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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
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- FOXN1 deficient nude severe combined immunodeficiency
- Phenotypic Analysis of T-Cells in Extensive Alopecia Areata Scalp Suggests Partial Tolerance
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