation site in N-glycoproteins. Backbone conformation of the peptide and possible intramolecular interaction between the Asn and Thr side chains were elucidated by means of n.m.r. spectroscopy. Temperature dependence of NH proton chemical shift and NOE experiments showed that Boc-Asn-Aib-Thr-Aib-OMe has a tendency to form a β-turn structure with a hydrogen bond involving Thr and Aib4 NH groups. Incorporation of Aib residues in the peptide model promotes folding of the peptide backbone. With folded backbone conformation, carboxyamide protons of the Asn residue are not involved in hydrogen bond network, while the OH group of the Thr residue is a candidate for a hydrogen bond in DMSO-d6 solution. 相似文献
35.
36.
Yuichi Fujita Yasuhiro Takahashi Takayuki Kohchi Haruo Ozeki Kanji Ohyama Hiroshi Matsubara 《Plant molecular biology》1989,13(5):551-561
The frxC gene, one of the unidentified open reading frames present in liverwort chloroplast DNA, shows significant homology with the nifH genes coding for the Fe protein, a component of the nitrogenase complex (Ohyama et al., 1986, Nature 322: 572–574). A truncated form of the frxC gene was designed to be over-expressed in Escherichia coli and an antibody against this protein was prepared using the purified product as an antigen. This antibody reacted with a protein in the soluble fraction of liverwort chloroplasts, which had an apparent molecular weight of 31 000, as revealed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, in good agreement with a putative molecular weight of 31945 deduced from the DNA sequence of the frxC gene. In a competitive inhibition experiment, the antigenicity of this protein was indicated to be similar to that of the over-expressed protein in E. coli. Therefore, we concluded that the frxC gene was expressed in liverwort chloroplasts and that its product existed in a soluble form. The molecular weight of the frxC protein was approximately 67 000, as estimated by gel filtration chromatography, indicating that the frxC protein may exist as a dimer of two identical polypeptides analogous to the Fe protein of nitrogenase. The results obtained from affinity chromatography supported the possibility that the frxC protein, which possesses a ATP-binding sequence in its N-terminal region that is conserved among various other ATP-binding proteins, has the ability to bind ATP. 相似文献
37.
38.
Yaichi Fukushima Harumichi Itoh Tetsuro Fukase Hiroshi Motai 《Applied microbiology and biotechnology》1989,30(6):604-608
Summary A chemostat culture system was investigated in order to produce protease by Aspergillus species effectively in the presence of 10% NaCl which was added to avid bacterial contamination. A salt tolerant fungus Aspegillus oryzae NISL 1913 produced protease even in the presence of 10% NaCl. The protease production by this strain was accelerated by proteins. Isolated soy protein or defatted soybean fluor (DSF) was used as a nitrogen source and an inducer of protease production, and starch was used as a carbon source. Continuous protease production was performed in a carbon-limited chemostat culture (dilution rate = 0.02). The maximum activity reached 2200 protease units (PU)/ml of the culture broth (130 PU/mg dry weight) with DSF as a nitrogen source. The culture could be continued for more than 50 days without any bacterial contamination. 相似文献
39.
Yoshikazu Izumi Pijush Kanti Nath Hiroshi Yamamoto Hideaki Yamada 《Applied microbiology and biotechnology》1989,30(4):337-342
Summary A convenient and efficient method of NADPH production from NADP+ has been established using a glucose dehydrogenase system involving whole cells and immobilized cells of Gluconobacter suboxydans IFO 3172. Using airdried cells of the bacterium, the optimum conditions for NADPH production were examined, including the cell and glucose concentrations, NADP+ concentration, pH, buffer and reaction temperature. Under suitable conditions, the conversion ratio and the amount of NADPH accumulated reached about 100% and 73 mg/ml of the reaction mixture, respectively, after 1-h reaction. Intact cells of the bacterium also showed high NADPH production even in the reaction mixture without a surfactant. The addition of Triton X-100 to the reaction mixture and freeze-thawing treatment of intact cells enhanced the production. The NADPH production method was further improved by using cells of the bacterium immobilized by entrapment in a -carrageenan gel lattice. The immobilized cells had almost the same enzymatic properties as the air-dried cells. The conditions for the continuous production of NADPH with an immobilized cell column were also investigated. NADPH was produced in a good yield (about 95%) with this continuous process. 相似文献
40.
Dr. Shigeru Sakiyama Yohko Nakamura Katsuo Tokunaga Hiroshi Takazawa Yoshinori Ohwaki Toshio Nagano 《Cell and tissue research》1989,258(2):225-231
Summary In-situ hybridization experiments have been performed using isoactin ( and )-specific riboprobes in various tissues of the rat and mouse. Distribution of the grains of actin mRNAs for both and types was similar throughout sections of the rat testis. Although both mRNAs were evenly distributed in the seminiferous tubule, extremely heavy labeling was observed in about 10% of the seminiferous tubules that could be identified as stage XII of spermatogenesis. At high magnification, grains of the mRNA were found in the cytoplasm of elongating spermatids and in the Sertoli cell cytoplasm at the adluminal side. Much higher density of the grains of mRNA was observed in the neck region of the spermatids at stage XII. Thus, the dense distribution of cytoskeletal actin mRNAs is stage-specific in the tubule during spermatogenesis in the rat. The high expression of both and actin mRNAs was also observed in the epithelial cells of the intestinal crypts. 相似文献