全文获取类型
收费全文 | 3497篇 |
免费 | 181篇 |
国内免费 | 1篇 |
出版年
2023年 | 5篇 |
2022年 | 6篇 |
2021年 | 34篇 |
2020年 | 19篇 |
2019年 | 26篇 |
2018年 | 50篇 |
2017年 | 44篇 |
2016年 | 76篇 |
2015年 | 114篇 |
2014年 | 115篇 |
2013年 | 428篇 |
2012年 | 222篇 |
2011年 | 228篇 |
2010年 | 138篇 |
2009年 | 139篇 |
2008年 | 239篇 |
2007年 | 225篇 |
2006年 | 252篇 |
2005年 | 198篇 |
2004年 | 191篇 |
2003年 | 202篇 |
2002年 | 189篇 |
2001年 | 34篇 |
2000年 | 30篇 |
1999年 | 30篇 |
1998年 | 40篇 |
1997年 | 39篇 |
1996年 | 34篇 |
1995年 | 44篇 |
1994年 | 31篇 |
1993年 | 24篇 |
1992年 | 13篇 |
1991年 | 20篇 |
1990年 | 16篇 |
1989年 | 15篇 |
1988年 | 11篇 |
1987年 | 6篇 |
1986年 | 8篇 |
1985年 | 6篇 |
1984年 | 12篇 |
1983年 | 7篇 |
1982年 | 16篇 |
1981年 | 17篇 |
1980年 | 8篇 |
1979年 | 12篇 |
1978年 | 12篇 |
1977年 | 6篇 |
1976年 | 11篇 |
1974年 | 9篇 |
1973年 | 5篇 |
排序方式: 共有3679条查询结果,搜索用时 734 毫秒
51.
Koichi Matsuzaki Mikio Kan Wallace L. McKeehan 《In vitro cellular & developmental biology. Animal》1996,32(6):345-360
Summary Two transmembrane serine-threonine kinases (type I and II receptors), a membrane-anchored proteoglycan (type III), and a homodimeric
ligand participate in the transforming growth factor beta type on (TGFβ1) signal transduction complex. The expression of recombinant
receptors in insect cells co-infected with up to three recombinant baculoviruses was employed to study interactions among
the ectodomains of the three types of receptors and the TGFβ1 ligand in absence of uncontrollable extrinsic factors in mammalian
cells. Multi-subunit complexes were assembled in intact cells and purified on glutathione-conjugated beads for analysis by
tagging one of the subunits with glutathione S-transferase (GST). Intrinsic ligand-independent interactions were observed
among receptor subunits as follows: type III–III type I–I, type III-I, and type II-I. The homeotypic complex of type II–II
receptors and the heterotypic type III-II interaction was ligand dependent. The type I, but not the type III, subunit displaced
about 50% of the type II component in either ligand-dependent homomeric type II-type II complexes or heteromeric type III-type
II complexes to form type II-I or type III-II-I oligomers, respectively. The type II subunit displaced type I subunits in
oligomers of the type I subunit. Specificity of type I receptors may result from differential affinity for the type II receptor
rather than specificity for ligand. A monomeric subunit of the TGFβ1 ligand bound concurrently to type III and type II or
type III and type I receptors, but failed to concurrently bind to the type II and type I subunits. The binding of TGFβ1 to
the type I kinase subunit appears to require an intact disulfide-linked ligand dimer in the absence of a type III subunit.
The combined results suggest a pentameric TGFβ signal transduction complex in which one unit each of the type III, type II,
and type I components is assembled around the two subunits of the dimeric TGFβ1 ligand. An immobilized GST-tagged subunit
of the receptor complex was utilized to assemble multi-subunit complexesin vitro and to study the phosphorylation events among subunits in the absence of extrinsic cell-derived kinases. The results revealed
that (a) a low level of ligand-independent autophosphorylation occurs in the type I kinase; (b) a high level of autophosphorylation
occurs in the type II kinase; (c) both the type III and type I subunits aretrans-phosphorylated by the type II subunit; and (d) the presence of both type I and II kinases complexed with the type III subunit
and dimeric TGFβ1 ligand in a pentameric complex causes maximum phosphorylation of all three receptor subunits. 相似文献
52.
53.
Koichi Chikuni Yutaka Mori Toshiyuki Tabata Masayoshi Saito Michiko Monma Motoaki Kosugiyama 《Journal of molecular evolution》1995,41(6):859-866
Nucleotide sequences for the -casein precursor proteins have been determined from the genomic DNAs or hair roots of the Ruminantia. The coding regions, exons 2, 3, and 4, were amplified separately via the three kinds of PCRs and then directly sequenced. The primers were designed from the sequence of bovine -casein gene; they were applicable for the amplification of the -casein genes from the 13 species in the Ruminantia except exon 2 of the lesser mouse deer. These results permitted an easy phylogenetic analysis based on the sequences of an autosomal gene. A phylogenetic tree was constructed from the mature K-casein sequences and compared with the tree of the cytochrome b genes which were sequenced from the same individuals. The Cervidae (sika deer, Cervus nippon) were separated from the branch of the Bovidae on the tree of -casein genes with a relatively high confidence level of the bootstrap analysis, but included in the branch of the Bovidae on the tree of cytochrome b genes. The -casein tree indicated a monophyly of the subfamily Caprinae, although the internal branches were uncertain in the Caprinae. The tree based on the nucleotide sequences of cytochrome b genes clearly showed the relationships of the closely related species in the genus Capricornis consisting of serow (C. smatorensis), Japanese serow (C. crispus), and Formosan serow (C. swinhoei). These results would be explained by the difference of resolving power between the -casein and the cytochrome b sequences.
Correspondence to: K. Chikuni 相似文献
54.
†Akihito Yamamoto †Shuji Yamashiro †Kogo Takamiya Mitsuru Atsuta †Hiroshi Shiku † Koichi Furukawa 《Journal of neurochemistry》1995,65(6):2417-2424
Abstract: Among various tissues of mouse, β1,4- N -acetylgalactosaminyltransferase (GM2/GD2 synthase) gene is expressed predominantly in the brain. Further analysis of the gene expression in the mouse CNS was performed by northern blotting and by enzyme assays using extracts from various parts of the CNS. In situ hybridization was also done to investigate the distribution of cells generating GM2/GD2 synthase. In northern blots, diverse levels of the gene expression were observed, depending on the regions examined. By in situ hybridization, pyramidal cells in the hippocampus, granular cells in dentate gyrus and cerebral cortex, Purkinje cells in cerebellum, and mitral cells in the olfactory bulb expressed high levels of the mRNA; these results corresponded to the results obtained by northern blot. Enzyme levels in these sites were accordingly high. However, enzyme levels in certain areas with low mRNA intensities, such as thalamus and pons medulla, were higher than expected from the results of northern blotting. The significance of the high gene expression in certain areas for brain function and the reason for the discrepancy between mRNA level and enzyme activity in some regions are discussed. 相似文献
55.
Hidekazu Nishimura Kanetsu Sugawara Peng Gao Yasushi Muraki Seiji Hongo Fumio Kitame Kiyoto Nakamura 《Microbiology and immunology》1995,39(9):737-740
The HMV-II cells infected with influenza C virus were labeled with inorganic [32P]phosphate to identify phosphorylated proteins. Analysis by radioimmunoprecipitation with antiviral serum or monoclonal antibodies revealed that three major structural proteins of the virus, hemagglutinin-esterase (HE), nucleoprotein (NP), and matrix protein (M1) are all phosphorylated in both infected cells and virions. It was also observed that, in the presence of trypsin (10 μg/ml), the unphosphorylated form of the HE glycoprotein was cleaved efficiently whereas the phosphorylated form was not, raising the possibility that phosphorylation of HE may influence its susceptibility to degradation by proteolytic enzymes. 相似文献
56.
Hideyuki Takahashi Mitsuharu Inaki Koichi Fujimoto Shigeru Katsuta Izumi Anno Mamoru Nütsu Yuji Itai 《European journal of applied physiology and occupational physiology》1995,71(5):396-404
We examined the effect of differences in exercise intensity on the time constant (t
c) of phosphocreatine (PCr) resynthesis after exercise and the relationships betweent
c and maximal oxygen uptake (VO2max) in endurance-trained runners (n = 5) and untrained controls (n = 7) (average VO2max = 66.2 and 52.0 ml · min–1 · kg–1, respectively). To measure the metabolism of the quadriceps muscle using phosphorus nuclear magnetic resonance spectroscopy, we developed a device which allowed knee extension exercise inside a magnet. All the subjects performed four types of exercise: light, moderate, severe and exhausting. The end-exercise PCr: [PCr + inorganic phosphate (Pi)] ratio decreased significantly with the increase in the exercise intensity (P < 0.01). Although there was little difference in the end-exercise pH, adenosine diphosphate concentration ([ADP]) and the lowest intracellular pH during recovery between light and moderate exercise, significant changes were found at the two higher intensities (P < 0.01). These changes for runners were smaller than those for the controls (P < 0.05). The
c remained constant after light and moderate exercise and then lengthened in proportion to the increase in intensity (P < 0.05). The runners had a lowert
c at the same PCr and pH than the controls, particularly at the higher intensity (P < 0.05). There was a significant correlation betweent
c and [ADP] in light exercise and betweent
c and both end-exercise PCr and pH in severe and exhausting exercise (P < 0.05). The threshold of changes in pH andt
c was a PCr: (PCr + Pi) ratio of 0.5. There was a significant negative correlation between the VO2max andt
c after all levels of exercise (P<0.05).However, in the controls a significant correlation was found in only light and moderate exercise (P < 0.05). These findings suggest the validity of the use oft
c at an end-exercise PCr:(PCr + Pi) ratio of more than 0.5 as a stable index of muscle oxidative capacity and the correlation between local and general aerobic capacity. Moreover, endurance-trained runners are characterized by the faster PCr resynthesis at the same PCr and intracellular pH. 相似文献
57.
Alcohol and aldehyde dehydrogenase genotypes and drinking behavior of Chinese living in Shanghai 总被引:12,自引:0,他引:12
Taro Muramatsu Wang Zu-Cheng Fang Yi-Ru Hu Kou-Bao Yan Heqin Koichi Yamada Susumu Higuchi Shoji Harada Hiroaki Kono 《Human genetics》1995,96(2):151-154
Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH), the principal enzymes responsible for oxidative metabolism of ethanol, exist in multiple, genetically determined molecular forms. Widely different kinetic properties in some of these isozymes account for the individual differences in alcohol sensitivity. In this study we used the polymerase chain reaction/restriction fragment length polymorphism method to determine the genotypes of the ADH2 and ALDH2 loci of alcoholic and nonalcoholic Chinese living in Shanghai. We also investigated the subjects' drinking patterns by means of semistructured interviews. The alcoholics had significantly lower frequencies of the ADH22 and ALDH22 alleles than did the nonalcoholics, suggesting the inhibitory effects of these alleles for the development of alcoholism. In the nonalcoholic subjects, ADH22 had little, if any, effect, despite the significant effect of the ALDH22 allele in decreasing the alcohol consumption of the individual. Taken together, these results fit the proposed hypothesis for the development of alcoholism, i.e., drinking behavior is greatly influenced by the individual's gentoypes of alcohol-metabolizing enzymes, and the risk of becoming alcoholic is proportionate with the ethanol consumption of the individual. 相似文献
58.
Susumu Asakawa Masayo Akagawa-Matsushita Hiroyuki Morii Yosuke Koga Koichi Hayano 《Current microbiology》1995,31(1):34-38
We isolated a methanogenic strain, designated as strain TMA (=DSM 9195), from an enrichment culture inoculated with a Japanese paddy field soil. Strain TMA was Gram positive and strictly anaerobic. Cell shape was pseudosarcina-like, and cells were nonmotile. The strain was able to use methylamines, methanol, H2–CO2, and acetate as substrates for methanogenesis, but did not utilize formate. The optimum temperature and optimum pH were 30–37°C and 6.5–7.5 respectively. The G+C content of the DNA was 42.1 mol %. Strain TMA had DNA-DNA hybridization values of more than 80% with Methanosarcina mazeii S-6T (T = type strain). On the basis of phenotypic and genotypic characteristics, we identified strain TMA as M. mazeii. This is the first methylotrophic methanogen isolated from a paddy field soil and identified to the species level. 相似文献
59.
60.
Data are presented on the cytokinin status of seeds and seed components, at different stages of development in Phaseolus coccineus L., as determined with the soybean callus growth bioassay: A change in cytokinin types according to developmental stage occurred: from biologically very active less polar types (zeatin=Z) at early stages to more polar types (zeatin glucoside=Z9G and zeatin riboside=Zr), with relatively low biological activity, at intermediate and late stages of seed development: When cytokinins were analyzed separately in embryos (embryo proper) and suspensors at two embryonic stages: heart-shaped (A) and middle cotyledonary embryos (stage B) respectively, it was found that: i) at stage A, the suspensor showed cytokinin activity at the level of Z, 2iPA (2-isopentenyladenosine) and Zr, whereas more polar cytokinins (Z9G, Zr) were present in the embryo; ii) at stage B, when the embryo seems to become autonomous for cytokinin supply, there was a relative abundance of active cytokinins (Z, 2iPA) in the embryo to which Z9G activity in the suspensor corresponded. It is concluded that the suspensor plays an essential role in embryogenesis by acting as a hormone source to the early embryo.Abbreviations GA
gibberellic acid
- 2iPA
2-isopentenyladenosine
- Stage A
heart-shaped embryo
- siage B
middle cotyledonary embryo
- Z
zeatin
- Z9G
zeatin glucoside
- Zr
Zeatin riboside 相似文献