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Research 811–840 of 1000+
- 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
- TRPV3 as a Therapeutic Target for Itch
- 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
- 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
- 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
- Telogen Effluvium: A 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
- Tannic acid-functionalized 3D porous nanofiber sponge for antibiotic-free wound healing with enhanced hemostasis, antibacterial, and antioxidant properties
- OCT4 maintains self-renewal and reverses senescence in human hair follicle mesenchymal stem cells through the downregulation of p21 by DNA methyltransferases
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Depositing α-mangostin nanoparticles to sebaceous gland area for acne treatment
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Clinical biochemistry of dihydrotestosterone
- Spatiotemporal Expression, Distribution, and Processing of POMC and POMC-derived Peptides in Murine Skin