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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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Novel Statistical Methods for Analyzing Gene Expression Data
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Statistical Method for Studying Genome-Wide Interaction and the Natural History of Alzheimer’s Disease
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Cell-type-specific Transcriptomic-wide Association Studies Detected 80 Independent Risk Genes for Alzheimer’s Disease Dementia
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Regional mechanisms governing developmental and regenerative morphology of intrahepatic bile ducts
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Temporal regulation of human reactive astrocytes reveals their capacity for antigen presentation
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Sympathetic Innervation Regulates Metabolic Flexibility of Skeletal Muscle
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A Phenome-Wide Association Studies in a GWAS with application to the UK Biobank
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Investigation of RNA-mediated Chromatin Organization in Normal and Disease State
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Co-activator Crosstalk: Yorkie and Taiman interact to regulate niche-to-stem cell signaling in the female Drosophila germline stem cell niche
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Investigating the Role of DNA Secondary Structures in Repetitive Satellite Regions
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Histone acetylation is heritable information across generations in spr-2 mutant C. elegans
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Mitigating symptoms of the Aicardi-Goutières Syndrome through gene editing by CRISPR-Cas9
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Exploring X-linked Contributions to Sex-Specific Prevalence Differences in Autism Spectrum Disorder (ASD)
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Epitranscriptomic Regulation of Candida albicans Pathogenicity by RNA Methylation
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MicroRNA-137 Dysregulation in Human Fragile X Syndrome Model
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ncBAF function in iPSCs: Investigating a feedback loop between BICRA and BICRAL
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Characterization Of a Human Dorsal Root Ganglion Organoid Patterning Recipe
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Understanding the contribution of Adgrb1 to oligodendrocyte function
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Extracellular vesicle-targeted GALT gene therapy in a rat model of classic galactosemia
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Targeting EP300/CBP to Overcome IMiD Resistance in Multiple Myeloma
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Characterizing Chromatin Changes Upon Inhibition of Chromatin Remodeling Complexes
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Exploiting a Saccharomyces cerevisiae model to characterize DNA repair defects and altered growth linked to histone H3G34V oncohistone
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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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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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Identifying Drivers of Human Astrocyte Development
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An Ao-kay thesis: A cytological approach to the molecular role of Abnormal Oocyte (ao)
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Memory B cells are instructed molecularly and epigenetically by CD4 T cells and EZH2
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Evolution and pathogenesis of the Neisseria meningitidis urethritis-causing clade, NmUC
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The Role of the Retinal Pigment Epithelium and Serpinf1 in Visual Outcomes after Light Damage Exposure
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Employing machine learning and high-throughput sequencing to uncover complex genetic and epigenetic contributors in neurological phenotypes
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The Multifaceted Functions of the Long Noncoding RNAs NEAT1 and GOMAFU are Regulated by the RNA-Binding Protein Quaking
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The epigenetic landscape of prematurity, as it relates to health and development
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The conserved RNA binding protein Nab2 regulates RNA targets critical for proper neuronal function
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The Protective Effect of Melanopsin on Retinal Vascular Development in a Mouse Model of Retinopathy of Prematurity
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Evaluating Stochastic Epigenetic Mutations as Potential Mechanism Translating Psychosocial Stressors into Risk for Postpartum Depression
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Epigenetic gene regulation in B and T lymphocytes and its role in cellular activation, differentiation, and autoimmune disease
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Investigating SWR1 Recruitment in the Maintenance of the epigenomic H2A.Z landscape
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Arabidopsis thaliana Transcriptome and Chromatin Dynamics during a Phosphate Starvation Response Reveal New Insights Into H3K27me3 and H2A.Z mediated gene regulation
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KipOTIA detoxifies 5-oxoproline and promotes growth of Clostridioides difficile
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The Drosophila EcR-Hippo component Taiman promotes epithelial cell fitness by control of the Dally-like glypican and Wg gradient
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Exploiting a Saccharomyces cerevisiae Model to Characterize Dysfunctional DNA Repair in a Pediatric High-Grade Glioma-Causing Oncohistone
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Characterizing the Genetic Influences of Prescription Opioid Misuse and the Coheritability with Depression and Anxiety
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Investigating the impact of TSC2 pathogenic variants on human neurodevelopment using 3-D cortical organoids
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Nuances of context-dependent transcription factor function
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Traffic Control: Investigating the lipoprotein trafficking stress response in Escherichia coli and Acinetobacter baumannii
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Identifying Novel Genetic Causes of Cleft Palate
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The intrinsic and extrinsic regulation of fragile X messenger ribonucleoprotein on human hippocampal development
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REDEFINING BILIARY ATRESIA: INTEGRATIVE MODELS AND METHODOLOGIES
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Investigating the dynamics of transcription initiation and nucleosome turnover in Arabidopsis thaliana
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Pathogen recognition, inflammation, and ovarian cancer
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LARGE EXOME SEQUENCING STUDY ANALYZING X-LINKED VARIATION IN AUTISM SPECTRUM DISORDER
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Examining the Relationship Between Neonatal Epigenetic Age Acceleration and Anthropometric Growth Outcomes of Very Preterm Infants
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EPIGENETIC MODIFICATIONS ASSOCIATED WITH PBB-153 ELIMINATION RATE IN A MICHIGAN COHORT: A PILOT STUDY
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Unlocking New Avenues in Multiple Myeloma Treatment: Targeting Anti-Apoptotic Genes to Enhance Drug Efficacy
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HUM-7, an unconventional myosin with a RhoGAP domain, is required for assembly of integrin adhesion complexes in muscle
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Brain microRNAs differentially expressed in age-related cerebral pathologies
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The Association Between Cardiometabolic Risk Factors and Related Methylation Risk Scores in Patients Undergoing In Vitro Fertilization (IVF)
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An aDNA Approach to Investigating Post-Admixture Selection in Mexico: Assessing the (Immuno)Genetic Consequences of European Colonization
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Investigating the contribution of coding de novo mutations to orofacial clefts
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Investigating the role of MRPL40 in cardiac development
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Investigating the Role of Fascin-1 in Axonal Development of Drosophila
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Exploring Bacterial Tolerance: A Hidden Culprit in Treatment Failure of Urinary Tract Infections
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Investigations of how phosphorylation on histone H3T45 orchestrates the RNA Exosome complex to mediate RNA processing
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Tet1 Function in Intestinal Stem Cell Differentiation
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Exploring the Driving Factors of Human Astrocyte Development
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A Study on the Relationship of the Core and Accessory Genome in S. aureus
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Characterizing Prenatal Metabolite Accumulation in GALT-null Rat Fetuses at Gestational Day 21
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Investigation of ectopic changes between healthy and Ataxia Telangiectasia cells
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Identification of Spatially Variable Genes (SVGs)
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Identify Unique Subtypes in Recurrent Major Depression Disorder
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A Longitudinal Analysis of Prenatal Metabolite Accumulation Through Gestation in GALT-null Rat Fetuses
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Impact of Vesicular Monoamine Transporter 2 Overexpression and Norepinephrine Transporter Inhibition on Neuromelanin-Induced Locus Coeruleus Neurodegeneration
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Investigating the Role of Spatial Structure in Genetic Hitchhiking and Sweep Detection
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Existence of Selective Pressure in G6PD Deficiency alleles on Various African Population Groups Throughout Time
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Investigating the role of the BAF Complex in Human Disease and Evolution
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Urinary RNA Biomarkers in Extracellular Vesicles from Post-DRE Urine to Predict Aggressive Prostate Cancer
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Efficient quantification of pattern similarity between spatial genomics and cell morphology
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Genomic legacy of the Black Death: investigating the evolutionary relationship between cystic fibrosis and the second plague pandemic
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Exploring the Association of Maternal Socioeconomic Adversity, Epigenetics of Genes Regulating Fetal Glucocorticoid Intrauterine Exposure, and the Risk of Small for Gestational Age (SGA) in Term Infants
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Ten-Eleven Translocation Proteins-Mediated Epigenetic Regulation in Alzheimer’s Disease
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Exploring Therapeutic Strategies Targeting Cardiomyocytes for Heart Regeneration
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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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Viral Evolution During Monoclonal Antibody Treatment of SARS-CoV-2 Patients
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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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Exploring The Phenotypic Effects of Toll Signaling Pathways In Tumor Progression in EGFR-driven Glioblastoma Models
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Local ecdysone synthesis in a wounded epithelium sustains developmental delay and promotes regeneration in Drosophila
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Defining the cis-regulatory sequence elements regulated by BAF complexes containing different ARID1 variants
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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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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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A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders
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