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Research 571–600 of 581
- Prophylactic Amotosalen-Treated Donor T-Cells Prevent Late CMV Infection in Allogeneic Bone Marrow Transplantation.
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Leishmaniasis in a dog native to Colorado
- Systematic characterization of the barrier function of diverse ex vivo models of damaged human skin
- Pathologic Quiz Case: A Cutaneous Nodule on the Left Temple
- Hair care: Stem cells control immune response during wound repair
- Methods of keratin extraction from wool and hair and prospects of their application in biomedicine and bioengineering
- Case Report: Pulsed electric field treatment of metastatic liver disease demonstrating a possible abscopal response
- Autoimmune alopecia areata due to thymoma without myasthenia gravis: a case report
- Neuroendokrine paraneoplastische Syndrome
- Gene expression profiling of human keratinocytes exposed to the hair-dying agent, m-aminophenol
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Angelica sinensis promotes cortical regeneration of the thymus in mice with acute thymic involution induced by short-term rapamycin treatment
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- RANK as a therapeutic target in cancer
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- The nude gene and the skin
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Mice Engrafted with Human Fetal Thymic Tissue and Hematopoietic Stem Cells Develop Pathology Resembling Chronic Graft-versus-Host Disease
- 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