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• +-Collections
  • EBiSC (2)
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• +-Disease Status [clear]
  • Acromesomelic dysplasia (0)
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  • Alport syndrome (0)
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  FTDP-17 (Frontotemporal dementia and parkinsonism linked to chromosome 17) has no ontology id. (0)
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  Usher syndrome and congenital eye defects (0)
  Various (0)
  X-linked creatine transporter deficiency (0)
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• +-Cell Type of Origin [clear]
  • adipose tissue derived mesenchymal stem cell (22)
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  fibroblast of dermis (2)
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• +-Tissue Of Origin [clear]
  • Frozen PBMC (0)
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  • Unspecified (2)
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• +-Depositor [clear]
  • Berlin Institute of Health (0)
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  CHDI Foundation Inc. (0)
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• +-Donor Sex [clear]
  • Female (2)
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• +-Donor Age [clear]
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  Neonate (0)
  Unspecified (4)
  Various (0)
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• +-Pluripotency Assay [clear]
  • Unspecified (2)
• +-Reprogramming Method [clear]
  • Episomal (1)
  • Lentivirus expressing CRE recombinase (0)
  • Sendai virus (3)
  • Transposon (0)
  Unspecified (0)
  Virus (1)
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• +-Access Conditions [clear]
  • For access by not-for-profit recipients and organisations only. Please read and complete the Material Transfer Agreement (MTA) carefully to check you are a valid recipient and agree to the conditions of use that apply. (0)
  • Unspecified (2)