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Research 421–450 of 1000+
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Schmallenberg virus infection suspected in a calf born to an imported heifer
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- Disorders in Male Sexual Differentiation Due to 5α-Reductase-2 Deficiency
- Receptors in trichology: Hot spots for hair regeneration
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Developing Human Skin Contains Lymphocytes Demonstrating a Memory Signature
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- The Human Papillomavirus Type 11 Upstream Regulatory Region Triggers Hair-Follicle-Specific Gene Expression in Transgenic Mice
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Long-lived proteins and DNA as candidate predictive biomarkers for tissue associated diseases
- Increased risk of alopecia areata in patients with autism spectrum disorders: A Korean nationwide population-based study
- Diagnosis and treatment of methylmalonic acidemia in 14 cases
- Non-invasive biomonitoring of infant exposure to environmental organic pollutants in north-western Spain based on hair analysis. Identification of potential sources
- Giant congenital cerebriform pigmented nevus of scalp: case report
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Adult Patients with Aphallia: Were they Fertile?
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Edar Signaling in the Control of Hair Follicle Development
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- C/EBPα and C/EBPβ Are Required for Sebocyte Differentiation and Stratified Squamous Differentiation in Adult Mouse Skin
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Ichthyosis with confetti: clinics, molecular genetics and management
- Miz1 is required for hair follicle structure and hair morphogenesis
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report