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Research 541–570 of 1000+
- Congenital atrichia and hypotrichosis
- Methods of hair loss evaluation: a comparison of TrichoScan<sup>®</sup>with the modified wash test
- Evaluating the Quality of TikTok Content on Alopecia: A Cross-Sectional DISCERN-Based Analysis
- The Effect of Parathyroid Hormones on Hair Follicle Physiology: Implications for Treatment of Chemotherapy-Induced Alopecia
- Thyroid hormone action on skin.
- Repeated Microneedle Stimulation Induces Enhanced Hair Growth in a Murine Model
- Inducing hair follicle neogenesis with secreted proteins enriched in embryonic skin
- Hair loss in children.
- Ether: Fiction or Reality? A Review
- Cyclosporin A-induced hair growth in mice is associated with inhibition of calcineurin-dependent activation of NFAT in follicular keratinocytes
- Central centrifugal cicatricial alopecia: challenges and solutions
- Microneedles mediated bioinspired lipid nanocarriers for targeted treatment of alopecia
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Editor's Choice
- The effects and mechanisms of collagen peptides for alleviating skin ageing
- Surgical Anatomy of the Scalp
- Alopecia Areata Ophiasic with Ciliary Madarosis in A Pediatric Patient: Case Report
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Overexpression of spermidine/spermine N1-acetyltransferase under the control of mouse metallothionein I promoter in transgenic mice: evidence for a striking post-transcriptional regulation of transgene expression by a polyamine analogue
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- FOXN1 deficient nude severe combined immunodeficiency
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin