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Research 751–780 of 1000+
- The Polish version of Skindex-29: psychometric properties of an instrument to measure quality of life in dermatology
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Dermal fibroblast in cutaneous development and healing
- Stem cells in embryonic skin development
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Keratoacanthoma of the lip: A case report with emphasis on histogenesis
- Faces of the Face
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Regulation of masculinization: androgen signalling for external genitalia development
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Advances in Lipid Nanoparticle‐Based Disease Treatment
- Association between Polymorphisms of OCT1 and Metabolic Response to Metformin in Women with Polycystic Ovary Syndrome
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Evaluation of loci to predict ear morphology using two SNaPshot assays
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele