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Research 151–180 of 366
- Alopecia Areata: Current Treatments and New Directions
- Drug repurposing: A novel strategy to target cancer stem cells and therapeutic resistance
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Frontiers in alopecia areata pathobiology research
- Hair regrowth in alopecia areata patients following Stem Cell Educator therapy
- TGFβ and cancer metastasis: an inflammation link
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Genetic Basis of Alopecia Areata
- A kindred with mutant IKAROS and autoimmunity
- Alopecia Areata: An Autoimmune Disease of Multiple Players
- Concise Review: Human Dermis as an Autologous Source of Stem Cells for Tissue Engineering and Regenerative Medicine
- Diverse Role of OX40 on T Cells as a Therapeutic Target for Skin Diseases
- Thymic Stromal Lymphopoietin in Cutaneous Immune-Mediated Diseases
- The role of WNT10B in physiology and disease: A 10-year update
- A transcriptomic map of murine and human alopecia areata
- Developing Human Skin Contains Lymphocytes Demonstrating a Memory Signature
- Innate type 2 immunity controls hair follicle commensalism by Demodex mites
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Induction of T cell exhaustion by JAK1/3 inhibition in the treatment of alopecia areata
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Targeted protein degradation of Wnt/β-catenin signaling pathway: an effective strategy for cancer therapy
- Oral Lichen Planus
- Decreased GATA3 levels cause changed mouse cutaneous innate lymphoid cell fate, facilitating hair follicle recycling