http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2013071357-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7927e4438412570281110b0f6b194820
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N5-0634
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filingDate 2012-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_035e577df09f5a1e49618a29329b01ad
publicationDate 2013-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2013071357-A1
titleOfInvention Identification, proliferation in situ, harvesting, separation, and transplantation of adult-derived regenerative pluripotent transitional blastomere-like stem cells and methods of treatment thereof
abstract Non-embryonic transitional blastomere-like stem cells are disclosed. Most preferably, such cells are obtained from the blood after induction by a plant-based compound to proliferate and reverse diapadese into the vasculature or from various tissues of postnatal mammals or humans (using tissue biopsied from the mammal or human), are in the range of 3-5 microns, have a normal karyotype, and do not spontaneously differentiate in situ (in vivo) or in serum-free medium without differentiation inhibitors. These non-embryonic transitional blastomere-like stem cells typically express CD66e, CEA-CAM-1, CD10, SSEA (SSEA-1, SSEA-3, and SSEA-4), telomerase, Sonic hedgehog, but do not typically express Nanog, Nanos, BCl-2 or CXCR-4. Such transitional blastomere-like pluripotent stem cells can be differentiated into epiblast-like stem cells, ectodermal, mesodermal, and endodermal tissues, but NOT placental tissues or germ cells. Moreover, when implanted into a mammal or human, such cells will not be teratogenic.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017176267-A1
priorityDate 2011-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 964.