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Research 661–690 of 1000+
- Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Celiac disease associated with alopecia areata: A multicenter case-control study
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- 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
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- An Early Hair Loss Detection and Prediction Method Based on Machine Learning
- From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Hair Sciences: An interview with Dr. Rodney Sinclair on female pattern hair loss
- Claves diagnósticas en displasias pilosas II
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- The Pathobiology of Skin Aging
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Polycystic ovary syndrome
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Biotin and biotinidase deficiency
- Adult female acne: a guide to clinical practice
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Pharmacologic interventions in aging hair