195 related articles for article (PubMed ID: 36624150)
1. Programmable A-to-Y base editing by fusing an adenine base editor with an N-methylpurine DNA glycosylase.
Tong H; Wang X; Liu Y; Liu N; Li Y; Luo J; Ma Q; Wu D; Li J; Xu C; Yang H
Nat Biotechnol; 2023 Aug; 41(8):1080-1084. PubMed ID: 36624150
[TBL] [Abstract][Full Text] [Related]
2. Programmable deaminase-free base editors for G-to-Y conversion by engineered glycosylase.
Tong H; Liu N; Wei Y; Zhou Y; Li Y; Wu D; Jin M; Cui S; Li H; Li G; Zhou J; Yuan Y; Zhang H; Shi L; Yao X; Yang H
Natl Sci Rev; 2023 Aug; 10(8):nwad143. PubMed ID: 37404457
[TBL] [Abstract][Full Text] [Related]
3. Adenine base editor incorporating the N-methylpurine DNA glycosylase MPGv3 enables efficient A-to-K base editing in rice.
Wu X; Ren B; Liu L; Qiu S; Li X; Li P; Yan F; Lin H; Zhou X; Zhang D; Zhou H
Plant Commun; 2023 Nov; 4(6):100668. PubMed ID: 37528583
[No Abstract] [Full Text] [Related]
4. Magnesium, essential for base excision repair enzymes, inhibits substrate binding of N-methylpurine-DNA glycosylase.
Adhikari S; Toretsky JA; Yuan L; Roy R
J Biol Chem; 2006 Oct; 281(40):29525-32. PubMed ID: 16901897
[TBL] [Abstract][Full Text] [Related]
5. Germ line variants of human N-methylpurine DNA glycosylase show impaired DNA repair activity and facilitate 1,N6-ethenoadenine-induced mutations.
Adhikari S; Chetram MA; Woodrick J; Mitra PS; Manthena PV; Khatkar P; Dakshanamurthy S; Dixon M; Karmahapatra SK; Nuthalapati NK; Gupta S; Narasimhan G; Mazumder R; Loffredo CA; Üren A; Roy R
J Biol Chem; 2015 Feb; 290(8):4966-4980. PubMed ID: 25538240
[TBL] [Abstract][Full Text] [Related]
6. Excised damaged base determines the turnover of human N-methylpurine-DNA glycosylase.
Adhikari S; Uren A; Roy R
DNA Repair (Amst); 2009 Oct; 8(10):1201-6. PubMed ID: 19616486
[TBL] [Abstract][Full Text] [Related]
7. Protein language models-assisted optimization of a uracil-N-glycosylase variant enables programmable T-to-G and T-to-C base editing.
He Y; Zhou X; Chang C; Chen G; Liu W; Li G; Fan X; Sun M; Miao C; Huang Q; Ma Y; Yuan F; Chang X
Mol Cell; 2024 Apr; 84(7):1257-1270.e6. PubMed ID: 38377993
[TBL] [Abstract][Full Text] [Related]
8. Glycosylase base editors enable C-to-A and C-to-G base changes.
Zhao D; Li J; Li S; Xin X; Hu M; Price MA; Rosser SJ; Bi C; Zhang X
Nat Biotechnol; 2021 Jan; 39(1):35-40. PubMed ID: 32690970
[TBL] [Abstract][Full Text] [Related]
9. CRISPR single base-editing: in silico predictions to variant clonal cell lines.
Dickson KA; Field N; Blackman T; Ma Y; Xie T; Kurangil E; Idrees S; Rathnayake SNH; Mahbub RM; Faiz A; Marsh DJ
Hum Mol Genet; 2023 Aug; 32(17):2704-2716. PubMed ID: 37369005
[TBL] [Abstract][Full Text] [Related]
10. A distinct TthMutY bifunctional glycosylase that hydrolyzes not only adenine but also thymine opposite 8-oxoguanine in the hyperthermophilic bacterium, Thermus thermophilus.
Back JH; Park JH; Chung JH; Kim DS; Han YS
DNA Repair (Amst); 2006 Aug; 5(8):894-903. PubMed ID: 16781198
[TBL] [Abstract][Full Text] [Related]
11. Adenine base-editing-mediated exon skipping induces gene knockout in cultured pig cells.
Zhu XX; Pan JS; Lin T; Yang YC; Huang QY; Yang SP; Qu ZX; Lin ZS; Wen JC; Yan AF; Feng J; Liu L; Zhang XL; Lu JH; Tang DS
Biotechnol Lett; 2022 Jan; 44(1):59-76. PubMed ID: 34997407
[TBL] [Abstract][Full Text] [Related]
12. [Recent advances and applications of base editing systems].
Xu X; Liu M
Sheng Wu Gong Cheng Xue Bao; 2021 Jul; 37(7):2307-2321. PubMed ID: 34327897
[TBL] [Abstract][Full Text] [Related]
13. Altered expression of the DNA repair protein, N-methylpurine-DNA glycosylase (MPG) in breast cancer.
Cerda SR; Turk PW; Thor AD; Weitzman SA
FEBS Lett; 1998 Jul; 431(1):12-8. PubMed ID: 9684856
[TBL] [Abstract][Full Text] [Related]
14. Cloning and expression in Escherichia coli of a human cDNA encoding the DNA repair protein N-methylpurine-DNA glycosylase.
Chakravarti D; Ibeanu GC; Tano K; Mitra S
J Biol Chem; 1991 Aug; 266(24):15710-5. PubMed ID: 1874728
[TBL] [Abstract][Full Text] [Related]
15. A novel fluorometric oligonucleotide assay to measure O( 6)-methylguanine DNA methyltransferase, methylpurine DNA glycosylase, 8-oxoguanine DNA glycosylase and abasic endonuclease activities: DNA repair status in human breast carcinoma cells overexpressing methylpurine DNA glycosylase.
Kreklau EL; Limp-Foster M; Liu N; Xu Y; Kelley MR; Erickson LC
Nucleic Acids Res; 2001 Jun; 29(12):2558-66. PubMed ID: 11410664
[TBL] [Abstract][Full Text] [Related]
16. The Bacillus subtilis counterpart of the mammalian 3-methyladenine DNA glycosylase has hypoxanthine and 1,N6-ethenoadenine as preferred substrates.
Aamodt RM; Falnes PØ; Johansen RF; Seeberg E; Bjørås M
J Biol Chem; 2004 Apr; 279(14):13601-6. PubMed ID: 14729667
[TBL] [Abstract][Full Text] [Related]
17. Interaction of the recombinant human methylpurine-DNA glycosylase (MPG protein) with oligodeoxyribonucleotides containing either hypoxanthine or abasic sites.
Miao F; Bouziane M; O'Connor TR
Nucleic Acids Res; 1998 Sep; 26(17):4034-41. PubMed ID: 9705516
[TBL] [Abstract][Full Text] [Related]
18. Effects of substrate specificity on initiating the base excision repair of N-methylpurines by variant human 3-methyladenine DNA glycosylases.
Connor EE; Wilson JJ; Wyatt MD
Chem Res Toxicol; 2005 Jan; 18(1):87-94. PubMed ID: 15651853
[TBL] [Abstract][Full Text] [Related]
19. N-terminal extension of N-methylpurine DNA glycosylase is required for turnover in hypoxanthine excision reaction.
Adhikari S; Uren A; Roy R
J Biol Chem; 2007 Oct; 282(41):30078-84. PubMed ID: 17716976
[TBL] [Abstract][Full Text] [Related]
20. Designing an Elusive C•G→G•C CRISPR Base Editor.
Gajula KS
Trends Biochem Sci; 2019 Feb; 44(2):91-94. PubMed ID: 30446374
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
