<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/007/SRR2970377/SRR2970377.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/006/SRR2970376/SRR2970376.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/001/SRR2970381/SRR2970381.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/000/SRR2970380/SRR2970380.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/002/SRR2970382/SRR2970382.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/009/SRR2970379/SRR2970379.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2970383/SRR2970383.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/005/SRR2970375/SRR2970375.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/004/SRR2970374/SRR2970374.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/008/SRR2970378/SRR2970378.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2970373/SRR2970373.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Human Genetics, Tel Aviv University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA304752</full_dataset_link><scientific_name>Homo sapiens</scientific_name><tag>xref:PubMed:26751173</tag><long_description>We exained using RNA-seq the effect of targeting selected p53-bound enhancers on the p53-induced response to oncogenic stress Overall design: RNA-seq was applied to examine transcriptional response to oncogenic stress (induced by RASG12V activation) in control and genetically manipulated hTERT-immortalized BJ cells</long_description><repository>ENA</repository><description_synonyms>beta-Tub60D, beta[[3]]-Tub, CG10873, DmelCG17117, dp53, Dmbeta3, Dm-HTH, p50, p53, BETA 60D, prac, beta3t, beta3-Tub, 143391_i_at, beta3 TU, LFS1, betaTub3, Tp53, l(3)05745, Xp53, 3t, DMP53, bbl, p53/tubulin, Dmp53, bfy, beta[[3]] tubulin, anon-EST:Liang-2.13, Tub60D, HTH, Hth, CG33336, beta-tub, 1323/07, clone 2.13, function., BCC7, D.m.BETA-60D, beta-Tub6D, dmp53, DmelCG33336, D-p53, beta60C, CG3401, beta3Tub, beta3TUB, T, DmP53, Dm-P53, l(3)86Ca, 1422/04, beta3, dtl, Tub, DTB3, B3t, Meis1, DmelCG3401, hth1, Trp53, hth2, Dp53, betatub60D, P53, betaTub60C, p44, bhy, beta3-tubulin, beta[[3]]-tubulin, TRP53, CG17117, CG31325, betaTub, p50/tubulin</description_synonyms><name_synonyms>Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man</name_synonyms></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>CRISPR-Cas9 based screen for p53-bound enhancers that function in oncogene-induced senescence</description><dates><last_updated>2025-09-24</last_updated><first_public>2015-12-04</first_public></dates><accession>PRJNA304752</accession><cross_references><GEO>GSE75627</GEO><taxon>9606</taxon><PubMed>26751173</PubMed></cross_references></HashMap>