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Research 30 of 826
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- The nude gene and the skin
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- 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
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Gsdma3 is required for hair follicle differentiation in mice
- 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
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- 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
- Genetically separable determinants of hair keratin gene expression
- FOXN1 deficient nude severe combined immunodeficiency
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Molecular Genetics of Alopecias
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus