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Research 601–630 of 1000+
- An Unusual Case of Elevated Testosterone: When Testosterone by Dialysis Saves the Day
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Optimized Methodology to Produce Platelet-Rich Plasma and Perform Platelet Aggregation in Patients With Coronary Artery Disease
- Serum vitamin D, ferritin, and TSH in patients with telogen effluvium: a retrospective epidemiological study
- 201 Analysis of mice skin distribution using MALDI-MSI after subcutaneous injections of a new potent novel inhibitor of human hair growth, FOL-005
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- FOXN1 deficient nude severe combined immunodeficiency
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Chronic overlapping pain conditions and nociplastic pain
- Evaluation of loci to predict ear morphology using two SNaPshot assays
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The molecular pathogenesis of Trichilemmal carcinoma
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Keratin disorders: from gene to therapy
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Predicting Human Appearance from DNA for Forensic Investigations
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene