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 metabolismSimultaneous amplification of the two most frequent mutations of infantile Tay-Sachs disease in single blastomeresPrevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycinDramatically Different Phenotypes in Mouse Models of Human Tay-Sachs and Sandhoff DiseasesTay-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 deviceExpression 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