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Research 841–870 of 1000+
- Glucocorticoid and Sex Hormone Receptors: Clinical Implications and Therapeutic Relevance
- Le gène<i>hairless</i>de la souris
- Epigenetic orchestration of RNA m<sup>6</sup>A methylation in wound healing and post-wound events
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- A Case Report of Male Systemic Lupus Erythematous with Antinuclear Antibodies-Negative: A Challenging Diagnosis
- Correlation Between Nongenomic Action of C19-Steroids and COVID-19 Severity
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Abstracts
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- The involvement of androgens in human hair growth
- Hair, Hormones, and High-Risk Prostate Cancer
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Development and Molecular Characterization of Human Placental Mesenchymal Stem Cells from Human Aborted Fetal Tissue as a Model to Study Mechanism of Spontaneous Abortion
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- FINASTERIDE INHIBITS 5?-REDUCTASE ACTIVITY IN HUMAN DERMAL FIBROBLASTS: PREDICTION OF ITS THERAPEUTIC APPLICATION IN ANDROGEN-RELATED SKIN DISEASES
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Detecting the Mechanism behind the Transition from Fixed Two-Dimensional Patterned Sika Deer (Cervus nippon) Dermal Papilla Cells to Three-Dimensional Pattern
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Minoxidil Cannot Be Used To Target Lysyl Hydroxylases during Postnatal Mouse Lung Development: A Cautionary Note
- Clinical, Dermoscopic and In-Vivo Reflectance Confocal Microscopy Evaluation of a Case of Graham Little-Piccardi-Lassueur Syndrome Successfully Treated with Narrowband-UVB Phototherapy
- Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia
- Role of the Wnt signaling pathway in keratoacanthoma
- Study of the composition of 140 shampoos: similarities and differences depending on the sales channel used