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- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- Keratin disorders: from gene to therapy
- Delivery Strategies of siRNA Therapeutics for Hair Loss Therapy
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
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