http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019162054-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_716e9a2606ffd4ba1a2a3917e4a402fd |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6888 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-10 |
filingDate | 2018-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44abf54d3aa86537a3363ec8e294c68f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1f4f64777bc6446625a966118cf517a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a71c0781baf1971f7f5f8af791143e6 |
publicationDate | 2019-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2019162054-A |
titleOfInvention | Efficient method for establishing induced pluripotent stem cells |
abstract | [Object] To provide a means for identifying a marker gene that is expressed at an earlier stage than TRA-1-60 and understanding the molecular mechanism of reprogramming using the marker gene. Also, to provide an efficient method for establishing iPS cells using the expression of the marker gene as an index. A method for producing iPS cells comprising the following steps: (i) culturing a somatic cell population into which the reprogramming factor has been introduced; (ii) selecting cells expressing the ESRG gene from the cultured cell population; and (iii) culturing the selected cells to obtain iPS cells. [Selection figure] None |
priorityDate | 2018-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 717.