毛囊中芳基硫酸酯酶C的测定。 - Suppr

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Determination of arylsulfatase C in hair follicles.

作者信息

Meyer J C, Grundmann H P, Schnyder U W

出版信息

Arch Dermatol Res. 1979 Aug;266(1):95-7. doi: 10.1007/BF00412868.

DOI:10.1007/BF00412868

PMID:507934

Abstract

摘要

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本文引用的文献

Measurement of the arylsulphatase of Patella vulgata with 4-methylumbelliferone sulphate.

Biochem J. 1967 Mar;102(3):905-9. doi: 10.1042/bj1020905.

Studies on sulphatases. 12. The arylsulphatases of human tissues.

Biochem J. 1956 Mar;62(3):500-7. doi: 10.1042/bj0620500.

Lesch-Nyhan syndrome: rapid detection of heterozygotes by use of hair follicles.

Science. 1971 May 7;172(3983):572-4. doi: 10.1126/science.172.3983.572.

Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells.

Ann Hum Genet. 1969 Oct;33(2):171-6. doi: 10.1111/j.1469-1809.1969.tb01642.x.

The specific assay of arylsulphatase C, a rat liver microsomal marker enzyme.

Biochem J. 1972 Jun;128(2):331-6. doi: 10.1042/bj1280331.

Studies on hair roots for carrier detection in hypoxanthine-quanine phosphoribosyl transferase deficiency.

Clin Genet. 1974;5(5):449-56. doi: 10.1111/j.1399-0004.1974.tb01718.x.

[Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)].

Arch Dermatol Forsch. 1973 Dec 5;248(2):149-72.

[Differential diagnosis of autosomal-dominant chthyosis vulgaris and X-chromosome ichthyosis].

Hautarzt. 1974 Jul;25(7):319-25.

[Ultrastructure of inborn errors of keratinization. IV. X-linked recessive ichthyosis (author's transl)].

Arch Dermatol Forsch. 1974 Feb 20;248(4):361-78.

Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.

Arch Neurol. 1974 Feb;30(2):153-6. doi: 10.1001/archneur.1974.00490320041005.

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