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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c4e6b1c32fe1e727fe1edd4bc57dd196
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01K67-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-85
filingDate 2013-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a35bc4f292ae07b79da0b8655627b15b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61d0eaa37ef81c23fa3f3615099e0697
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a70cafdf4f7362f34b82c4bcd954d007
publicationDate 2014-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103642836-A
titleOfInvention Method for establishing fragile X-syndrome non-human primate model on basis of CRISPR gene knockout technology
abstract The invention discloses a method for establishing a fragile X-syndrome non-human primate model on the basis of a CRISPR gene knockout technology. The method comprises the following steps: (1) establishing a FMR1 gene knockout machin model; (2) carrying out identification and related functional analysis on the machin model; (3) carrying out tests on the nerve characteristics and learning and memorizing ability of the machin model. The method utilizes a CRISPR gene knockout technology to establish a fragile X-syndrome non-human primate model. The model fills the blank of non-human primate model, can effectively stimulate the pathological process of human diseases, can be used as an optimum animal model for researching human diseases, can effectively predict the effect of novel vaccine, novel drug or novel diagnostic reagent in clinical applications, and thus greatly reduces the risk of novel drug development.
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