对马罗托-拉米综合征患者皮肤成纤维细胞中芳基硫酸酯酶B的研究，特别涉及电泳迁移率和产前诊断。 - Suppr

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Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis.

作者信息

Schwartz M, Brandt N J, Christensen E, Pedersen C

出版信息

J Inherit Metab Dis. 1980;3(3):99-100. doi: 10.1007/BF02312540.

DOI:10.1007/BF02312540

PMID:6775150

Abstract

摘要

相似文献

Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis.

J Inherit Metab Dis. 1980;3(3):99-100. doi: 10.1007/BF02312540.

Postnatal and prenatal diagnosis of Maroteaux-Lamy syndrome.

Acta Anthropogenet. 1985;9(1-3):109-16.

[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].

Arch Fr Pediatr. 1977 Apr;34(4):362-70.

Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.

Clin Chim Acta. 1979 Apr 2;93(1):85-92. doi: 10.1016/0009-8981(79)90247-x.

Arylsulphatase B (Maroteaux-Lamy factor): a part of the enzyme system responsible for sulphate release from mucopolysaccharide fragment.

FEBS Lett. 1976 May 15;65(1):63-8. doi: 10.1016/0014-5793(76)80622-9.

Prenatal diagnosis of Maroteaux-Lamy syndrome.

Am J Med Genet. 1981;8(2):235-42. doi: 10.1002/ajmg.1320080215.

Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.

Adv Exp Med Biol. 1976;68:239-51. doi: 10.1007/978-1-4684-7735-1_16.

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.

Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507.

Diagnosis of the mucopolysaccharidoses using cultured skin fibroblasts and amniotic fluid cells.

J Inherit Metab Dis. 1978;1(1):25-8. doi: 10.1007/BF01805711.

Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome.

Science. 1977 Nov 25;198(4319):834-6. doi: 10.1126/science.144321.

引用本文的文献

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.

Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507.

本文引用的文献

Protein measurement with the Folin phenol reagent.

J Biol Chem. 1951 Nov;193(1):265-75.

The assay of arylsulphatases A and B in human urine.

Clin Chim Acta. 1959 May;4(3):453-5. doi: 10.1016/0009-8981(59)90119-6.

Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy.

Am J Hum Genet. 1973 May;25(3):310-6.

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.

Biochem Biophys Res Commun. 1974 Jul 24;59(2):455-61. doi: 10.1016/s0006-291x(74)80001-x.

[Biochemical diagnosis of mucopolysaccharidoses in cell culture (author's transl)].

Monatsschr Kinderheilkd (1902). 1974 Jan;122(1):23-30.

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues.

Am J Dis Child. 1973 Dec;126(6):747-55. doi: 10.1001/archpedi.1973.02110190597003.

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome.

Biochem Biophys Res Commun. 1975 Jan 20;62(2):448-55. doi: 10.1016/s0006-291x(75)80159-8.

Hurler/Scheie phenotype. Report of an inbred sibship with tapeto-retinal degeneration and electron-microscopie examination of the conjuctiva.

Ophthalmologica. 1978;176(4):194-204. doi: 10.1159/000308739.

A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and B.

Clin Chim Acta. 1977 Sep 15;79(3):527-31. doi: 10.1016/0009-8981(77)90172-3.

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Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis.

作者信息

Schwartz M, Brandt N J, Christensen E, Pedersen C

出版信息

J Inherit Metab Dis. 1980;3(3):99-100. doi: 10.1007/BF02312540.

DOI:10.1007/BF02312540

PMID:6775150

Abstract

摘要

相似文献

Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis.

J Inherit Metab Dis. 1980;3(3):99-100. doi: 10.1007/BF02312540.

Postnatal and prenatal diagnosis of Maroteaux-Lamy syndrome.

Acta Anthropogenet. 1985;9(1-3):109-16.

[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].

Arch Fr Pediatr. 1977 Apr;34(4):362-70.

Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.

Clin Chim Acta. 1979 Apr 2;93(1):85-92. doi: 10.1016/0009-8981(79)90247-x.

Arylsulphatase B (Maroteaux-Lamy factor): a part of the enzyme system responsible for sulphate release from mucopolysaccharide fragment.

FEBS Lett. 1976 May 15;65(1):63-8. doi: 10.1016/0014-5793(76)80622-9.

Prenatal diagnosis of Maroteaux-Lamy syndrome.

Am J Med Genet. 1981;8(2):235-42. doi: 10.1002/ajmg.1320080215.

Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.

Adv Exp Med Biol. 1976;68:239-51. doi: 10.1007/978-1-4684-7735-1_16.

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.

Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507.

Diagnosis of the mucopolysaccharidoses using cultured skin fibroblasts and amniotic fluid cells.

J Inherit Metab Dis. 1978;1(1):25-8. doi: 10.1007/BF01805711.

Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome.

Science. 1977 Nov 25;198(4319):834-6. doi: 10.1126/science.144321.

引用本文的文献

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.

Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507.

本文引用的文献

Protein measurement with the Folin phenol reagent.

J Biol Chem. 1951 Nov;193(1):265-75.

The assay of arylsulphatases A and B in human urine.

Clin Chim Acta. 1959 May;4(3):453-5. doi: 10.1016/0009-8981(59)90119-6.

Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy.

Am J Hum Genet. 1973 May;25(3):310-6.

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.

Biochem Biophys Res Commun. 1974 Jul 24;59(2):455-61. doi: 10.1016/s0006-291x(74)80001-x.

[Biochemical diagnosis of mucopolysaccharidoses in cell culture (author's transl)].

Monatsschr Kinderheilkd (1902). 1974 Jan;122(1):23-30.

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues.

Am J Dis Child. 1973 Dec;126(6):747-55. doi: 10.1001/archpedi.1973.02110190597003.

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome.

Biochem Biophys Res Commun. 1975 Jan 20;62(2):448-55. doi: 10.1016/s0006-291x(75)80159-8.

Hurler/Scheie phenotype. Report of an inbred sibship with tapeto-retinal degeneration and electron-microscopie examination of the conjuctiva.

Ophthalmologica. 1978;176(4):194-204. doi: 10.1159/000308739.

A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and B.

Clin Chim Acta. 1977 Sep 15;79(3):527-31. doi: 10.1016/0009-8981(77)90172-3.