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Genomics|January 1, 1993
Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human geneH W Yoo, C A Warner, C H Chen, et al.
Human Genetics|January 1, 1985
delta-Aminolevulinate dehydratase: induced expression and regional assignment of the human gene to chromosome 9q13----qterA L Wang, K H Astrin, W F Anderson, et al.
Enzyme|January 1, 1989
Characterization of the defective beta-glucuronidase activity in canine mucopolysaccharidosis type VIIE H Schuchman, T K Toroyan, M E Haskins, et al.
Investigative Ophthalmology & Visual Science|July 1, 1986
Arylsulfatase B activity in cultured retinal pigment epithelium: regional studies in feline mucopolysaccharidosis VIL E Stramm, R J Desnick, M E Haskins, et al.
The Biochemical Journal|December 15, 1993
Catabolism of hirudin and thrombin-hirudin complexes in the ratJ Bichler, J W Baynes, S R Thorpe
Enzyme|January 1, 1985
Use of activators and inhibitors to define the properties of the active site of normal and Gaucher disease lysosomal beta-glucosidaseS Gatt, T Dinur, K Osiecki, et al.
Clinical Biochemistry|August 1, 1981
Comparison of the tartrate-resistant acid phosphatase in Gaucher's disease and leukemic reticuloendotheliosisK W Lam, C Y Li, L T Yam, et al.
The Biochemical Journal|June 11, 1998
Human alpha-galactosidase A: glycosylation site 3 is essential for enzyme solubilityY A Ioannou, K M Zeidner, M E Grace, et al.
Enzyme|January 1, 1981
An improved method for heterozygote identification in feline and human mucopolysaccharidosis VI, arylsulfatase-B deficiencyM M McGovern, D T Vine, M E Haskins, et al.
The Journal of Biological Chemistry|June 25, 1992
Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic formsT Takahashi, M Suchi, R J Desnick, et al.
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