Biblio

Author Title [ Type(Desc)] Year
Filters: First Letter Of Title is G and Author is McLenachan, Samuel  [Clear All Filters]
Journal Article
Zhang X, Zhang D, Thompson JA, Chen S-C, Huang Z, Jennings L, McLaren TL, Lamey TM, De Roach JN, Chen FK, et al. Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids. Mol Genet Genomic Med. 2021:e1601.
Zhang X, Moon SYoon, Zhang D, Chen S-C, Lamey T, Thompson JA, McLaren T, De Roach JN, McLenachan S, Chen FK. Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation. Stem Cell Res. 2019;37:101452.
Huang D, Zhang D, Chen S-C, Aung-Htut MThandar, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, et al. Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene. Stem Cell Res. 2021;54:102439.
Claassen JN, Zhang D, Chen S-C, Moon SYoon, Lamey T, Thompson JA, McLaren T, De Roach JN, McLenachan S, Chen FK. Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy. Stem Cell Res. 2018;34:101352.
Huang Z, Zhang D, Chen S-C, Thompson JA, McLaren T, Lamey T, De Roach JN, McLenachan S, Chen FK. Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations. Stem Cell Res. 2019;40:101549.
McLenachan S, Zhang D, Zhang X, Chen S-C, Lamey T, Thompson JA, McLaren T, De Roach JN, Fletcher S, Chen FK. Generation of two induced pluripotent stem cell lines from a patient with dominant PRPF31 mutation and a related non-penetrant carrier. Stem Cell Res. 2018;34:101357.
Jennings L, Zhang D, Chen S-C, Moon SYoon, Lamey T, Thompson JA, McLaren T, De Roach JN, Chen FK, McLenachan S. Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4. Stem Cell Res. 2020;48:101947.
Huang D, Zhang D, Chen S-C, Aung-Htut MThandar, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, et al. Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene. Stem Cell Res. 2021;54:102448.
Zhang D, McLenachan S, Chen S-C, Zaw K, Alziyadat Y, Zhang X, Lamey TM, Thompson JA, McLaren TL, Mellough C, et al. Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. Stem Cell Res. 2021;51:102154.
Moon SYoon, Zhang D, Chen S-C, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Chen FK, McLenachan S. Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1. Stem Cell Res. 2021;54:102403.