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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 |
---|---|---|---|---|---|---|---|---|---|
FX08-1 | Human iPS | Fragile X syndrome|Autism | Full mutation FXS iPS cell line that lacks FMR1 and FMRP expression | Male | 11 Years | No | No | ||
Human iPS | None reported | Female | 25 Years | Caucasian | No | No | |||
Human iPS | None reported | Female | 25 Years | Caucasian | No | No | |||
Human iPS | None reported | Female | 25 Years | Caucasian | No | No | |||
Human iPS | Down syndrome, Trisomy 21 | Female | 25 Years | Caucasian | No | No | |||
Human iPS | Down syndrome, Trisomy 21 | Female | 25 Years | Caucasian | No | No | |||
Human iPS | Down syndrome, Trisomy 21 | Female | 25 Years | Caucasian | No | No | |||
Human iPS | None reported | Female | No | No | |||||
Human iPS | None reported | Male | No | No | |||||
Modified Human iPS | None reported | C>T mutation in potassium channel gene | Female | 26 Years | Caucasian > European | No | No |