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101.
H Kamei 《Cell biology international reports》1989,13(3):291-300
AC54 monoclonal antibody (MAb), an anti-desmin MAb, recognizes both intermediate filaments (IFs) and nuclear granules in BHK21/C13 cells. To investigate nuclear granules, similar MAbs were obtained by using desmin fraction as an antigen. Among them, DSB389 MAb recognized mainly nuclear granules in HeLa and rat liver cells. The nuclear granules in HeLa cells were aligned in arrays, sometimes connected by, or part of, a rope-like structure, and stable against treatment with 0.5% Triton X-100 and 2 M NaCl. They located on or around the chromosomes during mitosis. Essentially the same results were obtained with DSB860 and AC54 MAbs. The distribution of the granules in liver nuclei recognized by DSB389 MAb was similar to that of DNA and was different from that of the nuclear pore complexes. The biological significance of the nuclear granules is discussed. 相似文献
102.
Kamei K Wu X Xu X Minami K Huy NT Takano R Kato H Hara S 《Analytical biochemistry》2001,295(2):203-213
Evanescent wave biosensor has been recently employed as a powerful tool for analyses of macromolecular interactions. In the present study, evanescent wave biosensor analysis was developed to analyze the heparin-protein interaction using as ligands a series of heparin derivatives regioselectively desulfated by chemical methods, particularly to evaluate the effect of each sulfate group of heparin. The method for immobilizing heparin on the cuvette of the evanescent wave biosensor equipment was optimized to obtain the high response required for accurate measurement. The best result was achieved when the amino group introduced at the reducing end of heparin was coupled with carboxymethyl dextran on the surface of the cuvette using glycolchitosan as a multivalent linker. The established system appeared to describe well the interactions of heparin with such proteins as acidic and basic fibroblast growth factors and tissue factor pathway inhibitor. 相似文献
103.
Facile enzymatic conversion of lactose into lacto-N-tetraose and lacto-N-neotetraose 总被引:1,自引:0,他引:1
Lacto-N-tetraose (Galbeta1 -3GlcNAcbeta1-3Galbeta1-4Glc, LNT) and lacto-N-neotetraose (Galbeta1-4GlcNAcbeta1-3Galbeta1-4Glc, LNnT) were enzymatically synthesized by consecutive additions of GlcNAc and Gal residues to lactose. Lacto-N-triose II (GlcNAcbeta1-3Galbeta1-4Glc) was prepared first by the transfer of GlcNAc from UDP-GlcNAc to lactose by beta-1,3-N-acetylglucosaminyltransferase from bovine serum. The resulting lacto-N-triose II was converted into LNT and LNnT utilizing two kinds of beta-D-galactosidase-mediated transglycosylations. Thus, beta-D-galactosidase from Bacillus circulans ATCC31382 induced regioselective galactosyl transfer from o-nitrophenyl beta-D-galactoside to the OH-3" position of lacto-N-triose II, and commercially available beta-D-galactosidase from B. circulans to the OH-4" position of lacto-N-triose II. These convenient processes are suitable for large-scale preparations of LNT and LNnT. As another method, LNT was directly synthesized from lactose as an initial substance, utilizing lacto-N-biosidase (Aureobacterium sp. L-101)-mediated transglycosylation with Galbeta1-3GlcNAcbeta-pNP donor. 相似文献
104.
Increased numbers of B-1 cells and enhanced responses against TI-2 antigen in mice lacking APS, an adaptor molecule containing PH and SH2 domains 下载免费PDF全文
Iseki M Kubo C Kwon SM Yamaguchi A Kataoka Y Yoshida N Takatsu K Takaki S 《Molecular and cellular biology》2004,24(6):2243-2250
APS (adaptor molecule containing PH and SH2 domains) is an intracellular adaptor protein that forms an adaptor family along with Lnk and SH2-B. While experiments using cultured cell lines have demonstrated that APS is phosphorylated in response to various stimuli, its in vivo functions remain unclear. We attempted to determine the physiological roles of APS by generating APS-deficient (APS(-/-)) mice. APS(-/-) mice were viable and fertile and showed no abnormalities or growth retardation. Immunologically, APS(-/-) mice showed normal development and distribution of lymphocytes and myeloid cells, except for increased numbers of B-1 cells in the peritoneal cavity. APS(-/-) mice exhibited an enhanced humoral immune response against trinitrophenol-Ficoll, a thymus-independent type 2 antigen, while APS(-/-) B-2 cells exhibited normal proliferative responses and tyrosine phosphorylation of intracellular proteins upon B-cell receptor (BCR) cross-linking. APS colocalized with filamentous actin (F-actin) accumulated during the capping of BCRs in APS-transgenic B cells. After BCR stimulation, F-actin contents were lower in APS(-/-) B-1 cells than in wild-type B-1 cells. Our results indicate that APS might have a novel regulatory role in actin reorganization and control of B-1 cell compartment size. 相似文献
105.
Chloroplast phylogeny indicates that bryophytes are monophyletic 总被引:3,自引:0,他引:3
Nishiyama T Wolf PG Kugita M Sinclair RB Sugita M Sugiura C Wakasugi T Yamada K Yoshinaga K Yamaguchi K Ueda K Hasebe M 《Molecular biology and evolution》2004,21(10):1813-1819
Opinions on the basal relationship of land plants vary considerably and no phylogenetic tree with significant statistical support has been obtained. Here, we report phylogenetic analyses using 51 genes from the entire chloroplast genome sequences of 20 representative green plant species. The analyses, using translated amino acid sequences, indicated that extant bryophytes (mosses, liverworts, and hornworts) form a monophyletic group with high statistical confidence and that extant bryophytes are likely sisters to extant vascular plants, although the support for monophyletic vascular plants was not strong. Analyses at the nucleotide level could not resolve the basal relationship with statistical confidence. Bryophyte monophyly inferred using amino acid sequences has a good statistical foundation and is not rejected statistically by other data sets. We propose bryophyte monophyly as the currently best hypothesis. 相似文献
106.
Kentaro?HayashiEmail author Masanori?Okazaki Norihiro?Itsubo Atsushi?Inaba 《The International Journal of Life Cycle Assessment》2004,9(1):13-22
Background Acidification is one of the important impact categories for life cycle impact assessment. Although its characterization has
progressed during this decade through the employment of midpoint approaches, only limited studies of endpoint approaches have
been performed. Objective. This study aimed at developing damage function of acidification for terrestrial ecosystems in Japan.
Damage function expresses a quantitative relationship between the inventory and endpoint damage.
Methods The geographical boundary was limited in Japan both for emission and impact. In this study, sulfur dioxide (SO2), nitrogen monoxide (NO), nitrogen dioxide (NO2) (NO and NO2 collectively mean NOx), hydrogen chloride (HC1), and ammonia (NH3) were considered as major causative substances of acidification. Net primary production (NPP) of existing vegetation was
adopted as an impact indicator of terrestrial ecosystems. The aluminum toxicity was adopted as the major factor of effect
on terrestrial ecosystems due to acidification. The leachate concentration of monomeric inorganic aluminum ions was selected
to express the plant toxicity of aluminum.
Results and Discussion The results of damage function gave utilizable factors both for a midpoint approach and an endpoint approach; Atmospheric
Deposition Factor (ADF) and Damage Factor (DF) applicable to the former and the latter, respectively. The ADF indicates an
increase of H+ deposition per unit area to an additional emission of causative sustance. The additional emission corresponds to some alternatives
in industry, not the baseline emission. The DF indicates the total NPP damage in all of Japan due to the additional emission
of causative substances. The derived NPP damage is on the order of one millionth of the NPP itself. HC1 and NH3 showed larger
ADFs and DFs than that of SO2 and NOx. The reason was ascribed to the relatively large source-receptor relationships (SRR) of HC1 and NH3. However, since the method applied to determine the SRR of HC1 and NH3 has larger uncertainties than that of SO2 and NOx, attention is needed to handle the difference.
Conclusion The damage function easily defines the concrete NPP damage due to an additional emission. The impact indica tor, NPP, also
has an advantage in its mass unit that is directly summable through the entire impact categories. Expansion of endpoints,
such as in aquatic ecosystems, material degradation, human health, and biodiversity aspects of terrestrial ecosystems, is
an important subject for future work. Further, uncertain analyses for major parameters will provide helpful information on
the reliability of damage function. 相似文献
107.
Role of follicular dendritic cells in the early HIV-1 infection: in vitro model without specific antibody 总被引:2,自引:0,他引:2
Taruishi M Terashima K Dewan Z Yamamoto N Ikeda S Kobayashi D Eishi Y Yamazaki M Furusaka T Sugimoto M Ishii M Kitamura K Yamamoto N 《Microbiology and immunology》2004,48(9):693-702
About 90% of HIV-1 RNA in the lymph nodes is reported to localize in follicular dendritic cellsnetwork (FDC-NW) as early as several days after infection and as much as that in the late stage. But the mechanism remains to be fully understood. To elucidate the role of follicular dendritic cells (FDC) in the early stage of HIV-1 infection, FDC-like cell strains (FDCLC) were established and they were characterized in the co-culture system with T cells for their effect on HIV-1 trapping and replication in p24 immunoassay, immunohistochemistry as well as confocal and electronmicroscopy. Established FDCLC were positive for CNA-42, S-100alpha and intercellular desmosome-like junctions. L-SIGN and DC-SIGN were also detected in FDCLC. Alu-HIV-1 PCR analysis showed no HIV-1 integration in FDCLC. FDCLC trapped HIV-1 and transferred them to uninfected MOLT-4 T cells (MOLT-4) efficiently in the absence of specific antibody. FDCLC also accelerated HIV-1 replication in HIV-1-pre-exposed MOLT-4. These unique FDCLC effects were explained, at least partly, by the fact that FDCLC up-regulated CD4 expression in MOLT-4 and helped T cells escape from apoptosis in the co-culture. These data suggest that FDC/FDCLC engage not only in trapping but also in active expansion of HIV-1 in the absence of specific antibody. 相似文献
108.
Murakami N Tamura S Koyama K Sugimoto M Maekawa R Kobayashi M 《Bioorganic & medicinal chemistry letters》2004,14(10):2597-2601
Two analogues possessing steric hindered substituents on C-15 of arenastatin A (1), a potent cytotoxic spongean depsipeptide, were synthesized and shown to enhance stability in mouse serum. Notably, 15-tert-butylanalogue (6) with higher cytotoxicity exhibited in vivo anti-tumor activity through iv administration different from 1. Additionally, conformation analysis among the two analogues and arenastatin A (1) indicated that the torsion angle from C-14 to C-20 is a conclusive factor for the potent cytotoxicity of 1. 相似文献
109.
Tanaka M Sagawa S Hoshi J Shimoma F Matsuda I Sakoda K Sasase T Shindo M Inaba T 《Bioorganic & medicinal chemistry letters》2004,14(20):5171-5174
We report herein synthesis of PKCbeta-selective inhibitors possessing the novel pharmacophore of anilino-monoindolylmaleimide. Several compounds of this series exhibited IC50's as low as 50 nM against human PKCbeta2. One of the most potent compounds, 6l, inhibited PKCbeta1 and PKCbeta2 with IC50 of 21 and 5 nM, respectively, and exhibited selectivity of more than 60-fold in favor of PKCbeta2 relative to other PKC isozymes (PKCalpha, PKCgamma, and PKCepsilon). 相似文献
110.
Qing G Ma LC Khorchid A Swapna GV Mal TK Takayama MM Xia B Phadtare S Ke H Acton T Montelione GT Ikura M Inouye M 《Nature biotechnology》2004,22(7):877-882
Overexpression of proteins in Escherichia coli at low temperature improves their solubility and stability. Here, we apply the unique features of the cspA gene to develop a series of expression vectors, termed pCold vectors, that drive the high expression of cloned genes upon induction by cold-shock. Several proteins were produced with very high yields, including E. coli EnvZ ATP-binding domain (EnvZ-B) and Xenopus laevis calmodulin (CaM). The pCold vector system can also be used to selectively enrich target proteins with isotopes to study their properties in cell lysates using NMR spectroscopy. We have cloned 38 genes from a range of prokaryotic and eukaryotic organisms into both pCold and pET14 (ref. 3) systems, and found that pCold vectors are highly complementary to the widely used pET vectors. 相似文献