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Research 991–1000 of 1000+
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Regulation of masculinization: androgen signalling for external genitalia development
- FOXN1 deficient nude severe combined immunodeficiency
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family