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991.
Identification of a novel interleukin-6 response element containing an Ets-binding site and a CRE-like site in the junB promoter. 总被引:10,自引:3,他引:7
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K Nakajima T Kusafuka T Takeda Y Fujitani K Nakae T Hirano 《Molecular and cellular biology》1993,13(5):3027-3041
Interleukin-6 (IL-6) activation of the immediate-early gene junB has been shown to require both a tyrosine kinase and an unknown 1-(5-isoquinolinesulfonyl)-2-methylpiperazine (H7)-sensitive pathway. Here we report the identification and characterization of an IL-6 immediate-early response element in the junB promoter (designated JRE-IL6) in HepG2 cells. The JRE-IL6 element, located at -149 to -124, contains two DNA motifs, an Ets-binding site (EBS) (CAGGAAGC) and a CRE-like site (TGACGCGA). Functional studies using variously mutated JRE-IL6 elements showed that both motifs were necessary and sufficient for IL-6 response of the promoter. The EBS of the JRE-IL6 element (JEBS) appears to bind a protein in the Ets family or a related protein which could also form a major complex with the EBSs of the murine sarcoma virus long terminal repeat or human T-cell leukemia virus type 1 long terminal repeat. The CRE-like site appears to weakly bind multiple CREB-ATF family proteins. Despite the similarity in the structure between the JRE-IL6 element and the polyomavirus enhancer PyPEA3, composed of an EBS and an AP1-binding site and known to be activated by a variety of oncogene signals, JRE-IL6 could not be activated by activated Ha-Ras, Raf-1, or 12-O-tetradecanoylphorbol-13-acetate. We show that IL-6 activates JRE-IL6 through an H7-sensitive pathway that does not involve protein kinase C, cyclic AMP-dependent kinase, Ca(2+)- or calmodulin-dependent kinases, Ras, Raf-1, or NF-IL6 (C/EBP beta). The combination of JEBS and the CRE-like site appears to form the basis for the selective and efficient response of JRE-IL6 to IL-6 signals, but not to signals generated by activated Ha-Ras, Raf-1, or protein kinase C. 相似文献
992.
Deletion of the immunoglobulin kappa chain intron enhancer abolishes kappa chain gene rearrangement in cis but not lambda chain gene rearrangement in trans. 总被引:16,自引:2,他引:14
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Immunoglobulins (Ig) secreted from a plasma cell contain either kappa or lambda light chains, but not both. This phenomenon is termed isotypic kappa-lambda exclusion. While kappa-producing cells have their lambda chain genes in germline configuration, in most lambda-producing cells the kappa chain genes are either non-productively rearranged or deleted. To investigate the molecular mechanism for isotypic kappa-lambda exclusion, in particular the role of the Ig kappa intron enhancer, we replaced this enhancer by a neomycin resistance (neoR) gene in embryonic stem (ES) cells. B cells heterozygous for the mutation undergo V kappa-J kappa recombination exclusively in the intact Ig kappa locus but not in the mutated Ig kappa locus. Homozygous mutant mice exhibited no rearrangements in their Ig kappa loci. However, splenic B cell numbers were only slightly reduced as compared with the wild-type, and all B cells expressed lambda chain bearing surface Ig. These findings demonstrate that rearrangement in the Ig kappa locus is not essential for lambda gene rearrangement. We also generated homozygous mutant mice in which the neoR gene was inserted at the 3' end of the Ig kappa intron enhancer. Unexpectedly, mere insertion of the neoR gene showed some suppressive effect on V kappa-J kappa recombination. However, the much more pronounced inhibition of V kappa-J kappa recombination by the replacement of the Ig kappa intron enhancer suggests that this enhancer is essential for V kappa-J kappa recombination. 相似文献
993.
Induction of anthocyanin synthesis occurs during metabolic differentiation in carrot suspension cultured cells grown in medium lacking 2,4-dichlorophenoxyacetic acid (2,4-D), and is closely correlated with embryogenesis. Anthocyanin synthesis may also be induced by light-irradiation under different culture conditions. The phenylalanine ammonia-lyase (PAL) gene (TRN-PAL), which was transiently induced by the transfer effect, was also rapidly induced after light-irradiation. However, TRN-PAL was not involved in anthocyanin synthesis. A second PAL gene, ANT-PAL, was involved in anthocyanin synthesis. ANT-PAL was induced during metabolic differentiation in medium lacking 2,4-D parallel with the induction of chalcone synthase (CHS). PAL genes in the carrot genome are expressed differentially depending on the nature of the environmental stimulus, e.g. transfer effect and light, and other parameters which also affect anthocyanin synthesis.Abbreviations CHS
chalcone synthase
- 2,4-D
2,4-dichlorophenoxyacetic acid
- GUS
-glucuronidase
- Luc
firefly luciferase
- PAL
phenylalanine ammonia-lyase
- UV
ultraviolet 相似文献
994.
Satoshi Hamada Yoshiko Moriyama Koji Yamaguchi Kunio Takeda 《Journal of Protein Chemistry》1994,13(4):423-428
The peptide bond between Asp66-Pro67 of -lactalbumin was cleaved with formic acid (cleaved-lactalbumin). Secondary structural changes of the cleaved-lactalbumin, in which the two separated polypeptides were joined by disulfide bridges, were examined in solutions of sodium dodecyl sulfate (SDS), urea, and guanidine hydrochloride. The structural changes of the cleaved-lactalbumin were compared with those of the intact protein. The relative proportions of secondary structures were determined by curve fitting of the circular dichroism spectrum. The cleaved-lactalbumin contained 29%-helical structure as against 34% for the intact protein. Some helices of the cleaved-lactalbumin which had been disrupted by the cleavage appeared to be reformed upon the addition of SDS of very low concentration (0.5mM). In the SDS solution, the helicities of both the intact and cleaved proteins increased, attaining 44% at 4mM SDS. On the other hand, the helical structures of the cleaved-lactalbumin began to be disrupted at low concentrations of guanidine hydrochloride and urea compared with that of the intact protein. However, no diffrence was observed in the thermal denaturations of the intact and cleaved proteins, except for the difference in the original helicities. The helicities of both proteins decreased with an increase of temperature up to 65°C and recovered upon cooling. 相似文献
995.
To assess the effect of management of a park on soil arthropods, communities of Oribatida and Collembola were analyzed at
11 sites of different vegetation in Tsurumi Park, an urban park of Osaka City. The type of canopy layer and soil density strongly
affected the community parameters, such as species diversity. Ordination revealed that soil density, contents of organic matter,
and shrub layer were important for variety in the oribatid community; the shrub layer was important for the collembolan community.
Species richness of both arthropod groups was highest in a mixed forest and lowest on bare land, while the abundance of Collembola
was highest on a lawn site. Areas of a common vegetation type had a similar oribatid community;Trichogalumma nipponica dominated in deciduous forests,Eohypochthonius crassisetiger in mixed forests and one of coniferous forests. On the other hand, collembolan communities did not correspond with the vegetation.Sminthurinus sp. was collected from every site, and the most abundant species wasCryptopygus thermophilus that exhibited an outbreak on lawn sites. A significant correlation existed between species diversities but not between abundances
of Oribatida and Collembola. 相似文献
996.
P. Yuan A. Ogawa T. Ramamurthy G. B. Nair T. Shimada S. Shinoda T. Takeda 《World journal of microbiology & biotechnology》1994,10(1):59-63
Using a 0.27 kb DNA probe specific for the heat-stable enterotoxin gene (nag-st) of Vibrio cholerae non-O1, 1109 strains representing 17 species of the genus Vibrio, isolated from clinical and environmental sources were examined. The nag-st gene was preponderantly associated with strains classified as V. mimicus; 16.8% of these strains hybridized. It was more frequent in the clinical isolates (22.6%) than in the environmental isolates (13.7%). The incidence of nag-st gene-positive strains of V. mimicus isolated from different countries was uniformly high and ranged between 8.7% (Bangladesh) and 57.1% (environmental strains from USA). The incidence of the nag-st gene was much lower among strains of V. cholerae non-O1 (3.6%). Probe-positive and-negative strains of V. mimicus and V. cholerae non-O1 were used to evaluate the performance of the conventional suckling mouse assay for detection of the NAG-ST enterotoxin. Of the 31 probe-positive strains, only five (16.1%) yielded a positive fluid accumulation ratio (FA ratio) when neat heated culture supernatant was used to perform the suckling mouse assay. All the 31 probe-positive strains gave a positive FA ratio when 20-fold concentrated and heated culture supernatants of the strains were used to perform the suckling mouse assay. The need to concentrate (by at least 20-fold) the culture supernatant of strains of V. mimicus and V. Cholerae non-O1 was identified as an important step to obtain consistent results when using the suckling mouse assay for detection of NAG-ST.P. Yuan, A. Ogawa and T. Takeda are with the Department of Infectious Disease Research, National Children's Medical Research Center, 3-35-31 Taishido, Setagaya-ku, Tokyo 154, Japan; P. Yuan is also with the National Institute for the Control of Pharmaceutical and Biological Products, Beijing, China. T. Ramamurthy and G.B. Nair are with the National Institute of Cholera and Enteric Diseases, Calcutta, India. T. Shimada is with the National Institute of Health, Tokyo 141, Japan. S. Shinoda is with the Faculty of Pharmaceutical Sciences, Okayama University, Japan. 相似文献
997.
998.
999.
Crystals of the bacteriophage λ Cro repressor protein that are suitable for X-ray diffraction studies have been obtained. Preliminary crystallographic analysis reveals that the space group is R32, the cell dimensions in the hexagonal system are , and there are three dimers per asymmetric unit. 相似文献
1000.
In order to assess the natural photophase effective for controlling the pupal diapause of Hyphantria cunea, larvae were exposed in the long-day season to natural conditions of light (through a window) for a period of 14 hr, 50 min. This photophase included different portions of either the dawn or dusk twilight period. Since the critical photophase was found to be 14 hr 35 min under natural daylight as well as under conditions of artificial light, 50% diapause was expected when the twilight intensity reached the threshold level 15 min after the onset (dawn) or before the end (dusk) of the exposure. The threshold intensities of twilight thus determined showed a significant asymmetry, being about 1 and 10 lux at dawn and dusk, respectively. From this, it was inferred that the photophase under natural conditions would begin about 40 min before sunrise and end about 20 min after sunset. This asymmetry in sensitivity seems to be caused by the conditions (light or dark) to which the larval photo-receptive system has been exposed. The larvae that had been kept under artificial light of 180–200 lux for 14 hr were sensitive to a subsequent 1 hr exposure to 0.5 lux or greater and averted diapause, whereas those held under 9,000 lux failed to avert diapause even when the photophase was supplemented by light of 7.5 lux for 1 hr
Résumé De facon à évaluer la photophase naturelle efficace pour maîtriser la diapause nymphale de Hyphantria cunea, les chenilles ont été exposées pendant la saison aux jours longs aux conditions naturelles d'éclairement (à travers une fenêtre) pendant une période de 14 h 50 min. Puisqu'il a été établi que la photophase critique est de 14 h 35 min sous éclairement naturel aussi bien qu'artificiel, 50% de diapause était prévu quand l'intensité crépusculaire atteignait le seuil 15 min après le début (aube) ou avant la fin (crépuscule) de l'exposition. Les intensités-seuil crépusculaires ainsi déterminées ont présenté une asymétrie significative, étant respectivement de 1 à 10 lux à l'aube et au crépuscule. Il a été déduit de ces observations que la photophase en conditions naturelles commencerait environ 40 min avant le lever du soleil et se terminerait environ 20 min après son coucher. L'asymétrie de cette sensibilité semble être due aux conditions (lumière ou obscurité) auxquelles le système photo-récepteur des chenilles a été exposé. Les chenilles qui ont été maintenues pendant 14 h sous éclairage artificiel de 180–200 lux sont sensibles à une exposition ultérieure de 0,5 lux ou plus et évitent la diapause, tandis que celles maintenues à 9000 lux ou plus n'évitent pas la diapause quand la photophase est prolongée par un éclairement de 7,5 lux pendant une heure.相似文献