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51.
52.
Collagen IV and laminin are important constituents of the basement membrane (BM). By use of immunocytochemistry we examined the occurrence and distribution of these two components in the BM beneath normal, mucoid and metaplastic epithelium of large bronchi in 22 adults suffering from chronic nonspecific lung diseases. Both collagen IV and laminin were expressed as a thin and continuous layer beneath the epithelium in most tissue specimens with normal epithelium. In a few specimens the layer showed interruptions with a patchy distribution of the immunoreactivity. Three patterns of distribution of BM components were found under the metaplastic epithelium. Total absence of immunoreactive collagen IV and laminin was the most common variant. Weak and scarce staining for both proteins in the BM characterized the second pattern. The third variant showed strong collagen IV immunoreactivity but lack of laminin. The BM beneath the mucoid epithelium was characterized by irregular distribution of collagen IV and laminin. We suggest that the occurrence and distributional pattern of the BM components are related to the type of overlying epithelium and connected with an altered synthesis of these components. 相似文献
53.
性激素对大白鼠胃粘液分泌的影响 总被引:2,自引:0,他引:2
通过雄、雌性大鼠去势,怀孕鼠,以及肌肉注射性激素的方法,观察内,外源性激素对胃粘液分泌的影响,采用Alcian blue与胃液和胃壁粘液中糖蛋白结合的方法进行胃粘液测定,结果表明:雄、雌鼠胃粘液分泌无性别差异,去势夺雄、雌鼠胃粘液分泌无明显影响;怀孕鼠胃粘液分泌增加,丙酶睾酮对去势雄、雌鼠胃粘液分泌无影响,而戊酸雌二醇和孕酮可增加胃粘液分泌,提示:怀孕鼠胃粘液分泌的增加可能与雌激素和孕激素分泌增多 相似文献
54.
This study was implemented to test the Episkin model of reconstructed epidermis in the evaluation of the efficacy of cosmetic or dermopharmaceutical products on cutaneous energy metabolism. The energy metabolism is evaluated by measuring the concentration of intracellular ATP by a method using an ultrasensitive bioluminescent reaction. The work presented compares results obtained in reconstructed epithelium and monolayer primary cultures of human keratinocytes.After application of a hydrosoluble product, the increase in intracellular ATP is identical in a monolayer culture of keratinocytes (+239±18% versus control) and in Episkin (+248±21% versus control). An emulsion was also tested on the two models. It is only possible to test the emulsion at a dilution of under 0.05% on a keratinocyte culture, and this means that the real efficacy of the product is underestimated (+145±18% versus control). The three-dimensional model enables the application of the undiluted emulsion, and the results show an increase in intracellular ATP of +420±80% versus control: products in final formulation can be tested in normal conditions of use.Abbreviations BPE
bovine pituitary extract
- DMEM
Dulbecco's modified Eagle's medium
- EDTA
ethylene diamine tetraacetic acid
- EGF
epidermal growth factor
- K-SFM
keratinocytes serum free medium
- MTT
3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide
- O/W
oil in water
- PBS
phosphate-buffered saline 相似文献
55.
Alison Moore Kathy M. Ensrud Thomas W. White Chris D. Frethem David W. Hamilton 《Molecular reproduction and development》1994,37(2):181-194
Monoclonal antibody 4E9, which was raised against a partially purified detergent extract of rat caudal epididymal sperm, recognizes the tail of sperm from the cauda, but not from caput epididymidis, as well as epithelial cells in a restricted region of the distal caput/corpus epididymidis and proteins in epididymal fluid from corpus and cauda epididymidis. The antigen is apparently a glycoprotein, since it is retained on a Ricinus communis agglutinin l lectin column. Epididymal fluid antigens have apparent MrS of 38–26 kD, whereas the memrane-associated form of the molecule has an Mr of 26 kD. Immunocytochemical data and Western immunoblot data suggest that the membrane antigen is derived from the fluid antigen, which, in turn, is secrteted by the epididymal epithelium. Characterization of the membrane antigen indicates that it is tightly associated with the sperm surface, behaving as though it is an integral membrane protein. The antigen persists on ejaculated sperm. © 1994 Wiley-Liss, Inc. 相似文献
56.
B. A. Baibakov T. A. Chipisheva V. I. Guelstein V. D. Ermilova E. B. Polevaya J. M. Vasiliev L. B. Margolis 《In vitro cellular & developmental biology. Animal》1994,30(8):490-495
Summary Blocks of breast tissue obtained during radical mastectomies from 23 patients with mammary gland carcinomas were used for
cultivation in native-state, gel-supported histocultures. We show that the human mammary gland can be successfully maintained
in this system so that normal epithelial breast structures proliferate and undergo differentiation for several weeks and a
well-developed system of ducts and lobules is formed. Using antibodies to individual keratins 17 and 8 we have shown for the
first time that ducts and alveoles developing in vitro undergo differentiation into the lining epithelium and myoepithelium
in the same way as mammary gland epithelium in vivo. Growth of epithelial structures in vitro is also accompanied by the development
of continuous basal membrane. 相似文献
57.
The presence of cilia was documented in the hindgut of larval Atlantic halibut ( Hippoglossus hippoglossus ) with the use of electron microscopy. Cilia were shown to be present as late as 8 and 9 day post hatch. These observations were compared to similar observations in more primitive teleosts. 相似文献
58.
K. M. L. Perera 《Journal of fish biology》1993,43(1):45-59
The ultrastructure of the primary epithelium, and the efferent half of the subepithelium, of the primary gill lamellae of slimy mackerel ( Scomber australasicus ) is described. The following cells are identified and described: light nucleated epithelial cells (surface and basal), dark nucleated cells, mucous cells, acidophilic cells, type 1 cells, type 2 cells, type 3 cells and chloride cells in the epithelial region, and subepithelial cells A and B, fibroblasts, chondrocytes, cells of the wall of efferent blood vessel and some blood cells in the subepithelium. 相似文献
59.
David G. Thomassen 《In vitro cellular & developmental biology. Animal》1993,29(6):498-504
Summary Factors regulating the proliferation of normal, preneoplastic, and neoplastic rat tracheal epithelial (RTE) cells were investigated
to identify changes taking place during the progression of RTE cells to neoplasia. Normal RTE cells exhibit clonal proliferation
in a serum-free medium containing pituitary extract, serum albumin, cholera toxin, epidermal growth factor, hydrocortisone,
and insulin. All combinations of these six factors were examined for their abilities to support clonal proliferation of normal,
preneoplastic, and neoplastic RTE cells. In general, preneoplastic RTE cells required fewer factors for proliferation than
normal RTE cells, and neoplastic cells required fewer factors than preneoplastic cells. A common pattern of reductions has
been identified in the growth factors required for the clonal proliferation of preneoplastic vs. normal RTE cells and for
neoplastic vs. preneoplastic and normal RTE cells. Normal RTE cells exhibit clonal proliferation in a serum-free medium supplemented
with a minimum of six factors: bovine serum albumin, bovine pituitary extract, cholera toxin, epidermal growth factor, hydrocortisone,
and insulin. Preneoplastic RTE cells exhibit clonal proliferation in a serum-free medium supplemented with four factors: bovine
serum albumin, bovine pituitary extract, hydrocortisone, and insulin. Finally, neoplastic RTE cells exhibit clonal proliferation
in a serum-free medium supplemented with two factors: bovine serum albumin and bovine pituitary extract. These results suggest
that the progression of RTE cells to neoplasia is associated with a series of changes in regulatory pathways that control
cell proliferation. 相似文献
60.
M. Kondo W. E. Finkbeiner J. H. Widdicombe 《In vitro cellular & developmental biology. Animal》1993,29(1):19-24
Summary Tracheal epithelial cells were grown on Nuclepore filters coated with human placental collagen. When grown immersed in medium
containing fetal bovine serum, cells displayed an undifferentiated ultrastructure (no cilia and a cell height of ∼ 10 μm).
Short-circuit current (Isc) was approximately 1/10 that of the native epithelium. By contrast, when grown in hormonally defined, serum-free medium with
an air interface, cells showed Isc equal to or greater than the original tissue, possessed cilia, and had a cell height of ∼ 50 μm. Responses in Isc to mediators were similar to those of the original tissue, but differed from those of dog or human tracheal epithelium. Given
the ready availability and low cost of the native tissues, bovine tracheal cultures grown in serum-free medium with an air
interface should prove useful in studies of airway epithelial physiology. 相似文献