Table 1.
Cellular Model | Genetic Disease |
---|---|
Native urine-derived stem cells | Fabry disease Inherited epidermolysis bullosa Spinal muscular atrophy Genetic kidney disorders |
Direct reprogrammed urine cells (MyoD, alginate microbeads-specific growth factors, transcriptional factors-neurotrophic factors) | Limb Girdle Muscular Dystrophy Duchenne Muscular Dystrophy Wilson’s disease |
Urine-induced pluripotent stem cells (iPSCs) | Hemophilia A Familial hypercholesterolemia Phenylketonuria Down syndrome Spinocerebellar ataxia Paroxysmal kinesigenic dyskinesia Cardiac diseases |