118 related articles for article (PubMed ID: 38653148)
1. Generation of a KCNQ1 (c.1032 + 2 T > C) mutant human embryonic stem cell line via CRISPR base editing.
Jiang X; Fu C; Liu Q; Gao J
Stem Cell Res; 2024 Jun; 77():103425. PubMed ID: 38653148
[TBL] [Abstract][Full Text] [Related]
2. Generation of a human embryonic stem cell line WAe009-A-79 carrying a long QT syndrome mutation in KCNQ1.
Wang H; Guo T; Lan F
Stem Cell Res; 2023 Aug; 70():103119. PubMed ID: 37244124
[TBL] [Abstract][Full Text] [Related]
3. Establishment of a KCNQ1 homozygous knockout human embryonic stem cell line by episomal vector-based CRISPR/Cas9 system.
Liu X; Zhang S; Chang Y; Wu F; Bai R
Stem Cell Res; 2021 Aug; 55():102467. PubMed ID: 34343827
[TBL] [Abstract][Full Text] [Related]
4. KCNQ1-deficient and KCNQ1-mutant human embryonic stem cell-derived cardiomyocytes for modeling QT prolongation.
Song Y; Guo T; Jiang Y; Zhu M; Wang H; Lu W; Jiang M; Qi M; Lan F; Cui M
Stem Cell Res Ther; 2022 Jun; 13(1):287. PubMed ID: 35765105
[TBL] [Abstract][Full Text] [Related]
5. Generation of induced pluripotent stem cell lines from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene.
Ren L; Jahng JWS; Belbachir N; Cook Z; Rivero GC; Perez MV; Wu JC
Stem Cell Res; 2024 Aug; 78():103443. PubMed ID: 38763038
[TBL] [Abstract][Full Text] [Related]
6. Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing.
Giri S; Purushottam M; Viswanath B; Muddashetty RS
Stem Cell Res; 2019 Aug; 39():101494. PubMed ID: 31280136
[TBL] [Abstract][Full Text] [Related]
7. Generation of a homozygous HDAC6 knockout human embryonic stem cell line by CRISPR/Cas9 editing.
Xie L; Huang J; Li X; Dai L; Lin X; Zhang J; Luo J; Zhang W
Stem Cell Res; 2019 Dec; 41():101610. PubMed ID: 31775087
[TBL] [Abstract][Full Text] [Related]
8. Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing.
Zhang S; Fan J; Sun H; Hao X; He Y
Stem Cell Res; 2024 Jun; 77():103399. PubMed ID: 38574666
[TBL] [Abstract][Full Text] [Related]
9. Generation of a TRPM8 knockout hESC line (WAe009-A-A) derived from H9 using CRISPR/Cas9.
Bai J; Zhang J; Fu W; Li S; Tian X; Li X; Zhao X; Dong J
Stem Cell Res; 2023 Mar; 67():103040. PubMed ID: 36796252
[TBL] [Abstract][Full Text] [Related]
10. Establishment of a human induced pluripotent stem cell line, KSCBi015-A, from a long QT syndrome type 1 patient harboring a KCNQ1 mutation.
Lee Y; Park H; Kyung Koo S; Kim JH
Stem Cell Res; 2021 Oct; 56():102521. PubMed ID: 34509919
[TBL] [Abstract][Full Text] [Related]
11. Generation of a Nrf2 homozygous knockout human embryonic stem cell line using CRISPR/Cas9.
Kim SJ; Habib O; Kim JS; Han HW; Koo SK; Kim JH
Stem Cell Res; 2017 Mar; 19():46-48. PubMed ID: 28413005
[TBL] [Abstract][Full Text] [Related]
12. Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A.
Yang X; Wu F; Zhong J; Li F
Stem Cell Res; 2021 Mar; 51():102194. PubMed ID: 33517120
[TBL] [Abstract][Full Text] [Related]
13. Generation of an ASGR1 homozygous mutant human embryonic stem cell line WAe001-A-6 using CRISPR/Cas9.
Xu Y; Wu Y; Guo D; Gao G; Lai K; Yang F; Wang K; Wu H; Lai L; Li J; Xu K; Li YX
Stem Cell Res; 2017 Jul; 22():29-32. PubMed ID: 28952928
[TBL] [Abstract][Full Text] [Related]
14. Generation of a human induced pluripotent stem cell line (JSPHi002-A) from a patient with long-QT syndrome type 1 caused by KCNQ1 c.773A > T mutation.
Wang Q; Zhang Y; Zhang F; Li Z; Cheng H; Lin Y; Zhu Y; Chen H; Cui C; Chen M
Stem Cell Res; 2022 Jul; 62():102810. PubMed ID: 35580545
[TBL] [Abstract][Full Text] [Related]
15. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.
Oertli A; Rinné S; Moss R; Kääb S; Seemann G; Beckmann BM; Decher N
Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33498651
[No Abstract] [Full Text] [Related]
16. Generation of NERCe003-A-3, a p53 compound heterozygous mutation human embryonic stem cell line, by CRISPR/Cas9 editing.
Li Y; Huang C; Zha L; Kong M; Yang Q; Zhu Y; Peng Y; Ouyang Q; Lu G; Lin G; Zhou D
Stem Cell Res; 2019 Jan; 34():101371. PubMed ID: 30658254
[TBL] [Abstract][Full Text] [Related]
17. Generation of a GDE heterozygous mutation human embryonic stem cell line WAe001-A-14 by CRISPR/Cas9 editing.
Xu G; Guo D; Wu F; Abbas N; Lai K; Yuan F; You K; Liu Y; Zhuang Y; Wu Y; Xu Y; Chen Y; Yang F; Pan T; Li YX
Stem Cell Res; 2018 Mar; 27():38-41. PubMed ID: 29310060
[TBL] [Abstract][Full Text] [Related]
18. Generation of a TBX20-knockout human embryonic stem line by CRISPR/Cas9 system.
Wu X; Wang X
Stem Cell Res; 2023 Jun; 69():103082. PubMed ID: 36963213
[TBL] [Abstract][Full Text] [Related]
19. Generation of a TLE1 homozygous knockout human embryonic stem cell line using CRISPR-Cas9.
Herring A; Messana A; Bara AM; Hazelbaker DZ; Eggan K; Barrett LE
Stem Cell Res; 2016 Sep; 17(2):430-432. PubMed ID: 27879218
[TBL] [Abstract][Full Text] [Related]
20. Establishment of human embryonic stem cell WAe009-A-88 carrying a long QT syndrome mutation in KCNH2.
Wen H; Sun L; Zhong J; Wu F
Stem Cell Res; 2022 Jul; 62():102795. PubMed ID: 35526388
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]