英语词汇“Tay-Sachs”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

adj.

家族黑蒙性白痴病的；

家族黑蒙性白痴；

英英释义

Tay-Sachs[ 'tei's?ks ]

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

学习怎么用

权威例句

Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component
Mouse 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

单词	Tay-Sachs
释义	Tay-Sachs 听听怎么读 ['tei's?ks] 是什么意思 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's?ks ] 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 学习怎么用权威例句 Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component Mouse 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
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