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81.
Neurotrophins are essential for the development and survival of the catecholaminergic neurons. GTP cyclohydrolase I (GCH) is the first and rate-limiting enzyme in the biosynthesis of 5,6,7,8-tertahydrobiopterin (BH4), the required cofactor for tyrosine hydroxylase. Previously, we reported that TH requires the Ras/mitogen-activated protein kinase kinase (MEK) pathway for its induction by nerve growth factor (NGF). Here, we examined intracellular signals required for NGF-induced expression of the GCH gene in PC12D cells. The activity of GCH was increased up to 5-fold after the NGF treatment, and the increase was repressed by pretreatment with U0126, an MEK1/2 inhibitor, but not with protein kinase A (PKA), phosphoinositide 3-kinase (PI3K), p38 mitogen-activated protein kinase (MAPK), and c-Jun NH2-terminal kinase (JNK) inhibitors. Induction of GCH mRNA by NGF was also abolished by pretreatment with U0126. The human GCH promoter activity was significantly enhanced by NGF treatment. Deletion analysis showed that the 465-bp 5'-flanking region is responsible for NGF-enhanced promoter activity. These data suggest that the Ras-MEK pathway is required for coordinate expression of the GCH and TH genes induced by neurotrophins. 相似文献
82.
83.
Abe N Kohu K Ohmori H Hayashi K Watanabe T Hozumi K Sato T Habu S Satake M 《Journal of immunology (Baltimore, Md. : 1950)》2005,175(7):4475-4482
84.
Zhang MR Maeda J Ito T Okauchi T Ogawa M Noguchi J Suhara T Halldin C Suzuki K 《Bioorganic & medicinal chemistry》2005,13(5):1811-1818
N-(5-Fluoro-2-phenoxyphenyl)-N-(2-[(18)F]fluoromethoxy-d(2)-5-methoxybenzyl)acetamide ([(18)F]2) is a potent ligand (IC(50): 1.71 nM) for peripheral benzodiazepine receptor (PBR). However, in vivo evaluation on rodents and primates showed that this ligand was unstable and rapidly metabolized to [(18)F]F(-) by defluorination of the [(18)F]fluoromethyl moiety. In this study, we designed a deuterium-substituted analogue, N-(5-fluoro-2-phenoxyphenyl)-N-(2-[(18)F]fluoromethoxy-d(2)-5-methoxybenzyl)acetamide ([(18)F]5) as a radioligand for PBR to reduce the in vivo metabolic rate of the non-deuterated [(18)F]2. The design principle was based on the hypothesis that the deuterium substitution may reduce the rate of defluorination initiated by cleavage of the C-H bond without altering the binding affinity for PBR. The non-radioactive 5 was prepared by reacting diiodomethane-d(2) (CD(2)I(2), 6) with a phenol precursor 7, followed by treatment with tetrabutylammonium fluoride. The ligand [(18)F]5 was synthesized by the alkylation of 7 with [(18)F]fluoromethyl iodide-d(2) ([(18)F]FCD(2)I, [(18)F]9). Compound 5 displayed a similar in vitro affinity to PBR (IC(50): 1.90 nM) with 2. In vivo evaluation demonstrated that [(18)F]5 was metabolized by defluorination to [(18)F]F(-) as a main radioactive component, but its metabolic rate was slower than that of [(18)F]2 in the brain of mice. The deuterium substitution decreased the radioactivity level of [(18)F]5 in the bone of mouse, augmented by the percentage of specific binding to PBR in the rat brain determined by ex vivo autoradiography. However, the PET image of [(18)F]5 for monkey brain showed high radioactivity in the brain and skull, suggesting a possible species difference between rodents and primates. 相似文献
85.
Shin Ohtani Yusuke Shinkai Akio Horibe Kentaro Katayama Takehito Tsuji Yoshibumi Matsushima Masayoshi Tachibana Tetsuo Kunieda 《Experimental Animals》2006,55(5):491-495
The WS4 mouse is an animal model for human Waardenburg syndrome type 4 (WS4), showing pigmentation anomalies, deafness and megacolon, which are caused by defects of neural crest-derived cells. We have previously reported that the gene responsible for the WS4 mouse is an allele of the piebald mutations of the endothelin B receptor gene (Ednrb). In this study, we examined the genomic sequence of the Ednrb gene in WS4 mice and found a 598-bp deletion in the gene. The deleted region contains the entire region of exon 2 and the 5' part of exon 3 and is flanked by inverted repeat sequences which are suggested to trigger the deletion. We concluded that the deletion in the Ednrb gene is the causative mutation for the phenotype of WS4 mice. 相似文献
86.
Water chestnut (genus Trapa) is an annual floating-leaved macrophyte that produces dense beds known to drastically modify freshwater ecosystems. Although Trapa displays a distinct phenology that should alter the innate seasonal dynamics of ecosystems, the seasonality of these effects has rarely been investigated. Therefore, we examined seasonal changes in physicochemical conditions and assemblages of zoobenthos and zooplankton, and whether these changes were correlated with the rise and decline of dense beds of Trapa japonica in Lake Mikata, a temperate shallow lake in central Japan. Our results suggested that the formation of dense Trapa beds during summer resulted in hypoxia, which significantly decreased the abundance of Chironomidae and Oligochaeta in the benthic community, as well as that of Calanoida among zooplankton. When dense Trapa beds formed, we also detected growth of other taxa that were resistant to hypoxia, including Cladocera, Cyclopoida, Ostracoda, and Nematoda. Chlorophyll a concentration declined across the lake during summer, when dense Trapa beds formed. The decline in Trapa beds from autumn to spring resulted in increased dissolved oxygen concentration, chlorophyll a concentration, and invertebrate abundance (Chironomidae, Oligochaeta and Calanoida), as well as a decrease in taxa utilizing the dense Trapa beds. Our results suggest that the phenology of dense Trapa beds can drastically change the seasonal dynamics of physicochemical conditions and the lower components of the food web in a shallow lake ecosystem. 相似文献
87.
88.
Takehito Nakazawa Shinya Kaneko Hitoshi Murata Takashi Kamada Kazuo Shishido 《Mycoscience》2009,50(5):331-342
89.
Abidur Rahman Maho Takahashi Kyohei Shibasaki Shuang Wu Takehito Inaba Seiji Tsurumi Tobias I. Baskin 《The Plant cell》2010,22(6):1762-1776
In the root, the transport of auxin from the tip to the elongation zone, referred to here as shootward, governs gravitropic bending. Shootward polar auxin transport, and hence gravitropism, depends on the polar deployment of the PIN-FORMED auxin efflux carrier PIN2. In Arabidopsis thaliana, PIN2 has the expected shootward localization in epidermis and lateral root cap; however, this carrier is localized toward the root tip (rootward) in cortical cells of the meristem, a deployment whose function is enigmatic. We use pharmacological and genetic tools to cause a shootward relocation of PIN2 in meristematic cortical cells without detectably altering PIN2 polarization in other cell types or PIN1 polarization. This relocation of cortical PIN2 was negatively regulated by the membrane trafficking factor GNOM and by the regulatory A1 subunit of type 2-A protein phosphatase (PP2AA1) but did not require the PINOID protein kinase. When GNOM was inhibited, PINOID abundance increased and PP2AA1 was partially immobilized, indicating both proteins are subject to GNOM-dependent regulation. Shootward PIN2 specifically in the cortex was accompanied by enhanced shootward polar auxin transport and by diminished gravitropism. These results demonstrate that auxin flow in the root cortex is important for optimal gravitropic response. 相似文献
90.
Long-term cryopreservation of mouse sperm 总被引:2,自引:0,他引:2
The objective was to determine if mouse sperm can maintain their fertilizing ability after being frozen for >10 y and whether the offspring derived from these sperm had normal fertilizing ability and phenotype. We cryopreserved sperm from six strains of mice (C57BL/6J, DBA/2N, BALB/cA, C3H/HeJ, B6D2F1 and B6C3F1) in a solution containing 18% (w/v) raffinose and 3% (w/v) skim milk, and preserved them in liquid nitrogen for >10 y. To assess the normality and fertilizing ability of these sperms, they were thawed and used for in vitro fertilization of oocytes of the same strains. Fertilization rates for C57BL/6J, DBA/2N, BALB/cA, C3H/HeJ, B6D2F1 and B6C3F1 were 66.4, 92.3, 72.8, 32.9, 60.3 and 53.7%, respectively. Furthermore, 38.3, 15.0, 43.3, 26.1, 38.3 and 16.7% of the embryos transferred to pseudopregnant females developed and produced live offspring that had normal phenotype and fertility. 相似文献