Histochemical demonstration of acid beta-D-galactosidase activity in cultured human skin fibroblasts and its application to single cell analyses.
Author:
Affiliation:
1. Department of Pediatrics, Osaka University Hospital
2. Department of Genetics, Hyogo Medical College
Publisher
Japan Society of Histochemistry & Cytochemistry
Subject
Cell Biology,Histology,Physiology,Biochemistry,Pathology and Forensic Medicine
Link
http://www.jstage.jst.go.jp/article/ahc1968/14/4/14_4_343/_pdf
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A family with pseudodeficiency of acid α-glucosidase;Clinical Genetics;2008-06-28
2. Correlation of subcellular localization of disease-specific inclusions and sphingolipid activator protein-1(SAP-1) in sulfatide sulfatase-deficient fibroblasts.;ACTA HISTOCHEMICA ET CYTOCHEMICA;1988
3. Complementation analysis of .BETA.-galactosidase deficiency by means of histochemical method.;The Tohoku Journal of Experimental Medicine;1985
4. Use of a fluorescent analogue of galactocerebroside for assay of galactocerebroside β-galactosidase activity in skin fibroblasts from patients with krabbe's disease;Clinica Chimica Acta;1984-01
5. A severe infantile sialidosis (?-galactosidase-?-neuraminidase deficiency) mimicking GM1-gangliosidosis type 1;European Journal of Pediatrics;1983-09
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