Search
for
Sort by
Research 721–750 of 1000+
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Actinic keratosis: a clinical and epidemiological revision
- Dynamic regulation of retinoic acid-binding proteins in developing, adult and neoplastic skin reveals roles for β-catenin and Notch signalling
- Pathology of Mouse Models of Accelerated Aging
- Critical Analysis on Characterization, Systemic Effect, and Therapeutic Potential of Beta-Sitosterol: A Plant-Derived Orphan Phytosterol
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Regulation of stem cell function by protein ubiquitylation
- Clinical biochemistry of dihydrotestosterone
- Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents
- 5α-Reduced glucocorticoids: a story of natural selection
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Teriflunomide: A Once-daily Oral Medication for the Treatment of Relapsing Forms of Multiple Sclerosis
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Ichthyosis with confetti: clinics, molecular genetics and management
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Emerging roles of transit‐amplifying cells in tissue regeneration and cancer
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- The role of WNT10B in physiology and disease: A 10-year update
- Clinical review of ejaculatory dysfunction
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Myc and Fgf Are Required for Zebrafish Neuromast Hair Cell Regeneration
- Skin-associated adipocytes in skin barrier immunity: A mini-review
- Palatogenesis and cutaneous repair: A two‐headed coin
- Epidermal stem cells: skin surveillance and clinical perspective
- [Retracted] Fibroblasts in Scar Formation: Biology and Clinical Translation