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Distinct roles for expression of vasoactive intestinal peptide in the behavioral polymorphism in white-throated sparrows (Zonotrichia albicollis)
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The nature of co-infection during outbreaks of infectious disease
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Identifying HELZ as a Novel DNA Double-Strand Break Repair Protein
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Using optogenetics to test the role of auditory cortex in memory retrieving
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Astrocyte Primary Cilia are Dynamic during Development
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Functionality of placental 5-hydroxymethylcytosine and associations with birthweight
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THE RNA EXOSOME: IMPLICATIONS FOR GENE EXPRESSION REGULATION AND NEUROLOGICAL PATHOLOGY
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Inter- and Intra-specific Interactions of Staphylococcus aureus Modeling Cystic Fibrosis Infection
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Divergence from the human astrocyte developmental trajectory in glioblastoma
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Local ecdysone synthesis in a wounded epithelium sustains developmental delay and promotes regeneration in Drosophila
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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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Genomic Architecture of Regional Measures of Cerebral Cortical Thickness
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A Genome-Wide Association Study of Resistance to Tuberculosis Infection in a Multi-Ancestry Brazilian Cohort
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Depression is associated with earlier onset of cognitive impairment in a population-based longitudinal cohort
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Exploring The Phenotypic Effects of Toll Signaling Pathways In Tumor Progression in EGFR-driven Glioblastoma Models
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Genome-wide TWAS of brain and blood tissues identifies novel risk genes for Alzheimer’s disease dementia
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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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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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Exploring the Genetics and Biological Pathways of Obesity through Computational Biology and Statistical Approaches
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Viral Evolution During Monoclonal Antibody Treatment of SARS-CoV-2 Patients
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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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Developing enrichment analyzing methods at sub-cell type level to generate novel insights on complex disease pathogenesis
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A benchmark of rare cell type detection methods for single-cell RNA sequencing data
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Potential biomarkers for ALS/FTD as a consequence of TDP-43 loss of function
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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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Investigating Whether or Not Long-Term Outcomes in Classic Galactosemia are Progressive
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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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Grip Strength in GALT Deficiency
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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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Defining the cis-regulatory sequence elements regulated by BAF complexes containing different ARID1 variants
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Genome-wide patterns of selection in pre- and post-European contact Caribbean populations
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Exploring Potential Correlations Among Developmental Deficits Experienced by Patients with Classic Galactosemia
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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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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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A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders
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Investigation of the factors that regulate sporulation initiation in Clostridioides difficile
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Maltreatment and Epigenetic Aging in Infants – A DNA Methylation Analysis
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The Impact of Genetic Variation on RGS and G protein Signaling in Physiology and Disease
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Examination of Brain Chromatin Accessibility in the Prairie Vole (Microtus ochrogaster)
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Evaluating Stochastic Epigenetic Mutations as Potential Mechanism Translating Psychosocial Stressors into Risk for Postpartum Depression
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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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Genetic and Neural Basis of Cultural Norm Acquisition
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Mitochondrial deficiencies influence variable penetrance of nuclear Nab3 granule accumulation
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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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Alzheimer's Disease Pathology Imputation and Risk Prediction Using Clinical Indices
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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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Placental microRNA expression as a mechanism in the developmental programming of long-term health outcomes
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Bayesian Functional Genome-wide Association Study using Standardized Individual-level and Summary-level GWAS Data
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Towards a Better Understanding of the Genetic Contributions to Epilepsy
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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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A genetics-first, rare variant approach to understanding the neurobiological substrates of schizophrenia and associated disorders
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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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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 role of H3K27me3 demethylases in B cell differentiation
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The role of lysine specific demethylase 1 (LSD1) and the functional consequences during development
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Pilot investigation of treatment effect modification by vitamin D binding protein isoforms on calcium and vitamin D effects on biomarkers of risk for colorectal cancer in the normal-appearing colorectal mucosa of colorectal adenoma patients
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Investigating genetic associations using power-optimizing analytic approaches
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Multiplexed approaches to investigate cellular mechanisms underlying HIV-1 transcriptional competence and viral replication
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Sickle Cell Disease and Food Addiction as Potential Contributors to the Racial Disparity in Cognitive and Behavioral Deficits in Young and Middle-Aged Black Americans
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Fungal pathogen genome stability and adaptive potential depend on host immune status and pathogen ploidy
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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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Information Flow in Spatially Structured Populations
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Metabolomic alterations in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) premutation carriers
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Association between Maternal Depression during Pregnancy and Newborn DNA Methylation
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Epigenetic Associations of Circulating Interleukin 6 among People with HIV
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Associations of DNA methylation with biomarkers of liver function among male veterans living with HIV
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TIGAR-V2 with nonparametric Bayesian eQTL weights estimated from GTEx V8 & Leveraging multiple reference panels to improve TWAS power by ensemble machine learning
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EDClust: An EM-MM hybrid method for cell clustering in population-level single cell RNA sequencing
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The Drosophila Nab2 RNA-Binding Protein Regulates Splicing Neuronal RNAs
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Characterization of growth in a galactose-1-phosphate uridylyltransferase-null rat model of classic galactosemia
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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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Localization of pezo-1 gene expression is responsible for transitioning meiotic to mitotic replication in oocytes of Caenorhabditis elegans
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Identification of novel histone locus body components in Drosophila melanogaster
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Deciphering the role of ACTIN-RELATED PROTEIN8 in Arabidopsis thaliana using CRISPR-Cas9 mutagenesis and coimmunoprecipitation (Co-IP)
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Modeling Dysregulation of Neurogenesis and Neurodevelopment in Tuberous Sclerosis Complex with Human Brain Organoids
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Identifying the causal variant of a rare skeletal disorder using whole-genome sequencing
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Phospho-SAMHD1 as a potential prognostic biomarker for triple negative breast cancer patients
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Chemical profiling of Inosine using a Click-Compatible Acrylamide and EndoV Protein
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Roles of DNA methylation and hydroxymethylation in aging, immunosenescence, and gene regulation
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Evidence for an Extended Externalizing Spectrum in Youth: Associations between Psychopathology, Personality, and Behavior
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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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