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Research 631–660 of 1000+
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- Comprehensive RNA sequencing in primary murine keratinocytes and fibroblasts identifies novel biomarkers and provides potential therapeutic targets for skin-related diseases
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- Characterization of the Promoter Regions of Two Sheep Keratin-Associated Protein Genes for Hair Cortex-Specific Expression
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Identification of microRNAs involved in growth arrest and cell death in hydrogen peroxide-treated human dermal papilla cells
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Progressive expression of PPARGC1α is associated with hair miniaturization in androgenetic alopecia
- Expression profile analysis of dermal papilla cells mRNA in response to WNT10B treatment
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Identification of key pathways and genes that regulate cashmere development in cashmere goats mediated by exogenous melatonin
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- The Role of Wnt10b/β-Catenin Signaling Pathway in Hair Follicle Development in Different Ages of Rex Rabbits
- Integrative Analysis of the Metabolome and Transcriptome Reveals the Mechanism Underlying Differences in Skin Development Between the New Zealand Rabbit and the Rex Rabbit
- Fibroblast Growth Factor-7 and Hair Biology: Bridging Basic Science and Therapeutic Applications