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- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Multiple follicular abnormalities in a 1‐year old cat consistent with basaloid follicular hamartomas
- Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses
- The hair shaft: normality, abnormality, and genetics
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Trichothiodystrophy: an ultrastructural study of the hair follicle
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Black Hair Follicular Dysplasia in Black and White Saluki Dogs: Differentiation from Color Mutant Alopecia in the Doberman Pinscher by Microscopic Examination of Hairs
- Das Trichorhinophalangealsyndrom
- Unexpected Autocrine Role of Vascular Endothelial Growth Factor in Squamous Cell Carcinoma
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Clinical Snippets
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Seventy‐MHz Ultrasound Detection of Early Signs Linked to the Severity, Patterns of Keratin Fragmentation, and Mechanisms of Generation of Collections and Tunnels in Hidradenitis Suppurativa
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Bubble Hair and the Usefulness of Trichoscopy
- Monilethrix: an ultrastructural study
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Morphological analyses in fragility of pili torti with Björnstad syndrome
- Ichthyosis hystrix
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- [Studies on monilethrix].
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue