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Research 901–930 of 1000+
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Harnessing miRNA Milk-Derived Exosomes for Hair Loss Disorders: In Vitro Modulation of WNT Signaling and Dermal Papilla Proliferation
- Cicatricial (Scarring) Alopecias
- The effects of synthetic 19-norprogestins on osteoblastic cell function are mediated by their non-phenolic reduced metabolites
- INOSITOL AND SPECTACLED EYE IN RATS
- Moxibustion improves ovarian function based on the regulation of the androgen balance
- Delivery Strategies of siRNA Therapeutics for Hair Loss Therapy
- Hair Loss: Pathogenesis and Prevention: A Literature Review
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- An Overview of Alopecias
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Regulation of stem cell function by protein ubiquitylation
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Female Pattern Hair Loss: a clinical and pathophysiological review
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- Increased rate of hair keratin gene loss in the cetacean lineage
- Priming mobilization of hair follicle stem cells triggers permanent loss of regeneration after alkylating chemotherapy
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Serum vitamin D3 level in patients with female pattern hair loss
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Histopathological change of age-related hearing loss in female advance-aged CBA/CaJ mice