scholarly article | Q13442814 |
P356 | DOI | 10.1038/S41417-020-00256-7 |
P698 | PubMed publication ID | 33191402 |
P50 | author | R Srikar | Q102063581 |
P2093 | author name string | Reena Rajkumari | |
K Sreedurgalakshmi | |||
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PTPN11 is the first identified proto-oncogene that encodes a tyrosine phosphatase | Q35616065 | ||
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Npm1 is a haploinsufficient suppressor of myeloid and lymphoid malignancies in the mouse | Q36508976 | ||
Targeting mutant KRAS with CRISPR-Cas9 controls tumor growth. | Q47554878 | ||
Computational correction of copy number effect improves specificity of CRISPR-Cas9 essentiality screens in cancer cells. | Q47627028 | ||
Deactivated CRISPR Associated Protein 9 for Minor-Allele Enrichment in Cell-Free DNA. | Q47644164 | ||
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Application of CRISPR-Cas9 Based Genome-Wide Screening Approaches to Study Cellular Signalling Mechanisms | Q52347926 | ||
Anti-tumor activity of osimertinib, an irreversible mutant-selective EGFR tyrosine kinase inhibitor, in NSCLC harboring EGFR Exon 20 Insertions | Q52430499 | ||
In vivo CRISPR screening unveils histone demethylase UTX as an important epigenetic regulator in lung tumorigenesis | Q52431419 | ||
Specific targeting of point mutations in EGFR L858R-positive lung cancer by CRISPR/Cas9. | Q53684294 | ||
Nrf2 Redirects Glucose and Glutamine into Anabolic Pathways in Metabolic Reprogramming | Q54497843 | ||
Comparison of p53 and epidermal growth factor receptor gene status between primary tumors and lymph node metastases in non-small cell lung cancers. | Q54652248 | ||
Receptor Tyrosine Kinase fusions and BRAF kinase fusions are rare but actionable resistance mechanisms to EGFR tyrosine kinase inhibitors. | Q54976676 | ||
SHP2 is required for growth of KRAS-mutant non-small-cell lung cancer in vivo. | Q54977899 | ||
Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants. | Q55289701 | ||
A CRISPR screen identifies MAPK7 as a target for combination with MEK inhibition in KRAS mutant NSCLC. | Q55339149 | ||
Pooled Lentiviral CRISPR-Cas9 Screens for Functional Genomics in Mammalian Cells | Q57454453 | ||
Modulation of mutant KrasG12D-driven lung tumorigenesis in vivo by gain or loss of PCDH7 function | Q58585653 | ||
The continuously evolving CRISPR barcoding toolbox | Q58699403 | ||
Selective targeting of KRAS oncogenic alleles by CRISPR/Cas9 inhibits proliferation of cancer cells | Q58796049 | ||
Co-occurring KRAS mutation/LKB1 loss in non-small cell lung cancer cells results in enhanced metabolic activity susceptible to caloric restriction: an in vitro integrated multilevel approach | Q59793918 | ||
Up-Regulated FGFR1 Expression as a Mediator of Intrinsic TKI Resistance in EGFR-Mutated NSCLC | Q60044591 | ||
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries | Q60142201 | ||
Lung cancer deficient in the tumor suppressor GATA4 is sensitive to TGFBR1 inhibition | Q64060566 | ||
Targeting exon 20 insertion mutations in non-small cell lung cancer | Q64118764 | ||
Retinoblastoma mutation predicts poor outcomes in advanced non small cell lung cancer | Q64236786 | ||
Delivery Aspects of CRISPR/Cas for in Vivo Genome Editing | Q64386928 | ||
EGFR exon 20 insertion mutations and response to osimertinib in non-small-cell lung cancer. | Q64949390 | ||
Fas-induced apoptosis is mediated by activation of a Ras and Rac protein-regulated signaling pathway | Q71574095 | ||
A CRISPR Test for Rapidly and Sensitively Detecting Circulating EGFR Mutations | Q89860704 | ||
Functional Gene Knockout of NRF2 Increases Chemosensitivity of Human Lung Cancer A549 Cells In Vitro and in a Xenograft Mouse Model | Q90055403 | ||
Low Abundance of Circulating Tumor DNA in Localized Prostate Cancer | Q90139206 | ||
Highly efficient DSB-free base editing for streptomycetes with CRISPR-BEST | Q90240255 | ||
Simple in Vivo Gene Editing via Direct Self-Assembly of Cas9 Ribonucleoprotein Complexes for Cancer Treatment | Q90363341 | ||
Mutant LKB1 Confers Enhanced Radiosensitization in Combination with Trametinib in KRAS-Mutant Non-Small Cell Lung Cancer | Q90697707 | ||
The KRASG12C Inhibitor MRTX849 Provides Insight toward Therapeutic Susceptibility of KRAS-Mutant Cancers in Mouse Models and Patients | Q90974072 | ||
The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity | Q91013772 | ||
EMT-Mediated Acquired EGFR-TKI Resistance in NSCLC: Mechanisms and Strategies | Q91083904 | ||
CRISPR-Cas: a tool for cancer research and therapeutics | Q91142488 | ||
In Vivo Epigenetic CRISPR Screen Identifies Asf1a as an Immunotherapeutic Target in Kras-Mutant Lung Adenocarcinoma | Q91343630 | ||
LKB1 and KEAP1/NRF2 Pathways Cooperatively Promote Metabolic Reprogramming with Enhanced Glutamine Dependence in KRAS-Mutant Lung Adenocarcinoma | Q91650846 | ||
Recent advances in aerosol gene delivery systems using non-viral vectors for lung cancer therapy | Q91696659 | ||
Discovery of a Covalent Inhibitor of KRASG12C (AMG 510) for the Treatment of Solid Tumors | Q91840546 | ||
Impact of MET alterations on targeted therapy with EGFR-tyrosine kinase inhibitors for EGFR-mutant lung cancer | Q91937343 | ||
Targeting FGFR overcomes EMT-mediated resistance in EGFR mutant non-small cell lung cancer | Q92035698 | ||
Cause-and-Effect relationship between FGFR1 expression and epithelial-mesenchymal transition in EGFR-mutated non-small cell lung cancer cells | Q92086302 | ||
STK11 and KEAP1 mutations as prognostic biomarkers in an observational real-world lung adenocarcinoma cohort | Q92091040 | ||
Acquired BRAF Rearrangements Induce Secondary Resistance to EGFR therapy in EGFR-Mutated Lung Cancers | Q92111772 | ||
Liquid Biopsy by Next-Generation Sequencing: a Multimodality Test for Management of Cancer | Q92191367 | ||
The AMPK-Related Kinases SIK1 and SIK3 Mediate Key Tumor-Suppressive Effects of LKB1 in NSCLC | Q92214297 | ||
CRISPR-mediated modeling and functional validation of candidate tumor suppressor genes in small cell lung cancer | Q92217305 | ||
Specificity Assessment of CRISPR Genome Editing of Oncogenic EGFR Point Mutation with Single-Base Differences | Q92256739 | ||
Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant | Q92296048 | ||
Applications of CRISPR/Cas9 Technology in the Treatment of Lung Cancer | Q92681575 | ||
AGK-BRAF is associated with distant metastasis and younger age in pediatric papillary thyroid carcinoma | Q92695843 | ||
CX Chemokine Receptor 7 Contributes to Survival of KRAS-Mutant Non-Small Cell Lung Cancer upon Loss of Epidermal Growth Factor Receptor | Q92758220 | ||
Translatable gene therapy for lung cancer using Crispr CAS9-an exploratory review | Q92920001 | ||
Epigenetic CRISPR screens identify Npm1 as a therapeutic vulnerability in non-small cell lung cancer | Q97535525 | ||
Adaptive and Acquired Resistance to EGFR Inhibitors Converge on the MAPK Pathway | Q36970403 | ||
EGFR exon 20 insertion mutations in lung adenocarcinomas: prevalence, molecular heterogeneity, and clinicopathologic characteristics. | Q37021792 | ||
Structure-based view of epidermal growth factor receptor regulation | Q37197992 | ||
EGFR family: structure physiology signalling and therapeutic targets | Q37272623 | ||
LHX6 acts as a novel potential tumour suppressor with epigenetic inactivation in lung cancer | Q37299656 | ||
The distribution of BRAF gene fusions in solid tumors and response to targeted therapy | Q37308973 | ||
EGFR T790M mutation: a double role in lung cancer cell survival? | Q37354807 | ||
MET gene amplification or EGFR mutation activate MET in lung cancers untreated with EGFR tyrosine kinase inhibitors | Q37399525 | ||
Nucleophosmin sets a threshold for p53 response to UV radiation | Q37424634 | ||
CRISPR-Mediated Drug-Target Validation Reveals Selective Pharmacological Inhibition of the RNA Helicase, eIF4A. | Q37649874 | ||
CRISPR/Cas9: molecular tool for gene therapy to target genome and epigenome in the treatment of lung cancer | Q38614582 | ||
IGF1R depletion facilitates MET-amplification as mechanism of acquired resistance to erlotinib in HCC827 NSCLC cells | Q38707122 | ||
A genetic interaction analysis identifies cancer drivers that modify EGFR dependency | Q38717620 | ||
Applications of the CRISPR/Cas9 system in murine cancer modeling | Q38858314 | ||
Discovery of cancer drug targets by CRISPR-Cas9 screening of protein domains | Q38876767 | ||
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells. | Q38895804 | ||
DNA sequencing and CRISPR-Cas9 gene editing for target validation in mammalian cells | Q38984711 | ||
DrugTargetSeqR: a genomics- and CRISPR-Cas9-based method to analyze drug targets | Q38984714 | ||
Evaluating TBK1 as a therapeutic target in cancers with activated IRF3. | Q39002218 | ||
MiR-21 overexpression is associated with acquired resistance of EGFR-TKI in non-small cell lung cancer | Q39044325 | ||
Cornerstones of CRISPR-Cas in drug discovery and therapy | Q39051110 | ||
In Vivo Delivery of CRISPR/Cas9 for Therapeutic Gene Editing: Progress and Challenges | Q39163867 | ||
Translating cancer epigenomics into the clinic: focus on lung cancer | Q39394558 | ||
ERK5/BMK1 is indispensable for optimal colony-stimulating factor 1 (CSF-1)-induced proliferation in macrophages in a Src-dependent fashion. | Q40005436 | ||
A mechanism of resistance to gefitinib mediated by cellular reprogramming and the acquisition of an FGF2-FGFR1 autocrine growth loop. | Q40289611 | ||
Rapidly evolving homing CRISPR barcodes | Q40441230 | ||
CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations. | Q41194695 | ||
Mutational analysis of single circulating tumor cells by next generation sequencing in metastatic breast cancer | Q41225190 | ||
Targeted nanoconjugate co-delivering siRNA and tyrosine kinase inhibitor to KRAS mutant NSCLC dissociates GAB1-SHP2 post oncogene knockdown | Q41729089 | ||
Simple and rapid in vivo generation of chromosomal rearrangements using CRISPR/Cas9 technology | Q41747565 | ||
Genetic disruption of oncogenic Kras sensitizes lung cancer cells to Fas receptor-mediated apoptosis | Q41775168 | ||
KEAP1 loss modulates sensitivity to kinase targeted therapy in lung cancer | Q41952724 | ||
Keap1 loss promotes Kras-driven lung cancer and results in dependence on glutaminolysis. | Q41992348 | ||
In vivo engineering of oncogenic chromosomal rearrangements with the CRISPR/Cas9 system. | Q42183080 | ||
The impact of MET, IGF-1, IGF1R expression and EGFR mutations on survival of patients with non-small-cell lung cancer | Q42337044 | ||
Evaluation of digital PCR for detecting low-level EGFR mutations in advanced lung adenocarcinoma patients: a cross-platform comparison study | Q42366577 | ||
CRISPR-Cas9-based target validation for p53-reactivating model compounds. | Q42577802 | ||
Drug for an 'undruggable' protein | Q42734596 | ||
Focal Adhesion Kinase Regulates the DNA Damage Response and Its Inhibition Radiosensitizes Mutant KRAS Lung Cancer. | Q44951464 | ||
Beyond ALK and ROS1: RET, NTRK, EGFR and BRAF gene rearrangements in non-small cell lung cancer | Q46512789 | ||
CUT-PCR: CRISPR-mediated, ultrasensitive detection of target DNA using PCR. | Q47162594 | ||
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage | Q47328087 | ||
CRISPR/Cas9 library screening for drug target discovery | Q47329392 | ||
P921 | main subject | CRISPR | Q412563 |
non-small-cell lung carcinoma | Q3658562 | ||
P577 | publication date | 2020-11-15 | |
P1433 | published in | Cancer Gene Therapy | Q15763088 |
P1476 | title | CRISPR-Cas deployment in non-small cell lung cancer for target screening, validations, and discoveries |
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