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Research 721–750 of 1000+
- A Clinical Review of Trichorrhexis Nodosa
- Evolution of long scalp hair in humans
- Simultaneous Alopecia Areata in Identical Twins: First Case Reported in Saudi Arabia
- Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- E-Poster
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Mite Burden and Immunophenotypic Response to <i>Demodex musculi</i> in Swiss Webster, BALB/c, C57BL/6, and NSG Mice
- Generalised Glucocorticoid Resistance
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- Hyperinnervation inhibits organ-level regeneration in mammalian skin
- Differential Expression of MITF, WNT3A, SLC7A11, and EDN3 in the Shoulder ‘Bider Marking’ of Dun Mongolian Horses
- An ear for an ear, but only if you are a deomyinid
- The Trotter collection: A review of Mildred Trotter's hair research and an update for studies of human variation
- Forensic DNA Phenotyping
- An Infant with Worsening Rash
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- The Spectrum of Scarring in Craniofacial Wound Repair
- The susceptibility of disulfide bonds to modification in keratin fibers undergoing tensile stress
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Volatile organic compounds: A proinflammatory activator in autoimmune diseases
- Identification of Genes Related to Hair Follicle Cycle Development in Inner Mongolia Cashmere Goat by WGCNA
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- WNT10B (wingless-type MMTV integration site family)
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice