{"database":"ENA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["University of Edinburgh"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA878471"],"scientific_name":["Homo sapiens"],"long_description":["Investigating transcription deregulation and interferon signaling activation in iPSC-derived neurons deficient for ATRX. Overall design: Comparative gene expression profiling analysis of Quantseq 3' mRNA-seq data for induced pluripotent stem cells, neural progenitors and derived forebrain neurons mutant or wild type for ATRX."],"repository":["ENA"],"description_synonyms":["Profiling, Transcriptome, X-linked, ATR2, postnatal development, Monitorings, A4, Gene, growth and development, Alpha thalassemia mental retardation syndrome, Alpha thalassemia intellectual disability syndrome, ALPHA-thalassemia/mental retardation syndrome, Xnp, XNP, TYPE, LGMD2C, SHS, Gene Expression Profilings, 4833408C14Rik, DAGA4, Alpha-thalassemia/intellectual disability syndrome, Gene Expression, Differential Display, Transcript Expression Analysis, development, mRNA Differential Displays, Transcript Expression Analyses, Gene Expression Pattern Analysis, ATRX, XLMR hypotonic face syndrome, nondeletion type, HP1-BP38, Gene Expression Monitorings, MRXS3, Alpha-thalassemia/mental retardation syndrome, SFM1, Cell., Analysis, Profilings, MAM, Alpha-thalassemia-X-linked intellectual disability syndrome, ATRX syndrome, mRNA Differential Display, SCG3, Gene Expression Monitoring, XH2, Nondeletion type, Transcriptome Profiling, DMDA1, Analyses, mRNA, Transcriptome Profilings, postnatal growth, MRXHF1, ZNF-HX, Transcriptomics, Differential Displays, Transcript Expression, Transcriptome Analysis, RAD54L, Transcriptome Analyses, Monitoring, Gene Expression Analysis, DXHXS6677E, ALPHA-thalassemia/intellectual disability syndrome, AI447451, Hp1bp2, Rad54, DMDA, Gene Expression Analyses, Alpha-thalassemia X-linked intellectual disability syndrome, SCARMD2, JMS, Expression Analysis, RAD54, Expression Analyses, growth, Hp1bp38, ATR"],"name_synonyms":["Profiling, Transcriptome, X-linked, ATR2, postnatal development, Monitorings, A4, Gene, growth and development, Alpha thalassemia mental retardation syndrome, Alpha thalassemia intellectual disability syndrome, ALPHA-thalassemia/mental retardation syndrome, Xnp, XNP, TYPE, LGMD2C, SHS, Gene Expression Profilings, 4833408C14Rik, DAGA4, Alpha-thalassemia/intellectual disability syndrome, Gene Expression, Differential Display, Transcript Expression Analysis, development, mRNA Differential Displays, Transcript Expression Analyses, Gene Expression Pattern Analysis, ATRX, XLMR hypotonic face syndrome, nondeletion type, HP1-BP38, Gene Expression Monitorings, MRXS3, Alpha-thalassemia/mental retardation syndrome, SFM1, Cell., Analysis, Profilings, MAM, Alpha-thalassemia-X-linked intellectual disability syndrome, ATRX syndrome, mRNA Differential Display, SCG3, Gene Expression Monitoring, XH2, Nondeletion type, Transcriptome Profiling, DMDA1, Analyses, mRNA, Transcriptome Profilings, postnatal growth, MRXHF1, ZNF-HX, Transcriptomics, Differential Displays, Transcript Expression, Transcriptome Analysis, RAD54L, Transcriptome Analyses, Monitoring, Gene Expression Analysis, DXHXS6677E, ALPHA-thalassemia/intellectual disability syndrome, AI447451, Hp1bp2, Rad54, DMDA, Gene Expression Analyses, Alpha-thalassemia X-linked intellectual disability syndrome, SCARMD2, JMS, Expression Analysis, RAD54, Expression Analyses, growth, Hp1bp38, ATR"],"additional_accession":[]},"is_claimable":false,"name":"Differential gene expression analysis at different stages of neuronal development in mutant and wild type ATRX cells","description":"Differential gene expression analysis at different stages of neuronal development in mutant and wild type ATRX cells","dates":{"last_updated":"2025-09-24","first_public":"2023-09-28"},"accession":"PRJNA878471","cross_references":{"GEO":["GSE212922"],"taxon":["9606"]}}