scholarly article | Q13442814 |
P2093 | author name string | Jie Zhang | |
Junjie Chen | |||
Nora M Navone | |||
Chao Wang | |||
Zhen Chen | |||
Gang Wang | |||
Xu Feng | |||
Mengfan Tang | |||
Mrinal Srivastava | |||
Peter Shepherd | |||
Megan E McLaughlin | |||
Glen Traver Hart | |||
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A Genome-wide CRISPR Screen in Toxoplasma Identifies Essential Apicomplexan Genes | Q27972929 | ||
The Causes and Consequences of Topological Stress during DNA Replication | Q28077125 | ||
Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice | Q28143813 | ||
Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal | Q28288215 | ||
Mammalian RNase H2 removes ribonucleotides from DNA to maintain genome integrity | Q28505683 | ||
ATR disruption leads to chromosomal fragmentation and early embryonic lethality | Q28591433 | ||
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RNaseH2 mutants that cause Aicardi-Goutieres syndrome are active nucleases | Q33779326 | ||
cGAS is essential for cellular senescence | Q33790789 | ||
A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression | Q33850539 | ||
Genome instability due to ribonucleotide incorporation into DNA. | Q34142849 | ||
Potentiation of tumor responses to DNA damaging therapy by the selective ATR inhibitor VX-970 | Q34221860 | ||
Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development. | Q34274334 | ||
Causes and consequences of replication stress | Q34394094 | ||
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection | Q34548112 | ||
The Molecular Taxonomy of Primary Prostate Cancer | Q34674332 | ||
Reduction of hRNase H2 activity in Aicardi-Goutières syndrome cells leads to replication stress and genome instability | Q34920730 | ||
AGS, SLE, and RNASEH2 mutations: translating insights into therapeutic advances | Q35242554 | ||
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. | Q35858015 | ||
SLFN11 inhibits checkpoint maintenance and homologous recombination repair | Q35866775 | ||
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Bridging the gap between in vitro and in vivo: Dose and schedule predictions for the ATR inhibitor AZD6738 | Q35999359 | ||
The novel ATR inhibitor VE-821 increases sensitivity of pancreatic cancer cells to radiation and chemotherapy | Q36289912 | ||
Protein kinase mutants of human ATR increase sensitivity to UV and ionizing radiation and abrogate cell cycle checkpoint control | Q36490482 | ||
Targeting ATR in vivo using the novel inhibitor VE-822 results in selective sensitization of pancreatic tumors to radiation. | Q36525188 | ||
RNase H2 catalytic core Aicardi-Goutières syndrome-related mutant invokes cGAS-STING innate immune-sensing pathway in mice. | Q36745063 | ||
Ribonuclease H2 mutations induce a cGAS/STING-dependent innate immune response | Q36866528 | ||
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndrome. | Q37022007 | ||
Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondria | Q37142690 | ||
A Genome-wide CRISPR Screen Identifies CDC25A as a Determinant of Sensitivity to ATR Inhibitors | Q37268724 | ||
Substantial interindividual and limited intraindividual genomic diversity among tumors from men with metastatic prostate cancer | Q37302524 | ||
ATR inhibitors as a synthetic lethal therapy for tumours deficient in ARID1A. | Q37508792 | ||
The essential kinase ATR: ensuring faithful duplication of a challenging genome. | Q38622938 | ||
Evaluation and Design of Genome-Wide CRISPR/SpCas9 Knockout Screens. | Q38706202 | ||
Genome-wide CRISPR screens reveal a Wnt-FZD5 signaling circuit as a druggable vulnerability of RNF43-mutant pancreatic tumors | Q38729876 | ||
Targeting the ATR-CHK1 Axis in Cancer Therapy | Q38817102 | ||
Measuring error rates in genomic perturbation screens: gold standards for human functional genomics | Q38978817 | ||
ATR pathway inhibition is synthetically lethal in cancer cells with ERCC1 deficiency | Q39012252 | ||
The impact of replication stress on replication dynamics and DNA damage in vertebrate cells. | Q39438600 | ||
Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR. | Q39559122 | ||
Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents. | Q42745810 | ||
Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagy | Q46289705 | ||
Genome-Wide CRISPR/Cas9 Screening for High-Throughput Functional Genomics in Human Cells. | Q47951609 | ||
The role of RNase H2 in processing ribonucleotides incorporated during DNA replication. | Q50212840 | ||
ATR inhibition induces synthetic lethality and overcomes chemoresistance in TP53- or ATM-defective chronic lymphocytic leukemia cells | Q50913049 | ||
Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models | Q52811875 | ||
Methylation of SLFN11 is a marker of poor prognosis and cisplatin resistance in colorectal cancer | Q52881647 | ||
Integrative Clinical Genomics of Advanced Prostate Cancer | Q53788627 | ||
CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions | Q59084697 | ||
The cGAS-cGAMP-STING pathway connects DNA damage to inflammation, senescence, and cancer | Q88286449 | ||
P433 | issue | 14 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | CRISPR | Q412563 |
P304 | page(s) | 2451-2463 | |
P577 | publication date | 2018-12-07 | |
P1433 | published in | Oncogene | Q1568657 |
P1476 | title | Genome-wide CRISPR screens reveal synthetic lethality of RNASEH2 deficiency and ATR inhibition | |
P478 | volume | 38 |
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