{"search_session":{},"preferences":{"l":"en","queryLanguage":"en"},"patentId":"101-586-850-552-198","frontPageModel":{"patentViewModel":{"ref":{"entityRefType":"PATENT","entityRefId":"101-586-850-552-198"},"entityMetadata":{"linkedIds":{"empty":true},"tags":[],"collections":[{"id":11616,"type":"PATENT","title":"Case Western Reserve University - Patent Portfolio","description":"","access":"OPEN_ACCESS","displayAvatar":true,"attested":false,"itemCount":4001,"tags":[],"user":{"id":91044780,"username":"Cambialens","firstName":"","lastName":"","created":"2015-05-04T00:55:26.000Z","displayName":"Cambialens","preferences":"{\"usage\":\"public\",\"beta\":false}","accountType":"PERSONAL","isOauthOnly":false},"notes":[{"id":8291,"type":"COLLECTION","user":{"id":91044780,"username":"Cambialens","firstName":"","lastName":"","created":"2015-05-04T00:55:26.000Z","displayName":"Cambialens","preferences":"{\"usage\":\"public\",\"beta\":false}","accountType":"PERSONAL","isOauthOnly":false},"text":"
Search Applicants and Owners separately: weste* reser* AND Univ*
Select more for logical variants. Add to collection. Select all patents in the collection and expand by simple families. Add to collection. Total patents: 2737
Search Applicants and Owners separately: weste* reser* AND Univ*
Select more for logical variants. Add to collection. Select all patents in the collection and expand by simple families. Add to collection. Total patents: 2737
a) providing: i) an in vitro culture comprising between 200 and 600 isolated mouse embryonic stem cells, each of said cells comprising a gene of interest; ii) a chemical agent capable of producing at least one modification in said gene of interest;\n
b) treating said mouse embryonic stem cells with said chemical agent under conditions such that i) it is at least 70% probable that at least one modification in every gene in said mouse embryonic stem cells is produced, and ii) a mixture of mouse embryonic stem cells comprising said gene of interest is produced, said mixture of mouse embryonic stem cells comprising mouse embryonic stem cells having a first modification in said gene of interest, and mouse embryonic stem cells having a second modification in said gene of interest, wherein said mixture of mouse embryonic stem cells is capable of producing a mouse having a germline, and wherein said germline comprises said at least one modification; and\n
c) isolating said mouse embryonic stem cells having a first modification in said gene of interest and said mouse embryonic stem cells having a second modification in said gene of interest, thereby producing an allelic series of modifications in said gene of interest in the isolated mouse embryonic stem cells."],"number":1,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein said treating is under conditions such that it is at least 85% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":2,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein said treating is under conditions such that it is at least 95% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":3,"annotation":false,"title":false,"claim":true},{"lines":["A method of producing an allelic series of modifications in a gene of interest in a mouse embryonic stem cell, comprising:\n
a) providing: i) an in vitro culture comprising between 200 and 600 isolated mouse embryonic stem cells, each of said cells comprising a gene of interest; ii) a chemical agent capable of producing at least one modification in said gene of interest;\n
b) treating said mouse embryonic stem cells with said chemical agent under conditions such that i) cell survival is 10 percent, ii) it is at least 70% probable that at least one modification in every gene in said mouse embryonic stem cells is produced, and iii) a mixture of viable mouse embryonic stem cells comprising said gene of interest is produced, said mixture of mouse embryonic stem cells comprising cells having a first modification in said gene of interest, and cells having a second modification in said gene of interest, wherein said mixture of mouse embryonic stem cells is capable of producing a mouse having a germline, and wherein said germline comprises said at least one modification; and\n
c) isolating said viable mouse embryonic stem cells having a first modification in said gene of interest and said viable mouse embryonic stem cells having a second modification in said gene of interest, thereby producing an allelic series of modifications in said gene of interest in the isolated mouse embryonic stem cells."],"number":4,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4, wherein said treating is under conditions that it is at least 85% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":5,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4, wherein said treating is under conditions such that it is at least 95% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":6,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1 wherein said gene of interest is associated with a disease."],"number":7,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 7, wherein said gene of interest is selected from the group consisting of the p53 gene, BRCA1 gene, CFTR gene, PKD1 gene, PKD2 gene, and PKD3 gene."],"number":8,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, further comprising step d) detecting at least one of said first and second modification in said gene of interest using fluorescent chemical cleavage of mismatch."],"number":9,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein said chemical agent is selected from the group consisting of N-ethyl-N-nitrosurea, methylnitrosourea, procarbazine hydrochloride, triethylene melamine, acrylamide monomer, chlorambucil, melphalan, cyclophosphamide, diethyl sulfate, ethyl methane sulfonate, methyl methane sulfonate, 6-mercaptopurine, mitomycin-C, procarbazine, N-methyl-N′-nitro-N-nitrosoguanidine, 3H2O, and urethane."],"number":10,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein said chemical agent is N-ethyl-N-nitrosurea."],"number":11,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4 wherein said gene of interest is associated with a disease."],"number":12,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 12, wherein said gene of interest is selected from the group consisting of the p53 gene, BRCA1 gene, CFTR gene, PKD1 gene, PKD2 gene, and PKD3 gene."],"number":13,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4, further comprising step d) detecting at least one of said first and second modification in said gene of interest using fluorescent chemical cleavage of mismatch."],"number":14,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4, wherein said chemical agent is selected from the group consisting of N-ethyl-N-nitrosurea, methylnitrosourea, procarbazine hydrochloride, triethylene melamine, acrylamide monomer, chlorambucil, melphalan, cyclophosphamide, diethyl sulfate, ethyl methane sulfonate, methyl methane sulfonate, 6-mercaptopurine, mitomycin-C, procarbazine, N-methyl-N′-nitro-N-nitrosoguanidine, 3H2O, and urethane."],"number":15,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 4, wherein said chemical agent is N-ethyl-N-nitrosurea."],"number":16,"annotation":false,"title":false,"claim":true},{"lines":["A method of producing an allelic series of modifications in a gene of interest in a mouse embryonic stem cell, comprising:\n
a) providing: i) an in vitro culture comprising between 200 and 600 isolated mouse embryonic stem cells, each of said cells comprising a gene of interest; ii) a chemical agent capable of producing at least one modification in said gene of interest;\n
b) treating said mouse embryonic stem cells with said chemical agent under conditions such that i) cell survival is less than 5 percent, ii) it is at least 70% probable that at least one modification in every gene in said mouse embryonic stem cells is produced, and iii) a mixture of viable mouse embryonic stem cells comprising said gene of interest is produced, said mixture of mouse embryonic stem cells comprising cells having a first modification in said gene of interest, and cells having a second modification in said gene of interest, wherein said mixture of mouse embryonic stem cells is capable of producing a mouse having a germline, and wherein said germline comprises said at least one modification; and\n
c) isolating said viable mouse embryonic stem cells having a first modification in said gene of interest and said viable mouse embryonic stem cells having a second modification in said gene of interest, thereby producing an allelic series of modifications in said gene of interest in the isolated mouse embryonic stem cells."],"number":17,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, wherein said treating is under conditions that it is at least 85% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":18,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, wherein said treating is under conditions such that it is at least 95% probable that at least one modification in every gene in said mouse embryonic stem cells is produced."],"number":19,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, wherein said gene of interest is associated with a disease."],"number":20,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 20, wherein said gene of interest is selected from the group consisting of the p53 gene, BRCA1 gene, CFTR gene, PKD1 gene, PKD2 gene, and PKD3 gene."],"number":21,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, further comprising step d) detecting at least one of said first and second modification in said gene of interest using fluorescent chemical cleavage of mismatch."],"number":22,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, wherein said chemical agent is selected from the group consisting of N-ethyl-N-nitrosurea, methylnitrosourea, procarbazine hydrochloride, triethylene melamine, acrylamide monomer, chlorambucil, melphalan, cyclophosphamide, diethyl sulfate, ethyl methane sulfonate, methyl methane sulfonate, 6-mercaptopurine, mitomycin-C, procarbazine, N-methyl-N′-nitro-N-nitrosoguanidine, 3H2O, and urethane."],"number":23,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 17, wherein said chemical agent is N-ethyl-N-nitrosurea."],"number":24,"annotation":false,"title":false,"claim":true}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}