Search Results - "Finney, Richard"
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CD47-Dependent Regulation of Immune Checkpoint Gene Expression and MYCN mRNA Splicing in Murine CD8 and Jurkat T Cells
Published in International journal of molecular sciences (30-01-2023)“…Elevated expression of CD47 in some cancers is associated with poor survival related to its function as an innate immune checkpoint when expressed on tumor…”
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Genetic Alterations Activating Kinase and Cytokine Receptor Signaling in High-Risk Acute Lymphoblastic Leukemia
Published in Cancer cell (14-08-2012)“…Genomic profiling has identified a subtype of high-risk B-progenitor acute lymphoblastic leukemia (B-ALL) with alteration of IKZF1, a gene expression profile…”
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3
The chromatin remodeling protein Lsh alters nucleosome occupancy at putative enhancers and modulates binding of lineage specific transcription factors
Published in Epigenetics (04-03-2019)“…Dynamic regulation of chromatin accessibility is a key feature of cellular differentiation during embryogenesis, but the precise factors that control access to…”
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4
LSH mediates gene repression through macroH2A deposition
Published in Nature communications (06-11-2020)“…The human Immunodeficiency Centromeric Instability Facial Anomalies (ICF) 4 syndrome is a severe disease with increased mortality caused by mutation in the LSH…”
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5
Lsh/HELLS is required for B lymphocyte development and immunoglobulin class switch recombination
Published in Proceedings of the National Academy of Sciences - PNAS (18-08-2020)“…Mutation of HELLS (Helicase, Lymphoid-Specific)/Lsh in human DNA causes a severe immunodeficiency syndrome, but the nature of the defect remains unknown. We…”
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The epigenetic regulator LSH maintains fork protection and genomic stability via MacroH2A deposition and RAD51 filament formation
Published in Nature communications (10-06-2021)“…The Immunodeficiency Centromeric Instability Facial Anomalies (ICF) 4 syndrome is caused by mutations in LSH/HELLS, a chromatin remodeler promoting…”
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Bambino: a variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM format
Published in Bioinformatics (15-03-2011)“…Bambino is a variant detector and graphical alignment viewer for next-generation sequencing data in the SAM/BAM format, which is capable of pooling data from…”
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Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma
Published in Hepatology (Baltimore, Md.) (01-12-2010)“…Primary liver cancer is the third most common cause of cancer‐related death worldwide, with a rising incidence in Western countries. Little is known about the…”
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Chromatic: WebAssembly-Based Cancer Genome Viewer
Published in Cancer Informatics (2018)“…Chromatic is a novel web-browser tool that enables researchers to visually inspect genomic variations identified through next-generation sequencing of cancer…”
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Discovery analysis of TCGA data reveals association between germline genotype and survival in ovarian cancer patients
Published in PloS one (21-03-2013)“…Ovarian cancer remains a significant public health burden, with the highest mortality rate of all the gynecological cancers. This is attributable to the late…”
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11
Development of a bicistronic anti-CD19/CD20 CAR construct including abrogation of unexpected nucleic acid sequence deletions
Published in Molecular therapy. Oncolytics (21-09-2023)“…To address CD19 loss from lymphoma after anti-CD19 chimeric antigen receptor (CAR) T cell therapy, we designed a bicistronic construct encoding an anti-CD19…”
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Combined immune checkpoint inhibition with durvalumab and tremelimumab with and without radiofrequency ablation in patients with advanced biliary tract carcinoma
Published in Cancer medicine (Malden, MA) (01-02-2024)“…Background Current standard of care for advanced biliary tract cancer (BTC) is gemcitabine, cisplatin plus anti‐PD1/PD‐L1, but response rates are modest. The…”
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Genomic Heterogeneity Within Individual Prostate Cancer Foci Impacts Predictive Biomarkers of Targeted Therapy
Published in European urology focus (01-05-2019)“…Most lethal prostate cancers progress from relapse of aggressive primary disease. Recently, the most significant advances in survival benefit from systemic…”
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Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB)
Published in Genome Research (01-07-2007)“…Systematic investigations of genetic changes in tumors are expected to lead to greatly improved understanding of cancer etiology. To meet the analytical…”
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15
Detecting false expression signals in high-density oligonucleotide arrays by an in silico approach
Published in Genomics (San Diego, Calif.) (01-03-2005)“…High-density oligonucleotide arrays have become a popular assay for concurrent measurement of mRNA expression at the genome scale. Much effort has been devoted…”
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Alview: Portable Software for Viewing Sequence Reads in BAM Formatted Files
Published in Cancer Informatics (01-01-2015)“…The name Alview is a contraction of the term Alignment Viewer. Alview is a compiled to native architecture software tool for visualizing the alignment of…”
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Journal Article Book Review -
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Genome-wide transcriptional sequencing identifies novel mutations in metabolic genes in human hepatocellular carcinoma
Published in Cancer genomics & proteomics (01-01-2014)“…We report on next-generation transcriptome sequencing results of three human hepatocellular carcinoma tumor/tumor-adjacent pairs. This analysis robustly…”
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A high-resolution multistrain haplotype analysis of laboratory mouse genome reveals three distinctive genetic variation patterns
Published in Genome research (01-02-2005)“…Understanding of the structure and the origin of genetic variation patterns in the laboratory inbred mouse provides insight into the utility of the mouse model…”
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Development of a Bicistronic Anti-CD19/CD20 CAR Construct Including Optimization to Abrogate Retroviral Recombination Events
Published in Blood (23-11-2021)“…Anti-CD19 chimeric antigen receptor (CAR) T cells can eliminate lymphoma, but CD19 loss from lymphoma can cause anti-CD19 CAR T-cell treatment failure. To…”
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Transcriptional alterations in hereditary and sporadic nonfunctioning pancreatic neuroendocrine tumors according to genotype
Published in Cancer (01-02-2018)“…BACKGROUND Nonfunctioning pancreatic neuroendocrine tumors (NFPanNETs) may be sporadic or inherited because of germline mutations associated with von…”
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