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The Journal of Investigative Dermatology|January 29, 2000
A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevusA Terrinoni, E Candi, S Oddi, et al.
The British Journal of Dermatology|July 24, 2009
Quality of life in patients with epidermolysis bullosaS Tabolli, F Sampogna, C Di Pietro, et al.
Human Gene Therapy|July 3, 1998
Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosaE Dellambra, J Vailly, G Pellegrini, et al.
The British Journal of Dermatology|October 6, 2007
Herlitz junctional epidermolysis bullosa: laminin-5 mutational profile and carrier frequency in the Italian populationM Castori, G Floriddia, N De Luca, et al.
Annals of Human Genetics|December 16, 2004
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.
The British Journal of Dermatology|November 16, 2004
Development of a novel ELISA system for detection of anti-BP180 IgG and characterization of autoantibody profile in bullous pemphigoid patientsF Mariotti, F Grosso, M Terracina, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
The British Journal of Dermatology|March 1, 2019
MicroRNA-145-5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblastsA G Condorelli, E Logli, F Cianfarani, et al.
The Journal of Investigative Dermatology|February 13, 2001
A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional epidermolysis bullosaL Ruzzi, H Pas, P Posteraro, et al.
Clinical and Experimental Rheumatology|February 10, 2006
New insights into the autoantibody-mediated mechanisms of autoimmune bullous diseases and urticariaM Blank, P Gisondi, D Mimouni, et al.
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