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Genomic Architecture of Regional Measures of Cerebral Cortical Thickness
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A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders
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Characterizing Human-Disease Mutations in the Essential RNA Exosome with the Budding Yeast Model System
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Uncovering the contribution of rare genetic variants in orofacial clefts
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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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Ten-Eleven Translocation Proteins-Mediated Epigenetic Regulation in Alzheimer’s Disease
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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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Elucidating the role of CHD5 domains in the recruitment of CHD5 to DNA double-strand break sites
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Defining the cis-regulatory sequence elements regulated by BAF complexes containing different ARID1 variants
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Local ecdysone synthesis in a wounded epithelium sustains developmental delay and promotes regeneration in Drosophila
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Exploring The Phenotypic Effects of Toll Signaling Pathways In Tumor Progression in EGFR-driven Glioblastoma Models
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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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Viral Evolution During Monoclonal Antibody Treatment of SARS-CoV-2 Patients
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Divergence from the human astrocyte developmental trajectory in glioblastoma
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Inter- and Intra-specific Interactions of Staphylococcus aureus Modeling Cystic Fibrosis Infection
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THE RNA EXOSOME: IMPLICATIONS FOR GENE EXPRESSION REGULATION AND NEUROLOGICAL PATHOLOGY
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Functionality of placental 5-hydroxymethylcytosine and associations with birthweight
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Astrocyte Primary Cilia are Dynamic during Development
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Using optogenetics to test the role of auditory cortex in memory retrieving
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Identifying HELZ as a Novel DNA Double-Strand Break Repair Protein
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