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Differentiation; Research in Biological Diversity|June 12, 1999
Characterization of loricrin regulation in vitro and in transgenic miceD DiSepio, J R Bickenbach, M A Longley, et al.Nature Genetics|July 1, 1995
Mutation of a type II keratin gene (K6a) in pachyonychia congenitaP E Bowden, J L Haley, A Kansky, et al.The Journal of Investigative Dermatology|May 1, 1994
Abnormal keratin 1 and 10 cytoskeleton in cultured keratinocytes from epidermolytic hyperkeratosis caused by keratin 10 mutationsM Huber, C Scaletta, M Benathan, et al.Experimental Dermatology|May 8, 1999
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosisM J Arin, M A Longley, W Küster, et al.Experimental and Molecular Pathology|January 11, 2002
The Mallory body as an aggresome: in vitro studiesN E Riley, J Li, S Worrall, et al.The Journal of Investigative Dermatology|March 20, 1999
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of SiemensM J Arin, M A Longley, E H Epstein, et al.Journal of Dermatological Science|July 1, 1994
Genetic disorders of keratin: are scarring alopecias a sub-set?J A Rothnagel, M A Longley, R A Holder, et al.Archives of Dermatology|November 1, 1993
Transgenic models of skin diseasesJ A Rothnagel, D A Greenhalgh, X J Wang, et al.The Journal of Investigative Dermatology|April 14, 1999
A novel substitution in keratin 10 in epidermolytic hyperkeratosisM J Arin, M A Longley, I Anton-Lamprecht, et al.Nature Genetics|August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of SiemensJ A Rothnagel, H Traupe, S Wojcik, et al.Pageof 5