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Research 271–300 of 518
- 5a Trichoepithelioma
- Follicular unit extraction hair transplant automation: Options in overcoming challenges of the latest technology in hair restoration with the goal of avoiding the line scar
- The mammary hair of <i>Monodelphis domestica</i> and homology of the mammary pilosebacous unit
- The molecular basis of human keratin disorders
- Dermatological concerns for women and girls with turner syndrome
- The use of dupilumab for the treatment of alopecia areata
- 877 Loss of UBE2N in keratinocytes leads to skin inflammation and immune infiltration through IRAK1/4-mediated processes
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Ginseng in Hair Growth and Viability
- Deregulated expression of c-Myc depletes epidermal stem cells
- Animal and in vitro Models for the Study of Hair Follicles
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Intercellular Adhesion Molecule-1 and Hair Follicle Regression
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- The immune response to COVID‐19: Does sex matter?
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- Pigmentary mosaicism: An update
- Optimized Depilation Method and Comparative Analysis of Hair Growth Cycle in Mouse Strains
- In Vivo Reflectance Confocal Microscopy in General Dermatology: How to Choose the Right Indication
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Decay of Skin-Specific Gene Modules in Pangolins
- Long-Term Effects of Sirolimus on Human Skin TSC2-Null Fibroblast‒Like Cells
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- On Telogen Effluvium
- Pigmented Rings With Central Clearing: A Dermoscopic Feature of Melasma
- Wokeness in Our Practice
- The Transcriptomics and Epigenomics of Hair Follicles