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Research 271–300 of 1000+
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Tissue Engineering and Regenerative Medicine: Achievements, Future, and Sustainability in Asia
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- A novel regio-specific cyclosporin hydroxylase gene revealed through the genome mining of <i>Pseudonocardia autotrophica</i>
- Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Liposome-Based Carriers for CRISPR Genome Editing
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Recent Advances in Genome-Editing Technology with CRISPR/Cas9 Variants and Stimuli-Responsive Targeting Approaches within Tumor Cells: A Future Perspective of Cancer Management
- ESDR303 – The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Analysis of the finasteride treatment and its withdrawal in the rat hypothalamus and hippocampus at whole-transcriptome level
- Minoxidil ameliorates myelodysplastic syndrome by targeting Wnt4 while sparing normal hematopoiesis
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- What Is the Male Polycystic Ovary Syndrome Phenotype?
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Opposing impacts on healthspan and longevity by limiting dietary selenium in telomere dysfunctional mice
- 200 Deep learning model to predict sentinel lymph node status in melanoma patients
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais