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Research 391–420 of 762
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- A missense mutation in Lama3 causes androgen alopecia
- 132 Genetics of Stress Hormone Concentrations in Hair of Healthy Nursery Pigs and Their Relationship with Back Test Responses
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Male pattern hair loss: Can developmental origins explain the pattern?
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Role of collagen VI in peripheral nerves and wound-induced hair regrowth
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Weakly supervised learning of biomedical information extraction from curated data
- Drug Repositioning: New Approaches and Future Prospects for Life-Debilitating Diseases and the COVID-19 Pandemic Outbreak
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Pathophysiological mechanisms implicated in postpartum depression
- FGF5 is a crucial regulator of hair length in humans
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases