Tay-Sachs
['tei'sæks]

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 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