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- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Hair Growth on Nude Mice Due to Cyclosporin A
- FOXN1 deficient nude severe combined immunodeficiency
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
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