Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture

Author:

Su Pei-Yin,Lee Winston,Zernant Jana,Tsang Stephen H.,Nagasaki Takayuki,Corneo Barbara,Allikmets Rando

Funder

NEI

Foundation Fighting Blindness Inc

Research to Prevent Blindness

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference5 articles.

1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat. Genet.,1997

2. Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease;Lee;Hum. Mol. Genet.,2021

3. A genotype-phenotype correlation matrix for Stargardt/ABCA4 disease based on long-term prognostic outcomes;Lee;JCI Insight.,2021

4. Establishment and characterization of two iPSC lines derived from healthy controls;Patel;Stem Cell Res.,2020

5. Yang, W., Mills, J.A., Sullivan, S., Liu, Y., French, D.L., Gadue, P., 2008. iPSC Reprogramming from Human Peripheral Blood Using Sendai Virus Mediated Gene Transfer, in: StemBook. Cambridge (MA).

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