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151.
Jinyoung Hur Mi Jung Kim Young-Wuk Cho 《Biochemical and biophysical research communications》2010,391(3):1526-59
Although glial cells play a major role in the pathogenesis of many neurological diseases by exacerbating neuronal and non-neuronal cell death, the mechanisms involved are unclear. We examined the effects of microglia-(MCM) or astrocyte-(ACM) conditioned media obtained by chemical ischemia on the neuronal injury in SH-SY5Y cells. Chemical ischemia was induced by the treatment with NaN3 and 2-deoxy-d-glucose for 2 h. MCM-treated SH-SY5Y cells showed reduced the viability, increased caspase-3 activity, decreased Bcl-2/Bax ratio, and increased cytochrome c release, increased inflammatory cytokines, and increased reactive oxygen species (ROS) generation. MCM also increased gp91phox nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, which was inhibited by NADPH oxidase inhibitor, apocynin, and gp91phox siRNA. However, ACM did not show any significant changes. The results suggest that microglia activated by ischemic insult may increase reactive oxygen species generation via activation of gp91phox NADPH oxidase, resulting in neuronal injury. 相似文献
152.
Aspicilia humida Lee is described as a new lichen-forming fungus from a wetland forest, South Korea. The new species is distinguishable from Aspicilia aquatica (Fr.) Körb., the most similar species, by the absence of prothallus, black disk without green color in water, olive-brown epihymenium, shorter hymenium, hymenium I + yellowish blue-green, wider paraphysial tips without a vivid pigment, smaller asci, smaller ascospores, and the presence of stictic acid. Molecular analyses employing internal transcribed spacer (ITS) and mitochondrial small subunit (mtSSU) sequences strongly support A. humida as a distinct species in the A. cinerea group. A surrogate key is provided to assist in the identification of all 28 aspicilioid species of Korea. 相似文献
153.
M Yamada S J Hur K Hashinaka K Tsuneoka T Saeki C Nishio F Sakiyama S Tsunasawa 《Archives of biochemistry and biophysics》1987,255(1):147-155
A cDNA encoding the carboxyl-terminal fragment of the human myeloperoxidase heavy chain was isolated and characterized. It was then used to determine the locations of the myeloperoxidase light and heavy chains in the polypeptide precursor. A cDNA library from poly(A)+ RNA from human leukemia HL-60 cells was constructed in pBR322 and screened by differential hybridization with enriched and depleted cDNA probes and then by hybridization with an oligonucleotide probe. A cDNA clone containing 1278 bp with an open reading frame of 474 bp and a 3' noncoding region of 804 bp was isolated. The amino acid sequence deduced from the nucleotide sequence consisted of 158 residues including a sequence of 14 amino acids known to be present in the heavy chain of the molecule. The cDNA also included a stop codon of TAG followed by a noncoding sequence that included a potential recognition site for polyadenylylation and a poly(A) tail. RNA transfer blot analysis with the cDNA probe indicated that myeloperoxidase mRNA was approximately 3.3 kb in length. In vitro translation of the mRNA selected by cDNA hybridization revealed preferential synthesis of a 74,000-Da polypeptide precursor that could be precipitated with anti-myeloperoxidase IgG. Antibodies specific for the heavy and light chains of myeloperoxidase were isolated from antiserum by affinity chromatography employing Sepharose columns covalently bound to the heavy or light chains. Antibodies specific for the light chain or the heavy chain readily precipitated the 74,000-Da precursor polypeptide. These results indicated that myeloperoxidase is synthesized as a single chain which undergoes processing into a light and heavy chain. Furthermore, the heavy chain of myeloperoxidase originates from the carboxyl terminus of the precursor polypeptide. 相似文献
154.
Induction of thioredoxin is required for nodule development to reduce reactive oxygen species levels in soybean roots 总被引:7,自引:0,他引:7 下载免费PDF全文
Lee MY Shin KH Kim YK Suh JY Gu YY Kim MR Hur YS Son O Kim JS Song E Lee MS Nam KH Hwang KH Sung MK Kim HJ Chun JY Park M Ahn TI Hong CB Lee SH Park HJ Park JS Verma DP Cheon CI 《Plant physiology》2005,139(4):1881-1889
Nodules are formed on legume roots as a result of signaling between symbiotic partners and in response to the activities of numerous genes. We cloned fragments of differentially expressed genes in spot-inoculated soybean (Glycine max) roots. Many of the induced clones were similar to known genes related to oxidative stress, such as thioredoxin and beta-carotene hydroxylase. The deduced amino acid sequences of full-length soybean cDNAs for thioredoxin and beta-carotene hydroxylase were similar to those in other species. In situ RNA hybridization revealed that the thioredoxin gene is expressed on the pericycle of 2-d-old nodules and in the infected cells of mature nodules, suggesting that thioredoxin is involved in nodule development. The thioredoxin promoter was found to contain a sequence resembling an antioxidant responsive element. When a thioredoxin mutant of yeast was transformed with the soybean thioredoxin gene it became hydrogen peroxide tolerant. These observations prompted us to measure reactive oxygen species levels. These were decreased by 3- to 5-fold in 7-d-old and 27-d-old nodules, coincident with increases in the expression of thioredoxin and beta-carotene hydroxylase genes. Hydrogen peroxide-producing regions identified with cerium chloride were found in uninoculated roots and 2-d-old nodules, but not in 7-d-old and 27-d-old nodules. RNA interference-mediated repression of the thioredoxin gene severely impaired nodule development. These data indicate that antioxidants such as thioredoxin are essential to lower reactive oxygen species levels during nodule development. 相似文献
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156.
Antibiotic evaluation and in vivo analysis of alkynyl Coenzyme A antimetabolites in Escherichia coli
Mercer AC Meier JL Hur GH Smith AR Burkart MD 《Bioorganic & medicinal chemistry letters》2008,18(22):5991-5994
Pantothenamides have been the subject of much study as potential inhibitors of CoA and carrier protein dependent biosynthetic pathways. Based on an initial observation of growth inhibition in Escherichia coli by 3, we have synthesized a small panel of pantetheine analogues and re-examined the inhibitory properties of this class of antibiotics with an emphasis on understanding the ability of these compounds to act as substrates of native CoA and carrier protein utilizing biosynthetic pathways. Our findings suggest that a secondary structure-activity relationship is an important factor in the antibiotic activity of these compounds. 相似文献
157.
Euphorbiasteroid,a component of Euphorbia lathyris L., inhibits adipogenesis of 3T3‐L1 cells via activation of AMP‐activated protein kinase 下载免费PDF全文
Su‐Jin Park Jae Ho Park Anna Han Munkhtugs Davaatseren Hyun Jin Kim Myung‐Sunny Kim Haeng Jeon Hur Mi‐Jeong Sung Jin‐Taek Hwang Hye Jeong Yang Dae Young Kwon 《Cell biochemistry and function》2015,33(4):220-225
The purpose of this study is to investigate the effects of euphorbiasteroid, a component of Euphorbia lathyris L., on adipogenesis of 3T3‐L1 pre‐adipocytes and its underlying mechanisms. Euphorbiasteroid decreased differentiation of 3T3‐L1 cells via reduction of intracellular triglyceride (TG) accumulation at concentrations of 25 and 50 μM. In addition, euphorbiasteroid altered the key regulator proteins of adipogenesis in the early stage of adipocyte differentiation by increasing the phosphorylation of AMP‐activated protein kinase (AMPK) and acetyl‐CoA carboxylase. Subsequently, levels of adipogenic proteins, including fatty acid synthase, peroxisome proliferator‐activated receptor‐γ and CCAAT/enhancer‐binding protein α, were decreased by euphorbiasteroid treatment at the late stage of adipocyte differentiation. The anti‐adipogenic effect of euphorbiasteroid may be derived from inhibition of early stage of adipocyte differentiation. Taken together, euphorbiasteroid inhibits adipogenesis of 3T3‐L1 cells through activation of the AMPK pathway. Therefore, euphorbiasteroid and its source plant, E. lathyris L., could possibly be one of the fascinating anti‐obesity agent. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
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160.
Coupling of L-type voltage-sensitive calcium channels to P2X(2) purinoceptors in PC-12 cells 总被引:1,自引:0,他引:1
Extracellular ATPelevates cytosolic Ca2+ by activating P2X and P2Ypurinoceptors and voltage-sensitive Ca2+ channels (VCCCs)in PC-12 cells, thereby facilitating catecholamine secretion. Weinvestigated the mechanism by which ATP activates VSCCs.2-Methylthioadenosine 5'-triphosphate (2-MeS-ATP) and UTP were used aspreferential activators of P2X and P2Y, respectively. Nifedipineinhibited the ATP- and 2-MeS-ATP-evoked cytosolic Ca2+concentration increase and [3H]norepinephrine secretion,but not the UTP-evoked responses. Studies with Ca2+ channelblockers indicated that L-type VSCCs were activated after the P2Xactivation. Mn2+ entry profiles and studies withthapsigargin revealed that Ca2+ entry, rather thanCa2+ release, was sensitive to nifedipine. AlthoughP2X2 and P2X4 receptor mRNAs were detected,studies with pyridoxal phosphate-6-azophenyl-2',4'-disulfonic acidrevealed that P2X2 was mainly coupled to the L-type VSCCs. The inhibitory effect of nifedipine did not occur in the absence ofextracellular Na+, suggesting that Na+ influx,which induces depolarization, was essential for theP2X2-mediated activation of VSCCs. We report thatdepolarization induced by Na+ entry through theP2X2 purinoceptors effectively activates L-type VSCCs inPC-12 cells. 相似文献