Ou L - Search Results

1

ZFN-Mediated In Vivo Genome Editing Corrects Murine Hurler Syndrome.

Ou L, DeKelver RC, Rohde M, Tom S, Radeke R, St Martin SJ, Santiago Y, Sproul S, Przybilla MJ, Koniar BL, Podetz-Pedersen KM, Laoharawee K, Cooksley RD, Meyer KE, Holmes MC, McIvor RS, Wechsler T, Whitley CB. Ou L, et al. Mol Ther. 2019 Jan 2;27(1):178-187. doi: 10.1016/j.ymthe.2018.10.018. Epub 2018 Nov 1. Mol Ther. 2019. PMID: 30528089 Free PMC article.

2

High-dose enzyme replacement therapy in murine Hurler syndrome.

Ou L, Herzog T, Koniar BL, Gunther R, Whitley CB. Ou L, et al. Mol Genet Metab. 2014 Feb;111(2):116-22. doi: 10.1016/j.ymgme.2013.09.008. Epub 2013 Sep 19. Mol Genet Metab. 2014. PMID: 24100243 Free PMC article.

3

Standardization of α-L-iduronidase enzyme assay with Michaelis-Menten kinetics.

Ou L, Herzog TL, Wilmot CM, Whitley CB. Ou L, et al. Mol Genet Metab. 2014 Feb;111(2):113-5. doi: 10.1016/j.ymgme.2013.11.009. Epub 2013 Nov 26. Mol Genet Metab. 2014. PMID: 24332804 Free PMC article.

4

Elements of lentiviral vector design toward gene therapy for treating mucopolysaccharidosis I.

Ou L, Przybilla MJ, Koniar BL, Whitley CB. Ou L, et al. Mol Genet Metab Rep. 2016 Aug 13;8:87-93. doi: 10.1016/j.ymgmr.2015.11.004. eCollection 2016 Sep. Mol Genet Metab Rep. 2016. PMID: 27556013 Free PMC article.

5

Proteomic analysis of mucopolysaccharidosis I mouse brain with two-dimensional polyacrylamide gel electrophoresis.

Ou L, Przybilla MJ, Whitley CB. Ou L, et al. Mol Genet Metab. 2017 Jan-Feb;120(1-2):101-110. doi: 10.1016/j.ymgme.2016.10.001. Epub 2016 Oct 11. Mol Genet Metab. 2017. PMID: 27742266 Free PMC article.

6

Phenotype prediction for mucopolysaccharidosis type I by in silico analysis.

Ou L, Przybilla MJ, Whitley CB. Ou L, et al. Orphanet J Rare Dis. 2017 Jul 4;12(1):125. doi: 10.1186/s13023-017-0678-1. Orphanet J Rare Dis. 2017. PMID: 28676128 Free PMC article.

7

RTB lectin-mediated delivery of lysosomal α-l-iduronidase mitigates disease manifestations systemically including the central nervous system.

Ou L, Przybilla MJ, Koniar B, Whitley CB. Ou L, et al. Mol Genet Metab. 2018 Feb;123(2):105-111. doi: 10.1016/j.ymgme.2017.11.013. Epub 2017 Nov 28. Mol Genet Metab. 2018. PMID: 29198892 Free PMC article.

8

SAAMP 2.0: An algorithm to predict genotype-phenotype correlation of lysosomal storage diseases.

Ou L, Przybilla MJ, Whitley CB. Ou L, et al. Clin Genet. 2018 May;93(5):1008-1014. doi: 10.1111/cge.13226. Epub 2018 Mar 5. Clin Genet. 2018. PMID: 29396849 Free PMC article.

9

Dose-Dependent Prevention of Metabolic and Neurologic Disease in Murine MPS II by ZFN-Mediated In Vivo Genome Editing.

Laoharawee K, DeKelver RC, Podetz-Pedersen KM, Rohde M, Sproul S, Nguyen HO, Nguyen T, St Martin SJ, Ou L, Tom S, Radeke R, Meyer KE, Holmes MC, Whitley CB, Wechsler T, McIvor RS. Laoharawee K, et al. Among authors: ou l. Mol Ther. 2018 Apr 4;26(4):1127-1136. doi: 10.1016/j.ymthe.2018.03.002. Epub 2018 Mar 10. Mol Ther. 2018. PMID: 29580682 Free PMC article.

10

Metabolomics profiling reveals profound metabolic impairments in mice and patients with Sandhoff disease.

Ou L, Przybilla MJ, Whitley CB. Ou L, et al. Mol Genet Metab. 2019 Feb;126(2):151-156. doi: 10.1016/j.ymgme.2018.09.005. Epub 2018 Sep 14. Mol Genet Metab. 2019. PMID: 30236619 Free PMC article.

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