http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2012083000-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-435
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-567
filingDate 2011-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3681420c6146d3c551ce4eea7add12f3
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publicationDate 2012-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2012083000-A1
titleOfInvention Neuropeptide Release Assay For Sodium Channels
abstract Methods and compositions for using genetically modified non-human animals are provided, wherein the genetic modification comprises a humanization of the one or more extracellular pore loops of a Na V 1.7 channel protein or a complete humanization of an endogenous Na V 1.7 gene. Methods for using isolated DRG cultures from genetically modified non-human animals are also provided, wherein the isolated DRG express a human or chimeric Na V 1.7 protein on the surface, in particular measuring primary nociceptive activation through the release of calcitonin gene-related peptide (CGRP) in isolated DRG in vitro, and wherein the isolated DRG cultures are capable of generating action potentials and communicating through an excitable signal via the expressed human or chimeric Na V 1.7 protein the cell surface. In vivo and in vitro methods for characterizing Na V 1.7-specific antagonists and evaluation of corresponding therapeutic potential for Na V 1.7-mediated disease are also provided.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10072076-B2
priorityDate 2010-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395986
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226433313
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15424
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527287

Total number of triples: 311.