Cell Model Catalogue

 
 
hPSCreg NameCell TypeICD CodeDiseaseSourceReprogramming Grade
UMGi108-AiPSCF84.0Childhood autismGingivaLentivirusResearch
UMGi110-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch
UMGi111-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch
UMGi112-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch
UMGi113-AiPSCWTWT/RelativeSkinLentivirusResearch
UMGi114-AiPSCWTWT/RelativeSkinLentivirusResearch
UMGi014-DiPSCWTWTSkinmRNAResearch
UMGi099-AiPSCQ87.8Alström syndromeSkinmRNAResearch
UMGi129-BiPSCI49.8Short QT syndromeSkinmRNAResearch
UMGi014-BiPSCWTWTSkinPlasmidResearch
UMGi029-AiPSCI42.2Hypertrophic cardiomyopathySkinPlasmidResearch
UMGi165-AiPSCQ87.1Noonan syndromeSkinPlasmidResearch
UMGi163-AiPSCWTWTFibroblastsPlasmidResearch
UMGi164-AiPSCQ87.1Noonan syndromeFibroblastsPlasmidResearch
UMGi256-AiPSCQ87.1Cardiofaciocutaneous syndromeFibroblastsPlasmidResearch
UMGi014-AiPSCWTWTBloodSendai VirusResearch
UMGi014-CiPSCWTWTSkinSendai VirusResearch
UMGi015-AiPSCWTWTBloodSendai VirusResearch
UMGi016-AiPSCWTWTBloodSendai VirusResearch
UMGi017-AiPSCWTWTBloodSendai VirusResearch