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Research 181–210 of 1000+
- Association of Acne Tarda with Endocrinological Disorders
- Author Index
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Order from disorder: Self-organization in mammalian hair patterning
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (Mus musculus musculus) of Wild Origin
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Genetic Basis of Male Pattern Baldness
- Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products
- Genetics of polycystic ovary syndrome: searching for the way out of the labyrinth
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair
- Genetic Disorders and Defects in Vitamin D Action
- Genetic prediction of male pattern baldness
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Genetic basis of skin appendage development
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Role of genetics and sex steroid hormones in male androgenetic alopecia and female pattern hair loss: An update of what we now know
- Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology
- Trichoscopy in genetic hair shaft abnormalities
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Genetics of Inherited Ichthyoses and Related Diseases
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes