Search
for
Sort by
Research 30 of 859
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- FOXN1 deficient nude severe combined immunodeficiency
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- `Cyclic alopecia' in<i>Msx2</i>mutants: defects in hair cycling and hair shaft differentiation
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Foxp1 Regulates the Proliferation of Hair Follicle Stem Cells in Response to Oxidative Stress during Hair Cycling
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Transcriptional Governance of Hair Follicle Stem Cell Quiescence and Niche Maintenance in Long-Term Tissue Regeneration
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- FOXO1, TGF-β Regulation and Wound Healing
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Elastogenesis Stimulation by Minoxidil or Nebivolol Reduces Premature Aging of the Aortic Wall in Diabetic Mice
- Molecular biology of hair morphogenesis: Development and cycling
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Inherited Disorders of the Hair
- Iron Deficiency-Induced Hair Loss Is Associated with ROS-Mediated Disruption of Wnt/β-Catenin Signaling