Liu L - Search Results

1

Impact of next generation sequencing on diagnostics in a genetic skin disease clinic.

Takeichi T, Nanda A, Liu L, Salam A, Campbell P, Fong K, Akiyama M, Ozoemena L, Stone KL, Al-Ajmi H, Simpson MA, McGrath JA. Takeichi T, et al. Among authors: liu l. Exp Dermatol. 2013 Dec;22(12):825-31. doi: 10.1111/exd.12276. Exp Dermatol. 2013. PMID: 24279917

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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