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Summary Seven new names at species rank are proposed in Memecylon sect. Afzeliana Jacq.-Fél., a group of forest shrubs and small trees confined to Guineo-Congolian Africa. The group is centred in Cameroon,
where 17 of the 20 species occur. A new flower type, the “star-flower” in Memecylon is revealed, and its taxonomic and ecological importance discussed. Three new, locally endemic species from the South West
Province of Cameroon are described, mapped and illustrated: M. kupeanum R. D. Stone, Ghogue & Cheek, M. bakossiense R. D. Stone, Ghogue & Cheek, and M. rheophyticum R. D. Stone, Ghogue & Cheek. Two new names, M. accedens R. D. Stone, Ghogue & Cheek and M. hyleastrum R. D. Stone & Ghogue and one new combination, M. mamfeanum (Jacq.-Fél.) R. D. Stone, Ghogue & Cheek are provided at species level for three taxa originally proposed as varieties of
M. afzelii G. Don. The taxon M. arcuatomarginatum var. simulans Jacq.-Fél. is also elevated to species status, as M. simulans (Jacq.-Fél.) R. D. Stone & Ghogue. Conservation assessments are provided for all the newly named taxa. A key is provided
to the species of Memecylon sect. Afzeliana. 相似文献
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Jean-Yves Berthon Rachida Nachat-Kappes Mathieu Bey Jean-Paul Cadoret Isabelle Renimel 《Free radical research》2017,51(6):555-567
As the largest organ in the human body, the skin has multiple functions of which one of the most important is the protection against various harmful stressors. The keratinised stratified epidermis and an underlying thick layer of collagen-rich dermal connective tissues are important components of the skin. The environmental stressors such as ultraviolet radiation (UVR) and pollution increase the levels of reactive oxygen species (ROS), contributing to clinical manifestations such as wrinkle formation and skin aging. Skin aging is related to the reduction of collagen production and decrease of several enzymatic activities including matrix metalloproteinases (MMPs), which degrade collagen structure in the dermis; and tissue inhibitor of metalloproteinases (TIMPs), which inhibit the action of MMPs. In addition to alterations of DNA, signal transduction pathways, immunology, UVR, and pollution activate cell surface receptors of keratinocytes and fibroblasts in the skin. This action leads to a breakdown of collagen in the extracellular matrix and a shutdown of new collagen synthesis. Therefore, an efficient antioxidants strategy is of major importance in dermis and epidermis layers. Marine resources have been recognised for their biologically active substances. Among these, marine algae are rich-sources of metabolites, which can be used to fight against oxidative stress and hence skin aging. These metabolites include, among others, mycosporine-like amino acids (MAAs), polysaccharides, sulphated polysaccharides, glucosyl glycerols, pigments, and polyphenols. This paper reviews the role of oxidative processes in skin damage and the action of the compounds from algae on the physiological processes to maintain skin health. 相似文献
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The Middle Palaeolithic mineral environment in the South of the Massif Central: preliminary petroarchaeological results. Five Middle-Palaeolithic assemblages coming from archaeological sites in the Haute-Loire and Ardèche dated to isotopic stages 7 to 5 have been studied using a petroarchaeological method based on the optimization of observation techniques at different scales with respect to genetic and postgenetic characteristics of flint raw materials. The method reveals a relatively large collection area for the middle mountain sites (Sainte-Anne I, Baume-Vallée, Le Rond-de-Saint-Arcons, Rochelimagne), but apparently a smaller one for the site of Payre, located nearby the side of the Rhône Valley. For all sites, gathering is predominantly local, but some distant sources are utilised too. The rare exogenous materials, for example the Bedoulian flint from Ardèche identified in the Velay assemblages (Sainte-Anne I, Baume-Vallée) are in fact located in the heart of the massif as well as in secondary deposits and thus do not allow one to establish firm circulation routes for, or certain contact between the relevant human groups. To cite this article: P. Fernandes et al., C. R. Palevol 5 (2006). 相似文献
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A cell surface marker for neural crest and placodal cells: further evolution in peripheral and central nervous system 总被引:11,自引:0,他引:11
The recent production of a monoclonal antibody (NC-1) recognizing migrating avian neural crest (NC) cells (M. Vincent, J. L. Duband , and J. P. Thiery , Dev. Brain Res. 9, 235-238, 1983) allowed us to detail their migration pathways at the trunk level of the chick embryo. Three routes can be recognized: NC cells facing the bulk of the somite accumulate to form a spinal ganglion, those facing the intersomitic space can readily reach periaortic areas to contribute to the primary sympathetic chain, and cells at intermediate levels between these two accumulate between the neural tube and the somite but some of them can escape between the sclerotome and the myotome and settle near the aorta. Histological and in vitro immunofluorescence patterns have demonstrated that the NC-1 antigen is a neuroectodermal feature. In addition to its presence on the great majority of NC cells, it persists at the surface of both neuronal and satellite cells of the peripheral ganglia. Moreover, it can be detected on neurogenic placodes and their derivatives. The appearance of the NC-1 antigen in the central nervous system coincides with the first noticeable morphological changes of the neutral tube and develops according to a rostro-caudal gradient which parallels its development: it seems, however, to be transiently expressed by the neuron cell bodies and to concentrate later on their processes. It is also present on non-neuronal cells derived from the neuroectoderm. The neuroectodermal character of NC-1 reactivity is further emphasized by its disappearance from the melanocytes and the mesectodermal derivatives of the NC. The loss by the latter, in ventral areas of the head, of the NC-1 epitope is discussed in relation to previous findings on the degree of commitment of the cephalic NC. The NC-1 epitope is associated with several high-molecular-weight polypeptides and may involve a carbohydrate moiety. 相似文献
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Crest cells individualized at the dorsal border of the neural tube, while they became surrounded by a fibronectin-rich matrix. Crest cells initiated their migration between the basement membranes of the neural tube and the ectoderm. In the vagal region, crest cells migrated in a fibronectin-rich environment between the ectoderm and the dermomyotome, very rapidly reaching the apex of the pharynx. In the trunk region, crest cells opposite the bulk of the somite accumulated at the junction between the somite, the neural tube, and the ectoderm; they resumed their migration at the onset of the dissociation of the somite into dermomyotome and sclerotome. Migration occurred more ventrally along the neural tube; nevertheless, the formation of the rapidly expanding sclerotome prevented crest cells from reaching the paranotochordal region. Thereafter, crest cells accumulated between the neural tube, the dermomyotome, and the sclerotome, where ultimately they formed the dorsal root ganglia. In contrast, cells opposite the intersomitic space did not encounter these obstacles and utilized a narrow pathway formed between the basement membranes of the two adjacent somites. This pathway allowed crest cells to reach the most ventral regions of the embryo very rapidly; they accumulated along the aorta to form the aortic plexuses, the adrenal medulla, and the sympathetic ganglia. The basic features of the migration pathways are (1) a strict delimitation by the fibronectin-rich basement membranes of the surrounding tissues, (2) a formation of space concomitant with the migration of crest cells, (3) a transient existence: continued migration is correlated with the presence of fibronectin, whereas cessation is correlated with its focal disappearance. The crest cells are characterized by their inability to traverse basement membranes and penetrate within tissues. We propose that the combination of active proliferation, unique motility properties, and the presence of narrow pathways are the major mechanisms ensuring correct directionality. Morphologically defined transient routes of migration along with developmentally regulated changes in the extracellular matrix and in the adhesive properties of crest cells are most probably involved in their stabilization in defined territories and their aggregation into ganglia. 相似文献