Search
for
Sort by
Research 421–450 of 1000+
- THE INFLUENCE OF SKIN MICROBIOME IMBALANCE ON SPECIFIC PATHOLOGICAL SKIN CONDITIONS
- Metabolic and Vascular Inflammation in Alopecia Areata: Linking Uric Acid, Lipid Imbalance and ICAM ‐1 Upregulation
- Analysis of skin mycobiota associated with alopecia in captive cynomolgus macaques (Macaca fascicularis) based on Oxford Nanopore Technologies
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- 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
- Role of UVA-driven cellular senescence via mTOR activation in dihydrotestosterone-induced hair loss in androgenetic alopecia mouse model
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Th1 effector CD4 T cells rely on IFN-γ production to induce alopecia areata
- Blue Light Therapy in Dermatological Practice: A Review
- The Mechanism and Research Progress of Skin Microbiota in Pathogenesis of Acne
- 523 Targeting NETosis to treat delayed wound healing in a humanized mouse model of sickle cell disease
- Identification of tpo, tg, tshr and ana antibodies associated with thyroid disorders
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- 8242 A Case of Ayme Gripp Syndrome
- 058 The pattern of Fas and Fas ligand expression in alopecia areata
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Molecular Basis of Hereditary Hair Diseases
- CD4+ Treg expansion arrests disease progression in a pre-clinical model of alopecia areata
- 1406 Environmental pathobiology of frontal fibrosing alopecia (FFA): A link between linalool sensitization and FFA development
- Dermatological diseases from a genetic perspective
- Acrodermatitis enteropathica – diagnostic challenges
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- 382 Environmental pathobiology of frontal fibrosing alopecia (FFA): Does linalool promote FFA development and progression by inducing epithelial hair follicle stem cell damage and MICA expression in the bulge?
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic