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排序方式: 共有50条查询结果,搜索用时 31 毫秒
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Kinoshita T Miura A Choi Y Kinoshita Y Cao X Jacobsen SE Fischer RL Kakutani T 《Science (New York, N.Y.)》2004,303(5657):521-523
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Teruhisa Yotsuya Takao Ichii Minoru Sawano Tetsu Nakanishi Takeshi Ozaki 《Scientia Horticulturae》1984,24(2):177-184
Leaf buds of Japanese pear were collected in early June and early November and regarded as summer and winter dormant buds, respectively. Bud explants with and without scales were prepared from each of them, and cultured in vitro for 75 days at 25°C with 14 h photoperiod, on a medium either without growth regulators, or supplied with BA and GAs (GA3 and GA4+7), singly or in combination.When either BA or GA4+7 was contained in the medium, bud expansion occurred. Thereafter, summer dormant buds grew into shoots in the presence of BA, while winter dormant buds, although they swelled profusely, remained in a rosette. In the presence of BA, GA4+7 markedly stimulated shoot elongation of summer dormant buds, but GA3 did not. In winter dormant buds, GA4+7 not only failed to stimulate shoot elongation, but also interfered with the BA-induced swelling described above.The presence of bud scales delayed expansion of summer dormant buds, while it had little effect on winter dormant buds. The delaying effect of scales on expansion of summer buds was effectively removed by application of GA4+7 to the medium. 相似文献
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Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome 总被引:1,自引:0,他引:1
Rodriguez-Viciana P Tetsu O Tidyman WE Estep AL Conger BA Cruz MS McCormick F Rauen KA 《Science (New York, N.Y.)》2006,311(5765):1287-1290
Cardio-facio-cutaneous (CFC) syndrome is a sporadic developmental disorder involving characteristic craniofacial features, cardiac defects, ectodermal abnormalities, and developmental delay. We demonstrate that heterogeneous de novo missense mutations in three genes within the mitogen-activated protein kinase (MAPK) pathway cause CFC syndrome. The majority of cases (18 out of 23) are caused by mutations in BRAF, a gene frequently mutated in cancer. Of the 11 mutations identified, two result in amino acid substitutions that occur in tumors, but most are unique and suggest previously unknown mechanisms of B-Raf activation. Furthermore, three of five individuals without BRAF mutations had missense mutations in either MEK1 or MEK2, downstream effectors of B-Raf. Our findings highlight the involvement of the MAPK pathway in human development and will provide a molecular diagnosis of CFC syndrome. 相似文献
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Okada K Inoue A Okada M Murata Y Kakuta S Jigami T Kubo S Shiraishi H Eguchi K Motomura M Akiyama T Iwakura Y Higuchi O Yamanashi Y 《Science (New York, N.Y.)》2006,312(5781):1802-1805
The formation of the neuromuscular synapse requires muscle-specific receptor kinase (MuSK) to orchestrate postsynaptic differentiation, including the clustering of receptors for the neurotransmitter acetylcholine. Upon innervation, neural agrin activates MuSK to establish the postsynaptic apparatus, although agrin-independent formation of neuromuscular synapses can also occur experimentally in the absence of neurotransmission. Dok-7, a MuSK-interacting cytoplasmic protein, is essential for MuSK activation in cultured myotubes; in particular, the Dok-7 phosphotyrosine-binding domain and its target in MuSK are indispensable. Mice lacking Dok-7 formed neither acetylcholine receptor clusters nor neuromuscular synapses. Thus, Dok-7 is essential for neuromuscular synaptogenesis through its interaction with MuSK. 相似文献
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Kazuhiro Kawai Tomohito Hayashi Yoshio Kiku Tomoyuki Chiba Hajime Nagahata Hidetoshi Higuchi Tetsu Obayashi Seigo Itoh Ken Onda Sachiko Arai Reiichiro Sato Toshio Oshida 《Animal Science Journal》2013,84(12):805-807
Somatic cell counts (SCC) measurements are typically performed using quantitative methods, such as the Breed method (Breed) and the Fossomatic method (FSCC). The DeLaval cell counter (DCC) developed recently is a quantitative somatic cell counter with a low initial cost and superior portability. However, since the DCC was specifically developed for measuring SCC of ≤ 4 × 106 cells/mL milk from bulk tanks or individual cows, its reliability for estimating SCC that exceed this concentration has not yet been clarified. This study therefore examined whether it is possible to accurately measure SCC by diluting milk samples with initial SCC of 4 × 106 cells/mL, as seen in clinical mastitis milk. We collected milk samples from 99 quarters of 99 Holstein cows with clinical mastitis. These milk samples were diluted 10‐fold with saline and thoroughly mixed before performing SCC measurement with the DCC. The correlation coefficients of SCC measured by the FSCC, Breed and DCC methods indicated strong correlations between each pair of methods. The findings showed that DCC can be used to identify bovine clinical mastitis milk and is useful as a quantitative SCC measurement device on farm sites. 相似文献
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中国砂梨7个自交不亲和新基因的分离与测序 总被引:2,自引:0,他引:2
S-RNase是配子体自交不亲和植物雌蕊的基因产物,它降解具有相同基因型的花粉mRNA或rRNA,导致植物的自交不亲和.借鉴日本梨S-RNase基因的分析方法,对中国砂梨5个品种的基因组DNA进行PCR-RFLP系统检测和DNA序列分析,从中发现了7个新的S-RNase等位基因,分别命名为S11-RNase、S12-RNase、S13-RNase、S14-RNase、S15-RNase、S16-RNase和S25-RNase基因,其部分序列已登录到GenBank. 相似文献