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Автор kruger, Warren D.
Автор Cox, David R.
Дата выпуска 1995
dc.description Mutations in the human cystathionine β-synthase (CBS) gene are known to cause homocystinuria and may also be a significant risk factor for premature atherosclerosis. We have previously shown that the human CBS protein can substitute for the endogenous yeast CBS protein in Saccharomyces cerevisiae. We now show that expression of three different CBS mutants known to be associated with reduced enzyme activity in humans fail to complement growth in the yeast assay. in addition, we have used the yeast CBS assay to identity eight mutant CBS alleles in cell lines from patients with CBS deficiency. These mutant alleles include two previously identified and five novel CBS mutations. Our results also demonstrate that the yeast CBS assay can detect a large percentage of individuals heterozygous for mutations in CBS. This system should be useful in determining the relationship between CBS mutations and human disease.
Формат application.pdf
Издатель Oxford University Press
Копирайт / 1995 Oxford University Press
Тема ARTICLES
Название A yeast assay for functional detection of mutations in the human cystathionine β-synthase gene
Тип research-article
Electronic ISSN 1460-2083
Print ISSN 0964-6906
Журнал Human Molecular Genetics
Том 4
Первая страница 1155
Последняя страница 1161
Аффилиация Department of Genetics, Stanford University, School of MedicineStanford, CA 94305, USA
Выпуск 7

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