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Research 271–300 of 567
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Perforins Expression by Cutaneous Gamma Delta T Cells
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- Unlocking the therapeutic potential of TRPV3: Insights into thermosensation, channel modulation, and skin homeostasis involving TRPV3
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Fibroblast bioelectric signaling drives hair growth
- Human Placenta Extract (HPH) Suppresses Inflammatory Responses in TNF-α/IFN-γ-Stimulated HaCaT Cells and a DNCB Atopic Dermatitis (AD)-Like Mouse Model
- Morphologic Markers of Acute and Chronic Stress in Child Abuse
- Methods of keratin extraction from wool and hair and prospects of their application in biomedicine and bioengineering
- The Protective and Regenerative Potential of Lactoferrin in Hair and Skin Health
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- JAK1 Signaling Is Involved in the Induction of Mechanical Alloknesis in Atopic Dermatitis
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Deciphering the molecular mechanisms of stem cell dynamics in hair follicle regeneration
- Gene expression profiling of human keratinocytes exposed to the hair-dying agent, m-aminophenol
- The cell-surface marker MTS24 identifies a novel population of follicular keratinocytes with characteristics of progenitor cells
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Malnutrition and Allergies: Tipping the Immune Balance towards Health
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Commensal Microbes and Hair Follicle Morphogenesis Coordinately Drive Treg Migration into Neonatal Skin
- Tracking adult stem cells
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Tregs: Where We Are and What Comes Next?
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- Pathology of Mouse Models of Accelerated Aging