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A case of colorectal cancer with ERBB2 c.2264T>C (p.Leu755Ser) mutation
Dataset
EGAD00001002252
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Anaplastic Thyroid Cancer somatic variants (MuTect)
Dataset
EGAD00001004129
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Genetic Analysis of Metopic Nonsyndromic Craniosynostosis
Study
phs001508
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Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Atherosclerosis Risk in Communities (ARIC)
Study
phs000223
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Genetic Modifiers of Duchenne Muscular Dystrophy
Study
phs003680
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Epigenetic Control of Topoisomerase 1 by MacroH2A1.1
Study
phs003729
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whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
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High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
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Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
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Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Study
EGAS00001002390
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
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Transcriptome_human_nasal_epithelium
Study
EGAS00001001294
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Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Pharmacogenomic Analysis Reveals New Therapeutic Options for Pleural Mesothelioma
Study
EGAS00001007866
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OMKar
Study
EGAS00001008245
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eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
WES Elucidation of Pathogenetic Mechanisms for Immune System Disorders and NIAID Pilot of Genetic Incidental Finding Management
Study
phs001561
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Charles R. Bronfman Institute for Personalized Medicine (IPM) BioBank Genome Wide Association Study of Cardiovascular, Renal and Metabolic Phenotypes
Study
phs000388
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
Molecular Etiology of Early-Onset Dystonia
Study
phs001733
-
Mechanism and Response of Thymoglobulin in Patients with Myelodysplastic Syndrome (MDS)
Study
phs000697
-
Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC)
Study
phs003510
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Framingham Heart Study (FHS)
Study
phs002911
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POU4F3 mutation screening in Japanese hearing loss patients.
Study
JGAS000093
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In this study, blood-brain barrier (BBB)-forming brain endothelial-like cells were generated from apolipoprotein E gene allele E4 (APOE4, high AD risk) and allele E3 (APOE3, lower AD risk) carrying patient-derived induced pluripotent stem cells (iPSCs). Cells were subsequently exposed to focused ultrasound and microbubbles (FUS+MB) to induce BBB opening and their transcriptome analysed. RNA sequencing (RNA-seq) results demonstrated minimal changes in the gene expression following FUS+MB suggesting safety of FUS+MB application in the clinical setting.
Study
EGAS00001005944