遗传学的

Genetic abnormalities on Chromosome 2p, 10q and l8q may be associated with the pathogenesis of central neurocytoma.

染色体2p、10q和18q的遗传学改变很可能与中枢神经细胞瘤的发病机制有关。

The paper's lead author, Duke University molecular genetics and microbiology post-doctoral Lee Chung-chang said: Nosema infection treatment is difficult, because we know little of its 50%% of AIDS patients suffered Nosema fungal infection Caused chronic diarrhea.

该论文的主要作者、杜克大学分子遗传学和微生物学博士后李颂昌说：微孢子虫感染很难治疗，因为我们对其知之甚少，50%%的艾滋病患者遭遇微孢子真菌感染，引发慢性腹泻。

Objective: To study the distribution of genetic polymorphism of VWA, FGA, PENTA E loci in Mongolia population and construct genetic database.

目的 ：了解内蒙古锡盟地区蒙古族人群 VWA、FGA、PENTA E三个 STR位点的遗传多态性分布，获得相应多态位点的群体遗传学数据。

Molecular Plant-Microbe Interactions is published by American Phytopathological Society, publishes significant research on the molecular genetics and molecular biology of pathological, symbiotic, and associative interactions of microbes and plants.

资源描述：《分子植物与微生物相互作用》由美国植物病理学协会负责出版，刊载研究论文和评论，内容包括：分子生物学、分子病理遗传学、微生物和植物的共生作用及其对栽培植物、野生植物和植物产品的影响。

Pombe which is not responsible for pseudouridylation of rRNA or snRNA. At last, genetic analyses of the functions of one pseudouridylation guide and two orphan guide snoRNAs were carried out by gene deletions.

最后，本文还利用同源重组方法对1个指导假尿嘧啶化修饰的功能snoRNA分子SP20和两个orphan-guide snoRNA分子SP12和SP16进行了基因缺失的遗传学分析。

The extra pronuclear of triploid zygotes after IVF is from sperm and the zygotes have no implantation value.

IVF后3PN卵子中多余的原核多为精子来源，没有移植价值；ICSI后3PN中多余的原核非精子来源，ICSI后3PN中二倍体率与IVF相比显著增高，在患者ICSI后无2PN卵子时可考虑行植入前遗传学诊断。

The present study aims to evaluate whether retinoid is involved in the pathophysiology of schizophrenia.

本研究的目的是：在中国汉族病例-对照人群中进行 ALDH1A1 ， ALDH1A2 ， ALDH1A3 ， CYP26A1，CYP26B1 和 CYP26C1 这 6 个基因与精神分裂症的关联分析，从遗传学角度考察维生素 A 代谢异常与精神分裂症是否相关。

Epigenetics is the study of processes that establish metastable that is, somatically heritable state of gene expression without altering the sequence.

表观遗传学是研究没有DNA序列变化，但可遗传的基因表达的改变。

These results suggest that P300 reduction in both symptomatological and genetic high risk groups of schizophrenia might have different origin of disturbance in the neural circuitry for P300 generation.

这些结果提示分裂症的症状学及遗传学高危人群存在 P300 减少，且可能存在有不同 P300 神经通路的失调。

"We now are given a hint as to what parts of RLS may be genetically determined," says John Winkelman, a sleep specialist at Harvard Medical School in Boston, Massachusetts.

&关于不宁腿综合症哪个部分是由遗传学决定的，我们现在已经得到一些线索&，来自麻萨诸塞州波士顿哈佛医学中心的睡眠学家John Winkelman说。

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。