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Research 601–630 of 1000+
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- Pathogenesis of Alopecia Areata and Vitiligo: Commonalities and Differences
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Review on Alopecia Areata in the Middle East and Africa: Landscape and Unmet Needs
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Editorial: Advances in reproductive biotechnologies in carnivores
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Insulin resistance as risk factor for the development of type 2 diabetes mellitus: a systematic approach
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Андроген-опосередковані й андрогенонезалежні причини алопеції та акне в жінок. Огляд літератури
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- Acne Vulgaris
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients