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Research 811–840 of 1000+
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- The hair follicle enigma
- The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase?
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Female pattern hair loss
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Frontal Fibrosing Alopecia: A Review
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- New developments in the molecular treatment of ichthyosis: review of the literature
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Making Waves with Hairs
- Managing hair loss in midlife women
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation