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- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Assessment of replication rates of human keratinocytes in engineered skin substitutes grafted to athymic mice
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Learning from nudity: lessons from the nude phenotype
- Phenotypic modulation of human hair matrix cells (trichocytes) by environmental influence in vitro and in vivo.
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Hedgehog signaling maintains hair follicle stem cell phenotype in young and aged human skin
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Neovascularization during healing of wounds treated with dermal substitutes and fibrin glue in nude mice
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Effect of P144® (Anti-TGF-β) in an “In Vivo” Human Hypertrophic Scar Model in Nude Mice
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Interfollicular epidermal stem-like cells for the recreation of the hair follicle epithelial compartment
- Discovery of a novel and highly selective JAK3 inhibitor as a potent hair growth promoter
- Feasibility of repairing full-thickness skin defects by iPSC-derived epithelial stem cells seeded on a human acellular amniotic membrane
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Hair transplantation in mice: Challenges and solutions
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies