NMD: a multifaceted response to premature translational termination

Cited by (559)

Items 101–200 of 559

1. Quality control systems for aberrant mRNAs induced by aberrant translation elongation and termination
   Toshifumi Inada · 2013 · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms
2. The RNA Helicase DHX34 Activates NMD by Promoting a Transition from the Surveillance to the Decay-Inducing Complex
   Nele Hug, Javier F. Cáceres · 2014 · Cell Reports
3. Plant nonsense-mediated mRNA decay is controlled by different autoregulatory circuits and can be induced by an EJC-like complex
   Tünde Nyikó, Farkas Kerényi, Levente Szabadkai, Anna Hangyáné Benkovics, Péter Major, Boglárka Sonkoly, Zsuzsanna Mérai, Endre Barta, Emilia Niemiec, Joanna Kufel et al. · 2013 · Nucleic Acids Research
4. EJC core component MLN51 interacts with eIF3 and activates translation
   Pierre-Etienne Chazal, Élisabeth Daguenet, Corinne Wendling, Nathalie Ulryck, Catherine Tomasetto, Bruno Sargueil, Hervé Le Hir · 2013 · Proceedings of the National Academy of Sciences
5. Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response
   Jennifer L. Johnson, Loredana Stoica, Yuwei Liu, Ping Zhu, Abhisek Bhattacharya, Shelly Alexandra Buffington, Redwan Huq, N. Tony Eissa, Ola Segnestam Larsson, Bo Torben Porse et al. · 2019 · Neuron
6. Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data
   Yitian Zhou, Kohei Fujikura, Souren Mkrtchian, Volker Martin Lauschke · 2018 · Frontiers in Pharmacology
7. Tumor diversity and the trade-off between universal cancer tasks
   Jean Hausser, Pablo Székely, Noam Bar, Anat Zimmer, Hila Sheftel, Carlos Caldas, Uri Alon · 2019 · Nature Communications
8. Poly(ADP-ribose) polymerase-13 and RNA regulation in immunity and cancer
   Tanya Todorova Kwan, Florian J. Bock, Paul Chang · 2015 · Trends in Molecular Medicine
9. Preservation of forelimb function by UPF1 gene therapy in a rat model of TDP-43-induced motor paralysis
   Kasey L. Jackson, Robert D. Dayton, Elysse A. Orchard, Shulin Ju, Dagmar Ringe, Gregory A. Petsko, Lynne E. Maquat, Ronald L. Klein · 2014 · Gene Therapy
10. Regulation of gene expression in mammalian nervous system through alternative pre-mRNA splicing coupled with RNA quality control mechanisms
    Karen Yap, Eugene V. Makeyev · 2013 · Molecular and Cellular Neuroscience
11. Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
    Fatih Bayraklı, Bülent Güçlü, Cengiz Yakıcıer, Hatice Balaban, Ugur Kartal, Bekir Ergüner, Mahmut Şamil Sağıroğlu, Şirin Yüksel, Ahmet Rasit Ozturk, Burak Kazancı et al. · 2013 · BMC Genetics
12. The genetic architecture of aniridia and Gillespie syndrome
    Hildegard Nikki Hall, Kathleen A. Williamson, David R FitzPatrick · 2018 · Human Genetics
13. Tying up loose ends: ribosome recycling in eukaryotes and archaea
    Elina Nürenberg‐Goloub, Robert Tampé · 2012 · Trends in Biochemical Sciences
14. The Ribosome as a Platform for mRNA and Nascent Polypeptide Quality Control
    Toshifumi Inada · 2016 · Trends in Biochemical Sciences
15. Mutations in TJP2 , encoding zona occludens 2, and liver disease
    Melissa Sambrotta, Richard J. Thompson · 2015 · Tissue Barriers
16. Intracellular calcium regulates nonsense-mediated mRNA decay
    Andrew Nickless, Erin Jackson, Jayne C. Marasa, Patrick Nugent, Robert W. Mercer, David R Piwnica-Worms, Zhongsheng You · 2014 · Nature Medicine
17. Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice
    Ranad Shaheen, Shams Anazi, Tawfeg Ben‐Omran, Mohammed Zain Seidahmed, Lura Brianna Caddle, Kristina J. Palmer, Rehab Ali, Tarfa A Alshidi, Samya T. Hagos, Leslie O. Goodwin et al. · 2016 · The American Journal of Human Genetics
18. Impaired Dendritic Development and Memory inSorbs2Knock-Out Mice
    Qiangge Zhang, Xian Gao, Chenchen Li, Cátia Feliciano, Dongqing Wang, Dingxi Zhou, Mei Yuan, Patrícia Monteiro, Michelle Anand, Shigeyoshi Itohara et al. · 2016 · Journal of Neuroscience
19. The Dharma of Nonsense-Mediated mRNA Decay in Mammalian Cells
    Maximilian Wei‐Lin Popp, Lynne E. Maquat · 2014 · Molecules and Cells
20. Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing
    Guangqian Xing, Jun Yao, Bin Wu, Tingting Liu, Qinjun Wei, Cheng Liu, Yajie Lu, Zhibin Chen, Heng Zheng, Xiaonan Yang et al. · 2014 · Genetics in Medicine
21. Targeted mutagenesis of zebrafish antithrombin III triggers disseminated intravascular coagulation and thrombosis, revealing insight into function
    Yang Liu, Colin A. Kretz, Morgan L. Maeder, Catherine E. Richter, Philip Tsao, Andy H. Vo, Michael C. Huarng, Thomas Rode, Zhilian Hu, Rohit Mehra et al. · 2014 · Blood
22. Perspectives on Allele-Specific Expression
    Siobhán Cleary, Cathal Seoighe · 2021 · Annual Review of Biomedical Data Science
23. Splicing repression allows the gradual emergence of new Alu-exons in primate evolution
    Jan Attig, Igor Ruiz de los Mozos, Nejc Haberman, Zhen Wang, Warren Emmett, Kathi Zarnack, Julian König, Jernej Ule · 2016 · eLife
24. A network of SMG-8, SMG-9 and SMG-1 C-terminal insertion domain regulates UPF1 substrate recruitment and phosphorylation
    Aurélien Deniaud, Manikandan Karuppasamy, Thomas Bock, Simonas Masiulis, Karine Huard, Frédéric Garzoni, Kathrin Kerschgens, Matthias W. Hentze, Andreas E. Kulozik, Martin Beck et al. · 2015 · Nucleic Acids Research
25. NMD: At the crossroads between translation termination and ribosome recycling
    Alper Celik, Stéphanie Kervestin, Allan Jacobson · 2014 · Biochimie
26. Transcriptome analysis of the filamentous fungus Aspergillus nidulans directed to the global identification of promoters
    Christopher Sibthorp, Huihai Wu, Gwendolyn Cowley, Prudence W. H. Wong, Paulius Palaima, Igor Y. Morozov, Gareth D. Weedall, Mark X. Caddick · 2013 · BMC Genomics
27. Full UPF3B function is critical for neuronal differentiation of neural stem cells
    Tahani Mohammed Ameen Alrahbeni, Francesca Sartor, Jihan Anderson, Zosia Miedzybrodzka, Colin McCaig, Berndt Müller · 2015 · Molecular Brain
28. The determinants of alternative RNA splicing in human cells
    Tatsiana V. Ramanouskaya, Vasily V. Grinev · 2017 · Molecular Genetics and Genomics
29. Nanomolar-potency ‘co-potentiator’ therapy for cystic fibrosis caused by a defined subset of minimal function CFTR mutants
    Puay‐Wah Phuan, Joseph‐Anthony Tan, Amber A. Rivera, Lorna T. Zlock, Dennis W. Nielson, Walter E. Finkbeiner, Peter M. Haggie, Alan S. Verkman · 2019 · Scientific Reports
30. Identification and characterization of transcript polymorphisms in soybean lines varying in oil composition and content
    Wolfgang Goettel, Eric Xia, Robert G. Upchurch, Ming-Li Wang, Pengyin Chen, Yong‐qiang Charles An · 2014 · BMC Genomics
31. New inducible genetic method reveals critical roles of GABA in the control of feeding and metabolism
    Fantao Meng, Yong Han, Dollada Srisai, Валерий Владимирович Белахов, Mónica Farías, Yong Xu, Richard D. Palmiter, Timor Baasov, Qi Wu · 2016 · Proceedings of the National Academy of Sciences
32. Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome
    Mohammed D. Saleem · 2018 · Pediatric Dermatology
33. An atlas of plant full-length RNA reveals tissue-specific and monocots–dicots conserved regulation of poly(A) tail length
    Jinbu Jia, Wenqin Lu, Bo Liu, Huihui Fang, Yiming Yu, Weipeng Mo, Hong Zhang, Xianhao Jin, Shu Yi, Yanping Long et al. · 2022 · Nature Plants
34. Nonsense‐mediated RNA decay – a switch and dial for regulating gene expression
    Jenna E. Smith, Kristian E. Baker · 2015 · BioEssays
35. Mutation of a novel ABC transporter gene is responsible for the failure to incorporate uric acid in the epidermis of ok mutants of the silkworm, Bombyx mori
    Lingyan Wang, Takashi Kiuchi, Tsuguru Fujii, Takaaki Daimon, Muwang Li, Yutaka Banno, Shingo Kikuta, Takahiro Kikawada, Susumu Katsuma, Toru Shimada · 2013 · Insect Biochemistry and Molecular Biology
36. Structural Basis for Regulation of RNA-Binding Proteins by Phosphorylation
    Roopa Thapar · 2014 · ACS Chemical Biology
37. The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene
    Annalaura Torella, Mariateresa Zanobio, Roberta Zeuli, Francesca Del Vecchio Blanco, Marco Savarese, Teresa Giugliano, Arcomaria Garofalo, Giulio Piluso, Luisa Politano, Vincenzo Nigro · 2020 · PLoS ONE
38. Uncovering the impacts of alternative splicing on the proteome with current omics techniques
    Marina Reixachs‐Solé, Eduardo Eyras · 2022 · Wiley Interdisciplinary Reviews - RNA
39. Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0
    Matthew R. Willmann, Nathan Berkowitz, Brian D. Gregory · 2013 · Methods
40. Human nonsense-mediated mRNA decay factor UPF2 interacts directly with eRF3 and the SURF complex
    Andrés López‐Perrote, Raquel Castaño, Roberto Melero, Marı́a Teresa Zamarro, Hitomi Kurosawa, Tetsuo Ohnishi, Akiko Uchiyama, Kyoko Aoyagi, Gretel Buchwald, Naoyuki Kataoka et al. · 2016 · Nucleic Acids Research
41. RNA virus evasion of nonsense-mediated decay
    Jared P. May, Xuefeng Yuan, Erika Sawicki, Anne E. Simon · 2018 · PLoS Pathogens
42. Reactivation of nonsense-mediated mRNA decay protects against C9orf72 dipeptide-repeat neurotoxicity
    Wangchao Xu, Puhua Bao, Xin Jiang, Haifang Wang, Meiling Qin, Ruiqi L. Wang, Tao Wang, Yi An Yang, Ileana Lorenzini, Lujian Liao et al. · 2019 · Brain
43. Emerging functions of alternative splicing coupled with nonsense-mediated decay
    Fursham Hamid, Eugene V. Makeyev · 2014 · Biochemical Society Transactions
44. Intron retention-dependent gene regulation in Cryptococcus neoformans
    Sara Gonzalez-Hilarion, Damien Paulet, Kyung-Tae ‍Lee, Chung-Chau Hon, Pierre Lechat, Estelle Gewiss Mogensen, Frédérique Moyrand, Caroline Proux, Rony Barboux, Giovanni Bussotti et al. · 2016 · Scientific Reports
45. Structural basis of mRNA-cap recognition by Dcp1–Dcp2
    Jeffrey S. Mugridge, Marcin Ziemniak, Jacek Jemielity, John D. Gross · 2016 · Nature Structural & Molecular Biology
46. Selenium-Related Transcriptional Regulation of Gene Expression
    Mikko Juhani Lammi, Chengjuan Qu · 2018 · International Journal of Molecular Sciences
47. Enhancement of premature stop codon readthrough in the CFTR gene by Ataluren (PTC124) derivatives
    Ivana Pibiri, Laura Lentini, Raffaella Melfi, Giulia Gallucci, Andrea Pace, Angelo Spinello, Giampaolo Barone, Aldo Di Leonardo · 2015 · European Journal of Medicinal Chemistry
48. A novel protein, Pho92, has a conserved YTH domain and regulates phosphate metabolism by decreasing the mRNA stability of PHO4 in Saccharomyces cerevisiae
    Hyun-Jun Kang, Sook-Jin Jeong, Kyung-Nam Kim, In-Joon Baek, Miwha Chang, Chang-Min Kang, Yong Sung Park, Cheol‐Won Yun · 2013 · Biochemical Journal
49. Serine/arginine-rich splicing factor 3 (SRSF3) regulates homologous recombination-mediated DNA repair
    Xiaolong He, Pei Zhang · 2015 · Molecular Cancer
50. The broader sense of nonsense
    Evangelos D. Karousis, Oliver Mühlemann · 2022 · Trends in Biochemical Sciences
51. Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans
    Hideki Mutai, Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda, Noriko Morimoto, Kiyomitsu Nara, Satoe Takahashi, Tatsuhiko Tsunoda et al. · 2020 · PLoS Genetics
52. Structure of the activated Edc1-Dcp1-Dcp2-Edc3 mRNA decapping complex with substrate analog poised for catalysis
    Jeffrey S. Mugridge, Ryan W. Tibble, Marcin Ziemniak, Jacek Jemielity, John D. Gross · 2018 · Nature Communications
53. Novel SUZ12 mutations in Weaver‐like syndrome
    Eri Imagawa, Edoarda Vasco de Albuquerque Albuquerque, Bertrand Isidor, Satomi Mitsuhashi, Takeshi Mizuguchi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Margaret Cristina da Silva Boguszewski, César Luiz Boguszewski et al. · 2018 · Clinical Genetics
54. Decoding complex patterns of genomic rearrangement in hepatocellular carcinoma
    Julio Fernandez-Banet, Nikki Pui Yue Lee, Kin Chan, Huan Gao, Xiao Liu, Wing-Kin Ken Sung, Winnie Tan, Sheung Tat Fan, Ronnie T. P. Poon, Shiyong Li et al. · 2014 · Genomics
55. Phenome-wide association studies (PheWASs) for functional variants
    Zhan Ye, John G. Mayer, Lynn C. Ivacic, Zhiyi Zhou, Min He, Steven J. Schrodi, David Page, Murray H. Brilliant, Scott Joseph Hebbring · 2014 · European Journal of Human Genetics
56. The exon junction complex in neural development and neurodevelopmental disease
    John J. McMahon, Emily E. Miller, Debra L. Silver · 2016 · International Journal of Developmental Neuroscience
57. Elimination of cap structures generated by mRNA decay involves the new scavenger mRNA decapping enzyme Aph1/FHIT together with DcpS
    Valério Taverniti, Bertrand Séraphin · 2014 · Nucleic Acids Research
58. Human Papillomavirus 16 Oncoprotein Expression Is Controlled by the Cellular Splicing Factor SRSF2 (SC35)
    Melanie McFarlane, Alasdair Iain Macdonald, Andrew Stevenson, Sheila V. Graham · 2015 · Journal of Virology
59. Truncated yet functional viral protein produced via RNA polymerase slippage implies underestimated coding capacity of RNA viruses
    Yuka Hagiwara‐Komoda, Sun Hee Choi, Masanao Sato, Go Atsumi, Junya Abe, Junya Fukuda, Mie N. Honjo, Atsushi J. Nagano, Keisuke Komoda, Kenji Nakahara et al. · 2016 · Scientific Reports
60. Developmental regulation of canonical and small ORF translation from mRNAs
    Pedro Patraquim, Muhammad Ali Mumtaz, José Ignacio Pueyo, Julie L. Aspden, Juan Pablo Couso · 2020 · Genome biology
61. Yeast Upf1 CH domain interacts with Rps26 of the 40S ribosomal subunit
    Ei Ei Min, Bijoyita Roy, Nadia Amrani, Feng He, Allan Jacobson · 2013 · RNA
62. Quantitative global studies reveal differential translational control by start codon context across the fungal kingdom
    Edward W. J. Wallace, Corinne Maufrais, Jade Sales-Lee, Laura Tuck, Luciana Márcia de Oliveira, Frank Feuerbach, Frédérique Moyrand, Prashanthi Natarajan, Hiten D. Madhani, Guilhem Janbon · 2020 · Nucleic Acids Research
63. Insights into the role of alternative splicing in plant temperature response
    Varvara Dikaya, Nabila El Arbi, Nelson Rojas-Murcia, Sarah Muniz Nardeli, Daniela Goretti, Markus Schmid · 2021 · Journal of Experimental Botany
64. The birth of piRNAs: how mammalian piRNAs are produced, originated, and evolved
    Yu Huining Sun, Brent Lee, Xin Zhiguo Li · 2021 · Mammalian Genome
65. The Exploding Genetic Code
    Edward A. Lemke · 2014 · ChemBioChem
66. The RNA helicase DHX34 functions as a scaffold for SMG1-mediated UPF1 phosphorylation
    Roberto Melero, Nele Hug, Andrés López‐Perrote, Akio Yamashita, Javier F. Cáceres, Óscar Llorca · 2016 · Nature Communications
67. Astroglial toxicity promotes synaptic degeneration in the thalamocortical circuit in frontotemporal dementia with GRN mutations
    Marsan, Elise, Velmeshev, Dmitry, Ramsey, Arren, Patel, Ravi K., Zhang, Jiasheng, Koontz, Mark, Andrews, Madeline G., de Majo, Martina, Mora, Cristina, Blumenfeld, Jessica et al. · 2023 · Journal of Clinical Investigation
68. The role of nonsense-mediated decay in neuronal ceroid lipofuscinosis
    Jake N. Miller, Chun‐Hung Chan, David A. Pearce · 2013 · Human Molecular Genetics
69. Cytoplasmic mRNA decay and quality control machineries in eukaryotes
    Megan E. Dowdle, Jens Lykke‐Andersen · 2025 · Nature Reviews Genetics
70. UPF2, a nonsense-mediated mRNA decay factor, is required for prepubertal Sertoli cell development and male fertility by ensuring fidelity of the transcriptome
    Jianqiang Bao, Chong Tang, Shuiqiao Yuan, Bo Torben Porse, Wei Yan · 2014 · Development
71. Plakophilins 1 and 3 Bind to FXR1 and Thereby Influence the mRNA Stability of Desmosomal Proteins
    Regina Fischer-Kešo, Sonja Breuninger, Sarah Hofmann, Manuela Henn, Theresa Röhrig, Philipp Ströbel, Georg Stoecklin, Ilse Hofmann · 2014 · Molecular and Cellular Biology
72. Transcriptome-wide identification and study of cancer-specific splicing events across multiple tumors
    Yi‐Hsuan Tsai, Daniel Dominguez, Shawn M. Gomez, Zefeng Wang · 2015 · Oncotarget
73. Pharmacological inhibition of the spliceosome subunit SF3b triggers exon junction complex-independent nonsense-mediated decay
    Teresa Carvalho, Sandra Martins, José Rino, Sérgio Pires Marinho, Maria Carmo‐Fonseca · 2017 · Journal of Cell Science
74. RNA degradomes reveal substrates and importance for dark and nitrogen stress responses of Arabidopsis XRN4
    Vinay K. Nagarajan, Patrick M Kukulich, Bryan von Hagel, Pamela J. Green · 2019 · Nucleic Acids Research
75. Cytoplasmic mRNA turnover and ageing
    Fivos Borbolis, Popi Syntichaki · 2015 · Mechanisms of Ageing and Development
76. Emerging roles for ribonucleoprotein modification and remodeling in controlling RNA fate
    Suzanne Rebecca Lee, Jens Lykke‐Andersen · 2013 · Trends in Cell Biology
77. Human UPF3A and UPF3B enable fault‐tolerant activation of nonsense‐mediated mRNA decay
    Damaris Wallmeroth, Jan‐Wilm Lackmann, Sabrina Kueckelmann, Janine Altmüller, Christoph Dieterich, Volker Boehm, Niels H. Gehring · 2022 · The EMBO Journal
78. Interaction between the poly(A)-binding protein Pab1 and the eukaryotic release factor eRF3 regulates translation termination but not mRNA decay in Saccharomyces cerevisiae
    Sylvain Roque, Marie Cerciat, Isabelle Gaugué, Liliana Mora, Aurélie G. Floch, Miklos de Zamaroczy, Valérie Heurgué‐Hamard, Stéphanie Kervestin · 2014 · RNA
79. Gentamicin-Induced Readthrough and Nonsense-Mediated mRNA Decay of SERPINB7 Nonsense Mutant Transcripts
    Yuka Ohguchi, Toshifumi Nomura, Shotaro Suzuki, Masae Takeda, T. Miyauchi, Osamu Mizuno, Satoru Shinkuma, Yasuyuki Fujita, Osamu Nemoto, Kota Ono et al. · 2017 · Journal of Investigative Dermatology
80. Upf proteins: highly conserved factors involved in nonsense mRNA mediated decay
    Puneet Gupta, Yan-Ruide Li · 2017 · Molecular Biology Reports
81. Dissecting the functions of SMG5, SMG7, and PNRC2 in nonsense-mediated mRNA decay of human cells
    Pamela Nicholson, Asimina Gkratsou, Christoph Josi, Martino Colombo, Oliver Mühlemann · 2018 · RNA
82. SUMOylation-modified Pelota-Hbs1 RNA surveillance complex restricts the infection of potyvirids in plants
    Linhao Ge, Buwei Cao, Rui Qiao, Hongguang Cui, Shaofang Li, Hongying Shan, Pan Gong, Mingzhen Zhang, Hao Li, Aiming Wang et al. · 2023 · Molecular Plant
83. RefSeq curation and annotation of stop codon recoding in vertebrates
    Bhanu Rajput, Kim D. Pruitt, Terence D. Murphy · 2018 · Nucleic Acids Research
84. The mRNA repressor TRIM71 cooperates with Nonsense-Mediated Decay factors to destabilize the mRNA of CDKN1A/p21
    Lucia Torres Fernández, Bettina Jux, Maximilian Bille, Yasmine Port, Karin Schneider, Matthias Geyer, Günter Mayer, Waldemar Kolanus · 2019 · Nucleic Acids Research
85. The RNA helicase Ddx5/p68 binds to hUpf3 and enhances NMD of Ddx17/p72 and Smg5 mRNA
    Verena Geißler, Simone Altmeyer, Benjamin Stein, Heike Uhlmann‐Schiffler, Hans D. Stahl · 2013 · Nucleic Acids Research
86. The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family
    Nawei Sun, Cara Nasello, L Deng, Ningyuan Wang, Y. Zhang, Zihui Xu, Zhi Jian Song, Kelvin Y. Kwan, Robert A. King, Zhiping P. Pang et al. · 2017 · Molecular Psychiatry
87. Nanoscale synapse organization and dysfunction in neurodevelopmental disorders
    Hanna L. Zieger, Daniel Choquet · 2021 · Neurobiology of Disease
88. Exploring the readthrough of nonsense mutations by non-acidic Ataluren analogues selected by ligand-based virtual screening
    Ivana Pibiri, Laura Lentini, Marco Tutone, Raffaella Melfi, Andrea Pace, Aldo Di Leonardo · 2016 · European Journal of Medicinal Chemistry
89. MtNF-YA1, A Central Transcriptional Regulator of Symbiotic Nodule Development, Is Also a Determinant of Medicago truncatula Susceptibility toward a Root Pathogen
    Thomas Rey, Philippe Laporte, Maxime Bonhomme, Marie‐Françoise Jardinaud, Stéphanie Huguet, Sandrine Balzergue, Bernard Dumas, Andréas Niebel, Christophe Jacquet · 2016 · Frontiers in Plant Science
90. Pan-Cancer Analysis Reveals the Diverse Landscape of Novel Sense and Antisense Fusion Transcripts
    Neetha Nanoth Vellichirammal, Abrar Albahrani, Jasjit Kaur Banwait, Nitish K. Mishra, You Li, Shrabasti Roychoudhury, Mathew J. Kling, Sameer Mirza, Kishor K. Bhakat, Vimla Band et al. · 2020 · Molecular Therapy — Nucleic Acids
91. Identification of Interactions in the NMD Complex Using Proximity-Dependent Biotinylation (BioID)
    Christoph Schweingruber, Paolo Soffientini, Marc‐David Ruepp, Angela Bachi, Oliver Mühlemann · 2016 · PLoS ONE
92. Tracking endogenous proteins based on RNA editing-mediated genetic code expansion
    Min Hao, Xinyu Ling, Yi Xin Sun, Xue Wang, Wenzhe Li, Liying Chang, Zhiying Zeng, Xiaomeng Shi, Mengxiao Niu, Liangyi Chen et al. · 2024 · Nature Chemical Biology
93. Long Open Reading Frame Transcripts Escape Nonsense-Mediated mRNA Decay in Yeast
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94. Neuronal RNA ‐binding proteins in health and disease
    Silvia Carolina Lenzken, Tilmann Achsel, Maria Teresa Carrı̀, Silvia M.L. Barabino · 2014 · Wiley Interdisciplinary Reviews - RNA
95. Serine/Arginine-rich protein family of splicing regulators: New approaches to study splice isoform functions
    Mitchell J. L. Morton, Nadia Al‐Tamimi, Haroon Butt, Anireddy S. N. Reddy, Magdy M. Mahfouz · 2019 · Plant Science
96. Pharmacological approaches for targeting cystic fibrosis nonsense mutations
    Jyoti Sharma, Kim M. Keeling, Steven Mark Rowe · 2020 · European Journal of Medicinal Chemistry
97. Eukaryotic mRNA decapping factors: molecular mechanisms and activity
    Feng He, Allan Jacobson · 2022 · FEBS Journal
98. Nonsense-mediated mRNA decay of collagen – emerging complexity in RNA surveillance mechanisms
    Yiwen Fang, John F. Bateman, Julian F. B. Mercer, Shireen R. Lamandé · 2013 · Journal of Cell Science
99. Alternative transcripts of the SERPINA1 gene in alpha-1 antitrypsin deficiency
    Nerea Matamala, María Teresa Martínez, Beatriz Lara, Laura Pérez, Irene Vázquez-Domínguez, Azucena Jimenez, Miguel Barquín, Ilaria Ferrarotti, Ignacio Blanco, Sabina M Janciauskiene et al. · 2015 · Journal of Translational Medicine
100. A novel mutation of IGSF1 in a Japanese patient of congenital central hypothyroidism without macroorchidism [Rapid Communication]
     Toshihiro Tajima, Akie Nakamura, Katsura Ishizu · 2013 · Endocrine Journal