186 related articles for article (PubMed ID: 32282910)
1. Aminoglycosides are efficient reagents to induce readthrough of premature termination codon in mutant B4GALNT1 genes found in families of hereditary spastic paraplegia.
Yesmin F; Bhuiyan RH; Ohmi Y; Ohkawa Y; Tajima O; Okajima T; Furukawa K; Furukawa K
J Biochem; 2020 Aug; 168(2):103-112. PubMed ID: 32282910
[TBL] [Abstract][Full Text] [Related]
2. Loss of Enzyme Activity in Mutated B4GALNT1 Gene Products in Patients with Hereditary Spastic Paraplegia Results in Relatively Mild Neurological Disorders: Similarity with Phenotypes of B4galnt1 Knockout Mice.
Bhuiyan RH; Ohmi Y; Ohkawa Y; Zhang P; Takano M; Hashimoto N; Okajima T; Furukawa K; Furukawa K
Neuroscience; 2019 Jan; 397():94-106. PubMed ID: 30521973
[TBL] [Abstract][Full Text] [Related]
3. Small molecule Y-320 stimulates ribosome biogenesis, protein synthesis, and aminoglycoside-induced premature termination codon readthrough.
Hosseini-Farahabadi S; Baradaran-Heravi A; Zimmerman C; Choi K; Flibotte S; Roberge M
PLoS Biol; 2021 May; 19(5):e3001221. PubMed ID: 33939688
[TBL] [Abstract][Full Text] [Related]
4. Stop codon context influences genome-wide stimulation of termination codon readthrough by aminoglycosides.
Wangen JR; Green R
Elife; 2020 Jan; 9():. PubMed ID: 31971508
[TBL] [Abstract][Full Text] [Related]
5. Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.
Bukowy-Bieryllo Z; Dabrowski M; Witt M; Zietkiewicz E
RNA Biol; 2016 Oct; 13(10):1041-1050. PubMed ID: 27618201
[TBL] [Abstract][Full Text] [Related]
6. Properties of Non-Aminoglycoside Compounds Used to Stimulate Translational Readthrough of PTC Mutations in Primary Ciliary Dyskinesia.
Dabrowski M; Bukowy-Bieryllo Z; Jackson CL; Zietkiewicz E
Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34066907
[TBL] [Abstract][Full Text] [Related]
7. Readthrough of dystrophin stop codon mutations induced by aminoglycosides.
Howard MT; Anderson CB; Fass U; Khatri S; Gesteland RF; Atkins JF; Flanigan KM
Ann Neurol; 2004 Mar; 55(3):422-6. PubMed ID: 14991821
[TBL] [Abstract][Full Text] [Related]
8. Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency.
Frew J; Baradaran-Heravi A; Balgi AD; Wu X; Yan TD; Arns S; Shidmoossavee FS; Tan J; Jaquith JB; Jansen-West KR; Lynn FC; Gao FB; Petrucelli L; Feldman HH; Mackenzie IR; Roberge M; Nygaard HB
Mol Neurodegener; 2020 Mar; 15(1):21. PubMed ID: 32178712
[TBL] [Abstract][Full Text] [Related]
9. Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy.
Howard MT; Shirts BH; Petros LM; Flanigan KM; Gesteland RF; Atkins JF
Ann Neurol; 2000 Aug; 48(2):164-9. PubMed ID: 10939566
[TBL] [Abstract][Full Text] [Related]
10. Readthrough of nonsense mutation W822X in the SCN5A gene can effectively restore expression of cardiac Na+ channels.
Teng S; Gao L; Paajanen V; Pu J; Fan Z
Cardiovasc Res; 2009 Aug; 83(3):473-80. PubMed ID: 19377070
[TBL] [Abstract][Full Text] [Related]
11. Effect of small molecule eRF3 degraders on premature termination codon readthrough.
Baradaran-Heravi A; Balgi AD; Hosseini-Farahabadi S; Choi K; Has C; Roberge M
Nucleic Acids Res; 2021 Apr; 49(7):3692-3708. PubMed ID: 33764477
[TBL] [Abstract][Full Text] [Related]
12. Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.
Li S; Li J; Shi W; Nie Z; Zhang S; Ma F; Hu J; Chen J; Li P; Xie X
Biomolecules; 2023 Jun; 13(6):. PubMed ID: 37371567
[TBL] [Abstract][Full Text] [Related]
13. Structural annotation of Beta-1,4-N-acetyl galactosaminyltransferase 1 (B4GALNT1) causing Hereditary Spastic Paraplegia 26.
Dad R; Malik U; Javed A; Minassian BA; Hassan MJ
Gene; 2017 Aug; 626():258-263. PubMed ID: 28536081
[TBL] [Abstract][Full Text] [Related]
14. Stop codons and the +4 nucleotide may influence the efficiency of G418 in rescuing nonsense mutations of the HERG gene.
Yu H; Meng Y; Zhang S; Tian C; Wu F; Li N; Li Q; Jin Y; Pu J
Int J Mol Med; 2019 Dec; 44(6):2037-2046. PubMed ID: 31573043
[TBL] [Abstract][Full Text] [Related]
15. Readthrough of ACTN3 577X nonsense mutation produces full-length α-actinin-3 protein.
Harada N; Hatakeyama A; Okuyama M; Miyatake Y; Nakagawa T; Kuroda M; Masumoto S; Tsutsumi R; Nakaya Y; Sakaue H
Biochem Biophys Res Commun; 2018 Jul; 502(3):422-428. PubMed ID: 29857001
[TBL] [Abstract][Full Text] [Related]
16. Nonselective TRPC channel inhibition and suppression of aminoglycoside-induced premature termination codon readthrough by the small molecule AC1903.
Baradaran-Heravi A; Bauer CC; Pickles IB; Hosseini-Farahabadi S; Balgi AD; Choi K; Linley DM; Beech DJ; Roberge M; Bon RS
J Biol Chem; 2022 Feb; 298(2):101546. PubMed ID: 34999117
[TBL] [Abstract][Full Text] [Related]
17. 2-Guanidino-quinazoline promotes the readthrough of nonsense mutations underlying human genetic diseases.
Bidou L; Bugaud O; Merer G; Coupet M; Hatin I; Chirkin E; Karri S; Demais S; François P; Cintrat JC; Namy O
Proc Natl Acad Sci U S A; 2022 Aug; 119(35):e2122004119. PubMed ID: 35994666
[TBL] [Abstract][Full Text] [Related]
18. The synthetic aminoglycoside ELX-02 induces readthrough of G550X-CFTR producing superfunctional protein that can be further enhanced by CFTR modulators.
Chen J; Thrasher K; Fu L; Wang W; Aghamohammadzadeh S; Wen H; Tang L; Keeling KM; Falk Libby E; Bedwell DM; Rowe SM
Am J Physiol Lung Cell Mol Physiol; 2023 Jun; 324(6):L756-L770. PubMed ID: 37014818
[TBL] [Abstract][Full Text] [Related]
19. Frontotemporal dementia non-sense mutation of progranulin rescued by aminoglycosides.
Kuang L; Hashimoto K; Huang EJ; Gentry MS; Zhu H
Hum Mol Genet; 2020 Mar; 29(4):624-634. PubMed ID: 31913476
[TBL] [Abstract][Full Text] [Related]
20. Cancer syndromes and therapy by stop-codon readthrough.
Bordeira-Carriço R; Pêgo AP; Santos M; Oliveira C
Trends Mol Med; 2012 Nov; 18(11):667-78. PubMed ID: 23044248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
