NMD: a multifaceted response to premature translational termination

P bodies and the control of mRNA translation and degradation

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The highways and byways of mRNA decay

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PTC124 targets genetic disorders caused by nonsense mutations

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The spliceosome deposits multiple proteins 20–24 nucleotides upstream of mRNA exon–exon junctions

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P bodies: at the crossroads of post-transcriptional pathways

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Nonsense surveillance regulates expression of diverse classes of mammalian transcripts and mutes genomic noise

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The exon–exon junction complex provides a binding platform for factors involved in mRNA export and nonsense‐mediated mRNA decay

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Endonucleolytic cleavage of eukaryotic mRNAs with stalls in translation elongation

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Binding of a novel SMG-1–Upf1–eRF1–eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decayPreprint

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Translational control in biology and medicine

Mathews, M. B., Sonenberg, N., & Hershey, J. W. B. (2007) · Cited by 661

Circular intronic long noncoding RNAs

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RefSeq: an update on mammalian reference sequences

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Complexity of the Alternative Splicing Landscape in Plants

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Nonsense-mediated mRNA decay: an intricate machinery that shapes transcriptomes

Lykke‐Andersen, S., & Jensen, T. H. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4063 · Cited by 843

Mechanism and regulation of the nonsense-mediated decay pathway

Hug, N., Longman, D., & Cáceres, J. F. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw010 · Cited by 535

Cancer-Associated SF3B1 Hotspot Mutations Induce Cryptic 3′ Splice Site Selection through Use of a Different Branch Point

Darman, R. B., Seiler, M., Agrawal, A. A., Lim, K., Peng, S., Aird, D. R., Bailey, S., Bhavsar, E. B., Chan, B., Colla, S., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.053 · Cited by 472

Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types

Seiler, M., Peng, S., Agrawal, A. A., Palacino, J. J., Teng, T., Zhu, P., Smith, P. G., Johnson, R., Demchok, J. A., Felau, I., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.088 · Cited by 445

Regnase-1 and Roquin Regulate a Common Element in Inflammatory mRNAs by Spatiotemporally Distinct Mechanisms

Mino, T., Murakawa, Y., Fukao, A., Vandenbon, A., Wessels, H.-H., Ori, D., Uehata, T., Tartey, S., Akira, S., Suzuki, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2015.04.029 · Cited by 390

Organizing Principles of Mammalian Nonsense-Mediated mRNA Decay

Popp, M. W., & Maquat, L. E. (2013) · Annual Review of Genetics · doi:10.1146/annurev-genet-111212-133424 · Cited by 387

Nonsense-mediated mRNA decay — Mechanisms of substrate mRNA recognition and degradation in mammalian cells

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A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

Helsmoortel, C., Vulto-van Silfhout, A. T., Coe, B. P., Vandeweyer, G., Rooms, L., van den Ende, J., Schuurs-Hoeijmakers, J. H. M., Marcelis, C. L., Willemsen, M. H., Vissers, L. E. L. M., et al. (2014) · Nature Genetics · doi:10.1038/ng.2899 · Cited by 354

Mutant Cohesin in Premature Ovarian Failure

Caburet, S., Arboleda, V. A., Llano, E., Overbeek, P. A., Barbero, J. L., Oka, K., Harrison, W. R., Vaiman, D., Ben‐Neriah, Z., García‐Tuñón, I., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1309635 · Cited by 303

Nonsense-Mediated mRNA Decay: Degradation of Defective Transcripts Is Only Part of the Story

He, F., & Jacobson, A. (2015) · Annual Review of Genetics · doi:10.1146/annurev-genet-112414-054639 · Cited by 303

The exon junction complex as a node of post-transcriptional networks

Hir, H. L., Saulière, J., & Wang, Z. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2015.7 · Cited by 280

Global analyses of UPF1 binding and function reveal expanded scope of nonsense-mediated mRNA decayPreprint

Hurt, J. A., Robertson, A. D., & Burge, C. B. (2013) · Genome Research · doi:10.1101/gr.157354.113 · Cited by 288

The combined human sperm proteome: cellular pathways and implications for basic and clinical science

Amaral, A., Castillo, J., Ramalho‐Santos, J., & Oliva, R. (2013) · Human Reproduction Update · doi:10.1093/humupd/dmt046 · Cited by 280

Cdc48-associated complex bound to 60S particles is required for the clearance of aberrant translation products

Defenouillère, Q., Yao, Y., Mouaikel, J., Namane, A., Galopier, A., Decourty, L., Doyen, A., Malabat, C., Saveanu, C., Jacquier, A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221724110 · Cited by 246

Roadblocks and resolutions in eukaryotic translation

Schuller, A. P., & Green, R. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0011-4 · Cited by 245

Nonsense-mediated decay in genetic disease: Friend or foe?

Miller, J. N., & Pearce, D. A. (2014) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2014.05.001 · Cited by 231

Primate-Specific ORF0 Contributes to Retrotransposon-Mediated Diversity

Denli, A. M., Narvaiza, I., Kerman, B. E., Pena, M., Benner, C. W., Marchetto, M. C., Diedrich, J. K., Aslanian, A., Ma, J., Moresco, J. J., et al. (2015) · Cell · doi:10.1016/j.cell.2015.09.025 · Cited by 244

Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy

Lee, J., Termglinchan, V., Diecke, S., Itzhaki, I., Lam, C. K., Garg, P., Lau, E., Greenhaw, M., Seeger, T., Wu, H., et al. (2019) · Nature · doi:10.1038/s41586-019-1406-x · Cited by 222

Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles

Coban-Akdemir, Z., White, J. J., Song, X., Jhangiani, S. N., Fatih, J. M., Gambin, T., Bayram, Y., Chinn, I. K., Karaca, E., Punetha, J., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.06.009 · Cited by 219

The SMG5–SMG7 heterodimer directly recruits the CCR4–NOT deadenylase complex to mRNAs containing nonsense codons via interaction with POP2Preprint

Loh, B., Jonas, S., & Izaurralde, E. (2013) · Genes & Development · doi:10.1101/gad.226951.113 · Cited by 212

Nonsense-Mediated mRNA Decay Begins Where Translation EndsPreprint

Karousis, E. D., & Mühlemann, O. (2018) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a032862 · Cited by 212

An Active Role for the Ribosome in Determining the Fate of Oxidized mRNA

Simms, C. L., Hudson, B. H., Mosior, J., Rangwala, A. S., & Zaher, H. S. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.042 · Cited by 211

Cap-binding complex (CBC)

Gonatopoulos-Pournatzis, T., & Cowling, V. H. (2013) · Biochemical Journal · doi:10.1042/bj20131214 · Cited by 208

Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans

Cenik, C., Cenik, E. S., Byeon, G. W., Grubert, F., Candille, S. I., Spacek, D., Alsallakh, B., Tilgner, H., Araya, C. L., Tang, H., et al. (2015) · Genome Research · doi:10.1101/gr.193342.115 · Cited by 208

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

van Bon, B. W. M., Coe, B. P., Bernier, R., Green, C., Gerdts, J., Witherspoon, K., Kleefstra, T., Willemsen, M. H., Kumar, R., Bosco, P., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.5 · Cited by 204

MOV10 Is a 5′ to 3′ RNA Helicase Contributing to UPF1 mRNA Target Degradation by Translocation along 3′ UTRs

Gregersen, L. H., Schueler, M., Munschauer, M., Mastrobuoni, G., Chen, W., Kempa, S., Dieterich, C., & Landthaler, M. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.03.017 · Cited by 209

Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genesPreprint

Lykke‐Andersen, S., Chen, Y., Ardal, B. K., Lilje, B., Waage, J., Sandelin, A., & Jensen, T. H. (2014) · Genes & Development · doi:10.1101/gad.246538.114 · Cited by 200

The intimate relationships of mRNA decay and translation

Roy, B., & Jacobson, A. (2013) · Trends in Genetics · doi:10.1016/j.tig.2013.09.002 · Cited by 177

Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia

Zech, M., Boesch, S., Maier, E. M., Borggraefe, I., Vill, K., Laccone, F. A., Pilshofer, V., Ceballos-Baumann, A., Alhaddad, B., Berutti, R., et al. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.10.010 · Cited by 178

Translation-dependent displacement of UPF1 from coding sequences causes its enrichment in 3′ UTRs

Zünd, D., Gruber, A. R., Zavolan, M., & Mühlemann, O. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2635 · Cited by 171

The Host Nonsense-Mediated mRNA Decay Pathway Restricts Mammalian RNA Virus Replication

Balistreri, G., Horváth, P., Schweingruber, C., Zünd, D., McInerney, G. M., Merits, A., Mühlemann, O., Azzalin, C. M., & Helenius, A. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.08.007 · Cited by 168

Functionally uncoupled transcription–translation in Bacillus subtilis

Johnson, G. E., Lalanne, J., Peters, M. L., & Li, G. (2020) · Nature · doi:10.1038/s41586-020-2638-5 · Cited by 175

The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processingPreprint

Vourekas, A., Zheng, K., Fu, Q., Maragkakis, M., Alexiou, P., Ma, J., Pillai, R. S., Mourelatos, Z., & Wang, P. J. (2015) · Genes & Development · doi:10.1101/gad.254631.114 · Cited by 168

Nonsense-Mediated Decay Serves as a General Viral Restriction Mechanism in Plants

Garcia, D., Garcia, S., & Voinnet, O. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.08.001 · Cited by 161

The CCAAT box-binding transcription factor NF-YA1 controls rhizobial infection

Laporte, P., Lepage, A., Fournier, J., Catrice, O., Moreau, S., Jardinaud, M., Mun, J., Larrainzar, E., Cook, D. R., Gamas, P., et al. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert392 · Cited by 161

Update on Selenoprotein Biosynthesis

Bulteau, A., & Chavatte, L. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6391 · Cited by 161

Synthetic Aminoglycosides Efficiently Suppress Cystic Fibrosis Transmembrane Conductance Regulator Nonsense Mutations and Are Enhanced by Ivacaftor

Xue, X., Mutyam, V., Tang, L., Biswas, S., Du, M., Jackson, L. A., Dai, Y., Белахов, В. В., Shalev, M., Chen, F., et al. (2013) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2013-0282oc · Cited by 161

Human Upf1 is a highly processive RNA helicase and translocase with RNP remodelling activities

Fiorini, F., Bagchi, D., Hir, H. L., & Croquette, V. (2015) · Nature Communications · doi:10.1038/ncomms8581 · Cited by 148

Mechanism and Regulation of Protein Synthesis in Saccharomyces cerevisiae

Dever, T. E., Kinzy, T. G., & Pavitt, G. D. (2016) · Genetics · doi:10.1534/genetics.115.186221 · Cited by 159

Current status and new features of the Consensus Coding Sequence database

Farrell, C. M., O’Leary, N. A., Harte, R., Loveland, J. E., Wilming, L. G., Wallin, C., Diekhans, M., Barrell, D. G., Searle, S. M. J., Aken, B. L., et al. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1059 · Cited by 142

Comparison of EJC-enhanced and EJC-independent NMD in human cells reveals two partially redundant degradation pathways

Metze, S., Herzog, V. A., Ruepp, M., & Mühlemann, O. (2013) · RNA · doi:10.1261/rna.038893.113 · Cited by 149

Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation

Veitia, R. A., Bottani, S., & Birchler, J. A. (2013) · Trends in Genetics · doi:10.1016/j.tig.2013.04.004 · Cited by 143

Quality control of transcription start site selection by nonsense-mediated-mRNA decay

Malabat, C., Feuerbach, F., Ma, L., Saveanu, C., & Jacquier, A. (2015) · eLife · doi:10.7554/elife.06722 · Cited by 134

Nonsense suppression by near-cognate tRNAs employs alternative base pairing at codon positions 1 and 3

Roy, B., Leszyk, J., Mangus, D. A., & Jacobson, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424127112 · Cited by 140

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis

Kaneb, H., Folkmann, A. W., Belzil, V., Jao, L.-E., Leblond, C. S., Girard, S., Daoud, H., Noreau, A., Rochefort, D. L., Hince, P., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu545 · Cited by 132

Rbfox2 controls autoregulation in RNA-binding protein networksPreprint

Jangi, M., Boutz, P. L., Paul, P., & Sharp, P. A. (2014) · Genes & Development · doi:10.1101/gad.235770.113 · Cited by 136

SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies

Davidsson, J., Puschmann, A., Tedgård, U., Bryder, D., Nilsson, L., & Cammenga, J. (2018) · Leukemia · doi:10.1038/s41375-018-0074-4 · Cited by 129

GNAS Mutations in Pseudohypoparathyroidism Type 1a and Related Disorders

Lemos, M. C., & Thakker, R. V. (2014) · Human Mutation · doi:10.1002/humu.22696 · Cited by 128

Simultaneous DNA and RNA Mapping of Somatic Mitochondrial Mutations across Diverse Human Cancers

Stewart, J. B., Alaei-Mahabadi, B., Sabarinathan, R., Samuelsson, T., Gorodkin, J., Gustafsson, C. M., & Larsson, E. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005333 · Cited by 126

An atlas of chromatoid body components

Meikar, O., Vagin, V. V., Chalmel, F., Sõstar, K., Lardenois, A., Hammell, M., Jin, Y., Ros, M. D., Wasik, K. A., Toppari, J., et al. (2014) · RNA · doi:10.1261/rna.043729.113 · Cited by 135

How to get away with nonsense: Mechanisms and consequences of escape from nonsense‐mediated RNA decay

Dyle, M. C., Kolakada, D., Cortázar, M. A., & Jagannathan, S. (2019) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1560 · Cited by 124

Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons

Havlicek, S., Kohl, Z., Mishra, H. K., Prots, I., Eberhardt, E., Denguir, N., Wend, H., Plötz, S., Boyer, L. F., Marchetto, M. C., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt644 · Cited by 122

Smg6/Est1 licenses embryonic stem cell differentiation via nonsense‐mediated mRNA decay

Li, T., Shi, Y. X., Wang, P., Guachalla, L. M., Sun, B., Jörß, T., Chen, Y., Groth, M., Krueger, A., Platzer, M., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201489947 · Cited by 128

Principles of Virus Uncoating: Cues and the Snooker Ball

Yamauchi, Y., & Greber, U. F. (2016) · Traffic · doi:10.1111/tra.12387 · Cited by 127

Temporal and spatial characterization of nonsense-mediated mRNA decayPreprint

Trcek, T., Sato, H., Singer, R. H., & Maquat, L. E. (2013) · Genes & Development · doi:10.1101/gad.209635.112 · Cited by 123

Surveillance pathways rescuing eukaryotic ribosomes lost in translation

Graille, M., & Séraphin, B. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3457 · Cited by 133

Transcripts from downstream alternative transcription start sites evade uORF-mediated inhibition of gene expression in Arabidopsis

Kurihara, Y., Makita, Y., Kawashima, M., Fujita, T., Iwasaki, S., & Matsui, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1804971115 · Cited by 119

Phospho-dependent and phospho-independent interactions of the helicase UPF1 with the NMD factors SMG5–SMG7 and SMG6

Chakrabarti, S., Bonneau, F., Schüssler, S., Eppinger, E., & Conti, E. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku578 · Cited by 115

Target Discrimination in Nonsense-Mediated mRNA Decay Requires Upf1 ATPase Activity

Lee, S. R., Pratt, G. A., Martinez, F. J., Yeo, G. W.-M., & Lykke‐Andersen, J. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.06.036 · Cited by 111

Changes in splicing factor expression are associated with advancing age in man

Holly, A. C., Melzer, D. R., Pilling, L. C., Fellows, A. D., Tanaka, T., Ferrucci, L., & Harries, L. W. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.05.006 · Cited by 111

Identification of SMG6 cleavage sites and a preferred RNA cleavage motif by global analysis of endogenous NMD targets in human cells

Schmidt, S. A., Foley, P. L., Jeong, D., Rymarquis, L. A., Doyle, F., Tenenbaum, S. A., Belasco, J. G., & Green, P. J. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1258 · Cited by 110

Quality control of chemically damaged RNA

Simms, C. L., & Zaher, H. S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2261-7 · Cited by 110

Ribosome‐based quality control of mRNA and nascent peptides

Simms, C. L., Thomas, E. N., & Zaher, H. S. (2016) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1366 · Cited by 108

Long-read sequencing of nascent RNA reveals coupling among RNA processing eventsPreprint

Herzel, L., Straube, K., & Neugebauer, K. M. (2018) · Genome Research · doi:10.1101/gr.232025.117 · Cited by 107

Canonical Poly(A) Polymerase Activity Promotes the Decay of a Wide Variety of Mammalian Nuclear RNAs

Bresson, S. M., Hunter, O. V., Hunter, A. C., & Conrad, N. K. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005610 · Cited by 112

Unique Aspects of Plant Nonsense-Mediated mRNA Decay

Shaul, O. (2015) · Trends in Plant Science · doi:10.1016/j.tplants.2015.08.011 · Cited by 106

Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells

Schwarz, N., Carr, A. F., Lane, A., Möller, F., Chen, L., Aguilà, M., Nommiste, B., Muthiah, M. N., Kanuga, N., Wolfrum, U., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu509 · Cited by 112

High-resolution profiling of NMD targets in yeast reveals translational fidelity as a basis for substrate selection

Celik, A., Baker, R., He, F., & Jacobson, A. (2017) · RNA · doi:10.1261/rna.060541.116 · Cited by 108

Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR

Panagiotou, E. S., Sanjurjo-Soriano, C., Poulter, J. A., Lord, E. C., Dzulova, D., Kondo, H., Hiyoshi, A., Chung, B. H., Chu, Y. W. Y., Lai, C. H. Y., et al. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.05.001 · Cited by 107

Lost in Translation: Ribosome-Associated mRNA and Protein Quality Controls

Karamyshev, A. L., & Karamysheva, Z. N. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00431 · Cited by 103

Targeting Nonsense Mutations in Diseases with Translational Read-Through-Inducing Drugs (TRIDs)

Nagel‐Wolfrum, K., Möller, F., Penner, I., Baasov, T., & Uwe Wolfrum, B. (2016) · BioDrugs · doi:10.1007/s40259-016-0157-6 · Cited by 101

A dynamic intron retention program in the mammalian megakaryocyte and erythrocyte lineages

Edwards, C. R., Ritchie, W., Wong, J. J. L., Schmitz, U., Middleton, R. M., An, X., Mohandas, N., Rasko, J. E. J., & Blobel, G. A. (2016) · Blood · doi:10.1182/blood-2016-01-692764 · Cited by 101

Emerging roles for RNA degradation in viral replication and antiviral defense

Abernathy, E., & Glaunsinger, B. A. (2015) · Virology · doi:10.1016/j.virol.2015.02.007 · Cited by 98

Translation‐coupled mRNA quality control mechanisms

Monaghan, L., Longman, D., & Cáceres, J. F. (2023) · The EMBO Journal · doi:10.15252/embj.2023114378 · Cited by 98

Transcriptome-wide modulation of splicing by the Exon Junction Complex

Wang, Z., Murigneux, V., & Hir, H. L. (2014) · Genome biology · doi:10.1186/preaccept-1827287072145398 · Cited by 97

Nonsense-mediated mRNA decay occurs during eIF4F-dependent translation in human cells

Durand, S., & Lykke‐Andersen, J. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2575 · Cited by 107

eIF4E-bound mRNPs are substrates for nonsense-mediated mRNA decay in mammalian cells

Rufener, S. C., & Mühlemann, O. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2576 · Cited by 107

UPF2-Dependent Nonsense-Mediated mRNA Decay Pathway Is Essential for Spermatogenesis by Selectively Eliminating Longer 3'UTR Transcripts

Bao, J., Vitting‐Seerup, K., Waage, J., Tang, C., Ge, Y. C., Porse, B. T., & Yan, W. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1005863 · Cited by 98

Identification of a DNA Damage–Induced Alternative Splicing Pathway That Regulates p53 and Cellular Senescence Markers

Chen, J., Crutchley, J., Zhang, D., Owzar, K., & Kastan, M. B. (2017) · Cancer Discovery · doi:10.1158/2159-8290.cd-16-0908 · Cited by 93

Interrelations between translation and general mRNA degradation in yeast

Huch, S., & Nissan, T. A. (2014) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1244 · Cited by 97

DHX34 and NBAS form part of an autoregulatory NMD circuit that regulates endogenous RNA targets in human cells, zebrafish and Caenorhabditis elegans

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