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Research 241–270 of 1000+
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Why Some Women Look Young for Their Age
- Decreased Serum Ferritin is Associated With Alopecia in Women
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Female pattern hair loss
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Review article: dermatological complications of immunosuppressive and anti-TNF therapy in inflammatory bowel disease
- Stem cell-derived motor neurons from spinal and bulbar muscular atrophy patients
- Androgenetic Alopecia: In Vivo Models
- Pharmacological Inhibition of Stearoyl CoA Desaturase in the Skin Induces Atrophy of the Sebaceous Glands
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Role for the Epidermal Growth Factor Receptor in Chemotherapy-Induced Alopecia
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- β-Catenin–Dependent Wnt Signaling: A Pathway in Acute Cutaneous Wounding [RETRACTED]
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Somatic mutations distinguish melanocyte subpopulations in human skin
- The Suppression of Very Long Chain Fatty Acids Is Associated with Skin Carcinogenesis
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Contents Vol. 2, 2016
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Developmental Toxicity of Levo-Alpha-Acetylmethadol (LAAM) in Tolerant Rats
- Isotretinoin
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Validation of a skin and coat scoring protocol in dogs
- MicroRNA in skin diseases