Lobel P - Search Results

1

Intracranial delivery of CLN2 reduces brain pathology in a mouse model of classical late infantile neuronal ceroid lipofuscinosis.

Passini MA, Dodge JC, Bu J, Yang W, Zhao Q, Sondhi D, Hackett NR, Kaminsky SM, Mao Q, Shihabuddin LS, Cheng SH, Sleat DE, Stewart GR, Davidson BL, Lobel P, Crystal RG. Passini MA, et al. Among authors: lobel p. J Neurosci. 2006 Feb 1;26(5):1334-42. doi: 10.1523/JNEUROSCI.2676-05.2006. J Neurosci. 2006. PMID: 16452657 Free PMC article.

2

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. Among authors: lobel p. Cancer Res. 1995 Aug 1;55(15):3424-30. Cancer Res. 1995. PMID: 7614483

3

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. Among authors: lobel p. 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.

4

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

Sleat DE, Lobel P. Sleat DE, et al. Among authors: lobel p. 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.

5

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. Among authors: lobel p. Biochem J. 1997 May 15;324 ( Pt 1)(Pt 1):33-9. doi: 10.1042/bj3240033. Biochem J. 1997. PMID: 9164838 Free PMC article.

6

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. Among authors: lobel p. Science. 1997 Sep 19;277(5333):1802-5. doi: 10.1126/science.277.5333.1802. Science. 1997. PMID: 9295267

7

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: lobel p. Genomics. 1998 Jun 1;50(2):206-12. doi: 10.1006/geno.1998.5328. Genomics. 1998. PMID: 9653647

8

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. Among authors: lobel p. Biochem J. 1998 Sep 15;334 ( Pt 3)(Pt 3):547-51. doi: 10.1042/bj3340547. Biochem J. 1998. PMID: 9729460 Free PMC article.

9

Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder.

Sleat DE, Gin RM, Sohar I, Wisniewski K, Sklower-Brooks S, Pullarkat RK, Palmer DN, Lerner TJ, Boustany RM, Uldall P, Siakotos AN, Donnelly RJ, Lobel P. Sleat DE, et al. Among authors: lobel p. Am J Hum Genet. 1999 Jun;64(6):1511-23. doi: 10.1086/302427. Am J Hum Genet. 1999. PMID: 10330339 Free PMC article.

10

Biochemical characterization of a lysosomal protease deficient in classical late infantile neuronal ceroid lipofuscinosis (LINCL) and development of an enzyme-based assay for diagnosis and exclusion of LINCL in human specimens and animal models.

Sohar I, Sleat DE, Jadot M, Lobel P. Sohar I, et al. Among authors: lobel p. J Neurochem. 1999 Aug;73(2):700-11. doi: 10.1046/j.1471-4159.1999.0730700.x. J Neurochem. 1999. PMID: 10428067 Free article.

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