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- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- The hair shaft: normality, abnormality, and genetics
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Epidemiology and burden of alopecia areata: a systematic review
- Inherited Disorders of the Hair
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Human Hair Keratin‐Associated Proteins (KAPs)
- Hair follicle-specific keratins and their diseases
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Inherited Epidermolysis Bullosa: A Clinical Case
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- 9 Role of 5α-reductase in health and disease
- Oestrogen functions in skin and skin appendages
- A genomic approach to susceptibility and pathogenesis leads to identifying potential novel therapeutic targets in androgenetic alopecia
- Beyond Expectations
- Against the Rules: Human Keratin K80
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Keratin 79 identifies a novel population of migratory epithelial cells that initiates hair canal morphogenesis and regeneration
- What does acne genetics teach us about disease pathogenesis?