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- Genetically separable determinants of hair keratin gene expression
- Learning from nudity: lessons from the nude phenotype
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- The genetics of alopecia areata
- The nude gene and the skin
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Autoimmunity: Alopecia Areata
- 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
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- THE PATHOGENESIS OF ALOPECIA AREATA
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- 9. Immunology and Genetics
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Cutaneous signals of immune system disease