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Research 691–720 of 1000+
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Comparative advantage and efficacy of natural products for polycystic ovary syndrome
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Diseases of Hair
- Diseases of Hair
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Cylindroma as Tumor of Hair Follicle Origin
- Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- The nude gene and the skin
- Genetic Basis of Alopecia Areata
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Immuno-Endocrinology of COVID-19: The Key Role of Sex Hormones
- The role of leptin in selected skin diseases
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- The significance of the apelinergic system in doxorubicin-induced cardiotoxicity
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine