204 related articles for article (PubMed ID: 38430393)
1. Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations.
Lebeda D; Fierenz A; Werfel L; Rosin-Arbesfeld R; Hofhuis J; Thoms S
J Mol Med (Berl); 2024 May; 102(5):641-653. PubMed ID: 38430393
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome.
Wong KM; Wegener E; Baradaran-Heravi A; Huppke B; Gärtner J; Huppke P
Int J Mol Sci; 2023 Jul; 24(14):. PubMed ID: 37511424
[TBL] [Abstract][Full Text] [Related]
3. Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutations.
Vecsler M; Ben Zeev B; Nudelman I; Anikster Y; Simon AJ; Amariglio N; Rechavi G; Baasov T; Gak E
PLoS One; 2011; 6(6):e20733. PubMed ID: 21695138
[TBL] [Abstract][Full Text] [Related]
4. Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model.
Brendel C; Belakhov V; Werner H; Wegener E; Gärtner J; Nudelman I; Baasov T; Huppke P
J Mol Med (Berl); 2011 Apr; 89(4):389-98. PubMed ID: 21120444
[TBL] [Abstract][Full Text] [Related]
5. Stop Codon Context-Specific Induction of Translational Readthrough.
Schilff M; Sargsyan Y; Hofhuis J; Thoms S
Biomolecules; 2021 Jul; 11(7):. PubMed ID: 34356630
[TBL] [Abstract][Full Text] [Related]
6. Aminoglycoside-mediated partial suppression of MECP2 nonsense mutations responsible for Rett syndrome in vitro.
Popescu AC; Sidorova E; Zhang G; Eubanks JH
J Neurosci Res; 2010 Aug; 88(11):2316-24. PubMed ID: 20623622
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Serum starvation enhances nonsense mutation readthrough.
Wittenstein A; Caspi M; David Y; Shorer Y; Nadar-Ponniah PT; Rosin-Arbesfeld R
J Mol Med (Berl); 2019 Dec; 97(12):1695-1710. PubMed ID: 31786671
[TBL] [Abstract][Full Text] [Related]
9. Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
Pitcher MR; Herrera JA; Buffington SA; Kochukov MY; Merritt JK; Fisher AR; Schanen NC; Costa-Mattioli M; Neul JL
Hum Mol Genet; 2015 May; 24(9):2662-72. PubMed ID: 25634563
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibiotics.
Brendel C; Klahold E; Gärtner J; Huppke P
Pediatr Res; 2009 May; 65(5):520-3. PubMed ID: 19190538
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Translational readthrough potential of natural termination codons in eucaryotes--The impact of RNA sequence.
Dabrowski M; Bukowy-Bieryllo Z; Zietkiewicz E
RNA Biol; 2015; 12(9):950-8. PubMed ID: 26176195
[TBL] [Abstract][Full Text] [Related]
14. Induction of Translational Readthrough across the Thalassemia-Causing Premature Stop Codon in β-Globin-Encoding mRNA.
Kar D; Sellamuthu K; Kumar SD; Eswarappa SM
Biochemistry; 2020 Jan; 59(1):80-84. PubMed ID: 31577420
[TBL] [Abstract][Full Text] [Related]
15. Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots.
Wan M; Lee SS; Zhang X; Houwink-Manville I; Song HR; Amir RE; Budden S; Naidu S; Pereira JL; Lo IF; Zoghbi HY; Schanen NC; Francke U
Am J Hum Genet; 1999 Dec; 65(6):1520-9. PubMed ID: 10577905
[TBL] [Abstract][Full Text] [Related]
16. Transcript-specific induction of stop codon readthrough using a CRISPR-dCas13 system.
Manjunath LE; Singh A; Devi Kumar S; Vasu K; Kar D; Sellamuthu K; Eswarappa SM
EMBO Rep; 2024 Apr; 25(4):2118-2143. PubMed ID: 38499809
[TBL] [Abstract][Full Text] [Related]
17. Effects of gentamicin inducing readthrough premature stop Codons: A study of alpha-L-iduronidase nonsense variants in COS-7 Cells.
Ngiwsara L; Sawangareetrakul P; Wattanasirichaigoon D; Tim-Aroon T; Dejkhamron P; Champattanachai V; Ketudat-Cairns JR; Svasti J
Biochem Biophys Res Commun; 2022 Dec; 636(Pt 1):147-154. PubMed ID: 36332477
[TBL] [Abstract][Full Text] [Related]
18. Factors Affecting Readthrough of Natural Versus Premature Termination Codons.
Beryozkin A; Nagel-Wolfum K; Banin E; Sharon D
Adv Exp Med Biol; 2023; 1415():149-155. PubMed ID: 37440028
[TBL] [Abstract][Full Text] [Related]
19. Pseudouridine-mediated stop codon readthrough in
Adachi H; Yu YT
RNA; 2020 Sep; 26(9):1247-1256. PubMed ID: 32434780
[TBL] [Abstract][Full Text] [Related]
20. Translation termination codons in protein synthesis and disease.
Lombardi S; Testa MF; Pinotti M; Branchini A
Adv Protein Chem Struct Biol; 2022; 132():1-48. PubMed ID: 36088072
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
