autosomal

autosomal怎么读

英式音标：[ˌɔ:tə\'səʊməl]

美式音标：[ˌɔtə\'soʊməl]

autosomal的意思释义

adj.

正染色体的，常染色体的；

英英释义

adj.of or relating to an autosome

\"autosomal gene\"

autosomal用法及例句

词组短语

autosomal dominant inheritance常染色体显性遗传

双语例句

用作形容词(adj.)

Xeroderma pigmentosum is an autosomal recessive disease.

着色性干皮病是一种常染色体的退行性疾病。

例句参考

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Friedreich\'s Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Friedreich\'s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)

Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson\'s Di...

autosomal相关例句

1. The Alzheimer in this ancestry appears as autosomal dominant genetic disease .

阿尔茨海默病在本家系中显示为常染色体显性遗传。

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2. They also found adermatoglyphia to be autosomal dominant, meaning only one parent needs to pass on the mutation for the child to show it.

他们也发现皮纹病是显性遗传，意味着只有一个父母将突变传给孩子去显现出来。

5. This disorder is inherited as an autosomal dominant trait.

本病作为常染色体显性传递。

7. Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.

脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。

8. The recurrence risk for this disease is, of course, 25% because of the autosomal recessive inheritance pattern.

因为它是常染色体隐性遗传的，所以它在家族中的发病率是25％。

9. Objective To evaluate the role of homozygosity mapping in the fine mapping of the genes responsible for the rare autosomal recessive diseases.

目的探讨纯合子定位法在罕见常染色体隐性遗传病致病基因精确定位中的作用。

10. Autosomal recessive inheritance was difficult to be evaluated because of few families remained.

常染色体隐性遗传因剩下的家系样本太少，难以预测；

11. Mutations in the cardiac sodium channel gene SCN5A also cause cardiac conduction disease and autosomal recessive sick sinus syndrome (SSS).

心脏钠离子通道基因SCN5A的突变也可导致心脏传导疾病和常染色体隐性病态窦房结综合征（SSS）。

12. Trichothiodystrophy is a rare hair disorder inherited in an autosomal recessive pattern.

毛发缺硫性失养症为一少见的常染色体隐性毛发疾病。

14. As part of the process, the team genotyped 1261 autosomal single-nucleotide polymorphisms in 829 individuals from 225 families.

作为病变的要素之一，在来自225个家族中的829个个体中，基因1261存在常染色体单核苷酸多态性。

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15. Certain autosomal translocations in the heterozygous state can be fully viable .

呈杂合子状态的某些常染色体易位完全可以生活的。

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16. Conclusions(1) HNPCC is of autosomal dominant inheritance (AD).

结论（1 ）该家族呈常染色体显性遗传；

17. Results The genetic pattern of the familial diabetes mellitus is mainly autosomal dominance inheritance and is not polygenic inheritance.

结果家族性糖尿病主要为常染色体显性遗传，不符合多基因遗传。

18. Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

结论：手掌小鱼际区真实花纹可能属于常染色体显性遗传。

23. Objective To explore the clinical features of autosomal recessive juvenile Parkinson disease(AR-JP).

目的探讨常染色体隐性遗传性青少年型帕金森病（AR-JP）的临床特征。

24. Trapped Neutrophil Syndrome is an autosomal recessive disease which results in mature neutrophils being unable to migrate from the bone marrow into the blood.

遗传性嗜中性白血球减少症是一种常染色体隐性遗传疾病，该疾病导致成体中性粒细胞无法从骨髓迁移到血液中。

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25. The hereditary mode of this family line is a autosomal dominant inheritance, which differs from those which have been reported.

本家系遗传方式为常染色体显性遗传，和其它学者报告不同。

26. It is also caused by mutations in genes associated with autosomal dominant cerebellar ataxia (ADCA), notably CAG/CAA repeat expansions in SCA2.

它还可能由常染色体显性遗传性小脑性共济失调相关基因突变引起，尤其是SCA2中的CAG/CAA重复扩增。

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27. Most mammals have just two kinds of photopigment in their retinas: one is encoded in the X chromosome and the other in an autosomal (non-sex) chromosome.

大部分哺乳动物的视网膜中只有两种感光色素：一种编码在X染色体中另一种寸在于正染色体中。

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28. WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.

WD是神经科较为常见的常染色体隐性遗传病，其唯一致病基因为ATP7B基因。

29. WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.

WD是神经科较为常见的常染色体隐性遗传病，其唯一致病基因为ATP7B基因。

30.autosomal abnormalities

常染色体异常

31.This disorder is inherited as an autosomal dominant trait.

本病作为常染色体显性传递。

38.a disorder of lipid metabolism that is inherited as an autosomal recessive trait.

油脂新陈代谢混乱的一种遗传病症。

-- 来源 -- 汉英 - 翻译参考

39.an autosomal recessive form of muscular dystrophy characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle.

一种常染色体退缩形式的肌营养不良。

-- 来源 -- 汉英 - 翻译参考