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Research 811–840 of 1000+
- Calcium and Vitamin D Supplementation with and Without Collagen on Bone Density and Skin Elasticity in Menopausal Women—A Randomized Controlled Study
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- In this Issue
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Selective inhibition of JAK3 signaling is sufficient to reverse alopecia areata
- Amnion bilayer for dressing and graft replacement for delayed grafting of full-thickness burns; A study in a rat model
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Managing Azathioprine-Induced Myelosuppression and Alopecia Totalis: Lessons from a SLE Patient
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Curl pattern classification: A potential tool for communication and risk stratification
- Adipose Tissue‐Derived Exosomes in the Treatment of Lichen Planopilaris: A Case Report
- Dermatological Changes during Menopause and HRT: What to Expect?
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Telogen Effluvium
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A Case of Linear Alopecia of the Scalp
- Low-dose oral minoxidil in a case of short anagen syndrome
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- AB023. An atypical clinical presentation of alopecia in two patients with systemic lupus erythematosus
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Zinc deficiency associated with hypothyroidism: An overlooked cause of severe alopecia
- EGFR signaling is required for regenerative proliferation in the cochlea: Conservation in birds and mammals
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Collagen/Chitosan Gels Cross-Linked with Genipin for Wound Healing in Mice with Induced Diabetes
- Nonhuman primate dermatology: a literature review