http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2019216638-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1b49b135f099e96a0e4cab2427a48ae8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K48-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-405
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-705
filingDate 2019-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa722001c46df86d816a6284dded0dab
publicationDate 2021-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2019216638-B2
titleOfInvention Identification of Channelopsin-2 (Chop2) mutations and methods of use
abstract The invention provides compositions and kits including at least one nucleic acid or polypeptide nmolecule encoding for a mutant ChR2 protein. Methods of the invention include administering a ncomposition comprising a mutant ChR2 to a subject to preserve, improve, or restore nphototransduction. Preferably, the compositions and methods of the invention are provided to a nsubject having impaired vision, thereby restoring vision to normal levels.
priorityDate 2012-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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