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Research 601–630 of 1000+
- Molecular Genetics of Alopecias
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Spironolactone May Reduce the Risk of Incident Rosacea
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- A Case of Relapsed Leprosy Successfully Treated With Sparfloxacin
- Function of KLF4 in Stem Cell Biology
- Le gène<i>hairless</i>de la souris
- How a Bird Gets Its Feathers: Insights from Chromatin Looping
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Androgen receptor gene polymorphism and biological age markers in men
- Inherited Epidermolysis Bullosa: A Clinical Case
- Study of Skin Expression of MicroRNA-146a in Patients with Alopacia Areata
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Dermatologic manifestations of endocrine disorders
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- 5-Alpha reductase deficiency
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A Systematic Approach to Afro-Textured Hair Disorders
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Generalised Glucocorticoid Resistance
- Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review
- Roles for Msx and Dlx homeoproteins in vertebrate development
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase