Search
for
Sort by
Research 811–840 of 1000+
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Alopecias in lupus erythematosus
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- Apoptosis resistance in peripheral blood lymphocytes of alopecia areata patients
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Ichthyosis with confetti: clinics, molecular genetics and management
- Efficacy of Platelet-Rich Plasma Therapy in Oral Lichen Planus: A Systematic Review
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Dermoscopic findings of alopecia areata in dark skinned individuals: An analysis of 116 cases
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- Skin manifestations associated with COVID-19
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Alopecia Areata: A Review of the Role of Oxidative Stress, Possible Biomarkers, and Potential Novel Therapeutic Approaches
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- ES Cell Differentiation Into the Hair Follicle Lineage In Vitro
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- Skin manifestations associated with systemic diseases – Part I
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Trichoscopic patterns of nonscarring alopecia's
- Ischemic modified albumin as a new biomarker in predicting of oxidative stress in alopecia areata
- Trichotillomania as a Manifestation of Dementia
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages