Cell Model Catalogue

 
 
hPSCreg NameCell TypeICD CodeDiseaseSourceReprogramming Distribution
UMGi108-AiPSCF84.0Childhood autismGingivaLentivirusProject
UMGi110-AiPSCQ21.3Tetralogy of FallotSkinLentivirusProject
UMGi111-AiPSCQ21.3Tetralogy of FallotSkinLentivirusProject
UMGi112-AiPSCQ21.3Tetralogy of FallotSkinLentivirusProject
UMGi113-AiPSCWTWT/RelativeSkinLentivirusProject
UMGi114-AiPSCWTWT/RelativeSkinLentivirusProject
UMGi014-DiPSCWTWTSkinmRNAUMG Collection
UMGi099-AiPSCQ87.8Alström syndromeSkinmRNAUMG Collection
UMGi129-BiPSCI49.8Short QT syndromeSkinmRNAUMG Collection
UMGi014-BiPSCWTWTSkinPlasmidUMG Collection
UMGi029-AiPSCI42.2Hypertrophic cardiomyopathySkinPlasmidUMG Collection
UMGi165-AiPSCQ87.1Noonan syndromeSkinPlasmidUMG Collection
UMGi163-AiPSCWTWTFibroblastsPlasmidUMG Collection
UMGi164-AiPSCQ87.1Noonan syndromeFibroblastsPlasmidProject
UMGi256-AiPSCQ87.1Cardiofaciocutaneous syndromeFibroblastsPlasmidProject
UMGi014-AiPSCWTWTBloodSendai VirusUMG Collection
UMGi014-CiPSCWTWTSkinSendai VirusUMG Collection
UMGi015-AiPSCWTWTBloodSendai VirusProject
UMGi016-AiPSCWTWTBloodSendai VirusProject
UMGi017-AiPSCWTWTBloodSendai VirusProject