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81.
KOWICHI JIMBOW JONG S. PARK FUMIHIRO KATO KUNINORI HIROSAKI KAZUTOMO TOYOFUKU CHEN HUA TOSHIHARU YAMASHITA 《Pigment cell & melanoma research》2000,13(4):222-229
Assembly, target‐signaling and transport of tyrosinase gene family proteins at the initial stage of melanosome biogenesis are reviewed based on our own discoveries. Melanosome biogenesis involves four stages of maturation with distinct morphological and biochemical characteristics that reflect distinct processes of the biosynthesis of structural and enzymatic proteins, subsequent structural organization and melanin deposition occurring in these particular cellular compartments. The melanosomes share many common biological properties with the lysosomes. The stage I melanosomes appear to be linked to the late endosomes. Most of melanosomal proteins are glycoproteins that should be folded or assembled correctly in the ER through interaction with calnexin, a chaperone associated with melanogenesis. These melanosomal glycoproteins are then accumulated in the trans Golgi network (TGN) and transported to the melanosomal compartment. During the formation of transport vesicles, coat proteins assemble on the cytoplasmic face of TGN to select their cargos by interacting directly or indirectly with melanosomal glycoproteins to be transported. Adapter protein‐3 (AP‐3) is important for intracellular transport of tyrosinase gene family proteins from TGN to melanosomes. Tyrosinase gene family proteins possess a di‐leucine motif in their cytoplasmic tail, to which AP‐3 appears to bind. Thus, the initial cascade of melanosome biogenesis is regulated by several factors including: 1) glycosylation of tyrosinase gene family proteins and their correct folding and assembly within ER and Golgi, and 2) supply of specific signals necessary for intracellular transport of these glycoproteins by vesicles from Golgi to melanosomes. 相似文献
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YURIKO NISHIYAMA-FUJITA AI KAWANA-TACHIKAWA TOSHIAKI ONO YUKIE TANAKA TAKAFUMI KATO HELEN E. HESLOP TOMOHIRO MORIO SATOSHI TAKAHASHI 《Cytotherapy》2018,20(9):1182-1190
Background: Restoration of virus-specific immunity by virus specific T cells (VSTs) offers an attractive alternative to conventional drugs, and can be highly effective in immunocompromised patients, including hematopoietic stem cell transplant (HSCT) recipients. However, conventional VSTs manufacture requires preparation of specialized antigen-presenting cells (APCs), prolonged ex vivo culture in serum-containing medium and antigen re-stimulation with viruses or viral vectors to provide viral antigens for presentation on APCs. Methods: To simplify this complex process, we developed a method to generate multiple VSTs by direct stimulation of peripheral blood mononuclear cells (PBMCs) with overlapping peptide libraries in serum-free medium. Results: We generated VSTs that targeted seven viruses (cytomegalovirus [CMV], Epstein-Barr virus [EBV], adenovirus [AdV], human herpesvirus 6 [HHV-6], BK virus [BKV], JC virus [JCV] and Varicella Zoster virus [VZV]) in a single line. The phenotype, growth and specificity of multiple VSTs produced in serum-free medium were equivalent to those generated in conventional serum-containing medium. Discussion: The use of serum-free medium allows this approach to be readily introduced to clinical practice with lower cost, greater reproducibility due to the absence of batch-to-batch variability in serum and without concerns for infectious agents in the serum used. This simplified approach will now be tested in recipients of Human Leukocyte Antigen (HLA)–matched sibling HSCT. 相似文献
84.
A nocturnal Provespa wasp species as the probable pollinator of epiphytic orchid Coelogyne fimbriata
Many vespid wasps visit flowers to forage nectar. These hymenopterans sometimes contribute to flower pollination. However, none of the nocturnal wasp species is a known pollinator. We collected individuals of light‐attracted Provespa nocturna workers in a montane rainforest on Peninsular Malaysia: some wasps collected bore orchid pollinia on their thoraxes. Among 114 trapped individuals, four bore pollinaria and nine bore only viscidia, suggesting that pollinia had been successfully transported. Molecular barcoding of the pollinia (based on their ITS sequences) assigned the orchid to a species in Coelogyne fimbriata complex. These findings and our other analyses suggest that this nocturnal wasp contributes to pollination of an epiphytic nectarless orchid that probably releases olfactory attractants. This discovery sheds light on the importance of mutualistic relationships between the nocturnal social wasps and epiphytic orchids in Southeast Asian tropical rainforest canopies. 相似文献
85.
DNA barcoding is a technique for identifying organisms based on a short, standardized fragment of genomic DNA. The standardized sequence region is called a DNA barcode because it is like a barcode tag for each taxon. Since the proposition of this concept and the launch of a large project named the Barcode of Life, this simple technique has attracted attention from taxonomists, ecologists, conservation biologists, agriculturists, plant‐quarantine officers and others, and the number of studies using the DNA barcode has rapidly increased. The extreme diversity of insects and their economical, epidemiological and agricultural importance have made this group a major target of DNA barcoding. However, there is some controversy about the utility of DNA barcoding. In this review, we present an overview of DNA barcoding and its application to entomology. We also introduce current advances and future implications of this promising technique. 相似文献
86.
Effects of forest loss and fragmentation on pollen diets and provision mass of the mason bee,Osmia cornifrons,in central Japan
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TERUYOSHI NAGAMITSU MIKI F. SUZUKI SHOTARO MINE HISATOMO TAKI KATO SHURI SATOSHI KIKUCHI TAKASHI MASAKI 《Ecological Entomology》2018,43(2):245-254
1. Habitat loss and fragmentation potentially affect the performance of bees that forage nectar and pollen of plants in their habitats. In forest landscapes, silvicultural conifer plantations often have reduced and fragmented natural broadleaf forests, which seem to provide more floral resources for bees than do the plantations. 2. This study evaluated the effects of forest characteristics (i.e. elevation, area, edge length, and tree size of natural forests) on pollen diets (plant taxa assemblages of pollen grains in provisions) and total provision mass in oviposited chambers in nests made by a standardised number of Osmia cornifrons bees at 14 sites in a forestry area in central Japan. 3. From April to May, the numbers of nests and chambers per nest increased, and the provision mass per chamber decreased. Main pollen sources were Prunus at higher elevations in April and Wisteria at lower elevations in May, foraging on which increased the numbers of nests and chambers per nest. The provision mass per chamber was smaller at higher elevations in more fragmented natural forests. Decreases in the area of natural forests within the foraging range (400‐m radii) of O. cornifrons increased the utilisation of Rubus pollen and decreased the total provision mass. 4. These findings suggest that the loss and fragmentation of natural broadleaf forests change pollen diets and reduce the provision mass of mason bees, which may reduce the number and size of their offspring. 相似文献
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Fertilization of sea urchin eggs fails to occur at a pH lower than 6.5. Analytical studies on this problem were made with Hemicentrotus pulcherrimus, Anthocidaris crassispina and Pseudocentrotus depressus. If the spermatozoa have been pretreated with egg water, eggs can be fertilized even at pH 6.5 and 6.0. The acrosome reaction is inhibited at a pH lower than 6.5. Intact spermatozoa fail to adhere to the fixed eggs in acidified sea water, whereas egg-water-treated spermatozoa adhere even at pH 6.5 and 6.0. From these results we infer that the failure of fertilization at pH 6.5–6.0 is caused by non-occurrence of the acrosome reaction, and that fertilization reactions other than the acrosome reaction, such as the binding and fusion of the gametes, are not inhibited in this range of pH. At pH 5.5, the spermatozoa become inert and fertilization is inhibited or suppressed, even though egg-water-treated spermatozoa are employed. 相似文献
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90.
The effect of trypsin on the fertilizing capacity of spermatozoa was studied with 6 species of sea urchins. Trypsin has no harmful effect on intact spermatozoa. However, spermatozoa which have undergone the acrosome reaction in egg-water lose the fertilizing capacity when treated with trypsin-sea water. Electron- microscopical examination revealed that trypsin does not produce any morphologically noticeable effect on intact spermatozoa, but does dissolve the material covering the acrosomal tubule of the spermatozoa which have undergone the acrosome reaction. It is likely that the loss of this material is closely correlated with the loss of fertilizing capacity of spermatozoa by the trypsin treatment. 相似文献