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Research 61–90 of 1000+
- HAIR AND SYSTEMATIC DISEASE
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hirsutism: diagnosis and treatment
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Congenital hair loss disorders: Rare, but not too rare
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Causes and Management of Hypertrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Answer
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Genetics of Alopecia
- Monilethrix – Case report of a rare disease
- Genetic Hair Disorders: A Review
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Trichoscopy in Hair Shaft Disorders
- Molecular Genetics of Alopecias
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Focal and Generalized Alopecia
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype