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Research 391–420 of 1000+
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Male pattern hair loss: Can developmental origins explain the pattern?
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Potassium Channel Openers Increase Aortic Elastic Fiber Formation and Reverse the Genetically Determined Elastin Deficit in the BN Rat
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- The Rotterdam Study: objectives and design update
- EMT Factors and Metabolic Pathways in Cancer
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- Vaccines, adjuvants and autoimmunity
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Antihepcidin antibody treatment modulates iron metabolism and is effective in a mouse model of inflammation-induced anemia
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- The Rotterdam Study: 2010 objectives and design update