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Research 211–240 of 1000+
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Congenital Atrichia: A Case Report
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Recently Identified Forms of Epidermolysis Bullosa
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Clinical Snippets
- Clinical Snippets
- Netherton Syndrome
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Inherited Epidermolysis Bullosa: A Clinical Case
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Woolly hair nevus
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Role of the Wnt signaling pathway in keratoacanthoma
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Subcellular localization of the five members of the human steroid 5α-reductase family
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis