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Research 361–390 of 1000+
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hairless is a nuclear receptor corepressor essential for skin function
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Identification of the cell lineage at the origin of basal cell carcinoma
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Regulatory pathway analysis of coat color genes in Mongolian horses
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Role of FGFR2-signaling in the pathogenesis of acne
- Disorders of Keratinization
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Analogs of human genetic skin disease in domesticated animals
- Hair Anomalies in a 6-Year-Old Girl
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
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- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness