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Research 421–450 of 1000+
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Exploring Mast Cell–CD8 T Cell Interactions in Inflammatory Skin Diseases
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- The Association Between Polycystic Ovary Syndrome and Its Dermatological Manifestations
- Comprehensive analysis of minoxidil effectiveness for hair growth
- 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes
- Тіе Modern treatment of androgenetic alopecia
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Mechanisms of autophagy and their implications in dermatological disorders
- Peran Multivitamin terhadap Pertumbuhan dan Kesehatan Rambut: Literature Review
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Medical Technologies: Pharmaceutical Cosmetology, Cosmeceuticals – Opportunities and Limitations
- 1343 Efficacy of asymmetric siRNA targeting androgen receptor for the treatment of androgenetic alopecia
- Third International Research Workshop on Alopecia Areata
- Assessment of androgenic hormones and other risk factors in Egyptian males with early onset androgenetic alopecia: a case control study
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis