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Research 601–630 of 1000+
- Types of Hair Loss and Treatment Options, Including the Novel Low-Level Light Therapy and Its Proposed Mechanism
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Cicatricial (Scarring) Alopecias
- Primary cicatricial alopecia: Recent advances in understanding and management
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Acquired scalp alopecia. Part I: A review
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Characterization of Hair Follicle Development in Engineered Skin Substitutes
- Congenital hair loss disorders: Rare, but not too rare
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Male pattern baldness: current treatments, future prospects
- A Microarray-Based Analysis Reveals that a Short Photoperiod Promotes Hair Growth in the Arbas Cashmere Goat
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Fluoroquinolone-induced serious, persistent, multisymptom adverse effects
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia