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Research 30 of 851
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Learning from nudity: lessons from the nude phenotype
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Rancangan televisyen: Menyangga atau menyanggah bahasa dan budaya?
- 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
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- FOXN1 deficient nude severe combined immunodeficiency
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The nude gene and the skin
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Genetically separable determinants of hair keratin gene expression
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Hair Growth Promoting Effect of Dermal Papilla Like Tissues from Canine Adipose-Derived Mesenchymal Stem Cells in Athymic Nude Mice
- Exogenous stimulation with Eclipta alba promotes hair matrix keratinocyte proliferation and downregulates TGF-β1 expression in nude mice
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production