Sleat DE - Search Results

1

Identification of sites of mannose 6-phosphorylation on lysosomal proteins.

Sleat DE, Zheng H, Qian M, Lobel P. Sleat DE, et al. Mol Cell Proteomics. 2006 Apr;5(4):686-701. doi: 10.1074/mcp.M500343-MCP200. Epub 2006 Jan 5. Mol Cell Proteomics. 2006. PMID: 16399764 Free article.

2

Transcriptional activity and mutational analysis of recombinant vesicular stomatitis virus RNA polymerase.

Sleat DE, Banerjee AK. Sleat DE, et al. J Virol. 1993 Mar;67(3):1334-9. doi: 10.1128/JVI.67.3.1334-1339.1993. J Virol. 1993. PMID: 8382299 Free PMC article.

3

Increased levels of glycoproteins containing mannose 6-phosphate in human breast carcinomas.

Sleat DE, Chen TL, Raska K Jr, Lobel P. Sleat DE, et al. Cancer Res. 1995 Aug 1;55(15):3424-30. Cancer Res. 1995. PMID: 7614483

4

Rat brain contains high levels of mannose-6-phosphorylated glycoproteins including lysosomal enzymes and palmitoyl-protein thioesterase, an enzyme implicated in infantile neuronal lipofuscinosis.

Sleat DE, Sohar I, Lackland H, Majercak J, Lobel P. Sleat DE, et al. J Biol Chem. 1996 Aug 9;271(32):19191-8. doi: 10.1074/jbc.271.32.19191. J Biol Chem. 1996. PMID: 8702598 Free article.

5

Ligand binding specificities of the two mannose 6-phosphate receptors.

Sleat DE, Lobel P. Sleat DE, et al. J Biol Chem. 1997 Jan 10;272(2):731-8. doi: 10.1074/jbc.272.2.731. J Biol Chem. 1997. PMID: 8995357 Free article.

6

alpha-Glucosidase and N-acetylglucosamine-6-sulphatase are the major mannose-6-phosphate glycoproteins in human urine.

Sleat DE, Kraus SR, Sohar I, Lackland H, Lobel P. Sleat DE, et al. Biochem J. 1997 May 15;324 ( Pt 1)(Pt 1):33-9. doi: 10.1042/bj3240033. Biochem J. 1997. PMID: 9164838 Free PMC article.

7

Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis.

Sleat DE, Donnelly RJ, Lackland H, Liu CG, Sohar I, Pullarkat RK, Lobel P. Sleat DE, et al. Science. 1997 Sep 19;277(5333):1802-5. doi: 10.1126/science.277.5333.1802. Science. 1997. PMID: 9295267

8

Mouse mutants lacking the cation-independent mannose 6-phosphate/insulin-like growth factor II receptor are impaired in lysosomal enzyme transport: comparison of cation-independent and cation-dependent mannose 6-phosphate receptor-deficient mice.

Sohar I, Sleat D, Gong Liu C, Ludwig T, Lobel P. Sohar I, et al. Biochem J. 1998 Mar 1;330 ( Pt 2)(Pt 2):903-8. doi: 10.1042/bj3300903. Biochem J. 1998. PMID: 9480908 Free PMC article.

9

Structural organization and sequence of CLN2, the defective gene in classical late infantile neuronal ceroid lipofuscinosis.

Liu CG, Sleat DE, Donnelly RJ, Lobel P. Liu CG, et al. Among authors: sleat de. Genomics. 1998 Jun 1;50(2):206-12. doi: 10.1006/geno.1998.5328. Genomics. 1998. PMID: 9653647

10

Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses.

Sleat DE, Sohar I, Pullarkat PS, Lobel P, Pullarkat RK. Sleat DE, et al. Biochem J. 1998 Sep 15;334 ( Pt 3)(Pt 3):547-51. doi: 10.1042/bj3340547. Biochem J. 1998. PMID: 9729460 Free PMC article.

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