Liu L - Search Results

1

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory.

Takeichi T, Liu L, Fong K, Ozoemena L, McMillan JR, Salam A, Campbell P, Akiyama M, Mellerio JE, McLean WH, Simpson MA, McGrath JA. Takeichi T, et al. Among authors: liu l. Br J Dermatol. 2015 Jan;172(1):94-100. doi: 10.1111/bjd.13190. Epub 2014 Nov 19. Br J Dermatol. 2015. PMID: 24947307

2

Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.

Liu L, Choy YS, Wessagowit V, Ozoemena L, Dopping-Hepenstal PJ, Fassihi H, McGrath JA. Liu L, et al. J Dermatol Sci. 2006 Oct;44(1):48-51. doi: 10.1016/j.jdermsci.2006.05.009. Epub 2006 Jun 30. J Dermatol Sci. 2006. PMID: 16814527 No abstract available.

3

Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.

Ee HL, Liu L, Goh CL, McGrath JA. Ee HL, et al. Among authors: liu l. J Am Acad Dermatol. 2007 May;56(5 Suppl):S77-81. doi: 10.1016/j.jaad.2006.10.017. J Am Acad Dermatol. 2007. PMID: 17434045 Review.

4

Five new homozygous mutations in the KIND1 gene in Kindler syndrome.

Lai-Cheong JE, Liu L, Sethuraman G, Kumar R, Sharma VK, Reddy SR, Vahlquist A, Pather S, Arita K, Wessagowit V, McGrath JA. Lai-Cheong JE, et al. Among authors: liu l. J Invest Dermatol. 2007 Sep;127(9):2268-70. doi: 10.1038/sj.jid.5700830. Epub 2007 Apr 26. J Invest Dermatol. 2007. PMID: 17460733 Free article. No abstract available.

5

Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.

Martignago BC, Lai-Cheong JE, Liu L, McGrath JA, Cestari TF. Martignago BC, et al. Among authors: liu l. Br J Dermatol. 2007 Dec;157(6):1281-4. doi: 10.1111/j.1365-2133.2007.08219.x. Epub 2007 Oct 4. Br J Dermatol. 2007. PMID: 17916195 No abstract available.

6

The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1.

Chan I, Liu L, Hamada T, Sethuraman G, McGrath JA. Chan I, et al. Among authors: liu l. Exp Dermatol. 2007 Nov;16(11):881-90. doi: 10.1111/j.1600-0625.2007.00608.x. Exp Dermatol. 2007. PMID: 17927570 Review.

7

Potential of fibroblast cell therapy for recessive dystrophic epidermolysis bullosa.

Wong T, Gammon L, Liu L, Mellerio JE, Dopping-Hepenstal PJ, Pacy J, Elia G, Jeffery R, Leigh IM, Navsaria H, McGrath JA. Wong T, et al. Among authors: liu l. J Invest Dermatol. 2008 Sep;128(9):2179-89. doi: 10.1038/jid.2008.78. Epub 2008 Apr 3. J Invest Dermatol. 2008. PMID: 18385758 Free article. Clinical Trial.

8

Autosomal dominant junctional epidermolysis bullosa.

Almaani N, Liu L, Dopping-Hepenstal PJ, Lovell PA, Lai-Cheong JE, Graham RM, Mellerio JE, McGrath JA. Almaani N, et al. Among authors: liu l. Br J Dermatol. 2009 May;160(5):1094-7. doi: 10.1111/j.1365-2133.2008.08977.x. Epub 2009 Dec 16. Br J Dermatol. 2009. PMID: 19120338

9

Kindler syndrome: a focal adhesion genodermatosis.

Lai-Cheong JE, Tanaka A, Hawche G, Emanuel P, Maari C, Taskesen M, Akdeniz S, Liu L, McGrath JA. Lai-Cheong JE, et al. Among authors: liu l. Br J Dermatol. 2009 Feb;160(2):233-42. doi: 10.1111/j.1365-2133.2008.08976.x. Epub 2008 Dec 11. Br J Dermatol. 2009. PMID: 19120339 Review.

10

New glycine substitution mutations in type VII collagen underlying epidermolysis bullosa pruriginosa but the phenotype is not explained by a common polymorphism in the matrix metalloproteinase-1 gene promoter.

Almaani N, Liu L, Harrison N, Tanaka A, Lai-Cheong J, Mellerio JE, McGrath JA. Almaani N, et al. Among authors: liu l. Acta Derm Venereol. 2009;89(1):6-11. doi: 10.2340/00015555-0605. Acta Derm Venereol. 2009. PMID: 19197535 Free article.

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