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Research 361–390 of 1000+
- Alopecia in Epidermolysis Bullosa
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Learning from nudity: lessons from the nude phenotype
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- 5-Alpha reductase deficiency
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Trichodystrophies: A hair-raising differential diagnosis
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Roles for Msx and Dlx homeoproteins in vertebrate development
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- [Regulation of hair follicle cycle].
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- The nude gene and the skin
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene