X-linked
释义
[医]伴性的，伴X染色体的，性连锁的；
英英释义
X-linked
adj.relating to genes or characteristics or conditions carried on the X chromosome
权威例句
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.X-linked IAP is a direct inhibitor of cell-death proteases.
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy
JM2, encoding a fork head–related protein, is mutated in X-linked autoimmunity–allergic disregulation syndrome
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SE...
CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM
Rett syndrome is caused by mutations in X-linked
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
1. Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia.
ALAS2基因的可遗传突变是人类X连锁铁粒幼细胞性贫血的原因。
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2. It is compatible with the X-linked recessive inheritance.
该病症符合X -连锁隐性遗传。
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3. This is an X-linked deficiency of one of the enzymes in the urea cycle.
这是一个X染色体缺陷导致的尿素循环酶缺乏症之一。
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4. They are lamellar, x-linked, and epidermolytic hyperkeratosis forms of ichthyosis.
他们是层状，X连锁，鱼鳞病及表皮角化的形式。
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5. Medically, the condition is called X-linked Severe Combined Immunodeficiency (X-SCID).
在医学上，这种情况称为X连锁重症联合免疫缺陷(X - SCID)。
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6. Objective To improve the recognition and diagnosis of X-linked hypophosphatemia (XLH).
目的提高对X -连低磷酸盐血症的认识和诊断。
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7. Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophy (ALD).
目的鉴定并分析1个新的肾上腺脑白质营养不良家系的基因突变类型和位点。
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8. At present, more than 200 diseases which have been identified are X-linked, these diseases only affect male fetuses.
目前，已有超过200种单基因遗传性疾病被认为是由X染色体连锁遗传引起的，这些疾病只影响男性胎儿。
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9. As an X-linked condition, choroideremia usually affects men, leading to severe vision loss or blindness in middle age.
作为一个X -连锁条件，通常会影响男性脉络膜，导致严重的视力减退或失明的中年。
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10. Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.
化综合征是一种X连锁的隐性遗传病，为男性假两性畸形中最常见的类型。
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11. Glycerol kinase deficiency (GKD), a rare X-linked recessive disorder, is classified into two types: isolated and complex.
甘油激酶缺乏症（GKD）是一种少见的X染色体隐性遗传性代谢缺陷病，可分为单纯型和复合型。
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12. Objective To investigate the clinical manifestations, diagnostic methods and treatment of X-linked agammaglobulinemia(XLA).
目的探讨X-连锁无丙种球蛋白血症的临床表现、诊断方法和治疗。
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13. Objective To investigate the typical clinical manifestations, biochemical change and treatment of X-linked adrenoleukodystrophy.
目的：研究X-连锁肾上腺脑白质营养不良的临床、生化改变及治疗情况。
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14. Objective To carry out prenatal molecular diagnosis on 3 fetuses from different pedigrees with X-linked adrenoleukodystrophy (ALD).
目的对3名来自不同家系的肾上腺脑白质营养不良(ALD)携带者所怀胎儿进行产前分子诊断。
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15. Objective To analyze the ABCD1 gene mutations in 5 cases of X-linked adrenoleukodystrophy (X-ALD) patients and 2 cases of their mothers.
目的对5例x -连锁肾上腺脑白质营养不良(X -ALD)患儿及其中2例的母亲进行ABCD 1基因突变分析。
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16. In a new study, researchers propose that Henry had an X-linked genetic disorder and a rare blood type that could explain many of his problems.
在一项新研究中，科研人员推断亨利八世的X染色体遗传障碍和罕见血型是导致其状况频发的罪魁祸首。
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17. The manifestations of this x-linked disease are more drastic than SEH; males suffer from lissencephaly, while females suffer from band heterotopia.
X-连锁性病变的现象比SEH更明显，男性表现为无脑回，女性表现为带状异位。
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18. There are three kinds of inherited patterns including autosomal dominant, autosomal recessive and X-linked recessive in inherited congenital cataract.
与遗传有关的先天性白内障有多种遗传方式，其致病基因、 基因突变的位点和引起先天性白内障的表现型相继被发现。
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19. Like other X-linked disorders such as color blindness and muscular dystrophy, genetic mutation causing a son's infertility could be passed from his mother.
像色盲，肌营养不良等X连锁的疾病一样，由遗传突变导致的不育可以从母亲传给儿子。
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20. Objective Using molecular biological method to determine the inherited modal of a family which was considered as X-linked high myopia by pedigree analysis.
目的应用分子生物学方法判定经家系分析初步认定为X连锁遗传的高度近视家系的遗传方式。
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21. Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天性小眼球是一种先天发育异常性眼科疾病，遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。
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22. Female mosaicism of the X chromosome has major implications for human health and disease and is the leading cause of female protection from X-linked genetic disorders.
女性作为X染色体的杂合子在人类的健康与疾病中及重要作用，并可避免X连锁遗产性疾病在女性中发生。
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23. FXS is characterized by X-linked mental retardation with additional features such as a long face with large protruding ears, macroorchidism, and eye-gaze avoidance etc.
其主要临床特征为智力低下、特殊的外貌特征（包括长脸、大耳廓、下颌突出、巨头、腭弓高、大睾丸等）、行为及认知障碍、多动、注意力难集中以及孤独、自闭等症状。
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24. A variety of approaches have been used to address this issue, the most common of which is the study of tumors in women, who are heterozygous for X-linked marker enzymes.
一系列的方法已被用来探讨这个问题，其中一个最常用的方法是研究女性肿瘤，她们是X连锁标记酶杂合子。
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25. The absence of ALAS2 leads to maturation arrest of primitive erythroid cells. Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia (XLSA).
ALAS2的缺失能导致红细胞发育的停滞，ALAS2基因的遗传性突变能引起X-连锁的成高铁红细胞贫血（XLSA）。
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26. 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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27. The methylation of histone H3-K27 was proved to be linked to several silencing phenomena including homeotic-gene silencing, X inactivation and genomic imprinting.
组蛋白H3第27位赖氨酸的甲基化与同源盒基因沉默、X染色体失活、基因印记等基因沉默现象有关；
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28. Objective to detect mutations of the RP2 gene in two Chinese families with X linked retinitis pigmentosa (XLRP).
目的检测引起2个家系产生X连锁视网膜色素变性的RP2基因突变。
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29. Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype.
目的探讨X-连锁迟发性脊椎骨骺发育不良（SEDL）基因逃避X染色体失活（XCI）及与临床表型的关系。
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30. Objective to identify the disease locus in X - linked retinitis pigmentosa (XLRP) families using genetic linkage analysis.
目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析，确定其致病基因的所在位点。
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X-linked
