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Research 391–420 of 1000+
- Fertility and Sterility Vol 101 No 4, April 2014
- British Society for Dermatopathology
- Male pattern hair loss: Taking one for the team: The selfless gene
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- A Case Report of Male Systemic Lupus Erythematous with Antinuclear Antibodies-Negative: A Challenging Diagnosis
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Understanding Polycystic Ovary Syndrome
- Emerging smart microneedle technologies in psoriasis: convergence of nanocarriers, machine learning, and personalized delivery
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Teriflunomide and Its Mechanism of Action in Multiple Sclerosis
- Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- An Update of Congenital Adrenal Hyperplasia
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Androgens and androgen receptor action in skin and hair follicles
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Biology and Genetics of Hair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men