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Research 541–570 of 1000+
- Skin signs of systemic diseases
- 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
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- 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
- 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
- Preclinical Pharmacology, Antitumor Activity, and Development of Pharmacodynamic Markers for the Novel, Potent AKT Inhibitor CCT128930
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- In vivo response of GsdmA3Dfl/+ mice to topically applied anti-psoriatic agents: effects on epidermal thickness, as determined by optical coherence tomography and H&E staining
- DNA phenotyping: current application in forensic science
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- New Three-dimensional Moving Field Radiation Therapy for Brain Tumors
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients