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Research 841–870 of 1000+
- Dermatologic care of patients with differences of sex development
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- A notch above bowl: Specification of niche cells in the Drosophila testis
- Data from A Phase Ib Study of Chemoimmunotherapy with Pegylated Liposomal Doxorubicin and Pembrolizumab in Estrogen Receptor–Positive Metastatic Breast Cancer
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Integrative transcriptomic and metabolomic analyses reveal the role of melatonin in promoting secondary hair follicle development in cashmere goats
- Role of DNA Methylation in the Pathogenesis of Skin Disorders: Mechanisms, Inhibitors of Methylation‐Related Enzyme, and Molecular Docking Studies
- Discovery Potential Hub Genes and Pathways in Keloid Fibroblast Development Based on Bioinformatics Analysis
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- Activation of the integrated stress response in human hair follicles
- eLife assessment: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Congenital Adrenal Hyperplasia
- miR-29a-5p Inhibits Prenatal Hair Placode Formation Through Targeting EDAR by ceRNA Regulatory Network
- Genome assembly and methylome analysis of the white wax scale insect provides insight into sexual differentiation of metamorphosis in hexapod
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Skin Development and Disease: A Molecular Perspective
- Biomedical applications of organoids in genetic diseases
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Hypoxia in Cell Reprogramming and the Epigenetic Regulations
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Nano-spanlastics-loaded dissolving microneedle patches for ketotifen fumarate: advanced strategies for allergic conjunctivitis treatment and molecular insights
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Identification of dual-purpose therapeutic targets implicated in aging and glioblastoma multiforme using PandaOmics - an AI-enabled biological target discovery platform