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Research 991–1000 of 993
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- DNA Methylation Mediates lncRNA2919 Regulation of Hair Follicle Regeneration
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- KRT17: A Key Driver of Cancer Therapy Resistance and Emerging Therapeutic Target