全文获取类型
收费全文 | 3048篇 |
免费 | 134篇 |
国内免费 | 1篇 |
出版年
2023年 | 11篇 |
2022年 | 11篇 |
2021年 | 42篇 |
2020年 | 32篇 |
2019年 | 34篇 |
2018年 | 50篇 |
2017年 | 31篇 |
2016年 | 59篇 |
2015年 | 108篇 |
2014年 | 128篇 |
2013年 | 201篇 |
2012年 | 171篇 |
2011年 | 206篇 |
2010年 | 109篇 |
2009年 | 119篇 |
2008年 | 181篇 |
2007年 | 183篇 |
2006年 | 177篇 |
2005年 | 181篇 |
2004年 | 193篇 |
2003年 | 170篇 |
2002年 | 171篇 |
2001年 | 45篇 |
2000年 | 28篇 |
1999年 | 42篇 |
1998年 | 41篇 |
1997年 | 27篇 |
1996年 | 22篇 |
1995年 | 23篇 |
1994年 | 20篇 |
1993年 | 24篇 |
1992年 | 29篇 |
1991年 | 30篇 |
1990年 | 29篇 |
1989年 | 24篇 |
1988年 | 16篇 |
1987年 | 21篇 |
1986年 | 9篇 |
1985年 | 16篇 |
1984年 | 17篇 |
1983年 | 14篇 |
1982年 | 17篇 |
1981年 | 10篇 |
1979年 | 23篇 |
1978年 | 9篇 |
1977年 | 9篇 |
1976年 | 14篇 |
1974年 | 9篇 |
1973年 | 7篇 |
1971年 | 8篇 |
排序方式: 共有3183条查询结果,搜索用时 15 毫秒
1.
Replication of X chromosomes in complete moles 总被引:1,自引:0,他引:1
Summary DNA replication patterns of X chromosomes in complete hydatidiform moles were studied using cultured fibroblasts from three 46,XX moles resulting from duplication of a haploid sperm, and from a 46,XY mole originating from dispermy. Control cultures included skin fibroblasts from an adult woman and a female fetus as well as PB lymphocytes from an adult woman. Cultures were treated with 5-bromodeoxyuridine for the last 2–4h of the S phase, and the chromosome slides prepared were stained by the Hoechst 33258-Giemsa procedure. Each of the three XX moles studied revealed one early-replicating and one late-replicating X chromosomes, while the XY mole revealed one early-replicating X chromosome. DNA replication patterns of molar X chromosomes were similar to those of adult and fetal fibroblasts, but different from those in adult lymphocytes. These findings indicate that DNA replication kinetics of molar fibroblasts are tissue-specific rather than origin- or developmental-stage specific. 相似文献
2.
3.
Mutations in the profilin 1 (PFN1) gene have been identified as a cause of familial amyotrophic lateral sclerosis (ALS), and neuropathological studies indicate that TDP-43 is accumulated in brains of patients with PFN1 mutation. Here, we investigated the role of PFN1 mutations in the formation of prion-like abnormal TDP-43. Expression of PFN1 with pathogenic mutations resulted in the formation of cytoplasmic aggregates positive for p62 and ubiquitin, and these aggregates sequestered endogenous TDP-43. TDP-43 accumulation was facilitated in the presence of proteasome or lysosome inhibitor. Co-expression of mutant PFN1 and TDP-43 increased the levels of detergent-insoluble and phosphorylated TDP-43, and this increase required the C-terminal region of TDP-43. Moreover, detergent-insoluble fractions prepared from cells expressing ALS-linked mutant PFN1 induced seed-dependent accumulation of TDP-43. These findings indicate that expression of PFN1 mutants induces accumulation of TDP-43, and promotes conversion of normal TDP-43 into an abnormal form. These results provide new insight into the mechanisms of TDP-43 proteinopathies and other diseases associated with amyloid-like protein deposition. 相似文献
4.
Takayoshi Kano 《Primates; journal of primatology》1982,23(3):453-457
Pygmy chimpanzees (Pan paniscus) of Wamba sometimes put leafy twigs on their bodies in a rain. In some cases, those twigs seemed to be effective against
the rain-impact. There is no record that common chimpanzees (Pan troglodytes) show the same behaviour, but similar or more elaborate use of twigs as rain cover is recorded among orang-utans (Pongo pygmaeus). 相似文献
5.
Nai-Chi Chen Masato Yoshimura Hong-Hsiang Guan Ting-Yu Wang Yuko Misumi Chien-Chih Lin Phimonphan Chuankhayan Atsushi Nakagawa Sunney I. Chan Tomitake Tsukihara Tzong-Yueh Chen Chun-Jung Chen 《PLoS pathogens》2015,11(10)
Betanodaviruses cause massive mortality in marine fish species with viral nervous necrosis. The structure of a T = 3 Grouper nervous necrosis virus-like particle (GNNV-LP) is determined by the ab initio method with non-crystallographic symmetry averaging at 3.6 Å resolution. Each capsid protein (CP) shows three major domains: (i) the N-terminal arm, an inter-subunit extension at the inner surface; (ii) the shell domain (S-domain), a jelly-roll structure; and (iii) the protrusion domain (P-domain) formed by three-fold trimeric protrusions. In addition, we have determined structures of the T = 1 subviral particles (SVPs) of (i) the delta-P-domain mutant (residues 35−217) at 3.1 Å resolution; and (ii) the N-ARM deletion mutant (residues 35−338) at 7 Å resolution; and (iii) the structure of the individual P-domain (residues 214−338) at 1.2 Å resolution. The P-domain reveals a novel DxD motif asymmetrically coordinating two Ca2+ ions, and seems to play a prominent role in the calcium-mediated trimerization of the GNNV CPs during the initial capsid assembly process. The flexible N-ARM (N-terminal arginine-rich motif) appears to serve as a molecular switch for T = 1 or T = 3 assembly. Finally, we find that polyethylene glycol, which is incorporated into the P-domain during the crystallization process, enhances GNNV infection. The present structural studies together with the biological assays enhance our understanding of the role of the P-domain of GNNV in the capsid assembly and viral infection by this betanodavirus. 相似文献
6.
Medha Raina Adil Moghal Amanda Kano Mathew Jerums Paul D. Schnier Shun Luo Rohini Deshpande Pavel V. Bondarenko Henry Lin Michael Ibba 《The Journal of biological chemistry》2014,289(25):17780-17790
Quality control operates at different steps in translation to limit errors to approximately one mistranslated codon per 10,000 codons during mRNA-directed protein synthesis. Recent studies have suggested that error rates may actually vary considerably during translation under different growth conditions. Here we examined the misincorporation of Phe at Tyr codons during synthesis of a recombinant antibody produced in tyrosine-limited Chinese hamster ovary (CHO) cells. Tyr to Phe replacements were previously found to occur throughout the antibody at a rate of up to 0.7% irrespective of the identity or context of the Tyr codon translated. Despite this comparatively high mistranslation rate, no significant change in cellular viability was observed. Monitoring of Phe and Tyr levels revealed that changes in error rates correlated with changes in amino acid pools, suggesting that mischarging of tRNATyr with noncognate Phe by tyrosyl-tRNA synthetase was responsible for mistranslation. Steady-state kinetic analyses of CHO cytoplasmic tyrosyl-tRNA synthetase revealed a 25-fold lower specificity for Tyr over Phe as compared with previously characterized bacterial enzymes, consistent with the observed increase in translation error rates during tyrosine limitation. Functional comparisons of mammalian and bacterial tyrosyl-tRNA synthetase revealed key differences at residues responsible for amino acid recognition, highlighting differences in evolutionary constraints for translation quality control. 相似文献
7.
Complete nucleotide sequences of the infectious cloned DNA components (DNA 1 and DNA 2) of mung bean yellow mosaic virus (MYMV) were determined. MYMV DNA 1 and DNA 2 consists of 2,723 and 2,675 nucleotides respectively. DNA 1 and DNA 2 have little sequence similarity except for a region of approximately 200 bases which is almost identical in the two molecules. Analysis of open reading frames revealed nine potential coding regions for proteins of mol. wt. > 10,000, six in DNA 1 and three in DNA 2. The nucleotide sequence of MYMV DNA was compared with that of bean golden mosaic virus (BGMV), tomato golden mosaic virus (TGMV) and African cassava mosaic virus (ACMV). The 200-base region common to the two DNAs of each virus had little sequence similarity, except for a highly conserved 33-36 base sequence potentially capable of forming a stable hairpin structure. The potential coding regions in the MYMV DNAs had counterparts in the BGMV, TGMV and ACMV, suggesting an overall similarity in genome organization, except for absence of 1L3 in MYMV DNA 1. The most highly conserved ORFs, MYMV 1R1, BGMV 1R1, TGMV 1R1 and ACMV 1R1, are the putative genes for the coat proteins of MYMV, BGMV, TGMV and ACMV, respectively. MYMV 1L1 has also a high degree of sequence similarity with BGMV 1L1, TGMV 1L1 and ACMV 1L1. 相似文献
8.
Yuichiro Higuchi Kenji Kawai Masahumi Yamamoto Miyuki Kuronuma Yasuhiko Ando Ikumi Katano Masato Nakamura Hiroshi Suemizu 《Experimental Animals》2014,63(1):55-62
The interaction between transplanted cells and host tissues is important for the growth
and maintenance of transplanted cells. To analyze the mechanisms of these interactions, a
systemic fluorescent protein-expressing mouse is a useful recipient. In this study, we
generated a novel NOG strain, which strongly expresses enhanced green fluorescent protein
(EGFP; PgkEGFP-NOG), especially in the liver, kidney, gastrointestinal tract, and testis.
Because the host tissues expressed EGFP, xenotransplanted human cancer cells were clearly
identified as EGFP-negative colonies in PgkEGFP-NOG mice. Immunohistochemical analysis
revealed that EGFP-expressing stromal tissues formed a complicated tumor microenvironment
within xenograft tissues. Moreover, a similar microenvironment was observed in human iPS
cell-derived teratomas. Collectively, these results indicated that a suitable
microenvironment is essential for the growth and maintenance of xenotransplanted cells and
that PgkEGFP-NOG mice represent a useful animal model for analyzing the mechanisms of
microenvironment formation. 相似文献
9.
Masato Asahina Toshio Niimura Tsutomu Yamaha Terue Takahashi 《Bioscience, biotechnology, and biochemistry》2013,77(5):711-718
The assimilation of sodium cyclamate (CHS-Na) by microorganisms was studied. Fifteen strains of cyclamate-assimilating bacteria were isolated from the feces of guinea pig excreting cyclohexylamine (CHA) in urine. The majority of the strain isolated seems to belong to the genera Pseudomonas and Corynebacterium. All strains were able to assimilate CHS-Na as a sole source of carbon and nitrogen, and accumulated clearly CHA in the culture medium. It was confirmed with the cell-free extract that the strains possessed the enzyme system which formed cyclohexanone (CHnone) from CHS-Na via CHA. It seems that the desulfation of CHS-Na to CHA is catalyzed by hydrolase, and that the deamination of CHA to CHnone is catalyzed by amine oxidase depending on oxygen. 相似文献
10.