Tay-Sachs
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n. 家族黑蒙性白痴
adj. 家族黑蒙性白痴病的
adj.
家族黑蒙性白痴病的；
n.
家族黑蒙性白痴；
英英释义
Tay-Sachs[ 'tei'sæks ]
n.a hereditary disorder of lipid metabolism occuring most frequently in individuals of Jewish descent in eastern Europe; accumulation of lipids in nervous tissue results in death in early childhood
同义词：Tay-Sachs diseaseSachs diseaseinfantile amaurotic idiocy
权威例句
Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase componentMouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism
Simultaneous amplification of the two most frequent mutations of infantile Tay-Sachs disease in single blastomeres
Prevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycin
Dramatically Different Phenotypes in Mouse Models of Human Tay-Sachs and Sandhoff Diseases
Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay.
Amplified microgravimetric quartz-crystal-microbalance analyses of oligonucleotide complexes: a route to a Tay–Sachs biosensor device
Expression of human beta-hexosaminidase alpha-subunit gene (the gene defect of Tay-Sachs disease) in mouse brains upon engraftment o...
Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.
Sensing and amplification of oligonucleotide-DNA interactions by means of impedance spectroscopy: a route to a Tay–Sachs sensor
Tay-Sachs
fatal inherited disorder, 1907, named in German (1901) by German neurologist Henryk Higier (1866-1942) from names of British ophthalmologist Warren Tay (1843-1927) and U.S. physician and neurologist Warren Sachs (1858-1944) who had independently described it in 1881 and 1887 respectively.
1. The former genes cause neurological diseases, such as Tay-Sachs, Gaucher's and Niemann-Pick.
前者会引发神经性疾病，如泰萨二氏病、脑苷脂沉积病和神经鞘磷脂沉积病；
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2. For some rare disorders, such as Huntington's and Tay-Sachs, genetic information is a diagnosis.
对一些罕见疾病，如亨廷顿氏舞蹈病和黑蒙性痴呆，通过基因信息就可以诊断。
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3. These enlarged, pale neurons are in a baby with Tay-Sachs disease, which is seen mostly in persons of European Jewish heritage.
Sachs病的婴儿会出现扩大的苍白色神经元，这在欧洲犹太后裔最常见。
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4. PGD is good for screening for specific genetic disorders such as cystic fibrosis and Tay-Sachs disease, and also can be used to select gender.
PGD适用于特殊遗传病的筛查，如囊性纤维化和神经节苷脂病，而且PGD也可以用于性别选择。
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5. So-called recessively inherited disorders, such as Tay-Sachs disease, cystic fibrosis and red blood cell disorders known as thalessemias are rare.
所谓隐性遗传疾病，像“泰-萨克斯病”、“囊性纤维化”，以及被称为“地中海贫血症”的血细胞疾病，都很罕见。
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6. For those thinking of starting a family, it could alert them to their risk of having a baby with cystic fibrosis, Tay-Sachs and other genetic disorders.
对那些打算建立家庭的人，它可以提醒他们所要的孩子是否会有囊性纤维化，泰萨二氏病和其他遗传疾病的风险。
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7. But Cassandra said she likes that I have different genes, arguing that when, for instance, Jews procreate with other Jews, they increase their kids' risk for breast cancer and Tay-Sachs.
但卡桑德拉说，她喜欢我的基因与她不同。例如，假如犹太人与其他犹太人生育，他们会增加孩子的乳腺癌和黑蒙性痴呆的风险。
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8. PGD has been offered by the NHS for more than a decade for serious diseases that come early in childhood, like cystic fibrosis or Tay Sachs, a neurological disease.
NHS提供PGD技术已经超过10年时间了，用来治疗一些早在儿童时期发病的严重疾病，例如囊性纤维化(属遗传性胰腺病)或者叫泰萨氏病的一种神经学疾病。
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9. PGD has been offered by the NHS for more than a decade for serious diseases that come early in childhood, like cystic fibrosis or Tay Sachs, a neurological disease.
NHS提供PGD技术已经超过10年时间了，用来治疗一些早在儿童时期发病的严重疾病，例如囊性纤维化(属遗传性胰腺病)或者叫泰萨氏病的一种神经学疾病。
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Tay-Sachs
