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Research 781–810 of 804
- Congenital Trichomegaly of the Eyelashes
- Clouston’s syndrome: a rare case report
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- DNCB 유발 피부염 생쥐에서 탄닌이 피부조직 모발주기 관련 유전자 발현에 미치는 영향
- 513 Demonstration of hair health benefits using an oral supplement
- Hair Loss in Children, Etiologies, and Treatment
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Methylene Blue: Its Efficacy and Safety as a Storage Solution in Hair Transplantation
- Monilethrix – Case report of a rare disease
- Oral Presentations
- Hair & Cutaneous Development
- Subject Index
- TONGUE, RED
- Female pattern hair loss: therapeutic update
- Effectiveness of Platelet-Rich Plasma in the Treatment of Androgenic Alopecia Compared to Placebo and Topical Minoxidil: A Systematic Review
- Comparison between topical cetirizine with minoxidil versus topical placebo with minoxidil in female androgenetic alopecia: a randomized, double-blind, placebo-controlled study
- The physiological and pharmacological roles of prostaglandins in hair growth
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Eyebrow Regrowth in Patients with Frontal Fibrosing Alopecia Treated with Low-Dose Oral Minoxidil
- Intercellular junctions in normal epidermis
- Protein S-Palmitoylation as Potential Therapeutic Target for Dermatoses
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS