Sleat DE - 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: sleat de. 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

Restricted replication of vesicular stomatitis virus in T lymphocytes is coincident with a deficiency in a cellular protein kinase required for viral transcription.

Sleat DE, Chikkala NF, Gautam S, Banerjee AK. Sleat DE, et al. J Gen Virol. 1992 Dec;73 ( Pt 12):3125-32. doi: 10.1099/0022-1317-73-12-3125. J Gen Virol. 1992. PMID: 1335023

3

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.

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

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

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: sleat de. 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. 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. 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: sleat de. J Neurochem. 1999 Aug;73(2):700-11. doi: 10.1046/j.1471-4159.1999.0730700.x. J Neurochem. 1999. PMID: 10428067 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

80 results

Search Page

Filters