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Research 961–990 of 1000+
- PCOS and Depression: Common Links and Potential Targets
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- The Proteins of Hair and Other Hard α-Keratins
- Evidence of Heterogeneity and Quantitative Differences of the Type 1 5α-Reductase Expression in Cultured Human Skin Cells – Evidence of its Presence in Melanocytes
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Scarless wound healing: Transitioning from fetal research to regenerative healing
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Regulated Proenkephalin Expression in Human Skin and Cultured Skin Cells
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Protein Kinase Cε, which Sensitizes Skin to Sun's UV Radiation–Induced Cutaneous Damage and Development of Squamous Cell Carcinomas, Associates with Stat3
- Protein Microarrays
- Edar Signaling in the Control of Hair Follicle Development
- The emerging progress on wound dressings and their application in clinic wound management
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- The Intermediate Filament Architecture as Determined by X-Ray Diffraction Modeling of Hard α-Keratin
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Targeting integrin pathways: mechanisms and advances in therapy