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Research 481–510 of 1000+
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Genetically separable determinants of hair keratin gene expression
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing
- Hair & Cutaneous Development
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- The Functional Organization of Cutaneous Low-Threshold Mechanosensory Neurons
- Quiescent Tissue Stem Cells Evade Immune Surveillance
- FGF5 is a crucial regulator of hair length in humans
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Runx3 is involved in hair shape determination
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Current evidence for the involvement of sex steroid receptors and sex hormones in benign prostatic hyperplasia
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- 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
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype