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Research 751–780 of 1000+
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Recent Advances in Biopolymeric Composite Materials for Tissue Engineering and Regenerative Medicines: A Review
- TRPV3 as a Therapeutic Target for Itch
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Breast implant illness: a topic in review
- Types of Hair Dye and Their Mechanisms of Action
- Hox genes in development and beyond
- Injectable Biomaterials for Dental Tissue Regeneration
- Pathology of Mouse Models of Accelerated Aging
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Insights into the angiogenic effects of nanomaterials: mechanisms involved and potential applications
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Free Testosterone: Pumping up the Tires or Ending the Free Ride?
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Telogen Effluvium: A Review
- Aldo-Keto Reductase (AKR) 1C3 inhibitors: a patent review
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- The biology and genetics of curly hair