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Human Molecular Genetics|December 1, 1992
A new Tay-Sachs disease B1 allele in exon 7 in two compound heterozygotes each with a second novel mutationM Fernandes, F Kaplan, M Natowicz, et al.Canadian Journal of Biochemistry|April 1, 1977
Characterization of an activating factor required for hydrolysis of Gm2 ganglioside catalyzed by hexosaminidase AP HechtmanAmerican Journal of Human Genetics|July 1, 1996
The Val192Leu mutation in the alpha-subunit of beta-hexosaminidase A is not associated with the B1-variant form of Tay-Sachs diseaseY Hou, G Vavougios, A Hinek, et al.Human Genetics|December 1, 1992
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French CanadaP Hechtman, B Boulay, M De Braekeleer, et al.Human Mutation|January 1, 1992
Novel Tay-Sachs disease mutations from ChinaN Akalin, H P Shi, G Vavougios, et al.The Journal of Biological Chemistry|January 10, 1997
Identification of candidate active site residues in lysosomal beta-hexosaminidase AM J Fernandes, S Yew, D Leclerc, et al.The Biochemical Journal|March 1, 1980
Interaction of activating protein and surfactants with human liver hexosaminidase A and GM2 gangliosideP Hechtman, Z KachraPediatric Research|October 1, 1992
Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growthM Dolenga, P HechtmanThe Biochemical Journal|December 1, 1977
Purification and properties of the hexosaminidase A-activating protein from human liverP Hechtman, D LeBlancJournal of Chromatography|April 4, 1980
High-capacity method for purification of human liver hexosaminidase B using hydrophobic chromatographyJ Hardwick, P HechtmanPageof 26