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Experimental Dermatology|February 25, 2000
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosisM J Arin, M A Longley, E H Epstein, et al.
The Journal of Investigative Dermatology|June 1, 1994
Retinoic acid suppression of loricrin expression in reconstituted human skin cultured at the liquid-air interfaceL J Brown, J C Geesin, J A Rothnagel, et al.
The Journal of Investigative Dermatology|January 1, 1994
Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencingJ A Rothnagel, M A Longley, R A Holder, et al.
The Journal of Biological Chemistry|November 15, 1987
The gene for mouse epidermal filaggrin precursor. Its partial characterization, expression, and sequence of a repeating filaggrin unitJ A Rothnagel, T Mehrel, W W Idler, et al.
The Journal of Investigative Dermatology|October 1, 1993
Identification of a calcium-inducible, epidermal-specific regulatory element in the 3'-flanking region of the human keratin 1 geneJ A Rothnagel, D A Greenhalgh, T A Gagne, et al.
The Journal of Investigative Dermatology|March 1, 1995
Loricrin expression is coordinated with other epidermal proteins and the appearance of lipid lamellar granules in developmentJ R Bickenbach, J M Greer, D S Bundman, et al.
The Journal of Investigative Dermatology|November 1, 1990
Targeting gene expression to the epidermis of transgenic mice: potential applications to genetic skin disordersJ A Rothnagel, M A Longley, D Bundman, et al.
The Journal of Investigative Dermatology|March 1, 1995
Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratodermaJ A Rothnagel, S Wojcik, K M Liefer, et al.
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