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{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/7281900","sourcedb":"PMC","sourceid":"7281900","source_url":"https://www.ncbi.nlm.nih.gov/pmc/7281900","text":"Here, we generated patient-specific, induced pluripotent stem cells (iPSCs) from a patient with TSC with a heterozygous, germline, nonsense mutation in exon 15 of TSC1 and established an isogenic set of heterozygous (Het), null, and corrected wild-type (Corr-WT) iPSCs using CRISPR/Cas9-mediated gene editing. We differentiated these iPSCs into neural progenitor cells (NPCs) and examined neurodevelopmental phenotypes, signaling, and changes in gene expression by RNA-seq.","tracks":[{"project":"testtesttest","denotations":[{"id":"T2","span":{"begin":45,"end":67},"obj":"Body_part"},{"id":"T3","span":{"begin":352,"end":368},"obj":"Body_part"}],"attributes":[{"id":"A2","pred":"uberon_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CL_0002248"},{"id":"A3","pred":"uberon_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/CL_0011026"},{"subj":"T2","pred":"source","obj":"testtesttest"},{"subj":"T3","pred":"source","obj":"testtesttest"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"testtesttest","color":"#e8ec93","default":true}]}]}}