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Research 481–510 of 1000+
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- This Month in Adult Urology
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- EBF1 expressed in the dermal papilla regulates hair type and length
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- A Short Report on Melanocyte/Melanoma Culture, Senescence, and Reproducibility
- Genomic Portraiture: The Science and Ethics of DNA Phenotyping in Identity Prediction
- Androgenetic Alopecia in Men: An Update On Genetics
- Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Advantages of Incomplete Digestion in Human Hair Shaft Proteomics, a Focus on Cuticular Keratins
- Autoimmune Polyglandular Syndrome Type 2 Presentation with Alopecia Universalis, Hashimoto’s Disease, and Addison’s Disease
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The causal relationship between androgenetic alopecia and serum uric acid: A bidirectional Mendelian randomization analysis
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Epigenetics of Colorectal Cancer
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss