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Research 451–480 of 1000+
- WNT10B (wingless-type MMTV integration site family)
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Agent: Minoxidil
- Clinical aspects of the metabolic syndrome
- Medications
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Teriflunomide efficacy, safety and tolerability in patients with relapsing forms of multiple sclerosis
- Neurosteroids on the Epilepsy Chessboard—Keeping Seizures in Check
- Modelling androgen synthesis and action during human sexual differentiation
- The variable cell
- Abstracts
- Wound Healing: A Cellular Perspective
- Epidermal homeostasis: a balancing act of stem cells in the skin
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Alopecia Areata
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- The Neurobiology of Sexual Function
- The Rotterdam Study: 2018 update on objectives, design and main results
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- The Rotterdam Study: 2016 objectives and design update
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Transforming growth factor-β in stem cells and tissue homeostasis
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- More than one way to skin . . .
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- A molecular wound response program associated with regeneration initiation in planarians
- Dermatoses of pregnancy
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes