Search Results - "Berger, Alice"
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All About That Ras: Novel Fusion Drives Ras Pathway Activation in Lung Cancer
Published in Clinical cancer research (15-07-2022)“…Lung cancers in never- and light-smokers often harbor targetable oncogenic mutations in Ras pathway genes. Here, a novel OCLN-RASGRF1 fusion is identified in…”
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A continuum model for tumour suppression
Published in Nature (London) (11-08-2011)“…Tumour suppression modelled The 'two-hit' hypothesis of tumorigenesis, originally proposed in 1971 by Alfred Knudson using retinoblastoma as a model, explained…”
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Haplo-insufficiency: a driving force in cancer
Published in The Journal of pathology (2011)“…It was originally proposed that tumour suppressor genes (TSGs) act in a recessive manner. Instead, numerous TSGs, including p53 and PTEN, exhibit…”
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Oncogenic KRAS alters splicing factor phosphorylation and alternative splicing in lung cancer
Published in BMC cancer (16-12-2022)“…Alternative RNA splicing is widely dysregulated in cancers including lung adenocarcinoma, where aberrant splicing events are frequently caused by somatic…”
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Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas
Published in Nature genetics (01-06-2016)“…Matthew Meyerson, Ramaswamy Govindan and colleagues examine the exome sequences and copy number profiles of 660 lung adenocarcinoma and 484 lung squamous cell…”
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Thrombolytic therapy based on fucoidan-functionalized polymer nanoparticles targeting P-selectin
Published in Biomaterials (01-02-2018)“…Injection of recombinant tissue plasminogen activator (rt-PA) is the standard drug treatment for thrombolysis. However, rt-PA shows risk of hemorrhages and…”
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High-throughput Phenotyping of Lung Cancer Somatic Mutations
Published in Cancer cell (08-08-2016)“…Recent genome sequencing efforts have identified millions of somatic mutations in cancer. However, the functional impact of most variants is poorly understood…”
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RNA isoform screens uncover the essentiality and tumor-suppressor activity of ultraconserved poison exons
Published in Nature genetics (01-01-2020)“…While RNA-seq has enabled comprehensive quantification of alternative splicing, no correspondingly high-throughput assay exists for functionally interrogating…”
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Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genome
Published in Cell reports (Cambridge) (31-08-2021)“…CRISPR screens have accelerated the discovery of important cancer vulnerabilities. However, single-gene knockout phenotypes can be masked by redundancy among…”
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Diagnostic accuracy of two commercial SARS-CoV-2 antigen-detecting rapid tests at the point of care in community-based testing centers
Published in PloS one (31-03-2021)“…Determine the diagnostic accuracy of two antigen-detecting rapid diagnostic tests (Ag-RDT) for SARS-CoV-2 at the point of care and define individuals'…”
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Mapping the Hallmarks of Lung Adenocarcinoma with Massively Parallel Sequencing
Published in Cell (14-09-2012)“…Lung adenocarcinoma, the most common subtype of non-small cell lung cancer, is responsible for more than 500,000 deaths per year worldwide. Here, we report…”
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Massively parallel phenotyping of coding variants in cancer with Perturb-seq
Published in Nature biotechnology (01-06-2022)“…Genome sequencing studies have identified millions of somatic variants in cancer, but it remains challenging to predict the phenotypic impact of most…”
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eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants
Published in PLoS computational biology (02-07-2021)“…While advancements in genome sequencing have identified millions of somatic mutations in cancer, their functional impact is poorly understood. We previously…”
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CRISPR base editor screens identify variant function at scale
Published in Molecular cell (18-02-2021)“…Cuella-Martin et al. (2021) and Hanna et al. (2021) showcase CRISPR base editing in large-scale pooled screens in human cells to discover both loss- and…”
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MET Exon 14 Mutation Encodes an Actionable Therapeutic Target in Lung Adenocarcinoma
Published in Cancer research (Chicago, Ill.) (15-08-2017)“…Targeting somatically activated oncogenes has revolutionized the treatment of non-small cell lung cancer (NSCLC). Mutations in the gene mesenchymal-epithelial…”
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Cell Painting predicts impact of lung cancer variants
Published in Molecular biology of the cell (15-05-2022)“…Most variants in most genes across most organisms have an unknown impact on the function of the corresponding gene. This gap in knowledge is especially acute…”
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Chromosome-level genome editing uncovers aneuploidy addiction in cancer
Published in Cell reports methods (23-10-2023)“…Publishing in Science, Girish and colleagues achieve chromosome-level genome editing to reveal a requirement for aneuploidy in breast and melanoma cancers…”
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Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2
Published in Proceedings of the National Academy of Sciences - PNAS (04-09-2012)“…We assessed somatic alleles of six receptor tyrosine kinase genes mutated in lung adenocarcinoma for oncogenic activity. Five of these genes failed to score in…”
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Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer
Published in Nature communications (09-08-2021)“…CRISPR-based cancer dependency maps are accelerating advances in cancer precision medicine, but adequate functional maps are limited to the most common…”
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Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation
Published in Genome medicine (20-12-2019)“…Variants of uncertain significance represent a massive challenge to medical genetics. Multiplexed functional assays, in which the functional effects of…”
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