Search
for
Sort by
Research 30 of 37
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Immunomodulators in the treatment of cutaneous lymphoma
- The clinical spectrum of parathyroid disease
- Hormones
- Dermatologic therapy: December 1987 to December 1988
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- The Role of Zinc in Gastrointestinal and Liver Disease
- Intestinal Intraepithelial Lymphocytes: Sentinels of the Mucosal Barrier
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Mice Engrafted with Human Fetal Thymic Tissue and Hematopoietic Stem Cells Develop Pathology Resembling Chronic Graft-versus-Host Disease
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Runx3 is involved in hair shape determination
- Developing stratified epithelia: lessons from the epidermis and thymus
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Advances in single-cell transcriptomics in animal research
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- 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
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>