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Identifying HELZ as a Novel DNA Double-Strand Break Repair Protein
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THE RNA EXOSOME: IMPLICATIONS FOR GENE EXPRESSION REGULATION AND NEUROLOGICAL PATHOLOGY
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Divergence from the human astrocyte developmental trajectory in glioblastoma
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Ectopic transcription due to inappropriately inherited histone methylation may interfere with the ongoing function of terminally differentiated cells
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Local ecdysone synthesis in a wounded epithelium sustains developmental delay and promotes regeneration in Drosophila
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Elucidating the role of CHD5 domains in the recruitment of CHD5 to DNA double-strand break sites
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The Identification and Mapping of a Gene Responsible for a Novel nonEmo Phenotype in C. elegans Oocytes
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Ten-Eleven Translocation Proteins-Mediated Epigenetic Regulation in Alzheimer’s Disease
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Development and characterization of synthetic modulators of nuclear receptor LRH-1: Driving divergent signaling using a common molecular scaffold
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The loss of H3T45 phosphorylation enhances histone deacetylase (HDAC) recruitment to histone H3 in hormone receptor-positive, PI3K-activated breast cancer
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The Role of Sox7 on the WNT Signaling Pathway in Lung Adenocarcinoma
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Investigation of the factors that regulate sporulation initiation in Clostridioides difficile
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The Impact of Genetic Variation on RGS and G protein Signaling in Physiology and Disease
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Investigating the role of epigenetics in the development of myopia and retinal degeneration in the interphotoreceptor retinoid-binding protein deficient mouse model
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Understanding the role of MRG-1 in C. elegans germline and somatic development
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The role of Drosophila CPEB protein, Orb2, during asymmetric neural stem cell division
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The PIX-1 Signaling Pathway that Includes the Rho GEF PIX-1 and the Rho GAP RRC-1 Direct Assembly and Stability of Integrin Adhesion Complexes in Striated Muscle
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The RNA binding protein Nab2 genetically interacts with multiple RNA exosome cofactors to regulate target RNAs
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The role of H3K27me3 demethylases in B cell differentiation
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Characterizing the role of recurrent histone H3 mutations in cancer initiation
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