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Research 691–720 of 1000+
- Topical drug delivery strategies for enhancing drug effectiveness by skin barriers, drug delivery systems and individualized dosing
- Factors associated with female pattern hair loss and its prevalence in Taiwanese women: A community-based survey
- Diverse Role of OX40 on T Cells as a Therapeutic Target for Skin Diseases
- Comparison of the efficacy and safety of a picosecond alexandrite laser and a Q-switched alexandrite laser for the treatment of freckles in Chinese patients
- Comprehensive RNA sequencing in primary murine keratinocytes and fibroblasts identifies novel biomarkers and provides potential therapeutic targets for skin-related diseases
- Erbium: YAG laser (2,940 nm) treatment stimulates hair growth through upregulating Wnt 10b and β-catenin expression in C57BL/6 mice.
- Advances in clinical applications of microneedle
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- 14-3-3σ Is Required for Club Hair Retention
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Acute COVID-19 Syndrome Predicts Severe Long COVID-19: An Observational Study
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Melatonin promotes the development of the secondary hair follicles by regulating circMPP5
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- Molecular Targets in Modern Cosmetic Science
- Stem Cell Secretome for Skincare: Of Cell Types, Exosomes, Extracellular Vesicles, and Soluble Fractions
- Emerging biomedical engineering strategies for hair follicle regeneration
- Hair Loss, Diagnosis, and Treatment Planning
- Bioactive Compound-Loaded Nanocarriers for Hair Growth Promotion: Current Status and Future Perspectives
- Metabolic Syndrome, Cardiovascular Disease and the Hair Growth Cycle: Addressing hair growth disruptions using Nourkrin® with Marilex® as a proteoglycan replacement therapy: A concise review
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family