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Research 241–270 of 1000+
- Transcriptome analysis reveals the genetic basis underlying the formation and seasonal changes of nuptial pads in Rana chensinensis
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis?
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits
- The switch from patented medicine to the generic one: an option or a necessity?
- Assessment of prescribing information for generic drugs manufactured in the Middle East and marketed in Saudi Arabia
- Laser therapy in superficial morphea lesions – indications, limitations and therapeutic alternatives
- Demodicosis in Different Age Groups and Alternative Treatment Options—A Review
- Large-Scale Plasma Proteomics and Genetic Integration Uncover Novel Biological Pathways in Male Pattern Baldness
- Biomedical applications of organoids in genetic diseases
- Exploring nanobioceramics in wound healing as effective and economical alternatives
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- First Report on Microbial-Derived Polydeoxyribonucleotide: A Sustainable and Enhanced Alternative to Salmon-Based Polydeoxyribonucleotide
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- เครองมอประมวลผลภาพดจทลสำหรบวดขอมลของเสนผมบนหนงศรษะของผปวยโรคผมบางทางพนธกรรม
- Scalp micropigmentation: a concealer for hair and scalp deformities.
- Alopecias in humans: biology, pathomechanisms and emerging therapies
- Causes and therapeutic limitations of clinical alopecia and the advent of human pluripotent stem cell follicular transplantation
- Vitiligo and alopecia areata: apples and oranges?
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Serum levels of vitamin C, vitamin E, and total antioxidant capacity in premature graying hair
- Epigenetic and transcriptional profiling of secondary hair follicle stem cells during cashmere growth