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Research 541–570 of 698
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Current Genetics in Hair Diseases
- 0847 The addition of collagen scaffolds to human cell therapy to modify skin identity
- Spiny Keratoderma
- Hypotrichosis in a child with olmsted syndrome
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Circle hairs are not rolled hairs
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- [Methotrexate to treat SAPHO syndrome with keloidal scars].
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- The epidermis: rising to the surface
- Basal cell carcinoma — molecular biology and potential new therapies
- Genetic hair and nail disorders
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Dermatologic adverse events in pediatric patients receiving targeted anticancer therapies: A pooled analysis
- Regionalisation of the skin
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita