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Melanocytes originate from the neural crest in vertebrates and migrate to the body surface where they differentiate into functional cells. Genes involved in melanocyte differentiation can be classified into two groups. One of them consists of the functional genes that control proteins specific to the function of the melanocyte. As the representative gene of this category, albino (c) locus in the mouse is considered to control tyrosinase, the key enzyme in melanogenesis. cDNA for mouse tyrosinase has been cloned and sequenced. The cDNA can be used to detect tyrosinase mRNA synthesized during melanocyte differentiation. On the other hand, genes such as brown (b) or pink-eyed dilution (p) have been assumed to control melanosome proteins. The other category consists of genes that regulate the expression of these functional genes directly or indirectly. In the mouse, so-called white-spotting genes and genes of the agouti series are considered to fall into this category. Based on the fact that mutations at the white-spotting loci result in the absence of melanocytes in a particular area of skin, it is assumed that some of these loci control the factors that promote either differentiation or migration of melanoblasts and are candidates for the classic regulator genes Genes at the agouti (a) locus in the mouse determine the type of melanin synthesized in hair follicle melanocytes, that is eumelanin or pheomelanin. An interesting feature of this locus is that the site of gene action is not within the melanocytes but in the cells surrounding them. The results of our study indicate that the gene product of the a-locus interacts with α-MSH at the α-MSH receptor site, regulates the cellular cAMP level via a signal transduction system and, in turn, determines the type of melanin synthesized in the cells. 相似文献
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SHIGEKO SUZUKI-MORIMOTO YOSHIHIRO YAMAMOTO TAKEO YAMAGUCHI 《Development, growth & differentiation》1985,27(6):729-736
Hydrocortisone is regarded as an initiator of keratinization in embryonic skin. The present investigation dealt with the effect of hydrocortisone on the proliferation of epidermal cells during early development: Cell kinetic analyses using 3 H-thymidine autoradiography were applied to a skin organ culture prepared from a 13-day chick embryo.
Hydrocortisone at a concentration between 0.01 and 1.0 μg/ml was effective in initiating a morphological change leading to the epidermal keratinization in vitro and caused a marked decrease in the mitotic and labeling indices of epidermal basal cells, the decrease being maximum at 2 days of culture previous to the morphological change.
During continuous labeling with3 H-thymidine, the number of labeled basal cells reached 100% within 2 days in the control and 4 days in the culture treated with hydrocortisone. This confirmed that the growth fraction of epidermal basal cells was 1.0 even after the administration of hydrocortisone.
The duration of each cell cycle phase at 2 days of culture was determined by percent labeled mitoses and double-labeling analyses. It was concluded that hydrocortisone extended the generation time of epidermal basal cells at this time point about three fold over the control. This extension was mainly due to the elongation of the G1 phase. 相似文献
Hydrocortisone at a concentration between 0.01 and 1.0 μg/ml was effective in initiating a morphological change leading to the epidermal keratinization in vitro and caused a marked decrease in the mitotic and labeling indices of epidermal basal cells, the decrease being maximum at 2 days of culture previous to the morphological change.
During continuous labeling with
The duration of each cell cycle phase at 2 days of culture was determined by percent labeled mitoses and double-labeling analyses. It was concluded that hydrocortisone extended the generation time of epidermal basal cells at this time point about three fold over the control. This extension was mainly due to the elongation of the G
4.
Macrophage Migration Inhibition by Serum from Desensitized Animals Previously Sensitized with Tubercle Bacilli 总被引:4,自引:0,他引:4
MIGRATION of peritoneal exudate cells removed from guinea-pigs or mice exhibiting delayed hypersensitivity is inhibited by specific antigen1–3. This in vitro macrophage migration inhibition has been regarded as a useful immunological test for delayed skin hypersensitivity4,5. Studies of the mechanism of this phenomenon revealed that, in contact with specific antigen, lymphocytes from sensitized animals released into the medium a specific substance (migration inhibitory factor; MIF) capable of inhibiting the migration of normal macrophages6,7. When injected intradermally into normal guinea-pigs, MIF elicits inflammatory reactions characterized by induration, erythema and mononuclear cell infiltration8. 相似文献
5.
Artificial induction of functional sex-reversal in genotypic females of the medaka (Oryzias latipes) 总被引:8,自引:0,他引:8
YAMAMOTO T 《The Journal of experimental zoology》1958,137(2):227-263
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MASAMICHI AIKAWA ALAN H. COCHRANE RUTH S. NUSSENZWEIG JOHN RABBEGE 《The Journal of eukaryotic microbiology》1979,26(2):273-279
Plasmodium cynomolgi, Plasmodium knowlesi, and Plasmodium berghei sporozoites, before and after incubation with immune serum, were studied after freeze-fracture by electron microscopy. There were evenly distributed numerous intramembranous particles (IMP) on the P face of the outer membrane. The E face of the plasma membrane had fewer IMP than its P face. The E face of the intermediate membrane had few IMP and also linear arrays of slightly raised ridges running the length of the parasite. The P face of the intermediate membrane had many IMP aligned along the long axis of the sporozoite. On the P face of the inner membrane. IMP were arranged in very distinct rows conforming to the long axis of the parasite; the E face of this membrane had a few randomly distributed IMP. A prominent change in the sporozoite incubated in immune serum was the appearance of a layer of aggregated particles around the parasite. The P face of the plasma membrane had several clear areas devoid of IMP and IMP aggregates. No changes were seen in the other fractured faces of the pellicle. These observations suggest that immune serum acts only on the P face of the plasma membrane. 相似文献
10.
NORIKO KAWAMOTO YAMAMOTO 《Development, growth & differentiation》1975,17(3):253-263
The effects of hypophysectomy on spermatogenesis in testes implanted to neuter individuals of the medaka, oryzias latipes , have been histologically studied.
The neuter fish produced by prolonged androgen treatment during larval life maintained the implanted testes for more than 8 months, irrespective of the genetic sex of the host. Histological examination revealed that all the implanted testes were filled with numerous cysts containing cells at all spermatogenetic stages, as in the normal testes. Each cyst contained only cells at the same stage. Furthermore, the implanted testes had fertile spermatozoa. In the experiment of regeneration of amputated anal fins, the implanted testes were found to be able to induce the formation of papillar processes, although the number of processes was one-half of that induced by normal testes.
Hypophysectomy of the fish was successfully achieved by orbital approach. The survival rate of the operated fish was 95% a week after the operation and still 50% 14 months later. Hypophysectomy inhibited the transformation of spermatogonia to spermatocytes in spermatogenesis.
The presence of the capacity to carry out normal spermatogenesis and induce papillar processes in the testis-implanted neuter fish suggests that the hypothalamus of the neuter fish was not seriously affected by prolonged androgen treatment. 相似文献
The neuter fish produced by prolonged androgen treatment during larval life maintained the implanted testes for more than 8 months, irrespective of the genetic sex of the host. Histological examination revealed that all the implanted testes were filled with numerous cysts containing cells at all spermatogenetic stages, as in the normal testes. Each cyst contained only cells at the same stage. Furthermore, the implanted testes had fertile spermatozoa. In the experiment of regeneration of amputated anal fins, the implanted testes were found to be able to induce the formation of papillar processes, although the number of processes was one-half of that induced by normal testes.
Hypophysectomy of the fish was successfully achieved by orbital approach. The survival rate of the operated fish was 95% a week after the operation and still 50% 14 months later. Hypophysectomy inhibited the transformation of spermatogonia to spermatocytes in spermatogenesis.
The presence of the capacity to carry out normal spermatogenesis and induce papillar processes in the testis-implanted neuter fish suggests that the hypothalamus of the neuter fish was not seriously affected by prolonged androgen treatment. 相似文献