BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 32810830)

  • 1. 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.
    Jennings L; Zhang D; Chen SC; Moon SY; Lamey T; Thompson JA; McLaren T; De Roach JN; Chen FK; McLenachan S
    Stem Cell Res; 2020 Oct; 48():101947. PubMed ID: 32810830
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene.
    Huang D; Zhang D; Chen SC; Aung-Htut MT; Lamey TM; Thompson JA; McLaren TL; De Roach JN; Fletcher S; Wilton SD; Chen FK; McLenachan S
    Stem Cell Res; 2021 Jul; 54():102448. PubMed ID: 34198153
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy.
    Claassen JN; Zhang D; Chen SC; Moon SY; Lamey T; Thompson JA; McLaren T; De Roach JN; McLenachan S; Chen FK
    Stem Cell Res; 2019 Jan; 34():101352. PubMed ID: 30634128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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.
    Huang D; Zhang D; Chen SC; Thandar Aung-Htut M; Lamey TM; Thompson JA; McLaren TL; De Roach JN; Fletcher S; Wilton SD; McLenachan S; Chen FK
    Stem Cell Res; 2021 Jul; 54():102439. PubMed ID: 34214897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Generation of two iPS cell lines (FRIMOi003-A and FRIMOi004-A) derived from Stargardt patients carrying ABCA4 compound heterozygous mutations.
    Riera M; Patel A; Burés-Jelstrup A; Corcostegui B; Chang S; Pomares E; Corneo B; Sparrow JR
    Stem Cell Res; 2019 Apr; 36():101389. PubMed ID: 30798147
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200.
    Zhang D; McLenachan S; Chen SC; Zaw K; Alziyadat Y; Zhang X; Lamey TM; Thompson JA; McLaren TL; Mellough C; De Roach JN; Chen FK
    Stem Cell Res; 2021 Mar; 51():102154. PubMed ID: 33429167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generation of two induced pluripotent stem cells lines from a Mucopolysaccharydosis IIIB (MPSIIIB) patient.
    Vallejo-Diez S; Fleischer A; Martín-Fernández JM; Sánchez-Gilabert A; Bachiller D
    Stem Cell Res; 2018 Dec; 33():180-184. PubMed ID: 30408744
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A gene.
    McLenachan S; Wong EYM; Zhang X; Leith F; Moon SY; Zhang D; Chen SC; Thompson JA; McLaren T; Lamey T; De Roach JN; Atlas MD; Dilley RJ; Chen FK
    Stem Cell Res; 2019 Apr; 36():101420. PubMed ID: 30904819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture.
    Su PY; Lee W; Zernant J; Tsang SH; Nagasaki T; Corneo B; Allikmets R
    Stem Cell Res; 2022 Dec; 65():102973. PubMed ID: 36455383
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1.
    Moon SY; Zhang D; Chen SC; Lamey TM; Thompson JA; McLaren TL; De Roach JN; Chen FK; McLenachan S
    Stem Cell Res; 2021 Jul; 54():102403. PubMed ID: 34034222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A.
    Suárez-Herrera N; Leijsten N; Albert S; Bax NM; Hoyng CB; Cremers FPM; Garanto A; Collin RWJ
    Stem Cell Res; 2023 Dec; 73():103252. PubMed ID: 37979432
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Generation of iPSC lines from three Stargardt patients carrying bi-allelic ABCA4 variants.
    Karjosukarso DW; Bukkems F; Duijkers L; Leijsten N; Hoyng CB; Collin RWJ
    Stem Cell Res; 2023 Sep; 71():103164. PubMed ID: 37441824
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation.
    Zhang X; Moon SY; Zhang D; Chen SC; Lamey T; Thompson JA; McLaren T; De Roach JN; McLenachan S; Chen FK
    Stem Cell Res; 2019 May; 37():101452. PubMed ID: 31059986
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation.
    Zhang X; Zhang D; Chen SC; Lamey T; Thompson JA; McLaren T; De Roach JN; Chen FK; McLenachan S
    Stem Cell Res; 2018 Aug; 31():147-151. PubMed ID: 30092450
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach.
    Pidishetty D; Maddileti S; Mahato S; Agrawal T; Pulimamidi VK; Naik M; Kannabiran C; Jalali S; Mariappan I
    Stem Cell Res; 2024 Jun; 77():103418. PubMed ID: 38615588
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic
    Garanto A; Duijkers L; Tomkiewicz TZ; Collin RWJ
    Genes (Basel); 2019 Jun; 10(6):. PubMed ID: 31197102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations.
    Huang Z; Zhang D; Chen SC; Thompson JA; McLaren T; Lamey T; De Roach JN; McLenachan S; Chen FK
    Stem Cell Res; 2019 Oct; 40():101549. PubMed ID: 31494449
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Generation of induced pluripotent stem cell (iPSC) line from Charcot-Marie-Tooth disease patient with MPZ mutation (CMT1B).
    Son D; Kang PJ; Yun W; You S
    Stem Cell Res; 2017 Oct; 24():5-7. PubMed ID: 29034895
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generation of three isogenic control lines from patient-derived iPSCs carrying bi-allelic ABCA4 variants underlying Stargardt disease.
    Karjosukarso DW; Bukkems F; Duijkers L; Leijsten N; Collin RWJ
    Stem Cell Res; 2023 Sep; 71():103169. PubMed ID: 37480818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene.
    Zaw K; Wong EYM; Zhang X; Zhang D; Chen SC; Thompson JA; Lamey T; McLaren T; De Roach JN; Wilton SD; Fletcher S; Mitrpant C; Atlas MD; Chen FK; McLenachan S
    Stem Cell Res; 2020 Dec; 50():102129. PubMed ID: 33360097
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.