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A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.

作者信息

Hickman S, Shapiro L J, Neufeld E F

出版信息

Biochem Biophys Res Commun. 1974 Mar 15;57(1):55-61. doi: 10.1016/s0006-291x(74)80356-6.

DOI:10.1016/s0006-291x(74)80356-6

PMID:4364008

Abstract

摘要

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A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.

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相似文献

A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.

Biochem Biophys Res Commun. 1974 Mar 15;57(1):55-61. doi: 10.1016/s0006-291x(74)80356-6.

N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycans.

Science. 1973 Aug 31;181(4102):866-7. doi: 10.1126/science.181.4102.866.

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.

Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.

Proc Natl Acad Sci U S A. 1972 Jul;69(7):1720-2. doi: 10.1073/pnas.69.7.1720.

Acid glycosidases in mucopolysaccharidoses fibroblasts.

Biochem Med. 1970 Sep;4(2):110-20. doi: 10.1016/0006-2944(70)90088-8.

-Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease.

Biochem Med. 1973 Jun;7(3):343-9. doi: 10.1016/0006-2944(73)90055-0.

Lysosomal enzymes in cultured cells from mucopolysaccharidoses.

Lab Invest. 1972 Dec;27(6):600-5.

Hurler's syndrome, an -L-iduronidase deficiency.

Biochem Biophys Res Commun. 1972 May 26;47(4):959-64. doi: 10.1016/0006-291x(72)90586-4.

Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.

Dev Med Child Neurol. 1974 Aug;16(4):534-9. doi: 10.1111/j.1469-8749.1974.tb03381.x.

Mucopolysaccharidosis.

Proc R Soc Med. 1972 Apr;65(4):339-41. doi: 10.1177/003591577206500412.

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Physiol Rev. 2018 Oct 1;98(4):2381-2430. doi: 10.1152/physrev.00024.2017.

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Adv Drug Deliv Rev. 2017 Sep 1;118:109-134. doi: 10.1016/j.addr.2017.05.004. Epub 2017 May 11.

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PLoS Genet. 2012 Sep;8(9):e1002943. doi: 10.1371/journal.pgen.1002943. Epub 2012 Sep 20.

Imiglucerase in the treatment of Gaucher disease: a history and perspective.

Drug Des Devel Ther. 2012;6:81-106. doi: 10.2147/DDDT.S14395. Epub 2012 Apr 18.

The insulin-like growth factor II/mannose-6-phosphate receptor : IGF-II/Man-6-P receptor.

Cytotechnology. 1989 Dec;2(4):287-305. doi: 10.1007/BF00364994.

Genetic therapy for the nervous system.

Hum Mol Genet. 2011 Apr 15;20(R1):R28-41. doi: 10.1093/hmg/ddr110. Epub 2011 Mar 23.

New strategies for enzyme replacement therapy for lysosomal storage diseases.

Rejuvenation Res. 2010 Apr-Jun;13(2-3):229-36. doi: 10.1089/rej.2009.0920.

Chemically modified beta-glucuronidase crosses blood-brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII.

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