全文获取类型
收费全文 | 8695篇 |
免费 | 468篇 |
国内免费 | 6篇 |
专业分类
9169篇 |
出版年
2022年 | 45篇 |
2021年 | 72篇 |
2020年 | 44篇 |
2019年 | 50篇 |
2018年 | 96篇 |
2017年 | 82篇 |
2016年 | 146篇 |
2015年 | 204篇 |
2014年 | 245篇 |
2013年 | 844篇 |
2012年 | 434篇 |
2011年 | 519篇 |
2010年 | 301篇 |
2009年 | 292篇 |
2008年 | 491篇 |
2007年 | 498篇 |
2006年 | 523篇 |
2005年 | 527篇 |
2004年 | 502篇 |
2003年 | 482篇 |
2002年 | 549篇 |
2001年 | 109篇 |
2000年 | 98篇 |
1999年 | 116篇 |
1998年 | 144篇 |
1997年 | 108篇 |
1996年 | 108篇 |
1995年 | 98篇 |
1994年 | 90篇 |
1993年 | 129篇 |
1992年 | 107篇 |
1991年 | 79篇 |
1990年 | 61篇 |
1989年 | 74篇 |
1988年 | 68篇 |
1987年 | 57篇 |
1986年 | 53篇 |
1985年 | 59篇 |
1984年 | 68篇 |
1983年 | 52篇 |
1982年 | 76篇 |
1981年 | 60篇 |
1980年 | 68篇 |
1979年 | 39篇 |
1978年 | 44篇 |
1977年 | 28篇 |
1976年 | 37篇 |
1975年 | 25篇 |
1973年 | 31篇 |
1972年 | 21篇 |
排序方式: 共有9169条查询结果,搜索用时 15 毫秒
1.
We examined whether actin filaments are involved in the cAMP-dependent activation of a high affinity sodium/glucose cotransporter (SGLT1) using epithelial expression systems. The expression of enhanced green fluorescent protein-tagged SGLT1 (EGFP-SGLT1) in Madin-Darby canine kidney (MDCK) cells was revealed by Western blotting and confocal laser microscopy. 8-Br-cAMP, a membrane permeable cAMP analog, enhanced [14C]-α-methyl glucopyranoside ([14C]-AMG) uptake. Both basal and 8-Br-cAMP-elicited [14C]-AMG uptakes were inhibited by N-(2{[3-(4-bromophenyl)-2-propenyl]-amino}-ethyl)-5-isoquinolinesulfonamide (H-89), a protein kinase A inhibitor, and cytochalasin D, an actin filament formation inhibitor. Furthermore, cytochalasin D inhibited the distribution of EGFP-SGLT1 at the apical surface. These results suggest that the EGFP-SGLT1 protein is functionally expressed in the apical membrane of MDCK cells, and is up-regulated by a cAMP-dependent pathway requiring intact actin filaments. 相似文献
2.
The effects of delayed mating on mouse preimplantation embryos (78 ± 1 hours) were studied by setting up different mating periods in relation to the estimated time of spontaneous ovulation. Copulation occurred even in the late morning and early afternoon after the night of spontaneous ovulation. However, females mated in the early afternoon had no viable embryos at the time of laparotomy. Although embryonic development was not affected in the groups mated 6 or 10 hours after estimated ovulation, the percentage of degenerated embryos was increased in these groups. These results suggest that prolonged intervals between the estimated time of ovulation and mating have some deleterious effects on preimplantation embryos. 相似文献
3.
A case of chromomycosis in which hyperthermia proved effective is reported. The patient was a 56-year-old male bean curd maker who, without any previous history of minor trauma, developed on the extensor side of the left upper arm an eczematous lesion that underwent gradual radial expansion. The lesion showed a well-defined, 7×10 cm infiltrated erythematous plaque with the central area healed and, at the upper and lower borders, adherent scales and crusts on the surface. Histological examination revealed granulomatous changes in the dermis, as well as sclerotic cells within giant cells and microabscesses. On culturing,Fonsecaea pedrosoi was isolated. The patient was treated with disposable chemical pocket warmers, which were secured over the lesion with a rather tight elastic bandage, so that they kept the affected area warm for 24 hours a day. After a month of such hyperthermic treatment, the erythema and infiltration had decreased considerably, and microscopic examination and culture of the crusts both yielded negative results. Examination of biopsy specimens of the lesion after the third month showed that it had cicatrized. The treatment was stopped after 4 months, and no relapse occurred. We also summarize the published results of local hyperthermic treatment of chromomycosis in Japan. 相似文献
4.
5.
Akira Shimizu 《Journal of Ethology》1992,10(2):85-102
Anoplius eous Yasumatsu (Hymenoptera, Pompilidae) exhibits some outstanding nesting behavior. Females excavate a unicellular or multicellular
nest in wet ground, or dig a single-celled nest in rotten wood, or build clustered mud cells in narrow spaces between walls
of such substances as wood or vinyl sheets. The latter nest-type has been unknown within the subfamily Pompilinae. Females
prepare a nest-cell before hunting, and construct it further after hunting, leaving the prey near the nest (behavior-formula:
IVPTIOC). They transport their prey backward on the ground, grasping it in their mandibles by any part of the legs, and forward
on the surface film of water or on the ground, grasping it by the middle part of the 1st or 2nd legs. Their only prey is the
adult female semi-aquatic spider,Pardosa pseudoannulata (Lycosidae). These nesting and provisioning behavior patterns are compared with those of other pompilids. The position of
the present species in the behavioral evolution of the Pompilidae is suggested. 相似文献
6.
Kitamura Akira; Matsui Kenji; Kajiwara Tadahiko; Hatanaka Akikazu 《Plant & cell physiology》1992,33(4):493-496
C6-Aldehydes emitted from intact tea leaves were analyzed quantitatively.Emission of the aldehydes increased temporarily in mid-May whenenzymatic activities involved in aldehyde formation from lipidsbegan to increase. Levels of C6-aldehydes in tea leaves alsoincreased temporarily. However, the accumulated C6-aldehydesdid not always correspond to emitted ones. (Received December 1, 1991; Accepted March 18, 1992) 相似文献
7.
H. Takahashi K. Takita T. Kishimoto T. Mitsui H. Hori 《Journal of Phytopathology》2002,150(10):529-535
Phenylalanine ammonia‐lyase (PAL, EC 4.3.1.5) activity in clubroot disease‐resistant turnip calli was transiently increased by 20 h after the inoculation with Plasmodiophora brassicae spores. The magnitude of the increase in PAL activity was four to six times higher than constitutive PAL activity. There was no transient increase in PAL activity in susceptible calli. Preincubation of calli in Ca2+‐free medium or the removal of Ca2+ from cell surfaces by ethylene glycol bis(2‐aminoethyl ether)‐N,N,N′,N′‐tetraacetic acid‐chelation, completely inhibited induced PAL activity. The influx of exogenous Ca2+ into cells appears necessary for this pathogen induced PAL activity. Verapamil and the calmodulin inhibitor W7 almost completely inhibited induced PAL activity at 1 and 0.1 mm , respectively. Neomycin, ruthenium red and (1‐(6‐[(17β‐3‐Methoxyestra‐1,3,5‐(10)‐trien‐17‐yl)amino]hexyl)‐1H‐pyrrole‐2,5‐dione) did not inhibit induced PAL activity. Thus, verapamil and N‐(6‐aminohexyl)‐5‐chloro‐1‐naphthalenesulphonamide hydrochloride‐sensitive Ca2+‐mediated signalling process appear necessary for P. brassicae induced PAL activity. As the protein synthesis inhibitor cycloheximide (CHX) blocked the induced increasing PAL activity, de novo synthesis of PAL appears to be required for turnip cell defence reactions against P. brassicae. 相似文献
8.
A new ribosomal protein of 38 kDa, named A0, was detected in yeast ribosomes on immunoblotting. The antibody used here was that against A1/A2, 13 kDa acidic ribosomal proteins which cross-reacted with A0. Although A0 and A1/A2 share common antigenic determinants, they differ in the following biochemical properties. While A1/A2 could be extracted from ribosomes with ethanol and ammonium sulfate, A0 could not. A0 gave two protein spots in a less acidic region than for A1/A2 on two-dimensional gel electrophoresis. The heterogeneity observed for A0 was ascribable to phosphorylation because one spot disappeared after treatment of the ribosomes with phosphatase. The syntheses of A0 and A1/A2 are directed by different mRNA species, as judged with a cell-free translation system, ruling out the possibility that A0 is a precursor of A1/A2. Although a mammalian ribosomal protein equivalent to A0 has been shown to be associated with 13 kDa acidic proteins in the cytoplasm, essentially no A0 was detected on immunoblotting in the yeast cytosol, while a small but detectable amount of A1/A2 was present. The possibility that A0 is a eukaryotic equivalent of L10 of Escherichia coli is discussed. 相似文献
9.
A radioimmunoassay for human pro-luteinizing hormone-releasing factor [pro-LRF(14-69)OH] 总被引:1,自引:0,他引:1
A Motoyama I Wakabayashi S Minami H Sugihara F Takahashi S Akira N Ling 《Endocrinologia japonica》1987,34(1):133-137
A radioimmunoassay (RIA) for human pro-LRF(14-69)OH was developed with an antiserum, generated in a rabbit, to [Tyr67]pro-LRF(47-67)NH2 conjugated to BSA. This antiserum bound 28-32% of [125I]pro-LRF(14-69)OH at a final dilution of 1:2500 and the binding was inhibited by pro-LRF(14-69)OH in a dose-dependent manner. The sensitivity of the RIA was 31.2-62.5 pg and the dose that inhibited 50% of the binding to the tracer was 280-320 pg. Intra- and inter-assay coefficients of variation at 50% inhibition were 8 and 12%, respectively. Neither LRF nor pro-LRF(14-37)OH was recognized by the antiserum. The dilution curve generated with human hypothalamic extract was parallel to that of pro-LRF(14-69)OH. In addition the extract yielded a major immunoreactive peak emerging in elution volumes concordant with [125I]pro-LRF(14-69)OH on Sephadex G-50 chromatography. 相似文献
10.
Komatsuna (Brassica campestris L. var. rapa) plants were grownhydroponically under various conditions with respect to thesupply of nitrate, and the variations in levels of natural 15Nabundance (15N) in nitrogenous fractions of leaf blades, petiolesplus midribs, and roots in these plants were analyzed. The fractionation of nitrogen isotopes during uptake of nitratewas null irrespective of the concentrations of nitrate in theculture medium. The roots had lower 15N values than that inthe nitrate applied to plants. The nitrate in the three tissuesexamined had higher 15N values than that in the nitrate applied:the values were highest in the leaf blades which were presumedto have highest activities in terms of reduction of nitrate.In contrast, the amino acids and residual fractions had lower15N values than those in the nitrate applied. These resultssuggest that reduction of nitrate is a critical step in thefractionation of nitrogen isotopes in plant tissues in vivo.
1Permanent address: Fukuoka Agricultural Experiment Station,Yoshiki 587, Chikushino, 818 Japan. (Received March 10, 1989; Accepted July 10, 1989) 相似文献