These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
230 related articles for article (PubMed ID: 35054841)
1. Premature Termination Codon in 5' Region of Desmoplakin and Plakoglobin Genes May Escape Nonsense-Mediated Decay through the Reinitiation of Translation. Vallverdú-Prats M; Brugada R; Alcalde M Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35054841 [TBL] [Abstract][Full Text] [Related]
2. Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells. Asimaki A; Protonotarios A; James CA; Chelko SP; Tichnell C; Murray B; Tsatsopoulou A; Anastasakis A; te Riele A; Kléber AG; Judge DP; Calkins H; Saffitz JE Circ Arrhythm Electrophysiol; 2016 Feb; 9(2):e003688. PubMed ID: 26850880 [TBL] [Abstract][Full Text] [Related]
3. [The NMD escape mechanism and its application in disease therapy]. Cheng MM; Cao YY Yi Chuan; 2020 Apr; 42(4):354-362. PubMed ID: 32312704 [TBL] [Abstract][Full Text] [Related]
4. Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia. Bauce B; Nava A; Beffagna G; Basso C; Lorenzon A; Smaniotto G; De Bortoli M; Rigato I; Mazzotti E; Steriotis A; Marra MP; Towbin JA; Thiene G; Danieli GA; Rampazzo A Heart Rhythm; 2010 Jan; 7(1):22-9. PubMed ID: 20129281 [TBL] [Abstract][Full Text] [Related]
5. Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients. Pilichou K; Lazzarini E; Rigato I; Celeghin R; De Bortoli M; Perazzolo Marra M; Cason M; Jongbloed J; Calore M; Rizzo S; Regazzo D; Poloni G; Iliceto S; Daliento L; Delise P; Corrado D; Van Tintelen JP; Thiene G; Rampazzo A; Basso C; Bauce B; Lorenzon A; Occhi G Circ Arrhythm Electrophysiol; 2017 Oct; 10(10):. PubMed ID: 29038103 [TBL] [Abstract][Full Text] [Related]
8. Nonsense suppression therapies in human genetic diseases. Martins-Dias P; Romão L Cell Mol Life Sci; 2021 May; 78(10):4677-4701. PubMed ID: 33751142 [TBL] [Abstract][Full Text] [Related]
9. Targeted pseudouridylation: An approach for suppressing nonsense mutations in disease genes. Adachi H; Pan Y; He X; Chen JL; Klein B; Platenburg G; Morais P; Boutz P; Yu YT Mol Cell; 2023 Feb; 83(4):637-651.e9. PubMed ID: 36764303 [TBL] [Abstract][Full Text] [Related]
10. Features and factors that dictate if terminating ribosomes cause or counteract nonsense-mediated mRNA decay. Embree CM; Abu-Alhasan R; Singh G J Biol Chem; 2022 Nov; 298(11):102592. PubMed ID: 36244451 [TBL] [Abstract][Full Text] [Related]
11. Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. Ohno S; Nagaoka I; Fukuyama M; Kimura H; Itoh H; Makiyama T; Shimizu A; Horie M Circ J; 2013; 77(6):1534-42. PubMed ID: 23514727 [TBL] [Abstract][Full Text] [Related]
12. Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy. Christensen AH; Benn M; Bundgaard H; Tybjaerg-Hansen A; Haunso S; Svendsen JH J Med Genet; 2010 Nov; 47(11):736-44. PubMed ID: 20864495 [TBL] [Abstract][Full Text] [Related]
13. Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Groeneweg JA; Ummels A; Mulder M; Bikker H; van der Smagt JJ; van Mil AM; Homfray T; Post JG; Elvan A; van der Heijden JF; Houweling AC; Jongbloed JD; Wilde AA; van Tintelen JP; Hauer RN; Dooijes D Heart Rhythm; 2014 Nov; 11(11):2010-7. PubMed ID: 25087486 [TBL] [Abstract][Full Text] [Related]
14. Transcripts expressed using a bicistronic vector pIREShyg2 are sensitized to nonsense-mediated mRNA decay. Shikama Y; Hu H; Ohno M; Matsuoka I; Shichishima T; Kimura J BMC Mol Biol; 2010 Jun; 11():42. PubMed ID: 20513249 [TBL] [Abstract][Full Text] [Related]
15. Nonsense mutation-dependent reinitiation of translation in mammalian cells. Cohen S; Kramarski L; Levi S; Deshe N; Ben David O; Arbely E Nucleic Acids Res; 2019 Jul; 47(12):6330-6338. PubMed ID: 31045216 [TBL] [Abstract][Full Text] [Related]
16. Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts. Vite A; Gandjbakhch E; Prost C; Fressart V; Fouret P; Neyroud N; Gary F; Donal E; Varnous S; Fontaine G; Fornes P; Hidden-Lucet F; Komajda M; Charron P; Villard E PLoS One; 2013; 8(9):e75082. PubMed ID: 24086444 [TBL] [Abstract][Full Text] [Related]
17. Autosomal-dominant biventricular arrhythmogenic cardiomyopathy in a large family with a novel in-frame DSP nonsense mutation. Singh SM; Casey SA; Berg AA; Abdelhadi RH; Katsiyiannis WT; Bennett MK; Mackey-Bojack S; Duncanson ER; Sengupta JD Am J Med Genet A; 2018 Jul; 176(7):1622-1626. PubMed ID: 30160835 [TBL] [Abstract][Full Text] [Related]
19. Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy. Lin X; Ma Y; Cai Z; Wang Q; Wang L; Huo Z; Hu D; Wang J; Xiang M BMC Cardiovasc Disord; 2020 Feb; 20(1):74. PubMed ID: 32046637 [TBL] [Abstract][Full Text] [Related]