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Research 391–420 of 1000+
- Emerging smart microneedle technologies in psoriasis: convergence of nanocarriers, machine learning, and personalized delivery
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Type-2 immunity associated with type-1 related skin inflammatory diseases: friend or foe?
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- Vaccines, Infections, and Alopecia Areata
- The pathogenesis of alopecia areata
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Main Plenary Sessions: Summaries of Papers
- Abstracts
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Anti-TNF antibody-induced psoriasiform skin lesions in patients with inflammatory bowel disease are characterised by interferon-γ-expressing Th1 cells and IL-17A/IL-22-expressing Th17 cells and respond to anti-IL-12/IL-23 antibody treatment
- Transforming growth factor-β in stem cells and tissue homeostasis
- Female pattern hair loss
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- The role of androgen and androgen receptor in skin-related disorders
- Drug-Induced Skin, Nail and Hair Disorders
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Review article: dermatological complications of immunosuppressive and anti-TNF therapy in inflammatory bowel disease
- High prevalence of chronic thyroiditis in patients with polycystic ovary syndrome
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- Type 1 interferon signature in the scalp lesions of alopecia areata
- Autoimmunity and autoimmune co-morbidities in psoriasis
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Male pattern baldness: current treatments, future prospects
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- MicroRNA in skin diseases