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Research 691–720 of 1000+
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Quantitative Models for the Study of Hair Growth <i>in Vivo</i><sup>a</sup>
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Hair Biology and Care Product Ingredients from Marine Organisms
- Hair follicle stem cells and the collapse of self-tolerance in alopecia: the interplay of barrier function, the microbiome, and immunity
- FC056 The ideal catagen of the hair
- 40 PRLR and PCCA variants associated with hair length in Brangus heifers
- Hair Diseases (Alopecia Areata and Androgenetic Alopecia)
- EVALUATION OF HAIR GROWTH PROMOTING POTENTIAL OF DURDHURADI TAILA THROUGH MODULATION OF 5Α-REDUCTASE GENE EXPRESSION
- Hair Changes Caused by Aging
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- THERAPEUTIC HOTLINE: Genetic variations in the androgen receptor gene and finasteride response in women with androgenetic alopecia mediated by epigenetics
- Becker nevus of the face with asymmetrical growth of beard hair
- Early androgenetic alopecia as a marker of insulin resistance
- An Overview of Alopecias
- Causes and therapeutic limitations of clinical alopecia and the advent of human pluripotent stem cell follicular transplantation
- Research Snippets
- Fortnightly review: Male pattern androgenetic alopecia
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Androgenetic Alopecia
- Alopecia Areata
- The autoimmune basis of alopecia areata: A comprehensive review
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Primary scarring alopecias. A literature review
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Immunology of alopecia areata
- Predicting Human Appearance from DNA for Forensic Investigations
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Keratosis follicularis spinulosa decalvans in a family
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats