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21.
Assignment of the pepsinogen gene complex (PGA) to human chromosome region 11q13 by in situ hybridization 总被引:5,自引:0,他引:5
The genes coding for human pepsinogen (PGA3, PGA4, and PGA5) were assigned to chromosome region 11q13 by in situ hybridization. Previously we localized the PGA gene complex to a centromeric region of chromosome 11 (p11----q13) by Southern blot analysis of mouse-human somatic cell hybrids. Our in situ hybridization results confirm this assignment and further localize the genes to a smaller region on the long arm. 相似文献
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The genes coding for insulin-like growth factors I and II and epidermal growth factor have been localized to human chromosomes 12q22----q24.1, 11p15, and 4q25----q27, respectively. 相似文献
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Summary Persistent estrus and diestrus was produced in rats by the administration of estrone for either 5 days or 30 days, respectively, immediately after birth. Female rats without any treatment were used for control. After these rats grew up, the anterior pituitaries were examined by electron microscopy. The identification criteria for two types of gonadotrophs, FSH-and LH-cells, proposed by Barnes were adopted. In the persistent estrous rats, FSH-gonadotrophs were almost normal, but LH-gonadotrophs were filled with an abundance of secretory granules which were probably suppressed in discharge. On the other hand, in the persistent diestrous rats, FSH-cells were few in number and strongly atrophic, containing a few secretory granules, while LH-cells were almost normal or rather slightly activated. These electron microscopic findings well coincide with the results of light microscopy of ovaries, which suggested that in the persistent estrous rats FSH secretion might be almost normal but the secretion of LH might be inhibited, while in the persistent diestrous rats FSH secretion might be almost totally abolished but LH might be moderately secreted. From these findings, identification of FSH-and LH-gonadotrophs in the anterior pituitary of the rat well coincides with that proposed by Barnes in mice. 相似文献
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At least two thyroid hormone receptor (hTR) genes are present in humans, but the significance of this multiplicity is unknown. These receptors could have differences in tissue distribution or possess different functions. We studied the distribution and abundance of three hTR mRNAs (hTR beta, hTR alpha 1, and hTR alpha 2) by Northern blot analysis. Three mRNAs were expressed in all tissues examined. hTR beta was strongly expressed in brain and prostate predominantly as a 10.0-kilobase (kb) mRNA. This mRNA was also expressed in thyroid and was much less abundant in liver, kidney, placenta, tonsil, and spleen. hTR alpha 1 is represented by two mRNAs with sizes of 6.0 and 3.2 kb. The 6.0-kb mRNA was constantly less abundant than the 3.2-kb mRNA. hTR alpha 2 was detected as a single mRNA with a size of 3.2 kb, using a probe unique for this mRNA. Both hTR alpha 1 and hTR alpha 2 were strongly expressed in brain, prostate, and thyroid and much less in other tissues. The relative amounts of the three hTR mRNAs were roughly parallel in each tissue. It is of interest that none of these hTRs was abundant in liver, which is the major thyroid hormone-responsive organ. Another hTR may be present in liver. 相似文献
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A Nakai C Hirayama K Ohtsuka K Hirayoshi K Nagata 《Journal of cellular physiology》1990,143(3):577-589
Using affinity chromatography on ATP-agarose, we have identified a major ATP-binding protein in Nonidet P-40 extracts of avian and mammalian cells labeled with [35S]methionine. After washing ATP-agarose beads with high-ionic-strength buffer (0.4 M NaCl), the 37-kD protein was shown to be one of the major ATP-binding proteins while p72 and grp78, which are members of the hsp70 family, also bound to ATP-agarose. This protein consisted of several spots on two-dimensional gel electrophoresis. The isoelectric point of the most basic spot was approximately 9.2 in chick embryo fibroblasts, whereas it was about 8.8 in mouse 3T3 cells. The identities of these proteins in mouse and chick cells were confirmed by peptide mapping. After heat-shock treatment of BALB/3T3 cells, the major heat-shock protein, hsp70, was shown to be induced very rapidly after heat shock and was recovered in the ATP-binding fraction. Besides hsp70, a 37-kD protein was also found to be induced by heat shock. This protein was drastically induced by treating the cells with alpha,alpha'-dipyridyl, an iron chelating reagent, but not with sodium arsenite, calcium ionophore, or tunicamycin. The synthesis and the total amount of this ATP-binding protein increased in mouse 3T3 cells transformed by simian virus 40, methylcholanthrene, or activated c-Ha-ras oncogene compared to their normal counterparts. The incorporation of [32P]orthophosphate was not detected in either normal or transformed cells. These studies established that a major ATP-binding protein of Mr = 37,000 is a heat-inducible protein and that the synthesis of this protein is regulated by malignant transformation. 相似文献