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Research 961–990 of 1000+
- Faculty Opinions recommendation of Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
- [Monilethrix is a hereditary hair shaft disorder].
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- 266 Myristoylphorbol Acetate (MPA) Enhances Metastasis Via Up-regulation of Eph A2 Transcription Activity
- The Investigation of LPA <sub>4</sub> Functions in Zebrafish
- Loss of PIKFyve Kinase Function Driven by Platelet Factor 4 Promoter Results in Platelet Lysosomal Storage Defects and Infiltration of Multiple Organs with Vacuolated Macrophages
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- In This Issue
- Criteria for Defining Polycystic Ovary Syndrome as a Predominantly Hyperandrogenic Syndrome: An Androgen Excess Society Guideline
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Current Guidelines for Diagnosing PCOS
- Beyond Wavy Hairs
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Tregs: Where We Are and What Comes Next?
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Ontogenetic Transition in Fetal Wound Transforming Growth Factor-β Regulation Correlates with Collagen Organization
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Commitment of Oral-Derived Stem Cells in Dental and Maxillofacial Applications
- Epidermal Growth Factor as a Biologic Switch in Hair Growth Cycle
- Actinic keratosis: a clinical and epidemiological revision
- Cytokeratin expression in trichoblastic fibroma (small nodular type trichoblastoma), trichoepithelioma and basal cell carcinoma
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice