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Research 751–780 of 1000+
- Linear trichoepithelioma on the neck of a 15-year-old girl
- Porphyria Cutanea Tarda – a Case Report
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Female Androgenetic (?) Alopecia
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Hair in the Wrong Place
- Ichthyosis
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Genetic Basis of Male Pattern Baldness
- Keratin gene mutations in disorders of human skin and its appendages
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Hair follicle-specific keratins and their diseases
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Hair: Its structure and response to cosmetic preparations
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes