Assay of ganglioside activity in human fibroblasts employing the natural activator protein — Diagnosis of variant forms of GM2 gangliosidosis
- 1 December 1980
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 108 (3), 361-368
- https://doi.org/10.1016/0009-8981(80)90342-3
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- The assay of sphingolipid hydrolases in white blood cells with labelled natural substratesClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Biochemistry and Genetics of gangliosidosesHuman Genetics, 1979
- Purification and Characterization of an Activator Protein for the Degradation of Glycolipids GM2and GA2by Hexosaminidase AHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1979
- Tay-sachs disease: An improved, fully-automated method for heterozygote identification by tear β-hexosaminidase assayClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- The Biochemistry of Sphingolipid Storage DiseasesAngewandte Chemie International Edition in English, 1977
- Human hexosaminidase isozymes: Chromatographic separation as an aid to heterozygote identificationClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Ganglioside GM2 N‐acetyl‐ß‐D‐gafactosaminidase and asialo GM2 (GA2) N‐acetyl‐ß‐D‐galactosaminidase; studies in human skin fibroblastsClinical Genetics, 1977
- Urinary hexosaminidase analysis for the identification of Tay-Sachs genotypesClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Sandhoff’s Disease: Studies on the Enzyme Defect in Homozygotes and Detection of HeterozygotesPublished by Springer Nature ,1972
- Enzymatische Untersuchungen im Blut von Überträgern einer Variante der Tay-Sachsschen Erkrankung (Variate O)Klinische Wochenschrift, 1971