autosomal
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adj.
正染色体的,常染色体的;
英英释义
autosomal[ ,ɔ:təu'səuməl ]
adj.of or relating to an autosome
"autosomal gene"
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。
权威例句
Mutations in PCSK9 cause autosomal dominant hypercholesterolemiaMutations 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...
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。
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3. The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
该病属常染色体隐性遗传,与X-染色体关联,所以,母亲是基因携带者的男性表现为发病。
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4. Study 2 - Cornell University : This study used comparative genomics to analyze 39, 440 autosomal SNPs in 10, 150 sequences from 15 African-Americans and 20 European-Americans.
研究小组2——康奈尔大学:这一研究运用了相匹配的基因组对15个非洲裔美国人及20个欧洲裔的美国人的39,440种常染色体SNP(单核苷酸多态性)的10,150 种不同序列进行了分析。
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5. This disorder is inherited as an autosomal dominant trait.
本病作为常染色体显性传递。
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6. Oculocutaneous albinism( OCA ) is a group of autosomal recessive disorders of melanin synthesis, which is characterized by congenital hypopigmentation of skin, hair and eyes.
眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
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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。
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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%。
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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。
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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;
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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)。
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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。
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13. BACKGROUND AND STUDY AIMS: Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder characterized by telangiectasia formation that can lead to small-bowel bleeding.
背景与研究目的:遗传性出血性毛细血管扩张症(HHT)为罕见的常染色体显性疾病,其特征为小肠毛细血管扩张、出血。
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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;
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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。
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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。
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19. Pedigree analysis indicated autosomal dominant inheritance.
呈常染色体显性遗传。
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20. It is shown that the mean relative lengths and centromeric indices of autosomal SCs agree closely with those of mitotic chromosomes.
结果表明,常染色体联会复合体的相对长度和着丝点指数与体细胞染色体的相应参数具有很好的吻合性。
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21. Progressive familial intrahepatic choleatasia(PFIC)is an autosomal recessive inherited children liver cholestasis characterized by severe jaundice and pruritus.
进行性家族性肝内胆汁淤积(PFIC)是一组常染色体隐性遗传肝细胞源性儿童胆汁淤积症。
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22. Objective To observe the clinical effect of laparoscopic renal cyst decortication (LRCD)for patients with autosomal dominant polycystic kidney disease (ADPKD).
目的观察腹腔镜肾囊肿去顶减压术(LRCD)在治疗常染色体显性遗传性多囊肾病(ADPKD)的临床效果。
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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。
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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。
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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。
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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。
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30. autosomal abnormalities
常染色体异常
-- 来源 -- 英汉 - 翻译参考[网络]
31. This disorder is inherited as an autosomal dominant trait.
本病作为常染色体显性传递。
-- 来源 -- 英汉 - 辞典例句
32. 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。
-- 来源 -- 英汉 - 辞典例句
33. a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results.
一种罕见的常染色体退缩疾病,症状是血小板不能正常凝固导致流血不止。
-- 来源 -- 汉英 - 翻译参考
34. An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.
除了正常染色体对以外,还存在有第二种同源染色体的非整倍体状态,被称为三体性。
-- 来源 -- 英汉 - 辞典例句
35. To discuss the role and value of high resolution ultrasonography in the diagnosis of autosomal recessive polycystic kidney disease(ARPKD)and to review literatures.
目的 :结合文献探讨高分辨率超声在常染色体隐性遗传性多囊肾 (autosomal recessive polycystic kid-ney disease,ARPKD)检查中的作用及价值。
-- 来源 -- 网友提供
36. Xeroderma pigmentosum is an autosomal recessive disease.
着色性干皮病是一种自发退行性疾
-- 来源 -- 英汉 - 辞典例句
37. autosomal inheritance
常染色体遗传
-- 来源 -- 英汉 - 翻译参考[网络]
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
autosomal




