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Research 451–480 of 763
- Causal effects of genetically determined metabolites on androgenetic alopecia: A two‐sample Mendelian randomization analysis
- Identification of VLDL as a biomarker for prewarning of androgenic alopecia
- Association between non-scarring alopecia and hypothyroidism: a bidirectional two-sample Mendelian randomization study
- Causal Effects of Lipids-Related Metabolites on Androgenic Alopecia: A Mendelian Randomization Study
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Commentary 2
- The Rotterdam Study: objectives and design update
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- Adipose‐Derived Stem Cells for Tissue Engineering and Regenerative Medicine Applications
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic
- Drug Repositioning: New Approaches and Future Prospects for Life-Debilitating Diseases and the COVID-19 Pandemic Outbreak
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- WNT Signaling in Disease
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Pathophysiological mechanisms implicated in postpartum depression
- FGF5 is a crucial regulator of hair length in humans
- The Pathobiology of Skin Aging
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- The Many Faces of Calcineurin Inhibitor Toxicity—What the FK?
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age