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Research 31–60 of 1000+
- Quantifying whole human hair scalp fibres of varying curl: A micro‐computed tomographic study
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- 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 Trotter collection: A review of Mildred Trotter's hair research and an update for studies of human variation
- Increased rate of hair keratin gene loss in the cetacean lineage
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Formation and Characterization of Hollow Microtubes by Thermal Treatment of Human Hair
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- EVALUATION OF ASSOCIATION OF ANTHROPOMETRIC INDICES WITH STRESS RESPONSE IN PCOS POPULATION
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Pathology of Mouse Models of Accelerated Aging
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Molecular and Functional Characterization of Clonogenic Human Thymic Epithelial Cells
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Scanning electron microscopy and morphometric analysis of the hair in dromedaries with SEM-EDX in relation to age
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Scaffolds for epithelial and hair follicle regeneration
- Woolly Antics between the Sheaths
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Keratin 17 null mice exhibit age- and strain-dependent alopecia