Tissue Culture Techniques as an Aid to Prenatal Diagnosis and Genetic Counselling in Homocystinuria
Open Access
- 1 June 1973
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 10 (2) , 120-121
- https://doi.org/10.1136/jmg.10.2.120
Abstract
Cystathionine synthase activity was studied in skin fibroblasts from a mother with homocystinuria and her husband and newborn baby. Enzyme studies were also undertaken on a fibroblast cell line derived from amniotic fluid taken at 16 weeks' gestation. The enzyme activity was very low in the mother, within the normal range in the father, and at an intermediate level consistent with heterozygosity in the infant. The activity present in the amnion fibroblasts was similar to that found in the cell line cultured from the infant's skin biopsy.Keywords
This publication has 8 references indexed in Scilit:
- Studies of the Mechanism of Pyridoxine-Responsive HomocystinuriaPediatric Research, 1972
- Cystathionine Synthase in Tissue Culture Derived from Human Skin: Enzyme Defect in HomocystinuriaScience, 1968
- Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway.1965
- Homocystinuria due to Cystathionine Synthetase Deficiency: The Mode of InheritanceScience, 1964
- Homocystinuria: An Enzymatic DefectScience, 1964
- The identification of homocystine in the urineBiochemical and Biophysical Research Communications, 1962
- Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern IrelandArchives of Disease in Childhood, 1962
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951