- 更多网络例句与二倍期相关的网络例句 [注：此内容来源于网络，仅供参考]
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Protein and triglyceride content in adductor muscle increased during gametogenesis, and then deceased in spawning.
在非繁殖期二倍体和三倍体性腺和闭壳肌生化成分含量受倍性影响不大。
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The autotetraploid plants were obtained by identifying the characteristics of morphology, cytology, agronomy,and nutrition quality.
采用不同质量浓度的秋水仙素处理子叶期二倍体萝卜茎尖生长点，通过对突变株进行形态学、细胞学、农艺学及营养品质鉴定，获得同源四倍体。
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Tetraploid embryos could be produced by electrofusion at the stage of two-cell embryos, which could develop to blastocysts followed by fusion of cytoplasm and nucleus and cleavage in vitro. During the fusion of cytoplasm, the DNA methylation levels of the fused embryos are as high as these of two-cell diploid embryos in vivo Then the embryos are rapidly demethylated when the nucleus begin to fuse, resulting in the lowest DNA methylation levels when the nucleus are fused completely. After that, the DNA methylation levels of the fused embryos are gradually increased until the morula stage. However, whereas an asymmetric distribution of DNA methylation is established in vivo-derived blastocysts with a higher methylation level in the inner cell mass than that in the trophectoderm, we can not detect the asymmetric distribution in most in vitro-derived tetraploid blastocysts.
结果表明：利用电融合方法制备的小鼠四倍体胚胎在体外培养体系中经历细胞质融合、细胞核融合及细胞继续分裂发育直到囊胚期的过程，在细胞质融合的时候胚胎卵裂球同体内体外培养二倍体胚胎一样，呈现高度甲基化状态；在细胞核开始融合的时候，甲基化水平急速下降，在细胞核完全融合的时候甲基化水平达到最低点；随着胚胎继续分裂，胚胎甲基化水平逐渐增加，在桑葚胚期甲基化水平最高；但是囊胚期四倍体胚胎内细胞团同滋养层细胞甲基化荧光信号没有差别，这与体内体外培养二倍体囊胚内细胞团细胞甲基化荧光强度高于滋养层细胞甲基化荧光强度不同。
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Tetraploid embryos could be produced by electrofusion at the stage of two-cell embryos, which could develop to blastocysts followed by fusion of cyto-plasm and nucleus and cleavage in vitro. During the fusion of cytoplasm, the DNA methylation levels of the fused embryos are as high as these of two-cell diploid embryos in vivo Then the embryos are rapidly demethylated when the nucleus begin to fuse, resulting in the lowest DNA methylation levels when the nucleus are fused completely. After that, the DNA methy-lation levels of the fused embryos are gradually increased until the morula stage. However, whereas an asymmetric distribu-tion of DNA methylation is established in vivo-derived blastocysts with a higher methylation level in the inner cell mass than that in the trophectoderm, we can not detect the asymmetric distribution in most in vitro-derived tetraploid blastocysts.
结果表明：利用电融合方法制备的小鼠四倍体胚胎在体外培养体系中经历细胞质融合、细胞核融合及细胞继续分裂发育直到囊胚期的过程，在细胞质融合的时候胚胎卵裂球同体内体外培养二倍体胚胎一样，呈现高度甲基化状态；在细胞核开始融合的时候，甲基化水平急速下降，在细胞核完全融合的时候甲基化水平达到最低点；随着胚胎继续分裂，胚胎甲基化水平逐渐增加，在桑葚胚期甲基化水平最高；但是囊胚期四倍体胚胎内细胞团同滋养层细胞甲基化荧光信号没有差别，这与体内体外培养二倍体囊胚内细胞团细胞甲基化荧光强度高于滋养层细胞甲基化荧光强度不同。
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Tetraploid embryos could be produced by electrofusion at the stage of two-cell embryos, which could develop to blastcysts fellowed by fusion of cytoplasm and nucleus and cleavage in vitro.After fusion of cytoplasm, the DNA methylation levels of the fused embryos was very high as well as two-cell diploid embryos in vivo.Then the embryos was rapiddly demethylated when the nucleus begin to fuse, resulting the lowest DNA methylation levels when the nucleus fused completely.After that, the DNA methylation levels of fused embryos were gradually increased until the blastocysts stage.However, whereas an asymmetric distribution of DNA methylation was established in an vivo-derived blastocysts with a higher methylation level in the inner cell mass than in the trophectoderm, in most vitro-derived tetraploid blastocysts, we can not detect the asymmetric distribution.
结果表明：利用电融合方法制备的小鼠四倍体胚胎在体外培养体系中经历细胞质融合、细胞核融合及细胞继续分裂发育直到囊胚期的过程，在细胞质融合的时候胚胎卵裂球同体内体外培养二倍体胚胎一样，呈现高度甲基化状态；在细胞核开始融合的时候，甲基化水平急速下降，在细胞核完全融合的时候甲基化水平达到最低点；随着胚胎继续分裂，胚胎甲基化水平逐渐增加，在囊胚期甲基化水平最高；但是囊胚期四倍体胚胎内细胞团同滋养层细胞甲基化荧光信号没有差别，这与体内体外培养二倍体囊胚内细胞团细胞甲基化荧光强度高于滋养层细胞甲基化荧光强度不同。
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Conclusions— The decrease in polyploidy and increase in diploidy after left ventricular assist device suggest a numeric increase in diploid cardiomyocytes (eg, through cell cycle progression with completion of mitosis or by increased stem cells).
结论-安置左室辅助装置以后，心肌细胞多倍体减少，二倍体明显增加增加（例如，通过细胞分裂周期完成有丝分裂期或增加干细胞数量）。
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The increased number of mitochondria in tetraploids seemed to adapt the demanding of more energy for fecundation in tetraploids because of larger size. 3 Biochemical compositions in gonad and adductor muscle between diploids and triploids in the Pacific oyster, Crassostrea gigas, during an annual period were examined.
三、对二倍体与三倍体太平洋牡蛎的性腺和闭壳肌生化组分含量2003.4-2004.3的年度变化的分析结果显示：二倍体牡蛎性腺糖原含量在配子发生过程中明显降低，至性腺成熟时降低了78.57%（P＜O.01），繁殖期维持在较低水平上，繁殖期过后逐渐升高，10月份至翌年3月份都保持较高的水平。
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Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.
结果 (1)ATP对U937细胞的增殖有按摩明显的阻抑作用，加药48h后增殖的抑制率可达43%以上；(2)ATP处理的U937细胞周期发生改变，G1期细胞数按摩明显增多，ATP作用24h时G1期前出现亚二倍体峰——凋亡峰，凋亡细胞数为3.4%，作用48h时凋亡细胞数增多为22.7%；(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜，逐渐向核膜外移动，进入胞浆内再移向质膜内外面，紧贴质膜外面再逐步脱离细胞体，进入细胞基质中，成为游离的凋亡小体。
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Methods Cell culture,flow cytometry,HE staining,Nigrosine staining and electron microscopy were used. Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.
结果 (1)ATP对U937细胞的增殖有明显的阻抑作用，加药48h后增殖的抑制率可达43%以上；(2)ATP处理的U937细胞周期发生改变，G1期细胞数明显增多，ATP作用24h时G1期前出现亚二倍体峰——凋亡峰，凋亡细胞数为3.4%，作用48h时凋亡细胞数增多为22.7%；(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜，逐渐向核膜外移动，进入胞浆内再移向质膜内外面，紧贴质膜外面再逐步脱离细胞体，进入细胞基质中，成为游离的凋亡小体。
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The flow cytometry was used to measure the DNA ploidy type and cell proliferous ratio of NP,BPH and PC.
PC组异倍体率为65.71%；NP组和BPH组均为DNA二倍体。PC组细胞增殖各期比值与BPH组、NP组差异有显著性(P.01)。
- 更多网络解释与二倍期相关的网络解释 [注：此内容来源于网络，仅供参考]
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diploid gametophyte apomixis：二倍配子体无融合生殖
二倍体 diploid | 二倍配子体无融合生殖 diploid gametophyte apomixis | 双线期 diplonema
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diploid parthenogenesis：多倍性单性生殖
diploidizotion 二倍体化 | diploid parthenogenesis 多倍性单性生殖 | diploid phase 二倍期
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diploidy：二倍型
diploid 二倍体 | diploidy 二倍型 | diplotene stage 双线期
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diplont：二倍體生物
二倍體期 diploid phase | 二倍體生物 diplont | 二倍體世代 diploid generation
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diplont plant：二倍性植物
diplont 二倍性植物,二倍体 | diplont plant 二倍性植物 | diplophase 二倍期
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diplophase：[生]二倍期,双倍期
quad pairing 四线对绞 | diplophase [生]二倍期,双倍期 | attraxin 趋向素
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diplophase：二倍期
diplont plant 二倍性植物 | diplophase 二倍期 | Diplopodos (拉)倍足类
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diplophase：二倍期 二倍体阶段
diplont 二倍体 | diplophase 二倍期 二倍体阶段 | diplopia 双像 复视
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diplophase：二倍期,双倍期
diploperistomous 双齿层的 | diplophase 二倍期,双倍期 | diplophyllous 二叶性的
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diploid intersexuality：二倍體間性
二倍體化 diploidization | 二倍體間性 diploid intersexuality | 二倍體期 diploid phase