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    Research 241–270 of 1000+

    1. Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery BMC Genomics · 2024 · 9 citations
    2. Characterisation of Four New Genes in the Ovine KAP19 Family International Journal of Molecular Sciences · 2025
    3. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis American journal of human genetics · 2019 · 53 citations
    4. Chronic overlapping pain conditions and nociplastic pain Human Genetics and Genomics Advances · 2024 · 16 citations
    5. Regulatory pathway analysis of coat color genes in Mongolian horses Hereditas · 2017 · 14 citations
    6. Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep Genes · 2024
    7. Must Hair Care Products That Target the Causes of Consumer Hair Loss Be More Popular? Advances in economics, management and political sciences · 2023
    8. Metal-Chelation-Assisted Deposition of Polydopamine on Human Hair: A Ready-to-Use Eumelanin-Based Hair Dyeing Methodology ACS biomaterials science & engineering · 2017 · 63 citations
    9. Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization Structure · 2017 · 24 citations
    10. Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans American journal of human genetics · 2009 · 234 citations
    11. Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome American journal of human genetics · 2016 · 119 citations
    12. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    13. Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction International Journal of Molecular Sciences · 2015 · 16 citations
    14. 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 American Journal of Medical Genetics Part A · 2021 · 10 citations
    15. Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza Scientific reports · 2020 · 8 citations
    16. Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep Frontiers in Veterinary Science · 2026
    17. miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway Animals · 2025
    18. A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism Frontiers in Genetics · 2025
    19. A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus American Journal of Medical Genetics Part A · 2025
    20. Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits International journal of molecular sciences · 2024
    21. <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i> New phytologist · 2023
    22. Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2 2022 · 8 citations
    23. Wool Keratin-Associated Protein Genes in Sheep—A Review Genes · 2016 · 98 citations
    24. Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families BMC Ophthalmology · 2024 · 6 citations
    25. Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits BMC Genomics · 2024 · 2 citations
    26. Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs 2021 · 12 citations
    27. Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease Translational Psychiatry · 2021 · 12 citations
    28. Forensic DNA Phenotyping: a review on SNP panels, genotyping techniques, and prediction models Research Square (Research Square) · 2023 · 2 citations
    29. A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing 2020
    30. Cyberspace Chat Hair transplant forum international · 2012