Literature DB >> 6256017

Purification and characterization of human alpha-galactosidase isozymes: comparison of tissue and plasma forms and evaluation of purification methods.

D F Bishop, K J Dean, C C Sweeley, R J Desnick.   

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Year:  1980        PMID： 6256017

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  2 in total

1.  Lysosomal alpha-galactosidase in endothelial cell cultures established from a Fabry hemizygous and normal umbilical veins.

Authors:  L Hasholt; S A Sørensen
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

2.  Fabry disease: preclinical studies demonstrate the effectiveness of alpha-galactosidase A replacement in enzyme-deficient mice.

Authors:  Y A Ioannou; K M Zeidner; R E Gordon; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-12-13       Impact factor: 11.025
  2 in total

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