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Human Mutation|February 5, 2000
Laminin 5 genes and Herlitz junctional epidermolysis bullosa: novel mutations and polymorphisms in the LAMB3 and LAMC2 genes. Mutations in brief no. 190. OnlineA Kon, L Pulkkinen, M Hara, et al.
The British Journal of Dermatology|May 8, 1999
Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motifC M Coleman, C S Munro, F J Smith, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1996
Prenatal diagnosis for recessive dystrophic epidermolysis bullosa in 10 families by mutation and haplotype analysis in the type VII collagen gene (COL7A1)A M Christiano, S LaForgia, A S Paller, et al.
The Journal of Investigative Dermatology|April 1, 1996
A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: evidence for a founder effectJ A McGrath, S Kivirikko, S Ciatti, et al.
The British Journal of Dermatology|August 1, 1996
Chronic sun exposure alters both the content and distribution of dermal glycosaminoglycansE F Bernstein, C B Underhill, P J Hahn, et al.
The Journal of Investigative Dermatology|June 1, 1984
Ultraviolet radiation-induced connective tissue changes in the skin of hairless miceK J Johnston, A I Oikarinen, N J Lowe, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 1, 1990
Type VI collagen. In situ hybridizations and immunohistochemistry reveal abundant mRNA and protein levels in human neurofibroma, schwannoma and normal peripheral nerve tissuesJ Peltonen, S Jaakkola, L L Hsiao, et al.
The Journal of Investigative Dermatology|May 1, 1988
Selectively enhanced procollagen gene expression in sclerosing (morphea-like) basal cell carcinoma as reflected by elevated pro alpha 1(I) and pro alpha 1(III) procollagen messenger RNA steady-state levelsR L Moy, L S Moy, L Y Matsuoka, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 1, 1988
Cellular differentiation and expression of matrix genes in type 1 neurofibromatosisJ Peltonen, S Jaakkola, M Lebwohl, et al.
International Journal of Tissue Reactions|January 1, 1989
Non-proteolytic activation of latent human neutrophil collagenase and its role in matrix destruction in periodontal diseasesT Sorsa, H Saari, Y T Konttinen, et al.
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