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Research 481–510 of 1000+
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- 643 Male pattern baldness and risk of incident skin cancer in a cohort of men
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Control of hair growth and follicle size by VEGF-mediated angiogenesis
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Obesity and the skin: Skin physiology and skin manifestations of obesity
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair
- <i>Hoxc13</i> mutant mice lack external hair
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- Towards a molecular understanding of hair loss and its treatment
- Critical Stages of Hair Development and Pigmentation in the Mouse
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- The diagnosis and treatment of iron deficiency and its potential relationship to hair loss
- Metformin: an old medication of new fashion: evolving new molecular mechanisms and clinical implications in polycystic ovary syndrome
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Wound Healing and the Use of Medicinal Plants
- Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell?
- An Update of Congenital Adrenal Hyperplasia