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Research 61–90 of 1000+
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Congenital hair loss disorders: Rare, but not too rare
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Causes and Management of Hypertrichosis
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Genetic Hair Disorders: A Review
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- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Disorders of hair in children
- Genetics of Structural Hair Disorders
- Monilethrix – Case report of a rare disease
- Hair and scalp disorders
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- Molecular Genetics of Alopecias
- Focal and Generalized Alopecia
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- CLINICAL UPDATES IN HAIR
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- Abstracts Pt.30
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses