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Cell Line | Cell Line Alias | Cell Type | Disease | Genetic Alteration/Mutation | Sex | Age at Collection | Ethnicity | Genetically Related Cell Lines | dbGaP Data |
|---|---|---|---|---|---|---|---|---|---|
C88 | Human iPS | Alexander disease (Type II) | C->T transition results in mutation at amino acid residue 88. | Male | 5 Years | No | No | ||
R88 | Modified Human iPS | None reported | Mutated allele corrected using CRISPR/Cas9 | Male | 5 Years | No | No | ||
Modified Human ES | None reported | Male | No | No | |||||
Modified Human ES | None reported | Male | No | No | |||||
Modified Human ES | None reported | Male | No | No | |||||
Modified Human ES | None reported | Female | No | No | |||||
Modified Human ES | None reported | Female | No | No | |||||
Modified Human ES | None reported | Female | No | No | |||||
WA09 inGFPhES#3 | Modified Human ES | None reported | Female | No | No | ||||
Modified Human ES | None reported | Female | No | No |