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Research 271–300 of 842
- RNA modifications: molecular orchestrators of wound healing
- Stress-induced sympathetic hyperactivation drives hair follicle necrosis to trigger autoimmunity
- Microbial allies in skin trauma recovery: from immune modulation to engineered probiotic therapeutics
- Exploring the Role of GLP‐1 Agents in Managing Diabetic Foot Ulcers: A Narrative and Systematic Review
- Research Progress on the Molecular Mechanism of Poultry Feather Follicle Development
- The Extract of Periplaneta americana (L.) Promotes Hair Regrowth in Mice with Alopecia by Regulating the FOXO/PI3K/AKT Signaling Pathway and Skin Microbiota
- The Impact of Sulforaphane on Sex-Specific Conditions and Hormone Balance: A Comprehensive Review
- Intermittent fasting triggers interorgan communication to suppress hair follicle regeneration
- Melatonin’s effect on hair follicles in a goat (Capra hircus) animal model
- The Pathogenesis and Treatment Progress of Androgenic Alopecia
- Harnessing mesenchymal aggregation for engineered organ‐level regeneration: Recent progress and perspective
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- 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
- Hair & Cutaneous Development
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- FOXN1 deficient nude severe combined immunodeficiency
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Foxn1 promotes keratinocyte differentiation by regulating the activity of protein kinase C
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Transcriptomics sequencing reveals Qu-shi-yu-fa Decoction promotes hair cycle and keratinization by upregulating FOXN1 and TGM3 to treat androgenetic alopecia
- Qu-Shi-Yu-Fa Decoction Promotes Hair Cycle and Keratinization by Upregulating Foxn1 and Tgm3 to Treat Androgenetic Alopecia
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)