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911.
Tomohiro Ueda Tomohisa Takagi Kazuhiro Katada Takaya Iida Katsura Mizushima Osamu Dohi Tetsuya Okayama Naohisa Yoshida Kazuhiro Kamada Kazuhiko Uchiyama Osamu Handa Takeshi Ishikawa Hideyuki Konishi Yuji Naito Yukio Nagasaki Yoshito Itoh 《Biochemical and biophysical research communications》2018,495(2):2044-2049
Background
Intestinal ischemia-reperfusion (I-R) injury is a serious abdominal condition leading to multiple organ failure with high mortality. However, no reliable treatment is available. A redox nanoparticle (RNPO) was recently developed, and its efficacy for several intestinal inflammatory conditions has been reported. To this end, the aim of this study was to investigate the therapeutic effects of RNPO on intestinal I-R injury in mice.Methods
Ischemia was induced in the small intestine of C57BL/6 mice by occluding the superior mesenteric artery for 45 min under anesthesia followed by reperfusion for 4 h. Mice were orally administered the vehicle or RNPO 1 h before ischemia. Inflammatory markers such as histological findings, thiobarbituric acid (TBA)-reactive substances as an index of lipid peroxidation, myeloperoxidase (MPO) activity as an index of neutrophil infiltration, and expression of pro-inflammatory cytokine mRNA in the intestinal mucosa were assessed.Results
Induction of I-R caused a significant increase in inflammatory markers (histological scores, TBA-reactive substances, MPO activity, and expression of keratinocyte chemoattractant mRNA). These changes were significantly attenuated in RNPO-treated mice as compared to vehicle-treated mice.Conclusion
Orally administered RNPO attenuated intestinal I-R injury in mice in association with reductions in neutrophil infiltration and lipid peroxidation, suggesting the possibly potential of RNPO as a therapeutic agent for intestinal I-R injury. 相似文献912.
913.
914.
Clara Shionyu-Mitsuyama Atsushi Hijikata Toshiyuki Tsuji Tsuyoshi Shirai 《Journal of structural and functional genomics》2016,17(4):135-146
The fast heuristic graph match algorithm for small molecules, COMPLIG, was improved by adding a structural superposition process to verify the atom–atom matching. The modified method was used to classify the small molecule ligands in the Protein Data Bank (PDB) by their three-dimensional structures, and 16,660 types of ligands in the PDB were classified into 7561 clusters. In contrast, a classification by a previous method (without structure superposition) generated 3371 clusters from the same ligand set. The characteristic feature in the current classification system is the increased number of singleton clusters, which contained only one ligand molecule in a cluster. Inspections of the singletons in the current classification system but not in the previous one implied that the major factors for the isolation were differences in chirality, cyclic conformations, separation of substructures, and bond length. Comparisons between current and previous classification systems revealed that the superposition-based classification was effective in clustering functionally related ligands, such as drugs targeted to specific biological processes, owing to the strictness of the atom–atom matching. 相似文献
915.
Georges St. Laurent Yuri Vyatkin Denis Antonets Maxim Ri Yao Qi Olga Saik Dmitry Shtokalo Michiel?J.L. de?Hoon Hideya Kawaji Masayoshi Itoh Timo Lassmann Erik Arner Alistair R.R. Forrest The FANTOM consortium Estelle Nicolas Timothy A. McCaffrey Piero Carninci Yoshihide Hayashizaki Claes Wahlestedt Philipp Kapranov 《Nucleic acids research》2016,44(7):3233-3252
916.
Tomi T Shibata Y Ikeda Y Taniguchi S Haik C Mataga N Shimada K Itoh S 《Biochimica et biophysica acta》2007,1767(1):22-30
A photosynthetic reaction center (RC) complex was isolated from a purple bacterium, Acidiphilium rubrum. The RC contains bacteriochlorophyll a containing Zn as a central metal (Zn-BChl a) and bacteriopheophytin a (BPhe a) but no Mg-BChl a. The absorption peaks of the Zn-BChl a dimer (P(Zn)), the accessory Zn-BChl a (B(Zn)), and BPhe a (H) at 4 K in the RC showed peaks at 875, 792, and 753 nm, respectively. These peaks were shorter than the corresponding peaks in Rhodobacter sphaeroides RC that has Mg-BChl a. The kinetics of fluorescence from P(Zn)(*), measured by fluorescence up-conversion, showed the rise and the major decay with time constants of 0.16 and 3.3 ps, respectively. The former represents the energy transfer from B(Zn)(*) to P(Zn), and the latter, the electron transfer from P(Zn) to H. The angle between the transition dipoles of B(Zn) and P(Zn) was estimated to be 36 degrees based on the fluorescence anisotropy. The time constants and the angle are almost equal to those in the Rb. sphaeroides RC. The high efficiency of A. rubrum RC seems to be enabled by the chemical property of Zn-BChl a and by the L168HE modification of the RC protein that modifies P(Zn). 相似文献
917.
Fukumoto K Kikuchi S Itoh N Tamura A Hata M Yamagishi H Tsukita S Tsukita S 《Biochimica et biophysica acta》2007,1772(3):298-306
ERM (ezrin/radixin/moesin) proteins are organizers of apical actin cortical layer in general. We previously reported that the knockout of radixin resulted in Rdx(-/-) mice with displacement/loss of the canalicular transporter Mrp2, giving rise to Dubin-Johnson syndrome-like conjugated hyperbilirubinemia in the mixed genetic background (C57BL/6-129/Sv) (Kikuchi, et al. (2002) Nature Genetics 31, 320-325). However, when these mice were kept under mixed genetic background for years (late mixed backgrounds; LMB), the conjugated hyperbilirubinemia gradually became inconspicuous, while evidence of liver injury increased. We examined the effect of genetic background by backcrossing LMB Rdx(-/-) mice to C57BL/6 and 129/Sv wild type mice with the result that the Rdx(-/-) congenic mice regained hyperbilirubinemia with reduced hepatocellular damage. As revealed by immunofluorescence and western blots, the localization/expression of apical transporters, Mrp2, CD26, P-gps, and Bsep were not influenced by backcrossing, though those of a basolateral transporter, Mrp3, were strikingly increased by backcrossing. 相似文献
918.
919.
We studied five carcinogens for (a) organ-specific mutagenicity and expression time in the transgenic (TG) mouse mutation assay and (b) clastogenicity in the peripheral blood micronucleus assay in the same mice. Groups of mice were injected intraperitoneally (ip) with N-nitroso-di-n-propylamine (NDPA), propylnitrosourea (PNU), 7, 12-dimethylbenz[a]anthracene (DMBA), 4-nitroquinoline-1-oxide (4NQO), or procarbazine (PCZ); 4NQO was also administered orally. LacZ mutant frequencies (MF) of various organs, sampled 7, 14 and 28 days after treatment, were analyzed by galE positive selection. At least 5 organs were analyzed in each experiment. Bone marrow, liver, and testis were always analyzed, as were each chemical's target organs. All chemicals, except NDPA, induced micronuclei. All chemicals increased lacZ MF in all of their target organs for carcinogenesis and, to a lesser extent, in some non-target organs. That suggests that an organ that has a positive response to a chemical in the TG mouse mutation assay is likely to develop tumors on exposure to that chemical, but it does not always happen. The time-course of MF increases (7-28 days) differed among tissues. In general, time-dependent increase in MF occurred in organs with a low cell proliferation rate whereas no increase, or even a decrease, occurred in organs with a high proliferation rate. Our results demonstrated that the TG mouse mutation assay is effective for the detection of chemical mutagenesis in the target organs for carcinogenesis, and organ and time-course variations in chemical mutagenesis are important issues for the establishment of an optimal protocol for the assay. 相似文献
920.
Shin-ya Miyagishima Ryuuichi Itoh Kyoko Toda Haruko Kuroiwa Tsuneyoshi Kuroiwa 《Planta》1999,207(3):343-353
The time courses of chloroplast and mitochondrial division and the morphological changes in the plastid-dividing ring (PD
ring) and mitochondrion-dividing ring (MD ring) during chloroplast and mitochondrial division were studied in Cyanidioschyzon merolae De Luca, Taddei and Varano. To accomplish this, chloroplast and cell division of living cells were continuously video-recorded
under light microscopy, and the morphological changes in the PD and MD rings were analyzed quantitatively and three-dimensionally
by transmission electron microscopy (TEM). Under the light microscope, the diameters of the chloroplast and the cell decreased
at uniform velocities, the speed depending on the temperature. To study in detail the sequential morphological change of the
mitochondrion in M phase and the contractile mechanism in the divisional planes of the chloroplast and the mitochondrion,
we observed the PD and MD rings, which are believed to promote contraction, under TEM, using the diameter of the chloroplast
as an index of the time. Three PD rings (an outer PD ring on the cytoplasmic face of the outer envelope, a middle PD ring
in the intermembrane space, and an inner PD ring on the stromal face of the inner envelope) were clearly observed, but only
the outer MD ring could be observed. The PD ring started to contract soon after it formed, while the contraction of the MD
ring did not occur immediately after formation, but was delayed until the contraction of the PD ring was almost complete.
Once the MD ring began to contract, the rate of decrease of its circumference was 4 times as high as that of the PD ring.
As the outer PD and MD rings contracted, they grew thicker and maintained a constant volume, while the thickness of the inner
PD ring did not change and its volume decreased at a constant rate with contraction. In the early stage of contraction, the
widths of the three PD rings increased in order, from the outer to the inner ring. With contraction, their widths changed
at different rates until they came to have much the same width. In cross-section, the MD ring was wider where it was next
to the chloroplast than at the opposite side, adjacent to the nucleus in the early stage of contraction. By the late stage,
the widths of the two sides became equal. In our observations, the microbody elongated along the outer MD ring and touched
the outer PD ring during contraction of the PD and MD rings. These results clearly revealed differences between the mode of
contraction of the outer, middle, and inner PD rings, and between the PD and the MD rings. They also revealed the coordinated
widening of the three PD rings, and suggested that the microbody plays a role in the contraction of the PD and MD rings.
Received: 1 July 1998 / Accepted: 1 September 1998 相似文献