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Research 361–390 of 1000+
- Androgen-associated and androgen-independent causes of alopecia and acne in women. Literature review
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- Gene Therapy: Recent Advances and Applications in Dermatology
- Potential of fermented small black soybean-lactobacillus complex for hair health: a study on hair growth and follicle gene expression
- Understanding the Molecular Landscape of Alopecia Areata: Key Genes, Regulatory Networks, and Therapeutic Targets
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- The TNFRSF1B Connection: Implications for Androgenetic Alopecia Pathogenesis and Treatment
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- 131 Exploring the Scalp Microbiome Landscape: A Cross-Sectional Study of Female Pattern Hair Loss in Indian Women
- Effects of Natural Herbal Marker Compounds on Human Dermal Papilla Cell Growth Regulation
- KASUS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA-MITIS YANG TERDIAGNOSIS PADA SAAT LANJUT USIA
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- TLR3 Activation Stimulates Autophagy Gene Expression in Keratinocytes
- Identification of Biomarkers in Affected Hair Follicles from Chronic Discoid LupusErythematosus by Weighted Gene Co-Expression Network Analysis
- Clinical cases of Darier-White follicular dyskeratosis
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Highlights
- Two females with hair loss
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Gene Variant in Amish a Clue to Better Aging