基因等位

The allele frequency of ALDH2*1 between alcoholic cardiomyopathy group and alcohol dependent group was significantly higher than that in controls and the allele frequency of ALDH2*2 between alcoholic cardiomyopathy group and alcohol dependent group was significantly lower than that in controls.

嗜酒组和酒精性心肌病组ALDH2*1等位基因的频率高於对照(P.01)，ALDH2*2等位基因的频率低於对照组(P.01)。

The most common allele was allele 5 with a frequency of 70.6%.

最常见的等位基因是5等位基因（DRD4＊5），频率为70.6％。

Mapping of microsatellite markers in two wheat crosses segregating for Pm23 and Pm4b, respectively, in combination with the reported mapping of Pm4a, indicated that the three genes were all linked to the marker Xgwm356 with a distance of 3-5 cM. Allelism between Pm4b and Pm23 was then confirmed, when the progenies of a cross between VPM1 (Pm4b) and Line 81-7241, were shown to be all resistant to a B.

利用获得的8个标记对Pm4b进行遗传作图，结果表明，4个标记与Pm4b连锁(Xgwm356、Xgdm93、Xbar76和Xbarc122)。3个抗白粉病基因(Pm4a、Pm4b和Pm23)均与标记Xgwm356连锁，遗传距离为3-5cM，等位性测验证明Pm23与Pm4b为等位基因。

Gene mutations were detected in 25 patients and a 18-year-old girl among 16 families. Trinucleotide repeats of CAG were 73～79. The fragments of abnormal alleles were 380～402bp, and all patients were heterozygous. The copy numbers of normal alleles were 18～40, fragments from 202～270bp. SCV reduction was much obvious compared to MCV, MCV and SCV in lower limb ?ere much more slow than that in upper's. BAEP, VEP were also delayed in latency. The anticipation in parental sex bias were much more obvioius than that in matental's. Cerebellar ataxia was most severe, the next were dysarthria and bulging eyes. Amytrophy was seen only in bed ridden patients. Cerebellar atrophy was more severe than brain stem, cord atrophy was n't observed in all MJD.

结果检出10个家系25例病人及1例症状前18岁女孩有MJD基因突变，CAG三核苷酸重复73～79次，异常等位基因片段长380～402bp，均为杂合子；正常人CAG三核苷酸重复18～40次，等位片段长200～270bp，电生理发现MJD的SCV减慢比MCV明显，而下肢的MCV、SCV又较上肢明显，BAEP、VEP均有不同程度的潜伏期延长或波的异常；MJD的父亲遗传早于母亲，进展也较块，临床以小脑性共济失调为突出症状，其次为构音障碍、突眼等，肌肉萎缩仅见于晚期病人；MRI示小脑萎缩较明显，脑干萎缩并不严重，未见明显的颈髓萎缩。

These were controlled by multiple allels or by loci with allels that segregate independently whereby epistasis also may have played a role.

这些是受复等位基因或含分离等位基因的位点支配的，上位性也可能靠它而起了作用。

A new RHAG mutation was found firstly in Chinese population,it is a 582 C＞T homozygosity mutation in RHAG gene.

首次在中国人群RhD变异型标本中发现一例新的RHAG等位基因，该等位基因是RHAG外显子第582位C＞T杂合突变。

The main clime features included ataxia, hypopsia, axanthocyanopsia and retinal pigmental degeneration. Alleles from 7 to 9 repeats were seen in the other 4 healthy members. GAG repeats from 6 to 21 were found in other 126 SCA patients, 71 family members and 60 healthy controls.

该家系内表型正常的4位成员SCA7等位基因CAG重复数目为7~9，另126例临床表现为SCA的患者、71名表型正常的家系成员及60名健康对照者SCA7等位基因内CAG三核苷酸重复数为6~21。

The analytic results showed frequencies of allele B or A and allele C were significantly different (P.01), while Taihe Silkies chickens and Baier chickens were different (P.05), it could conclude that the SNP may have relationship with thiamine content.

等位基因A和B的频率极显著高于等位基因C的频率，且泰和乌骨鸡与白耳鸡差异显著，故推测所检测到的基因座与肌肉硫胺素含量相关。

Studies on relationship between population size and sampling proportion revealed that population size had evident impact on the sampling proportion and retainment of variations in core collection.

以36对SSR引物的37个位点和2708份核心种质材料进行取样比例的研究结果认为，随着压缩比例的增大压缩群体的基因多样性指数先升高再降低，等位基因的数量和等位基因覆盖率持续下降并且速率逐渐加大。

The results showed that activities of the forward sequence of both genotypes were higher than that of reverse sequence. Promoter activity of the recombinants with A allele was about one third lower than that with C allele.

实验结果表明，2种基因型的正向序列启动子活性均高于相应的反向序列，含有A等位基因的启动子片段活性比含有C等位基因的片段低约1/3。

Plunder melds and run with this jewel!

掠夺melds和运行与此宝石！

My dream is to be a crazy growing tree and extend at the edge between the city and the forest.

此刻，也许正是在通往天国的路上，我体验着这白色的晕旋。