http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003512300-A
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K48-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K2319-00 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-47 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K48-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-47 |
filingDate | 2000-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2003-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2003512300-A |
titleOfInvention | Axonal outgrowth and induction by tenascin-C |
abstract | (57) [Summary]nWe have developed a test method to quantify the neurite response at the sensitive support interface, and when poly-L-lysine or fnA-D is given as an interfacial option, the neurites become fnA It has been found that it shows a strong priority for -D. In addition, axons were found to favor cells that overexpress the largest, but not the least, tenascin-C splice variant over the choice of control cells and cells transfected with tenascin-C. . The permissive guidance cue for large tenascin-C expressed by cells was mapped to fnA-D, indicating that neurite outgrowth and induction is promoted by distinct sequences within fnA-D. Thus, neurite outgrowth and neurite outgrowth, regulated by alternatively inherited regions of tenascin-C, are discrete events that can be independently regulated. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008506355-A |
priorityDate | 1999-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 194.