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- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Genetics of Structural Hair Disorders
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Biology and Genetics of Hair
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Congenital hair loss disorders: Rare, but not too rare
- Estrogen modulates mesenchymal-epidermal interactions in the adult nipple
- Differences in cell subsets between sun-exposed and unexposed skin: preliminary single-cell sequencing and biological analysis from a single case
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
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