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Research 361–390 of 494
- Beyond Wavy Hairs
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Vitamin D and the Skin: An Update for Dermatologists
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Keratins and disease at a glance
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Pathology of Mouse Models of Accelerated Aging
- The molecular basis of human keratin disorders
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Role of FGFR2-signaling in the pathogenesis of acne
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Epidermal Growth Factor Promotes Proliferation and Migration of Follicular Outer Root Sheath Cells via Wnt/β-Catenin Signaling
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Expression patterns of programmed cell death 4 protein in normal human skin and some representative skin lesions
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome