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Research 511–540 of 1000+
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Ovarian Hypertension: Polycystic Ovary Syndrome
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- The effect of weight loss and treatment with metformin on serum vaspin levels in women with polycystic ovary syndrome
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Genetically-manipulated adult stem cells as therapeutic agents and gene delivery vehicle for wound repair and regeneration
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Congenital atrichia and hypotrichosis
- Diseases of Periocular Hair
- Mouse notch: expression in hair follicles correlates with cell fate determination.
- The cDNA-deduced amino acid sequence for trichohyalin, a differentiation marker in the hair follicle, contains a 23 amino acid repeat.
- Alopecia in Children: The Most Common Causes
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Study of Skin Expression of MicroRNA-146a in Patients with Alopacia Areata
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Evaluation of Eclipta alba L. selections for higher biomass and bioactive compound
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Dermatologic manifestations of endocrine disorders
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- The role of vitamin D receptor mutations in the development of alopecia
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses