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Items: 5

1.
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening
M.‐L. Lovgren, M.A. McAleer, A.D. Irvine, N.J. Wilson, S. Tavadia, M.E. Schwartz, C. Cole, A. Sandilands, F.J.D. Smith, M. Zamiri
Br J Dermatol. 2017 May; 176(5): 1345–1350. Published online 2017 Apr 2. doi: 10.1111/bjd.14973
PMCID:
PMC5485079
AbstractArticlePDF–760K
2.
Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma
Martha B. Dua-Awereh, Yutaka Shimomura, Liv Kraemer, Muhammad Wajid, Angela M. Christiano
J Dermatol Sci. Author manuscript; available in PMC 2014 Apr 15.
Published in final edited form as: J Dermatol Sci. 2009 Mar; 53(3): 192–197. Published online 2009 Jan 20. doi: 10.1016/j.jdermsci.2008.11.005
PMCID:
PMC3986861
AbstractArticlePDF–502K
3.
Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation
Robert M. Harmon, Cory L. Simpson, Jodi L. Johnson, Jennifer L. Koetsier, Adi D. Dubash, Nicole A. Najor, Ofer Sarig, Eli Sprecher, Kathleen J. Green
J Clin Invest. 2013 Apr 1; 123(4): 1556–1570. Published online 2013 Mar 25. doi: 10.1172/JCI65220
PMCID:
PMC3613912
AbstractArticlePDF–4.5M
4.
Desmoglein as a target in skin disease and beyond
Masayuki Amagai, John R. Stanley
J Invest Dermatol. Author manuscript; available in PMC 2012 Sep 1.
Published in final edited form as: J Invest Dermatol. 2012 Mar; 132(3 0 2): 776–784. Published online 2011 Dec 22. doi: 10.1038/jid.2011.390
PMCID:
PMC3279627
AbstractArticlePDF–487K
5.
Loss of Desmoplakin Tail Causes Lethal Acantholytic Epidermolysis Bullosa
Marcel F. Jonkman, Anna M. G. Pasmooij, Suzanne G. M. A. Pasmans, Maarten P. van den Berg, Henk J. ter Horst, Albertus Timmer, Hendri H. Pas
Am J Hum Genet. 2005 Oct; 77(4): 653–660. Published online 2005 Aug 17. doi: 10.1086/496901
PMCID:
PMC1275614
AbstractArticlePDF–3.3M

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