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51.
Clustering of neurotransmitter receptors in the postsynaptic membrane is critical for efficient synaptic transmission. During
neuromuscular synaptogenesis, clustering of acetylcholine receptors (AChRs) is an early sign of postsynaptic differentiation.
Recent studies have revealed that the earliest AChR clusters can form in the muscle independent of motorneurons. Neurally
released agrin, acting through the muscle-specific kinase MuSK and rapsyn, then causes further clustering and localization
of clusters underneath the nerve terminal. AChRs themselves are required for agrin-induced clustering of several postsynaptic
proteins, most notably rapsyn. Once formed, AChR clusters are stabilized by several tyrosine kinases and by components of
the dystrophin/utrophin glycoprotein complex, some of which also direct postnatal synaptic maturation such as formation of
postjunctional folds. This review summarizes these recent results about AChR clustering, which indicate that early clustering
can occur in the absence of nerves, that AChRs play an active role in the clustering process and that partly different mechanisms
direct formation versus stabilization of AChR clusters.
Received 10 April 2002; received after revision 4 June 2002; accepted 10 June 2002 相似文献
52.
Melanocortin receptors: their functions and regulation by physiological agonists and antagonists 总被引:14,自引:0,他引:14
Abdel-Malek ZA 《Cellular and molecular life sciences : CMLS》2001,58(3):434-441
The melanocortins are a family of bioactive peptides derived from proopiomelanocortin, and share significant structural similarity.
Those peptides are best known for their stimulatory effects on pigmentation and steroidogenesis. Melanocortins are synthesized
in various sites in the central nervous system and in peripheral tissues, and participate in regulating multiple physiological
functions. Research during the past decade has provided evidence that melanocortins elicit their diverse biological effects
by binding to a distinct family of G protein-coupled receptors with seven transmembrane domains. To date, five melanocortin
receptor genes have been cloned and characterized. Those receptors differ in their tissue distribution and in their ability
to recognize the various melanocortins and the physiological antagonists, agouti signaling protein and agouti-related protein.
These advances have opened new horizons for exploring the significance of melanocortins, their antagonists, and their receptors
in a variety of important physiological functions.
Received 5 October 2000; accepted 10 November 2000 相似文献
53.
Schaefer U Schneider A Rudroff C Neugebauer E 《Cellular and molecular life sciences : CMLS》2003,60(9):1968-1981
During agonist-dependent long-term stimulation of cells, histamine receptor subtypes are frequently down-regulated. However, the mechanisms underlying the modulation of receptor expression during long-term histamine stimulation have yet to be resolved. Based on our recently reported results showing an H1-mediated down-regulation of histamine H2 receptor mRNA in endothelial cells, our aim was to characterize the mechanism controlling rapid and long-term histamine-mediated modulation of H2 receptor expression in more detail. We were able to show that the histamine-induced down-regulation of H2 receptor mRNA and cell surface expression lasting for 24 h was accompanied by augmentation of the receptor protein level in the cytoplasmatic fraction of endothelial cells for this time period. Furthermore, changes in receptor protein levels in whole-cell lysate were negligible, indicating that the rapid and prolonged modulation of cell surface H2 receptor levels by histamine was regulated solely via internalization. The role of nitric oxide (NO) as a key mediator in histamine-stimulated cell responses was underlined by subsequent studies showing the attenuation of histamine-induced H2 receptor mRNA down-regulation and protein trafficking following NO synthase isozyme inhibition.Received 11 March 2003; received after revision 11 June 2003; accepted 17 June 2003 相似文献
54.
Resveratrol-type oligostilbenes from Iris clarkei antagonize 20-hydroxyecdysone action in the Drosophila melanogaster B(II) cell line 总被引:2,自引:0,他引:2
Bioassay-guided high-performance liquid chromatography analysis of a MeOH extract of Iris clarkei seeds yielded the resveratrol-type oligomeric stilbenes, ampelopsin B and α-viniferin, which antagonize the action of 20-hydroxyecdysone; with a 20-hydroxyecdysone concentration of 50 nM, the ED50 values were 33 μM and 10 μM, respectively. The structures of these compounds were determined by spectroscopic analysis, notably
ultraviolet, liquid secondary ion mass spectrometry and modern one- and two-dimensional nuclear magnetic resonance techniques.
Received 4 November 1999; accepted 13 December 1999 相似文献
55.
为了解生长激素受体(GHR)基因多态性在江苏汉族人群中的分布,通过多重PCR及PCR-RFLP的方法对269例江苏地区正常汉族人进行GHR基因3个位点的多态性分析,并与文献中报道的其它种族和地区的人群进行比较分析.结果显示江苏地区汉族正常人群中GHR基因型以fl/fl、I/L、P/P发生频率最高,这种分布在男女之间没有差异,与其它地区汉族人比较没有明显差异,与日本人差异也不明显,而与法国、俄罗斯人差异明显.研究表明,GHR基因3个位点多态性在不同种族之间分布存在着明显的差异,这种差异有可能是导致不同种族间人体测量学差异及对一些疾病的易感性及对药物的反应性不同的因素之一. 相似文献
56.
57.
Summary Using thaw-mount autoradiography for steroid hormones, we obtained direct evidence for a nuclear localization of ecdysteroid binding sites in target organs of blowfly (Calliphora vicina) larvae. The binding sites revealed properties of ecdysteroid receptors. Endocrine cells of the ring gland were found to be target tissues of ecydysteroids. This observation provides morphological evidence for a network of complex interendocrine regulation. In the central nervous system receptorcontaining neurons were identified which include many, if not all, neurosecretory cells of the brain. A map of ecdysteroid sensitive cells of the larval brain is presented. 相似文献
58.
Visual pigment: G-protein-coupled receptor for light signals 总被引:5,自引:0,他引:5
The visual pigment present in photoreceptor cells is a prototypical G-protein-coupled receptor (GPCR) that receives a light
signal from the outer environment using a light-absorbing chromophore, 11-cis-retinal. Through cis-trans isomerization of the chromophore, light energy is transduced into chemical free energy, which
is in turn utilized for conformational changes in the protein to activate the retinal G-protein. In combination with site-directed
mutagenesis, various spectroscopic and biochemical studies identified functional residues responsible for chromophore binding,
color regulation, intramolecular signal transduction and G-protein coupling. Extensive studies reveal that these residues
are localized into specific domains of visual pigments, suggesting a highly manipulated molecular architecture in visual pigments.
In addition to the recent findings on dysfunctional mutations in patients with retinitis pigmentosa or congenital night blindness,
the mechanism of intramolecular signal transduction in visual pigments and their evolutionary relationship are discussed.
Received 20 July 1998; received after revision 9 September 1998; accepted 23 September 1998 相似文献
59.
60.
M. K. Ticku 《Cellular and molecular life sciences : CMLS》1989,45(5):413-418
Summary Ethanol has a pharmacological profile similar to that of classes of drugs like benzodiazepines and barbiturates, which enhance GABAergic transmission in the mammalian CNS. Several lines of behavioral, electrophysiological and biochemical studies suggest that ethanol may bring about most of its effects by enhancing GABAergic transmission. Recently, ethanol at relevant pharmacological concentrations has been shown to enhance GABA-induced36Cl-fluxes in cultured spinal cord neurons, synaptoneurosomes and microsacs. These enhancing effects of ethanol were blocked by GABA antagonists. Ro15-4513, an azido analogue of classical BZ antagonist Ro15-1788, reversed most of the behavioral effects of ethanol and other effects involving36Cl-flux studies. The studies summarized below indicate that most of the pharmacological effects of ethanol can be related to its effects on GABAergic transmission. 相似文献