The study concluded that "the mechanism of this weight loss is unknown [but] it would appear reasonable to include grapefruit in a weight reduction diet."
研究得出结论是这种减轻体重的机制还未知道，但相信包括葡萄柚等类似的减肥饮食的合理原因会浮出水面的。
In this dark realm, at a loss and fear of the unknown, wrapped in the dark, wrapped around her remaining courage.
就存在于这片黑暗的领域里，对未知领域的茫然与恐惧透过深邃的黑暗缠绕着，包裹着，蚕食着她仅存的勇气。
Parkinson's disease is caused by the degeneration of neurons in the midbrain. The mechanisms leading to the loss of these neurons, however, are largely unknown.
帕金森氏症是由中脑中神经细胞的退化导致的疾病。这种机制导致了这些神经的缺失，然而现金大部分机制还不清楚。
The Newton iteration method is used to solve the economic pressure on the unknown node, so as to calculate the economic head loss and economic pipe diameter of each section,.
采用牛顿迭代法来求解各未知节点的经济水压，进而得出各管段的经济水头损失、经济管径和水源二级泵站的经济扬程。
In combination with the Bayes estimator for the parameter of linear exponential model under the same loss function, the nonparametric empirical Bayes estimator of the unknown parameter was obtained.
然后结合线性指数模型未知参数在相同损失函数之下的贝叶斯估计得到了未知参数的非参数经验贝叶斯估计。
Mechanism based on priority to prevent the white list, without any loss of function of the circumstances, prevent the use of known and unknown security vulnerabilities.
白名单基于优先阻止机制，在不损失任何功能的情况下，阻止利用已知或未知安全漏洞的攻击。
For corrosion loss due to unknown causes, deductible per accident for first-time accident is 20% of the loss and for second-time accident the deductible per accident is 50% of the loss.
由于不明原因造成的腐蚀损失，第一次事故的免赔率为损失金额的20%，第二次事故的免赔率为损失金额的50%。
Travelling in an unknown territory will lead the employer and the employees into an undesirable end which is loss.
在未知领域的旅行将导致雇主和雇员有一个不愉快的结尾，这是一个损失。
However, the gene expression changes associated with iron deficiency hearing loss are unknown.
铁缺乏对缺铁耳聋大鼠基因表达的影响尚不清楚。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
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