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BMI1 is a novel, preclinical target in fusion-positive rhabdomyosarcoma
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Investigating rare genetic disorders to gain insight into human biology
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IRF4 controls cell fate outcomes during the initial stages of B cell differentiation
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The Drosophila Nab2 RNA-Binding Protein Regulates Splicing Neuronal RNAs
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The Disease-Associated Proteins Drosophila Nab2 and Ataxin-2 Interact with Shared RNAs and Coregulate Neuronal Morphology
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Roles of DNA methylation and hydroxymethylation in aging, immunosenescence, and gene regulation
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Integrating human brain transcriptomes and proteomes with genome-wide association data identifies risk genes shared between depression and Alzheimer’s disease
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The role of Lsd1 in the development of the retina and retinoblastoma
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Relationship of the ciliary GTPase, ARL13B, and the GPCR, SMOOTHENED
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The Ciliary Protein Arl13b Regulates Axon Guidance in the Developing Mouse Hindbrain
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DNA Methylation of CD4+ T-cells Reveals Association of ITGB7 in Pediatric Crohn’s Disease
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The Polyadenosine RNA Binding Protein ZC3H14 is Required in Mice for Proper Working Memory, Synaptosomal Composition, and Dendritic Spine Density and Morphology
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Fundamental Principles of 3D Genomic Organization
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Genome-wide studies of transcriptional dynamics in fear learning
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An Investigation of the Role of the Histone Demethylase LSD1, and Its Disordered Domain, in Neuronal Maintenance and Tau-Mediated Neurodegeneration
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A Multidimensional Investigation of 3q29 Deletion Syndrome
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Genomic Scan of Recent Positive Selection Differentiating Aggression in Chimpanzees and Bonobos
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Regulation of the base excision DNA repair pathway is critical for proper cell function
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Meiotic Synapsis: a Novel Role for Dynein Light Chain 1 in Synapsis Regulation and Sex-specific Processes in Meiotic Prophase I
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Maximizing the ability to detect modifying genetic factors of rare complex disorders – Fragile X-Associated Primary Ovarian Insufficiency and Down Syndrome - Congenital Heart Defects
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