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Research 811–840 of 1000+
- Inherited Disorders of the Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Selected topics in pediatric hair loss
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- The G1/S transition in mammalian stem cells in vivo is autonomously regulated by cell size
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Neuroactive Steroids and Ethanol Exposure: Relevance to Ethanol Sensitivity and Alcohol Use Disorders Risk
- 258 11β-hydroxysteroid dehydrogenase type 1 inhibition attenuates the adverse effects of glucocorticoids on dermal papilla cells
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- Generalised Glucocorticoid Resistance
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Treatment of Girolando cattle dermatophilosis using a combination of different plant extracts in the municipality of Abomey-Calavi, Republic of Benin
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Aged differentiated cells reverse into native stemness-like state by niche cytokines to sustain lifelong homeostasis and tissue repair
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- The genetic basis of dermatophytosis skin infection susceptibility
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Paraoxonase Enzyme Activity and Determination of Phenotypic Polymorphism in Patients with Acne Vulgaris
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism