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Research 781–810 of 1000+
- Recent advances in the genetics of alopecia areata
- Editorial: Machine Learning Techniques on Gene Function Prediction Volume II
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Polycystic Ovary Syndrome-Associated Acne: The Interplay of Hyperandrogenism, Insulin Resistance, and Therapeutic Strategies
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats
- Optimizing the production of true shallot seed by inducing flowering in various shallot genotypes
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Androgen excess: a hallmark of polycystic ovary syndrome
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Chapter 14 Low-Level Laser Therapy and Stem Cells
- Effects of LED radiation on the skin – what is new in recent research? Part II. In skin remodeling processes and hair growth
- Evolution in action: highlighting a role for the Agouti gene in development?
- Editors' Picks
- Australasian Society for Dermatology Research Meeting, May 2006
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Regulation of Involucrin Gene Expression
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Compendium of polycystic ovarian syndrome and its relevance in glycation and diabetes
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Update of Congenital Adrenal Hyperplasia
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction