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Alzheimer's Disease Pathology Imputation and Risk Prediction Using Clinical Indices
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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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Mitochondrial deficiencies influence variable penetrance of nuclear Nab3 granule accumulation
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Genetic and Neural Basis of Cultural Norm Acquisition
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Placental microRNA expression as a mechanism in the developmental programming of long-term health outcomes
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Towards a Better Understanding of the Genetic Contributions to Epilepsy
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A genetics-first, rare variant approach to understanding the neurobiological substrates of schizophrenia and associated disorders
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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 role of the histone demethylase LSD1 in hippocampal neuron survival and tau-mediated neurodegeneration.
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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 Drosophila RNA-binding Protein Nab2 Interacts with the Planar Cell Polarity Pathway to Regulate Neurodevelopment
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The role of H3K27me3 demethylases in B cell differentiation
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Cellular Transcriptional Profiling Reveals Multiple B Cell Differentiation Branching Points in Mus musculus Spleen Exposed to Lipopolysaccharides (LPS) and NP-4-Hydroxy-3- Nitrophenylacetic (NPF)
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Web Tool for Clinic Trio Based Sequence Data Analysis to Identify Potential Pathogenic Variants for Rare Genetic Diseases
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Molecular Epidemiology of a Type 4 Dengue Virus Outbreak in Paraguay, 2019-2020
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DNA Methylation as a Potential Mediator of the Association Between Prenatal Tobacco and Alcohol Exposure and Child Neurodevelopment in a South African Birth Cohort
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Analyzing the Developmental and Transcriptomic response of Callosobruchus maculatus to Alternative Bean Hosts
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Characterizing clinical and genomic factors of IDH-wildtype glioblastoma
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Investigation of the Germline Functions of CFP-1 and MRG-1 in Caenorhabditis elegans
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Understanding the rise of SARS-CoV-2 Delta variants in Atlanta and Georgia
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Characterizing the role of recurrent histone H3 mutations in cancer initiation
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A characterization of prenatal metabolites in GALT-null rat fetuses
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Towards identifying genetic modifiers of Fragile X-Associated Tremor/Ataxia Syndrome
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Understanding the Evolutionary History of Ancient Indigenous Individuals in Uruguay
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Integrate Proteomics Data with GWAS Summary data for Studying Alzheimer’s Disease by Nonparametric Bayesian Method
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Bayesian Functional Genome-wide Association Study using Standardized Individual-level and Summary-level GWAS Data
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Higher expression levels of MSL2 in D. virilis lead to histone locus binding that is not seen in other Drosophila species.
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The Epigenetics of Aging: Exploring Biomarkers and the Interplay Within the Aging Epigenome
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The Role of Transcription Elongation, Cohesin, and Condensin II in Mediating Gene Looping in Drosophila melanogaster
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Indoles Derived from Commensal Gut Bacteria Regulate Host Somatic and Reproductive Aging via the Interferon Pathway
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Integrative Prioritization of Genetic Loci for Nicotine Consumption
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Tissue-Specific Analysis of UDP-sugar Levels and Ratios in a Rat Model of Classic Galactosemia
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Investigating the Roles of ACLY in Multiple Myeloma Biology and Drug Sensitivity
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Interrelationships Between Body Composition, Physical Functioning, and Quality of Life in Adults with Cystic Fibrosis
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Relationship of the ciliary GTPase, ARL13B, and the GPCR, SMOOTHENED
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Identifying the Genetic Drivers of 3q29 Deletion-Associated Phenotypes
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Evaluate the host genetic effects of tuberculosis-associated variants on diabetes
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Investigation of MBD9’s Role in H2A.Z Deposition in Arabidopsis thaliana
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Investigating genetic associations using power-optimizing analytic approaches
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An integrative approach to investigate treatment-resistant lung adenocarcinoma
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Hypomorphic maternal LSD1 in mice leads to long-term defects in survival and imprinting
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A new high-throughput variant annotation and classification method and its implementation in the investigation of schizophrenia-associated copy number regions
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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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Associations of polygenic risk score and polybrominated biphenyl exposure on age at menarche in the Michigan polybrominated biphenyl registry
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Gain of Chromosome 1q is Associated with Early Progression in Multiple Myeloma Patients Treated with Lenalidomide, Bortezomib, and Dexamethasone
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Cell-type specific alteration of DNA methylation in Alzheimer’s Disease
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IDA3-mediated IFT Transport of the Ciliary Inner Dynein Arm I1
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The development of a temporally controllable lineage system for labeling enteric neural crest precursors in D. rerio and assessment of the possible role of ETV1 as a transcriptional regulator of ENS specification
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Influence of CYP3A4 inhibition on the tamoxifen metabolic pathway and the implications for breast cancer recurrence in a pre-menopausal cohort
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