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Research 211–240 of 1000+
- Topology of Feather Melanocyte Progenitor Niche Allows Complex Pigment Patterns to Emerge
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Hidradenitis suppurativa treated with finasteride
- Treatment of Lymphocutaneous and Visceral Sporotrichosis with Fluconazole
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Clinical and Hormonal Effects of Chronic Gonadotropin Releasing Hormone Agonist Treatment in Polycystic Ovarian Disease*
- The Effect of Finasteride on the Expression of Vascular Endothelial Growth Factor and Microvessel Density: A Possible Mechanism for Decreased Prostatic Bleeding in Treated Patients
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- <i>Polycystic Ovary Syndrome in Adolescence</i>
- Laser Hair Removal
- The protective role of the immunomodulator AS101 against chemotherapy-induced alopecia studies on human and animal models
- Severe Acute Respiratory Syndrome (SARS)
- The role of pregnane neurosteroids in ethanol withdrawal: behavioral genetic approaches
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Development and progression of alopecia in the vitamin D receptor null mouse
- Neural Potential of a Stem Cell Population in the Hair Follicle
- 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
- Multidisciplinary treatment of obesity with a protein-sparing modified fast: results in 668 outpatients.
- Topical minoxidil for hair regrowth
- What causes hidradenitis suppurativa ?—15 years after
- Management of acne
- Structure and function of skin, hair and nails
- Gene-wide association study between the aromatase gene (<i>CYP19A1</i>) and female pattern hair loss
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Template for Skin Regeneration
- A review of acitretin, a systemic retinoid for the treatment of psoriasis