配子体的

Such a gamete may be produced by tetraploid tissues, or it may be the result of faulty meiosis.

这样的配子可能是通过四倍体组织或者是错误的减数分裂产生的。

The results from adductor muscle suggesting adductor muscle is an important organ for energy storage and mobilization, and during gametogenesis, glycogen break down in adductor muscle provided energy for gonad maturity, protein and triglycerides also break down to provided energy during spawning.

四、对糖原磷酸化酶和糖原合成酶活力的季节变化研究结果显示，在配子发生期间，二倍体性腺总糖原磷酸化酶和糖原磷酸化酶活性形式的活力随着糖原含量的下降而下降，繁殖期间，糖原含量保持在较低的水平上，GPT和GPa活力有上升趋势，但无统计学差异；繁殖期后，糖原水平逐渐回升，GPT和GPa有下降趋势。

Aim To observe changes of peroxisome proliferator activated receptor γ mRNA, ATP-binding cassette transporter A1 (ABCA1) mRNA and CD36 mRNA in foam cells which come from the peritoneal macrophage of apolipoprotein E knock out mice with giant knotweed rhizome, hawthorn and both of them, and discuss possible mechanism of anti-atherosclerosis on gene level.

目的 观察中药虎杖、山楂配伍对载脂蛋白E基因敲除小鼠巨噬细胞源性泡沫细胞内过氧化体增殖物激活型受体γ、三磷酸腺苷结合盒转运子A1及CD36 mRNA表达的影响，从基因水平探讨虎杖和山楂配伍对动脉粥样硬化泡沫细胞形成的干预机制。

Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

发现~(125)I-Trx-nsLTP144、~(125)I-Trx-nsLTP110与水稻细胞质膜均具有特异性结合，而且结合是饱和性的、可被竞争的，符合配体-受体结合的典型特征，同时用于对照实验的蛋白质~(125)I-Thioredoxin没有此特性，表明水稻细胞质膜上存在nsLTP的受体；利用可氧化糖基的NaIO_4和水解糖基的N\'-糖苷酶F处理水稻细胞质膜，再进行结合实验，结合活性几乎不受影响；而利用胰蛋白酶处理细胞膜则使得结合能力几乎完全丧失，表明其受体为没有经过糖基化修饰的蛋白质；利用交联剂BS~3交联配体一受体后，再进行SDS-PAGE分离和放射自显影，结果显示水稻细胞质膜上的nsLTP受体中有一个60kDa的蛋白质可以与nsLTP144发生特异性的结合，可能是其受体；细胞外碱化实验表明，nsLTP144不能促使拟南芥原生质体细胞培养液的细胞外碱化反应，却能猝灭来自植物病原菌的激发子Cryptogein刺激拟南芥原生质体产生的细胞外碱化反应，表明nsLTP和Cryptogein结合细胞膜上相同的位点，保护了植物细胞免受Cryptogein导致的细胞程序性死亡，并诱导系统获得性抗性的产生；体外Pull-down实验表明，nsLTP144和水稻的OsCaM1具有相互作用，暗示了nsLTP144和OsCaM1可能同在一个信号通路上起作用。

As with the male gametes the remaining cytoplasma binding serves the synchronization of the division and maturation of the cells: just as for the 1rst polar body at the time of the termination of the 2nd meiosis.

和雄性配子一样，这些残留的细胞质连接有助于细胞分裂和成熟的同步化：就像第二次减数分裂结束时的第一极体一样。

Fertilization results in triploid or tetraploid individuals.

这是由于染色体在第一次减数分裂的后期没有分离而导致了多倍的而不是单倍体的配子，受精后产生了三倍或四倍体。

Two mode of plastid inheritance, uniparental maternal and biparental inheritance, were discovered in angiosperms at the beginning of this contury, and our knowledge of the mode and cytological basis of cytoplasmic inheritance, esp. plastid, has been improved in many respects following the new cytological and molecular techniques, eg. electron microscopy, DNA fluorescence and RFLP.

近几年由于电镜、DNA的荧光检测及RFLP等新的细胞学和分子生物学技术的发展，使对植物细胞质遗传形式及其细胞学基础有了一定的了解，但多是单一的方法或对雌、雄配子发生、发育个别发育时期研究的结果，对大部分植物种的质体遗传方式或细胞学基础仍不清楚，在有些植物种间应用不同的研究方法得出的结论也不一致。

Moreoer, c-Fos and phospho–c-Jun protein expression was inhibited by PPARα agonists, indicating that PPARα ligands suppress OPN expression through negatie cross talk with AP-1–dependent transactiation of the OPN promoter.

另外，c-Fos及磷酸化c-Jun蛋白表达可被PPARα激动剂抑制，说明PPARα配体通过OPN启动子AP-1依赖型转录激活的负交互作用而抑制OPN表达。

PPARα ligands suppressed OPN promoter actiity, and an actiator protein-1 consensus site conferred this repression. Oerexpression of c-Fos and c-Jun reersed the inhibitory effect of PPARα ligands on OPN transcription, and, in chromatin immunoprecipitation assays, PPARα ligands inhibited c-Fos and phospho–c-Jun binding to the OPN promoter.

PPARα配体可抑制OPN启动子活性，一个激活蛋白-1的一致序列位点与这种抑制有关。c-Fos和c-Jun的过表达可逆转 PPARα配体对OPN转录的抑制作用，并且在免疫沉淀实验中，PPARα配体可抑制c-Fos及磷酸化c-Jun与OPN启动子的结合。

A liquid crystal with pyridine group was synthesized from reactants of pyrogallic acid and isonicotinato by esterification reaction.

以焦性没食子酸和异烟酸为原料合成了带吡啶官能团的液晶配体。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。