Liao H - Search Results

1

Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy.

Allen EHA, Atkinson SD, Liao H, Moore JE, Pedrioli DML, Smith FJD, McLean WHI, Moore CBT. Allen EHA, et al. Among authors: liao h. Invest Ophthalmol Vis Sci. 2013 Jan 17;54(1):494-502. doi: 10.1167/iovs.12-10528. Invest Ophthalmol Vis Sci. 2013. PMID: 23233254 Free PMC article.

2

Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex.

Atkinson SD, McGilligan VE, Liao H, Szeverenyi I, Smith FJ, Moore CB, McLean WH. Atkinson SD, et al. Among authors: liao h. J Invest Dermatol. 2011 Oct;131(10):2079-86. doi: 10.1038/jid.2011.169. Epub 2011 Jun 30. J Invest Dermatol. 2011. PMID: 21716320 Free article.

3

Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy.

Liao H, Irvine AD, Macewen CJ, Weed KH, Porter L, Corden LD, Gibson AB, Moore JE, Smith FJ, McLean WH, Moore CB. Liao H, et al. PLoS One. 2011;6(12):e28582. doi: 10.1371/journal.pone.0028582. Epub 2011 Dec 12. PLoS One. 2011. PMID: 22174841 Free PMC article.

4

siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy.

Courtney DG, Atkinson SD, Allen EH, Moore JE, Walsh CP, Pedrioli DM, MacEwen CJ, Pellegrini G, Maurizi E, Serafini C, Fantacci M, Liao H, Irvine AD, McLean WH, Moore CB. Courtney DG, et al. Among authors: liao h. Invest Ophthalmol Vis Sci. 2014 May 6;55(5):3352-60. doi: 10.1167/iovs.13-12957. Invest Ophthalmol Vis Sci. 2014. PMID: 24801514

5

A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease.

Liao H, Zhao Y, Baty DU, McGrath JA, Mellerio JE, McLean WH. Liao H, et al. J Invest Dermatol. 2007 Feb;127(2):298-300. doi: 10.1038/sj.jid.5700523. Epub 2006 Aug 17. J Invest Dermatol. 2007. PMID: 16917491 Free article.

6

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.

Liao H, Sayers JM, Wilson NJ, Irvine AD, Mellerio JE, Baselga E, Bayliss SJ, Uliana V, Fimiani M, Lane EB, McLean WH, Leachman SA, Smith FJ. Liao H, et al. J Dermatol Sci. 2007 Dec;48(3):199-205. doi: 10.1016/j.jdermsci.2007.07.003. Epub 2007 Aug 24. J Dermatol Sci. 2007. PMID: 17719747

7

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

Liao H, Waters AJ, Goudie DR, Aitken DA, Graham G, Smith FJ, Lewis-Jones S, McLean WH. Liao H, et al. J Invest Dermatol. 2007 Dec;127(12):2795-8. doi: 10.1038/sj.jid.5700971. Epub 2007 Jul 26. J Invest Dermatol. 2007. PMID: 17657246 Free article.

8

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.

Sandilands A, O'Regan GM, Liao H, Zhao Y, Terron-Kwiatkowski A, Watson RM, Cassidy AJ, Goudie DR, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: liao h. J Invest Dermatol. 2006 Aug;126(8):1770-5. doi: 10.1038/sj.jid.5700459. Epub 2006 Jun 29. J Invest Dermatol. 2006. PMID: 16810297 Free article.

9

Filaggrin null mutations are associated with increased asthma severity in children and young adults.

Palmer CN, Ismail T, Lee SP, Terron-Kwiatkowski A, Zhao Y, Liao H, Smith FJ, McLean WH, Mukhopadhyay S. Palmer CN, et al. Among authors: liao h. J Allergy Clin Immunol. 2007 Jul;120(1):64-8. doi: 10.1016/j.jaci.2007.04.001. Epub 2007 May 25. J Allergy Clin Immunol. 2007. PMID: 17531295

10

Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults.

Basu K, Palmer CN, Lipworth BJ, McLean WH, Terron-Kwiatkowski A, Zhao Y, Liao H, Smith FJ, Mitra A, Mukhopadhyay S. Basu K, et al. Among authors: liao h. Allergy. 2008 Sep;63(9):1211-7. doi: 10.1111/j.1398-9995.2008.01660.x. Epub 2008 Feb 25. Allergy. 2008. PMID: 18307574

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