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Research 901–930 of 1000+
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells
- Types I and II Keratin Intermediate Filaments
- Essential Oils and Their Single Compounds in Cosmetics—A Critical Review
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- The Pathogenesis of Primary Cicatricial Alopecias
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Trichoscopy in genetic hair shaft abnormalities
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome