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Research 181–210 of 227
- Disorders of Keratinization
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Ichthyosis hystrix
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Trichorrhexis Invaginata and Netherton’s Syndrome
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Proteome Analysis of Human Hair Shaft
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Chronic graft versus host disease and skin
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Genetic disorders of keratin: are scarring alopecias a sub-set?