References
- Guo H., et al. Gap-junctional protein connexin 43 is expressed in dermis and epidermis of human skin: differential modulation by retinoids. J. Invest. Dermatol. 1992; 99: 460–467
- Heathcote K., et al. A connexin 26 mutation causes a syndrome of sensorineural bearing loss and palmoplantar hyperkeratosis. J. Med. Genet. 2000; 37: 50–51
- Kelsell D. P., et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997; 387: 80–83
- Labarthe M. P., et al. Upregulation of connexin 26 between keratinocytes of psoriatic lesions. J. Invest. Dermatol. 1998; 111: 72–76
- Lamartine J., et al. Mutations in GJB6 cause hidrotic ectodermal dysplasia. Nat. Genet. 2000; 26: 142–144
- Limat A., et al. Successful treatment of chronic leg ulcers with epidermal equivalents generated from cultured autologous outer root sheath cells. J. Invest. Dermatol. 1996; 107: 128–135
- Lucke T., et al. Upregulation of connexin 26 is a feature of keratinocyte differentiation in hyperproliferative epidermis, vaginal epithelium, and buccal epithelium. J. Invest. Dermatol. 1999; 112: 354–361
- Macari E., et al. Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis. Am. J. Hum. Genet. 2000; 67: 1296–301
- Maesrrini E., et al. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Hum. Mol. Genet. 1999; 8: 1237–1243
- Masgrau-Peya E., et al. In vivo modulation of connexins 43 and 26 of human epidermis by topical retinoic acid treatment. J. Histochem. Cytochem. 1997; 45: 207–215
- Richard G., et al. Mutations in the human connexin gene GJ63 cause erythrokeratodermia variabilis. Nat. Genet. 1998a; 20: 366–369
- Richard G., et al. Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. Hum. Genet. 1998b; 103: 393–399
- Rivas M. V., et al. Identification of aberrantly regulated genes in diseased skin using the cDNA differential display technique. J. Invest. Dermatol. 1997; 108: 188–194
- Salomon D., et al. Topography of mammalian connexins in human skin. J. Invest. Dermatol. 1994; 103: 240–247
- Wilgenbus K. K., et al. Expression of Cx26, Cx32 and Cx43 gap junction proteins in normal and neoplastic human tissues. Int. J. Cancer 1992; 51: 522–529
- Wiszniewski L., et al. Differential expression of connexins during stratification of human keratinocytes. J. Invest. Dermatol. 2000; 115: 278–285
- Zelante L. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNBI) in Mediterraneans. Hum. Mol. Genet. 1997; 6: 1605–1609