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Research 481–510 of 789
- Retinoid-mediated stimulation of steroid sulfatase activity in myeloid leukemic cell lines requires RARα and RXR and involves the phosphoinositide 3-kinase and ERK-MAP kinase pathways
- EVALUATION OF EFFICACY AND SAFETY OF PLATELET RICH PLASMA (PRP) IN THE TREATMENT OF ANDROGENIC ALOPECIA AND BACTERIAL ULCERATIVE LESION
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- The molecular basis of human keratin disorders
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Nilotinib-Induced Keratosis Pilaris
- The Dermatology Life Quality Index (DLQI) used as the benchmark in validation of 101 quality‐of‐life instruments: A systematic review
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- AN UPDATE OF HAIR SHAFT DISORDERS
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Ectodermal Dysplasia: Variable Expressions
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Trichoscopy in genetic hair shaft abnormalities
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Genetic Hair Disorders: A Review
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Keratosis follicularis spinulosa decalvans in a female
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma