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Research 361–390 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- Skin manifestations among<i>GATA2</i>-deficient patients
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Yellow and orange in cutaneous lesions: clinical and dermoscopic data
- Hair and Nail Relationship
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Disease causing homozygous variants in the human hairless gene
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Oral Presentations
- 9. Immunology and Genetics
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- The Potential Role of Minoxidil in the Hair Transplantation Setting
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Abstracts
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness