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Research 31–60 of 1000+
- Scarring Folliculitis in the Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Claudin tight junctionwhat's your function? The role of Claudin 6 in epidermal and hair follicle differentiation
- Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin
- Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: Use of the method for analysis of keratins and filaggrin
- Prolactin—a novel neuroendocrine regulator of human keratin expression<i>in situ</i>
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- In vivo Alteration of the Keratin 17 Gene in Hair Follicles by Oligonucleotide-directed Gene Targeting
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Overexpression of insulin-like growth factor-1 induces hyperplasia, dermal abnormalities, and spontaneous tumor formation in transgenic mice
- Histological and dermatoscopic description of sphynx cat skin
- Genetics of Structural Hair Disorders
- Late onset nevus comedonicus of scalp: a rare site for an uncommon condition
- Hair: Its structure and response to cosmetic preparations
- Trichorhinophalangeal Syndrome
- A new type of pachyonychia congenita.
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Inherited Disorders of the Hair
- Circle hairs involving the extremities in a young girl
- Ritlecitinib and brepocitinib demonstrate significant improvement in scalp alopecia areata biomarkers
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The structure of hair and follicles of mice carrying the naked (<i>N</i>) gene
- Follicular ichthyosis