Search
for
Sort by
Research 31–60 of 1000+
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Regulatory T cells in inflammatory skin disease: from mice to humans
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Exogenous stimulation with Eclipta alba promotes hair matrix keratinocyte proliferation and downregulates TGF-β1 expression in nude mice
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Therapeutic potential and pharmacological insights of total glucosides of paeony in dermatologic diseases: a comprehensive review
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- FOXN1 deficient nude severe combined immunodeficiency
- DNCB 유발 피부염 생쥐에서 탄닌이 피부조직 모발주기 관련 유전자 발현에 미치는 영향
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- The potential of regulatory T cell-based therapies for alopecia areata
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Stepwise acquisition of unique epigenetic signatures during differentiation of tissue Treg cells
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Hox in hair growth and development
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Molecular Genetics of Human Hair Diseases
- A bibliometric analysis of T cell and atherosclerosis
- Malt1 Protease Is Critical in Maintaining Function of Regulatory T Cells and May Be a Therapeutic Target for Antitumor Immunity
- Therapeutic Potential of Brassinosteroids in Biomedical and Clinical Research
- The expanding impact of T-regs in the skin
- Stress-induced sympathetic hyperactivation drives hair follicle necrosis to trigger autoimmunity