Lai-Cheong JE - Search Results

1

Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation.

Lai-Cheong JE, Parsons M, Tanaka A, Ussar S, South AP, Gomathy S, Mee JB, Barbaroux JB, Techanukul T, Almaani N, Clements SE, Hart IR, McGrath JA. Lai-Cheong JE, et al. Am J Pathol. 2009 Oct;175(4):1431-41. doi: 10.2353/ajpath.2009.081154. Epub 2009 Sep 17. Am J Pathol. 2009. PMID: 19762710 Free PMC article.

2

Kindler syndrome.

Lai-Cheong JE, McGrath JA. Lai-Cheong JE, et al. Dermatol Clin. 2010 Jan;28(1):119-24. doi: 10.1016/j.det.2009.10.013. Dermatol Clin. 2010. PMID: 19945624 Review.

3

What is Kindler syndrome?

Lai-Cheong JE, McGrath JA. Lai-Cheong JE, et al. Skinmed. 2011 May-Jun;9(3):145-6. Skinmed. 2011. PMID: 21675491 No abstract available.

4

Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome.

Lai-Cheong JE, Ussar S, Arita K, Hart IR, McGrath JA. Lai-Cheong JE, et al. J Invest Dermatol. 2008 Sep;128(9):2156-65. doi: 10.1038/jid.2008.58. Epub 2008 Jun 5. J Invest Dermatol. 2008. PMID: 18528435 Free PMC article.

5

The role of kindlins in cell biology and relevance to human disease.

Lai-Cheong JE, Parsons M, McGrath JA. Lai-Cheong JE, et al. Int J Biochem Cell Biol. 2010 May;42(5):595-603. doi: 10.1016/j.biocel.2009.10.015. Epub 2009 Oct 23. Int J Biochem Cell Biol. 2010. PMID: 19854292 Review.

6

Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology.

Clements SE, Techanukul T, Lai-Cheong JE, Mee JB, South AP, Pourreyron C, Burrows NP, Mellerio JE, McGrath JA. Clements SE, et al. Br J Dermatol. 2012 Jul;167(1):134-44. doi: 10.1111/j.1365-2133.2012.10888.x. Epub 2012 May 14. Br J Dermatol. 2012. PMID: 22329826

7

Novel and recurrent FERMT1 gene mutations in Kindler syndrome.

Techanukul T, Sethuraman G, Zlotogorski A, Horev L, Macarov M, Trainer A, Fong K, Lens M, Medenica L, Ramesh V, McGrath JA, Lai-Cheong JE. Techanukul T, et al. Acta Derm Venereol. 2011 May;91(3):267-70. doi: 10.2340/00015555-1063. Acta Derm Venereol. 2011. PMID: 21336475 Free article.

8

Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.

Arita K, South AP, Hans-Filho G, Sakuma TH, Lai-Cheong J, Clements S, Odashiro M, Odashiro DN, Hans-Neto G, Hans NR, Holder MV, Bhogal BS, Hartshorne ST, Akiyama M, Shimizu H, McGrath JA. Arita K, et al. Am J Hum Genet. 2008 Jan;82(1):73-80. doi: 10.1016/j.ajhg.2007.09.002. Am J Hum Genet. 2008. PMID: 18179886 Free PMC article.

9

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. Acta Derm Venereol. 2009;89(1):6-11. doi: 10.2340/00015555-0605. Acta Derm Venereol. 2009. PMID: 19197535 Free article.

10

Sporadic Kindler syndrome with a novel mutation.

Almeida HL Jr, Heckler GT, Fong K, Lai-Cheong J, McGrath J. Almeida HL Jr, et al. An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):212-5. doi: 10.1590/abd1806-4841.20132173. An Bras Dermatol. 2013. PMID: 24346923 Free PMC article.

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