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A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders
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Uncovering the contribution of rare genetic variants in orofacial clefts
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Characterizing Human-Disease Mutations in the Essential RNA Exosome with the Budding Yeast Model System
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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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Exploring Potential Correlations Among Developmental Deficits Experienced by Patients with Classic Galactosemia
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Genome-wide patterns of selection in pre- and post-European contact Caribbean populations
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A Tale of Two Opioids: Comparing the Potency of Methadone and Morphine in Analgesia and Abuse Liability in Female Mice
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Grip Strength in GALT Deficiency
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Brain GALT restoration by intrathecal injection of scAAV9-hGALT enables partial metabolic correction in adolescent GALT-null rats
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Investigating Whether or Not Long-Term Outcomes in Classic Galactosemia are Progressive
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Investigation into the effect of RNASEH2B mutation on R-loop dysregulation in the pathogenesis of Aicardi-Goutières syndrome (AGS)
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Potential biomarkers for ALS/FTD as a consequence of TDP-43 loss of function
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A benchmark of rare cell type detection methods for single-cell RNA sequencing data
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Developing enrichment analyzing methods at sub-cell type level to generate novel insights on complex disease pathogenesis
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The Role of Sox7 on the WNT Signaling Pathway in Lung Adenocarcinoma
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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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Viral Evolution During Monoclonal Antibody Treatment of SARS-CoV-2 Patients
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Exploring the Genetics and Biological Pathways of Obesity through Computational Biology and Statistical Approaches
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Investigating the role of SAMHD1 in response to Camptothecin and Sacituzumab Govitecan in triple-negative breast cancer cell line MDA-MB-231
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