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The Journal of Investigative Dermatology|December 1, 1992
Abnormal lamellar granules in harlequin ichthyosisM E Milner, W M O'Guin, K A Holbrook, et al.Prenatal Diagnosis|June 11, 1998
Regional difference in expression of characteristic abnormality of harlequin ichthyosis in affected fetusesM Akiyama, B A Dale, L T Smith, et al.The Journal of Biological Chemistry|November 25, 1992
Characterization of the human epidermal profilaggrin gene. Genomic organization and identification of an S-100-like calcium binding domain at the amino terminusR B Presland, P V Haydock, P Fleckman, et al.Journal of Immunological Methods|August 23, 2001
Detection of beta-defensins secreted by human oral epithelial cellsD L Diamond, J R Kimball, S Krisanaprakornkit, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|November 4, 1998
Translocation of profilaggrin N-terminal domain into keratinocyte nuclei with fragmented DNA in normal human skin and loricrin keratodermaA Ishida-Yamamoto, H Takahashi, R B Presland, et al.Biochemistry|March 13, 1984
High-molecular-weight precursor of epidermal filaggrin and hypothesis for its tandem repeating structureJ D Lonsdale-Eccles, K A Resing, R L Meek, et al.The Journal of Biological Chemistry|November 25, 1993
Independent regulation of two cytoplasmic processing stages of the intermediate filament-associated protein filaggrin and role of Ca2+ in the second stageK A Resing, N al-Alawi, C Blomquist, et al.The Journal of Biological Chemistry|January 13, 1995
Decreased profilaggrin expression in ichthyosis vulgaris is a result of selectively impaired posttranscriptional controlW Nirunsuksiri, R B Presland, S G Brumbaugh, et al.Clinical Otolaryngology and Allied Sciences|October 1, 1986
The Patterson operation for decompression of the orbitN P von Haacke, J A Wilson, B A Dale, et al.Journal of Craniofacial Genetics and Developmental Biology|April 1, 1992
Chromosomal localization of the retinol binding protein gene and its elimination as a candidate gene for the repeated epilation (Er) mutation in miceB A Dale, A H Jones, R Presland, et al.Pageof 11