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Research 601–630 of 1000+
- Congenital atrichia with papular lesions
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Use of fluorescent light energy for the management of bacterial skin infection associated with canine calcinosis cutis lesions
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Connexin mutations in human disease
- Hypoxia inducible factor-1α promotes trichogenic gene expression in human dermal papilla cells
- Refractory/relapse thrombocytopenia in a patient with Evans' syndrome successfully treated with zanubrutinib
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- NTP Toxicology and Carcinogenesis Studies of C.I. Acid Orange 3 (CAS No. 6373-74-6) in F344/N Rats and B6C3F1 Mice (Gavage Studies).
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Diagnostic Signs and Symptoms of Cyanocobalamin Deficiency at Rural Setting in India: Novel Method of Supplementation
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Clouston’s syndrome: a rare case report
- Female Androgenetic (?) Alopecia
- The Modulation of Aromatase and Estrogen Receptor Alpha in Cultured Human Dermal Papilla Cells by Dexamethasone: A Novel Mechanism for Selective Action of Estrogen via Estrogen Receptor Beta?
- Seborrheic dermatitis and pityriasis sicca: A review
- Corticotropin-releasing hormone: An autocrine hormone that promotes lipogenesis in human sebocytes
- Matriptase: Potent Proteolysis on the Cell Surface
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Applications of Tea (Camellia sinensis) and its Active Constituents in Cosmetics