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Research 241–270 of 566
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Thymic Mesenchymal Cells Have a Distinct Transcriptomic Profile
- 17β-Estradiol Enhances Contact Hypersensitivity in a Hair Cycle-Dependent Manner and Retards Thymic Atrophy with Age
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Angelica sinensis promotes cortical regeneration of the thymus in mice with acute thymic involution induced by short-term rapamycin treatment
- Dyad of infantile cutaneous and thymic Langerhans cell histiocytosis: Is it rare?
- 751 Thymic stromal lymphopoeitin controls hair growth
- Thymic epithelial cells : relatives of multipotent stem cells of the skin
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Molecular and Functional Characterization of Clonogenic Human Thymic Epithelial Cells
- Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis
- Patterns of expression of trichocytic and epithelial cytokeratins in mammalian tissues II. Concomitant and mutually exclusive synthesis of trichocytic and epithelial cytokeratins in diverse human and bovine tissues (hair follicle, nail bed and matrix, lingual papilla, thymic reticulum)
- The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- RANK as a therapeutic target in cancer
- (Neuro-)endocrinology of epithelial hair follicle stem cells
- The nude gene and the skin
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Pleiotropic effects of the nude mutation.
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Lineage potential, plasticity and environmental reprogramming of epithelial stem/progenitor cells
- Case 18-2018: A 45-Year-Old Woman with Hypertension, Fatigue, and Altered Mental Status
- Decision letter: IL18 signaling promotes homing of mature Tregs into the thymus
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development