Search
forResearch 10 of 201
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →