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• Altered molecular size of N-acetylglucosamine 1-phosphotransferase in I-cell disease and pseudo-Hurler polydystrophy.

  Ben-Yoseph Y, Potier M, Mitchell DA, Pack BA, Melançon SB, Nadler HL. Ben-Yoseph Y, et al. Biochem J. 1987 Dec 15;248(3):697-701. doi: 10.1042/bj2480697. Biochem J. 1987. PMID: 2829837 Free PMC article.
• Quantitative Proteome Analysis of Mouse Liver Lysosomes Provides Evidence for Mannose 6-phosphate-independent Targeting Mechanisms of Acid Hydrolases in Mucolipidosis II.

  Markmann S, Krambeck S, Hughes CJ, Mirzaian M, Aerts JM, Saftig P, Schweizer M, Vissers JP, Braulke T, Damme M. Markmann S, et al. Mol Cell Proteomics. 2017 Mar;16(3):438-450. doi: 10.1074/mcp.M116.063636. Epub 2017 Jan 6. Mol Cell Proteomics. 2017. PMID: 28062798 Free PMC article.
• Structural requirements for sulfation of asparagine-linked oligosaccharides of lutropin.

  Green ED, Morishima C, Boime I, Baenziger JU. Green ED, et al. Proc Natl Acad Sci U S A. 1985 Dec;82(23):7850-4. doi: 10.1073/pnas.82.23.7850. Proc Natl Acad Sci U S A. 1985. PMID: 3865202 Free PMC article.
• Mucolipidoses II and III variants with normal N-acetylglucosamine 1-phosphotransferase activity toward alpha-methylmannoside are due to nonallelic mutations.

  Ben-Yoseph Y, Mitchell DA, Yager RM, Wei JT, Chen TH, Shih LY. Ben-Yoseph Y, et al. Am J Hum Genet. 1992 Jan;50(1):137-44. Am J Hum Genet. 1992. PMID: 1309624 Free PMC article.
• Heterozygosity for phosphodiester glycosidase deficiency: a novel human mutation of lysosomal enzyme processing.

  Alexander D, Deeb M, Talj F. Alexander D, et al. Hum Genet. 1986 May;73(1):53-9. doi: 10.1007/BF00292664. Hum Genet. 1986. PMID: 3011646