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Research 30 of 871
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- 131 Mutational landscape of extramammary Paget disease
- 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
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- The nude gene and the skin
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Gsdma3 is required for hair follicle differentiation in mice
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- FOXN1 deficient nude severe combined immunodeficiency
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Learning from nudity: lessons from the nude phenotype
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Genetically separable determinants of hair keratin gene expression
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis