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Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|February 15, 2013
Revertant mosaicism in the skinJ E Lai-Cheong, J A McGrath
The International Journal of Biochemistry & Cell Biology|October 27, 2009
The role of kindlins in cell biology and relevance to human diseaseJ E Lai-Cheong, M Parsons, J A McGrath
Clinical and Experimental Dermatology|April 6, 2005
Molecular abnormalities of the desmosomal protein desmoplakin in human diseaseJ E Lai Cheong, V Wessagowit, J A McGrath
The Journal of Investigative Dermatology|June 6, 2008
Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndromeJ E Lai-Cheong, S Ussar, K Arita, et al.
Clinical and Experimental Dermatology|May 14, 2011
New homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree with Netherton syndromeK Fong, S Akdeniz, H Isi, et al.
The British Journal of Dermatology|August 12, 2009
New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosisA Tanaka, K Arita, J E Lai-Cheong, et al.
The British Journal of Dermatology|July 28, 2012
Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndromeJ E Lai-Cheong, G Sethuraman, M Ramam, et al.
The British Journal of Dermatology|November 20, 2008
Novel truncating mutations in PKP1 and DSP cause similar skin phenotypes in two Brazilian familiesA Tanaka, J E Lai-Cheong, M E M Café, et al.
Clinical and Experimental Dermatology|July 24, 2012
MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvansK Fong, E K Wedgeworth, J E Lai-Cheong, et al.
The British Journal of Dermatology|January 6, 2009
Kindler syndrome: a focal adhesion genodermatosisJ E Lai-Cheong, A Tanaka, G Hawche, et al.
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