homozygous
adj. 纯合子的;同型结合的
2026-04-13 10:09 浏览次数 14
adj. 纯合子的;同型结合的
"these two fruit flies are homozygous for red eye color"
homozygous dominants纯合显性
homozygous mutations纯合子突变
homozygous deletion纯合子缺失
homozygous genotype纯合基因型
homozygous individual纯合个体
homozygous dominance纯合显性
homozygous mutation同型接合子突变
homozygous s纯合子
methionine homozygous甲硫胺酸合子
however, most (90%) of homozygous mutant mice die within 24 hours after birth, and 63% of them show severe air dilatation and lack milk in stomach and intestine.
然而大部分(90%)的纯合子突变小鼠都在出生后24小时以内陆续死亡。其中63%的肠胃都出现 有严重的气体胀大与缺乏奶水。
in genetics, refers to an allele that is expressed in both the heterozygous and homozygous condition.
指等位基因在杂合状态和纯合状态都有表达的现象。
homozygous non-metallic (nm nm): two copies of the 「non-metallic」 gene.
纯非金属(波长纳米) :一式两份,非金属'基因。
conclusion compound homozygous mutations r450h and d727e lead to ch. compound heterozygous mutations r450h and d727e may be the cause of subclinical hypothyroidism.
结论r450h/d727e纯合子突变导致先天性甲减,r450h/d727e杂合子突变可发生亚临床甲减。
the hybrid of parents that differ at only one gene locus, for which each parent is homozygous with a different allele.
杂交的双亲只有一个基因位置不同,对它来说,每个亲本是有一个不同的等位基因混合的。
methods exon 4~9 of pten were amplified by polymerase chain reaction (pcr) for homozygous deletions in 110 tumor samples of patients with bone and soft tissue tumors, 3 tumor cell lines.
方法应用聚合酶链反应(pcr)分析骨及软组织肿瘤患者110例肿瘤标本,3个肿瘤细胞系pten基因第4~9外显子有无纯合性缺失。
to distinguish between the phenotypically identical aa and aa, these can be backcrossed to the homozygous recessive parent aa.
为了鑒定表现型完全相同的aa与aa ,我们用纯合的隐性亲本aa 来进行回交。
besides, t-dna insertion mutant lines of pollen surface proteins have been purchased, and through t-dna insertion and locus analysis, 96 homozygous mutant lines have been acquired.
此外,购买了花粉表面蛋白质t-dna插入突变体,通过分子生物学方法进行了t-dna插入鑒定以及插入位点鑒定,并获得了96个突变体株系的纯合植株。
their newborn daughter died last year from a devastating dwarfism-related disease called homozygous achondroplasia.
他们的新生女儿去年死于一种破坏性很强的侏儒相关性疾病,叫做纯合软骨发育不良。
the two options available to us for treating children with very severe homozygous form of the disease are to one either perform ldl apheresis.
这两种选择可用于治疗儿童该病非常严重纯合子形式。 方式之一是进行ldl单采。
altogether, half the offspring will be homozygous at that particular locus .
加在一起,将有半数的后代在那个特定的位点上是纯合的。
most plants carry a large genetic load for deleterious recessive genes of which a few are homozygous and depress growth.
多数植物带有大量有害的隐性基因的「遗传负荷」,其中少数是纯合的,因而降低了生长。
the paper introduces the breeding methods of the homozygous two-type line, temporary maintainer line and complete sterile line with a recessive epistasis nuclear male sterile.
对甘蓝型油菜隐性上位细胞核雄性不育纯合两型系、临保系和全不育系的转育方法进行了介绍。
purpose:to research the association between homozygous deletion of p16 gene and primary epithelial ovarian neo-plasms.
目的:探讨p16基因的纯合性丢失和原发性上皮性卵巢癌发生及发展的相关性。
this locus occurs in over 40% of the population and is associated with increased risk of 40% in homozygous and 15 to 20% in heterozygous.
该位点出现在40%以上的人群中,其与纯合子风险增大40%以及杂合子风险增大20%的现象相关。
the homozygous form is fatal.
纯合子是致命的。
homozygous tetraploid is a relatively balanced system, the continued selection is invalid.
纯合的四倍体是一个相对平衡的系统,继续选择是无效的。
contributing factors, harm and control measure of homozygous restoration line in the sorghum sterile line or male sterile maintainer were studied.
叙述了高粱不育系或保持系中同质恢复系产生的原因、危害及防治措施。
homozygous mutant mice showed expected ratio and no obvious defect in sizes and morphologies at all embryonic stages examined.
纯合子突变小鼠在各个胚 胎时期都有预期中的出现比例,在大小与型态上并没有明显的缺陷。
the functional defect affecting the heparin-binding site confers moderate risk of vte to heterozygous and high risk of vte to homozygous individuals.
影响肝素结合位点的功能性缺陷,使杂合子个体有中度风险患vte、纯合子个体有高度风险患vte。
according to conventional theory, little genomic changes should occur in homozygous and stable amphiploids of the grass family, particularly those involving polyploid wheat as a parent.
根据传统理论,在禾本科特别是在含有多倍体小麦为亲本的禾本科纯合、稳定的双二倍体中应存在极少的基因组变异。
people who were homozygous for cyp1a2*1a -meaning they carried two copies of gene for fast caffeine-metabolism - actually reduced their risk of heart attack by drinking coffee.
而那些携带有同型结合的cyp1a2*1a基因(即携带有两份快速代谢咖啡因基因)的人,喝咖啡却能减少他们心脏病发作的危险。
instead of looking for homozygous variants where each parent carried an allele, the researchers were looking for heterozygous variants that were also not present in the parents.
研究人员寻找不存在与父母中的杂合变异体,而不是寻找每位亲本携带一个等位基因的纯合变异体。