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Research 541–570 of 1000+
- Engineering a New Mouse Model for Vitiligo
- Genetic Control/Involvement in Hair Fiber Traits
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Premature hair graying: a multifaceted phenomenon
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- Medical Dermatology
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- 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
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- The Genetics of Acne
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Causal Effects of Lipids-Related Metabolites on Androgenic Alopecia: A Mendelian Randomization Study
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits