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- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
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