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Research 31–60 of 154
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genetic Hair Disorders: A Review
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Management of congenital ichthyoses: European guidelines of care, part two
- Evolving approaches to profiling the microbiome in skin disease
- Advances in Hair Diseases
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genetic Control/Involvement in Hair Fiber Traits
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Trichodystrophies: A hair-raising differential diagnosis
- Genetics
- Restoration of hair-inductive activity of cultured human follicular keratinocytes by co-culturing with dermal papilla cells
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Skin, Genetic Defects, and Aging
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Comparative Spatial Transcriptomic and Single-Cell Analyses of Human Nail Units and Hair Follicles Show Transcriptional Similarities between the Onychodermis and Follicular Dermal Papilla
- New developments in the molecular treatment of ichthyosis: review of the literature