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Research 961–990 of 1000+
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Unhealthy diet and lifestyle factors linked to female androgenetic alopecia: a community-based study from Jidong study, China
- Discovery Potential Hub Genes and Pathways in Keloid Fibroblast Development Based on Bioinformatics Analysis
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Extemporaneous Topical Minoxidil Solutions for the Treatment of Androgenetic Alopecia- Stability Studies and Incorporation Tests of Active Pharmaceutical Ingredients in Aloplus Total Base.
- Formulation and Evaluation of Minoxidil Loaded Submicron Emulsion Based Topical Gel for Treatment of Alopecia
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Establishment and validation of a hair fall atlas for Chinese men based on trichoscopy
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Virtual Insights into Natural Compounds as Potential 5α-Reductase Type II Inhibitors: A Structure-Based Screening and Molecular Dynamics Simulation Study
- Risk of Psychiatric Disorders following Polycystic Ovary Syndrome: A Nationwide Population-Based Cohort Study
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- The role of pregnane neurosteroids in ethanol withdrawal: behavioral genetic approaches
- Alopecia areata and risk of atopic and autoimmune conditions: population-based cohort study
- Male pattern baldness and prostate cancer risk in a population-based case–control study
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Prevalence and types of androgenetic alopecia in north Anatolian population: A community-based study.
- Mining and analysis of adverse event signals of isotretinoin based on the real-world data of FAERS database
- Exploring the Mechanisms and Molecular Targets of Taohong Siwu Decoction for the Treatment of Androgenetic Alopecia Based on Network Analysis and Molecular Docking
- Exploring the mechanism of Platycladi Cacumen in intervening androgenetic alopecia based on network pharmacology, molecular docking, and molecular dynamics simulation
- Anemia Assessment among the First-trimester Pregnant Women: A Cross-sectional Hospital-based Study in Mysore District, Karnataka, India
- Perspectives of Chinese Adult Patients with Alopecia Areata on Janus Kinase Inhibitors Therapy: A Qualitative Analysis Based on Social Media Platforms
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Evaluation of the Hemogram of Breast Cancer Patients Treated by Therapeutic Protocol Based on Immunohistochemical Analysis: A Retrospective Study
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- Post-marketing safety profile of cladribine in multiple sclerosis: a disproportionality analysis based on the FDA adverse event reporting system
- Disproportionality analysis comparing safety profiles of sonidegib and vismodegib based on the FAERS database