查询词典 heterozygous
- 与 heterozygous 相关的网络例句 [注:此内容来源于网络,仅供参考]
-
The gene targeted mice are commonly produced by breeding the heterozygous targeted mice following microinjecting the homologous recombinant ES cells into the blastocoele cavity of 3.5dpc embryos at the blastocyst stage to give birth to chimeric mice.
传统基因敲除获得某一突变基因的纯合体动物首先要利用打靶胚胎干细胞获得嵌合体动物;随后用嵌合体动物与野生型个体交配得到突变基因的杂合体动物;最后才能通过杂合体动物之间的交配来生产纯合体动物。
-
There are 2 alleles at a marker locus and they are codominant. We assumed that the sires used were heterozygous at all marker loci with known linkage phases and were mated to females which are randomly sampled from a population being in HardyWeinberg equilibrium.For further understanding of the values of treating QTL effect as random effect and the importance of estimating the variance component of QTL, we estimated the additive QTL effect under several factors combinations assuming that the QTL vanance component to be known.
为了进一步明确将QTL效应作为随机效应处理,并估计其方差组分的重要意义,本文在方差组分真值给定的前提下,采用随机QTL效应模型和单标记及侧翼标记信息,研究了不同试验设计、不同群体结构、不同QTL等位基因类型、不同遗传力和不同QTL方差贡献等因素组合下,TM-BLUP种畜遗传评定的效果。
-
In Small Tail Han sheep, Chinese Merino sheep, Corriedale sheep and South African Mutton Merino sheep, frequency of AA genotype was 0.58, 0.98, 0.96, 1.00, frequency of AB genotype was 0.40, 0.02, 0.04, 0.00, frequency of BB genotype was 0.02, 0.00, 0.00, 0.00, respectively. The ewes with mutation homozygous genotype BB or mutation heterozygous genotype AB had 1.45 at 305 bp of exon 3 of BMP4 gene in the BB genotype in comparison to the AA genotype, and this mutation resulted in an amino acid change: alanine—?aspartic acid. The ewes with genotype BB had 0.61 P
结果表明:小尾寒羊、中国美利奴绵羊、考力代绵羊在INHA基因5'调控区发生了1处碱基突变(316C→T),南非肉用美利奴绵羊没有发生这种突变;小尾寒羊、中国美利奴绵羊、考力代绵羊、南非肉用美利奴绵羊AA基因型频率分别为0.58、0.98、0.96、1.00,AB基因型频率分别为0.40、0.02、0.04、0.00,BB基因型频率分别为0.02、0.00、0.00、0.00;突变纯合型和突变杂合型小尾寒羊平均产羔数分别比野生型多1.45只P
-
Dihyborid An organism that is heterozygous at two loci, formed by crossing homozygous parents with different alleles at two given loci: for example, Mendel ' s cross between yellow round and green wrinkled garden peas to give a yellow round dihybrid.
双因子杂交:用两个基因位点上具有不同等位基因的纯合亲本杂交形成的杂合生物体。例如,在孟德尔的杂交试验中,黄圆和绿皱杂交生成杂合子黄圆。
-
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。
-
We now report a subsequent analysis of HIF2A in a cohort of 75 erythrocytosis patients and identify 4 additional patients with novel heterozygous Met535Val and Gly537Arg mutations.
我们报道对75例红细胞增多症病人的分析,发现有4人的杂合子Met535Val和Gly537Arg发生突变。
-
RESULTS: These familial keloids mainly occurred during adolescence, showing the equal chance of being affected between male and female subjects. The affected person could be heterozygous, and a child of an affected parent had a 50% chance of being affected. Thirteen subjects displayed familiar keloid, 1 suspected keloid, 2 did not present keloid as obligate carriers, and 1 did not present keloid as doubtful carrier. One pedigree displayed keloid in 3 generations, two displayed in 2 generations. The traits of familial keloids were transmitted interruptedly, revealing incomplete penetrance. The clinical phenotypes of familial keloids presented variable expression among the different affected.
结果:这些瘢痕疙瘩家系以青春期发病为主,男女患病的机会均等;杂合体即可发病,双亲之一发病其半数子女可能发病;3个瘢痕疙瘩家系发病13人,可疑发病1人,2个未发病肯定携带者,1个未发病可疑携带者;3代发病家系1个,2代发病家系2个;瘢痕疙瘩性状存在间断传递、外显不完全现象;临床表型存在个体差异。
-
The relationship between the genetic deficiencies and hemorrhagic disorder were characterized. The homozygosity of the Thr359Met in the propositus with FⅦ: C activity 2% was related to severe clinical symptoms; The proband with double heterozygous lesions of Arg152Leu and one single nucleotide deletion at position 11487-9, combined with Arg304Trp in exon 8 with FⅦ activity 1% suffered severe clinical bleeding tendency. one proband with double heterozygous mutations (Agr304Trp and Arg304Gln) with 10% of FⅦ activities characterized asymptom. the heterozygous mutations (Thr359Met, Arg152Gln,-55C→T) with FⅦ: C 1%~5. 5% showed moderate or mild clinical symptoms.
其中8961 G>T(Arg152Leu)和10966-8delC两种突变为国际首次报道,IFSla+5g>a突变导致的异常剪接为国际首次报道。1个F7及F10基因联合缺陷家系,其中,F10基因28139 G>T(Val384Phe)突变为国际首次报道;发现了1个由F7及组织因子(tissue factor,TF)两种基因联合缺陷导致的出血家系,其突变分别为F7基因启动子区-55C>T杂合突变;TF 9363 C>T(Arg131Trp)杂合多态性(频率2.63%)。6种F7基因突变发生在催化区;2种突变发生在裂解位点;1种发生在启动子区;1种突变发生在剪接位点,除一种缺失突变外,其余均为点突变;所有家系的基因突变都来自先证者的父亲和/或母亲。
-
Objective To evaluate the applicability of partial loss of heterozygous criteria in tumor tissues with Identifiler system.
目的 对肿瘤组织中部分杂合性丢失(partial loss of heterozygous, pLOH)的判定标准在Identifiler系统中的适用性进行评估。
-
Deduced by the proportion of typical sterile plants and normal fertile plants in segregative generations derived from WA zhenqiuA/6078 that:I gene could inhibit the expression of Rf gene completely by the heterozygosity of 1 pair of Rf in genotype;and only reduce the expression of Rf genes with two heterozygous Rf genes in genotype ;but it would never inhibit the expression of Rf genes if the genotype included 3 pairs of heterozygous Rf genes. When Rf gene was homozygous,the / gene could not inhibit the expression of it.
根据认叭真秋刀6078各衍生分离世代中典型不育株和正常可育株所占比例推断:基因型中仅包含1对杂合的Rf基因时,I对Rf的表达起完全抑制作用;基因型中包含2对杂合的Rf基因时,I仅对Rf的表达起削弱作用;当基因型中包含3对杂合的对基因时,I对Rf的表达不起抑制作用;I对纯合位点的Rf的表达不起抑制作用。
- 推荐网络例句
-
But we don't care about Battlegrounds.
但我们并不在乎沙场中的显露。
-
Ah! don't mention it, the butcher's shop is a horror.
啊!不用提了。提到肉,真是糟透了。
-
Tristan, I have nowhere to send this letter and no reason to believe you wish to receive it.
Tristan ,我不知道把这信寄到哪里,也不知道你是否想收到它。