Cell Model Catalogue

 
 
hPSCreg NameCell TypeICD CodeDisease SourceReprogrammingGrade
UMGi168-AiPSCQ87.1Noonan syndromeSkinSendai VirusResearch
UMGi165-AiPSCQ87.1Noonan syndromeSkinPlasmidResearch
UMGi164-AiPSCQ87.1Noonan syndromeFibroblastsPlasmidResearch
UMGi177-AiPSCQ87.1Noonan syndromeSkinSendai VirusResearch
UMGi274-AiPSCQ87.1Noonan syndromeSkinSendai VirusResearch
UMGi273-AiPSCQ87.1Noonan syndromeFibroblastsSendai VirusResearch
UMGi100-AiPSCQ87.1Noonan syndrome with multiple lentiginesFibroblastsSendai VirusResearch
UMGi089-AiPSCQ87.8Peroxisome biogenesis disorder spectrumFibroblastsSendai VirusResearch
UMGi095-AiPSCE34.8Progeroid syndromeFibroblastsSendai VirusResearch
UMGi097-AiPSCE34.8Progeroid syndromeFibroblastsSendai VirusResearch
UMGi178-AiPSCE34.8Progeroid syndromeFibroblastsSendai VirusResearch
UMGi120-AiPSCI49.8Short QT syndromeFibroblastsSendai VirusResearch
UMGi129-AiPSCI49.8Short QT syndromeSkinSendai VirusResearch
UMGi129-BiPSCI49.8Short QT syndromeSkinmRNAResearch
UMGi160-AiPSCI49.8Short QT syndromeSkinSendai VirusResearch
UMGi133-AiPSCI49.8Short QT syndromeSkinSendai VirusResearch
UMGi171-AiPSCI51.81Takotsubo syndromeSkinSendai VirusResearch
UMGi110-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch
UMGi111-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch
UMGi112-AiPSCQ21.3Tetralogy of FallotSkinLentivirusResearch