Intergenic complementation after fusion of fibroblasts from different patients with beta-galactosidase deficiency.

@article{Hoeksema1979IntergenicCA,
  title={Intergenic complementation after fusion of fibroblasts from different patients with beta-galactosidase deficiency.},
  author={H. Hoeksema and O. V. van Diggelen and H. Galjaard},
  journal={Biochimica et biophysica acta},
  year={1979},
  volume={566 1},
  pages={
          72-9
        }
}
Abstract Acid β-galactosidase from human liver consists, after gel filtration at pH 7.0, of a monomeric isoenzyme, β-galactosidase A and small amounts of a multimer, β-galactosidase B (Norden, A.G.W., Tennant, L.; and O'Brien, J.S. (1974) J. Biol. Chem. 249, 7969–7976). Our studies showed identical gel filtration patterns for β-galactosidase from human liver and cultured skin fibroblasts. Gel filtration in the buffer used for enzyme assays (pH 4.5) however, revealed primarily dimeric… Expand
The genetic defect in the various types of human β-galactosidase deficiency
Correction of combined beta-galactosidase/neuraminidase deficiency in human fibroblasts.
A neutral beta-galactosidase from the hepatopancreas of the shrimp Penaeus monodon (Crustacea: Decapoda): dimeric and sialyated.
  • N. Chuang
  • Biology, Medicine
  • Comparative biochemistry and physiology. B, Comparative biochemistry
  • 1990
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