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Research 151–180 of 289
- The Genetics of Human Skin Disease
- Organoid‐Guided Precision Medicine: From Bench to Bedside
- Regeneration of a bioengineered 3D integumentary organ system from iPS cells
- SOX9 in organogenesis: shared and unique transcriptional functions
- Tracing the developmental origin of tissue stem cells
- The Role of Bovine Milk-Derived Exosomes in Human Health and Disease
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- Food hypersensitivity-induced chronic gastrointestinal inflammation in a non-human primate model of diet-induced obesity
- Bilateral Temporal Triangular Alopecia Associated with Phakomatosis Pigmentovascularis Type IV Successfully Treated with Follicular Unit Transplantation
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Diagnosis and differential diagnosis of tertiary androgenetic alopecia with severe alopecia areata based on high‐resolution MRI
- Pilot study of a novel treatment for androgenetic alopecia using enriched cell culture medium: clinical trials
- Alopecia types, current and future treatment
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- Acne and Hidden Iodides
- Kerion Celsi due to <i>Microsporum canis</i> in an Adult Woman, Treated Successfully with Fosravuconazole
- Free Androgen Index (FAI): Marker of Premature Androgenetic Alopecia in Men
- Presence and future of dermoscopy
- Small Intestinal Organoid-Derived SP Cells Contribute to Repair of Irradiation-Induced Skin Injury
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Coexistent frontal fibrosing alopecia with ophiasis pattern alopecia areata in a young female: A case report and review of the literature
- From local to systemic: endoscopic findings reshape the diagnostic paradigm of satoyoshi syndrome – a case report
- S2608 A Rare Case of Iron Deficiency Anemia: Cronkhite-Canada Syndrome
- Cronkhite–Canada syndrome: from clinical features to treatment
- Evidence of Heterogeneity and Quantitative Differences of the Type 1 5α-Reductase Expression in Cultured Human Skin Cells – Evidence of its Presence in Melanocytes
- Skin manifestations of celiac disease
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Role of Lactoferrin in Chronic Telgon Effluvium
- Dermoscopic Assessment of Nail Alterations in Egyptian Patients with Alopecia Areata