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Research 121–150 of 1000+
- Genetic Basis of Alopecia Areata
- Newborn infant skin gene expression: Remarkable differences versus adults
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Demodicosis and rosacea: Epidemiology and significance in daily dermatologic practice
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- FOXN1 deficient nude severe combined immunodeficiency
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- Alopecia Areata
- Alopecia areata
- Dandruff lesional scalp skin exhibits epidermal T cell infiltration and a weakened hair follicle immune privilege
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- The antiandrogen enzalutamide downregulates TMPRSS2 and reduces cellular entry of SARS-CoV-2 in human lung cells
- SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
- Transcriptional profiling of putative human epithelial stem cells
- COVID-19 infection leading to acute pustular dermatoses
- Local Corticosteroids for Alopecia Areata: A Narrative Review
- Human Hair Follicle-Derived Mesenchymal Stromal Cells from the Lower Dermal Sheath as a Competitive Alternative for Immunomodulation
- The therapeutic efficacy of mesenchymal stem cells and their extracellular vesicles in the treatment of diverse skin diseases
- Serum levels of ifn-γ, complement component c3 c4 and vitamin d3 in the prognosis of patients with alopecia areata prospective teachers
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Interferon in the treatment of cutaneous T-cell lymphoma
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Stem Cell-Based Tissue Engineering for the Treatment of Burn Wounds: A Systematic Review of Preclinical Studies
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations