{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Shen H"],"funding":["NIEHS NIH HHS"],"pagination":["10-22"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4914802"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["151(1)"],"pubmed_abstract":["Though current functional genomic screening systems are useful for investigating human susceptibility to chemical toxicity, they have limitations. Well-established, high-throughput yeast mutant screens identify only evolutionarily conserved processes. RNA interference can be applied in human cells but is limited by incomplete gene knockout and off-target effects. Human haploid cell screening is advantageous as it requires knockdown of only a single copy of each gene. A human haploid cell mutant library (KBM7-Mu), derived from a chronic myeloid leukemia (CML) patient, was recently developed and has been used to identify genes that modulate sensitivity to infectious agents and pharmaceutical drugs. Here, we sought to improve the KBM7-Mu screening process to enable efficient screening of envi"],"journal":["Toxicological sciences : an official journal of the Society of Toxicology"],"pubmed_title":["Identification of Genes That Modulate Susceptibility to Formaldehyde and Imatinib by Functional Genomic Screening in Human Haploid KBM7 Cells."],"pmcid":["PMC4914802"],"funding_grant_id":["P42 ES004705","R01 ES017452"],"pubmed_authors":["McHale CM","Haider SI","Zhang L","Zhang S","Smith MT","Shen H","Jung C"],"additional_accession":[]},"is_claimable":false,"name":"Identification of Genes That Modulate Susceptibility to Formaldehyde and Imatinib by Functional Genomic Screening in Human Haploid KBM7 Cells.","description":"Though current functional genomic screening systems are useful for investigating human susceptibility to chemical toxicity, they have limitations. Well-established, high-throughput yeast mutant screens identify only evolutionarily conserved processes. RNA interference can be applied in human cells but is limited by incomplete gene knockout and off-target effects. Human haploid cell screening is advantageous as it requires knockdown of only a single copy of each gene. A human haploid cell mutant library (KBM7-Mu), derived from a chronic myeloid leukemia (CML) patient, was recently developed and has been used to identify genes that modulate sensitivity to infectious agents and pharmaceutical drugs. Here, we sought to improve the KBM7-Mu screening process to enable efficient screening of envi","dates":{"release":"2016-01-01T00:00:00Z","publication":"2016 May","modification":"2026-05-30T09:00:05.62Z","creation":"2019-03-27T02:16:34Z"},"accession":"S-EPMC4914802","cross_references":{"pubmed":["27008852"],"doi":["10.1093/toxsci/kfw032"]}}