Coupling mRNA processing with transcription in time and space

Expansion of the eukaryotic proteome by alternative splicing

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Nascent RNA Sequencing Reveals Widespread Pausing and Divergent Initiation at Human Promoters

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Widespread Shortening of 3′UTRs by Alternative Cleavage and Polyadenylation Activates Oncogenes in Cancer Cells

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Structural Basis of Transcription: RNA Polymerase II at 2.8 Ångstrom Resolution

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Regulation of Alternative Splicing by Histone Modifications

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R Loops: From Transcription Byproducts to Threats to Genome Stability

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DNA sequence required for efficient transcription termination in yeast

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CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing

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The C-terminal domain of RNA polymerase II couples mRNA processing to transcription

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Rapidly Growing Protein-Centric Technologies to Extensively Identify Protein–RNA Interactions: Application to the Analysis of Co-Transcriptional RNA Processing

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TINTIN, at the interface of chromatin, transcription elongation, and mRNA processing

Bhat, W., Ahmad, S., & Côté, J. (2015) · RNA Biology · doi:10.1080/15476286.2015.1026032 · Cited by 9

Nxf1 Natural Variant E610G Is a Semi-dominant Suppressor of IAP-Induced RNA Processing Defects

Concepcion, D., Ross, K. D., Hutt, K. R., Yeo, G. W.-M., & Hamilton, B. A. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005123 · Cited by 9

Rapid and Efficient Co-Transcriptional Splicing Enhances Mammalian Gene Expression

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RNA Pol II–dependent transcription efficiency fine-tunes A-to-I editing levelsPreprint

Szabo, B., Mandl, T. C., Woldrich, B., Diensthuber, G., Martin, D., Jantsch, M. F., & Licht, K. (2024) · Genome Research · doi:10.1101/gr.277686.123 · Cited by 8

NusG–Spt5 Transcription Factors: Universal, Dynamic Modulators of Gene Expression

Mooney, R. A., Zhu, J., Saba, J., & Landick, R. C. (2024) · Journal of Molecular Biology · doi:10.1016/j.jmb.2024.168814 · Cited by 9

UBE3D Regulates mRNA 3′-End Processing and Maintains Adipogenic Potential in 3T3-L1 Cells

Heller-Trulli, D., Liu, H., Mukherjee, S., & Moore, C. L. (2022) · Molecular and Cellular Biology · doi:10.1128/mcb.00174-22 · Cited by 8

RNA structure in alternative splicing regulation: from mechanism to therapy

Bao, N., Wang, Z., Fu, J., Dong, H., & Jin, Y. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024119 · Cited by 9

High-throughput single-molecule screen for small-molecule perturbation of splicing and transcription kinetics

Day, C. R., Chen, H., Coulon, A., Meier, J. L., & Larson, D. R. (2015) · Methods · doi:10.1016/j.ymeth.2015.11.025 · Cited by 8

Interactions between RNAP III transcription machinery and tRNA processing factors

Arimbasseri, G. A. (2018) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2018.02.003 · Cited by 8

Genome-wide characterization of nascent RNA processing in plants

Qin, Y., Long, Y., & Zhai, J. (2022) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2022.102294 · Cited by 8

Transcription-coupled RNA surveillance in human genetic diseases caused by splice site mutations

Vaz‐Drago, R., Pinheiro, M. T., Martins, S., Enguita, F. J., Carmo‐Fonseca, M., & Custódio, N. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv039 · Cited by 8

Measuring Nascent Transcripts by Nascent-seq

Chen, F., Marshall, S. A., Deng, Y., & Tianjiao, S. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7514-3_2 · Cited by 7

Human co-transcriptional splicing kinetics and coordination revealed by direct nascent RNA sequencingPreprint

Drexler, H. L., Choquet, K., & Churchman, L. S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/611020 · Cited by 8

Splicing-dependent restriction of the HBZ gene by Tax underlies biphasic HTLV-1 infection

Liang, Y., Lyu, C., Xu, S., Tan, C., Jiang, Q., Liu, B., Yang, S., Huang, W., Zhou, R., Yuan, X., et al. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013381 · Cited by 7

Slow Transcription of the 99a/let-7c/125b-2 Cluster Results in Differential MiRNA Expression and Promotes Melanoma Phenotypic Plasticity

Sheinboim, D., Parikh, S., Parikh, R., Menuchin, A., Shapira, G., Kapitansky, O., Elkoshi, N., Ruppo, S., Shaham, L., Golan, T., et al. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.03.036 · Cited by 7

Cheminformatics and Bioinformatics at the Interface with Systems Biology

Kaushik, A. C., Mehmood, A., Wei, D., Nawab, S., Sahi, S., & Kumar, A. (2023) · Royal Society of Chemistry eBooks · doi:10.1039/9781839166037 · Cited by 7

Pan-Cancer Profiling of Intron Retention and Its Clinical Significance in Diagnosis and Prognosis

Huang, L., Zeng, X., Ma, H., Yang, Y., Akimoto, Y., Wei, G., & Ni, T. (2023) · Cancers · doi:10.3390/cancers15235689 · Cited by 7

CCAT1 lncRNA is chromatin-retained and post-transcriptionally spliced

Bohrer, C., Varon, E., Peretz, E., Reinitz, G., Kinor, N., Halle, D., Nissan, A., & Shav‐Tal, Y. (2024) · Histochemistry and Cell Biology · doi:10.1007/s00418-024-02294-w · Cited by 7

Repression of pervasive antisense transcription is the primary role of fission yeast RNA polymerase II CTD serine 2 phosphorylation

Boulanger, C., Haidara, N., Yague‐Sanz, C., Larochelle, M., Jacques, P., Hermand, D., & Bachand, F. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae436 · Cited by 7

Statistical inference of the rate of RNA polymerase II elongation by total RNA sequencing

Kawamura, Y., Koyama, S., & Yoshida, R. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty886 · Cited by 7

The prevention and resolution of DNA replication–transcription conflicts in eukaryotic cells

Wu, W., Hickson, I. D., & Liu, Y. (2020) · Genome Instability & Disease · doi:10.1007/s42764-020-00012-z · Cited by 8

PiRNA Biogenesis and Their Role in Human Cancers and Other Diseases: A Narrative Review

Shirzad, H. (2021) · Iranian Journal of Public Health · doi:10.18502/ijph.v50i12.7930 · Cited by 7

CFIm25 regulates human stem cell function independently of its role in mRNA alternative polyadenylation

Ran, Y., Huang, S., Shi, J., Feng, Q., Deng, Y., Xiang, A. P., & Yao, C. (2022) · RNA Biology · doi:10.1080/15476286.2022.2071025 · Cited by 7

3� Rapid Amplification of cDNA Ends (3� RACE) Using Arabidopsis Samples

Rodr�guez-Cazorla, E., And�jar, A., Ripoll, J. J., Bailey-Steinitz, L. J., Mart�nez-Laborda, A., Yanofsky, M. F., & Vera, A. (2015) · BIO-PROTOCOL · doi:10.21769/bioprotoc.1604 · Cited by 7

In vitro assembly and proteomic analysis of RNA polymerase II complexes

Joo, Y. J., Ficarro, S. B., Marto, J. A., & Buratowski, S. (2019) · Methods · doi:10.1016/j.ymeth.2019.03.001 · Cited by 7

NET-prism enables RNA polymerase-dedicated transcriptional interrogation at nucleotide resolution

Mylonas, C., & Tessarz, P. (2019) · RNA Biology · doi:10.1080/15476286.2019.1621625 · Cited by 7

Tales around the clock: Poly(A) tails in circadian gene expression

Beta, R. A. A., & Balatsos, N. A. A. (2018) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1484 · Cited by 8

Aging-associated changes in transcriptional elongation influence metazoan longevityPreprint

Debès, C., Papadakis, A., Grönke, S., Karalay, Ö., Tain, L. S., Mizi, A., Nakamura, S., Hahn, O., Weigelt, C. M., Josipović, N., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/719864 · Cited by 7

Circular RNAs in Cardiovascular Physiopathology: From Molecular Mechanisms to Therapeutic Opportunities

Capirossi, G., Brasini, S., Tremoli, E., Binatti, A., & Roncarati, R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199725 · Cited by 6

Phase Separation of TAF15 C‐Terminal LC Domain Enables RNA ‐Binding Protein‐Mediated Transcriptional Regulation

Lee, J., & Kwon, I. (2025) · The FASEB Journal · doi:10.1096/fj.202502096r · Cited by 6

Bioinspired Backbone Editing Strategies for Rewriting Synthetic Polymers

Guo, S., Fu, J., Cui, S., Hu, J., Deng, Z., & Liu, S. (2026) · Angewandte Chemie International Edition · doi:10.1002/anie.202522451 · Cited by 6

Translation initiation and its relationship with metabolic mechanisms in cancer development, progression and chemoresistance

Muñoz-Ayala, A., Chimal‐Vega, B., & García‐González, V. (2022) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2022.05.011 · Cited by 6

Selective neuronal vulnerability to deficits in RNA processing

Zuniga, G., & Frost, B. E. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102500 · Cited by 8

CTDP1 and RPB7 stabilize Pol II and permit reinitiation

Zheng, H., Xu, Q., Ji, D., Yang, B., & Ji, X. (2025) · Nature Communications · doi:10.1038/s41467-025-57513-2 · Cited by 6

Construction of a De Novo Nucleotide Biosynthesis Pathway in Artificial Cells for RNA Transcription

Liu, Y., Zhang, M., Zhao, J., Ren, Y., Li, S., Wang, W., Mu, W., & Han, X. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c09375 · Cited by 6

RNAPII CTD: A key regulator in eukaryotic gene expression system

Kashif, M., Ahmad, A., Siddiqui, S., Kumar, B., & Khan, M. J. (2018) · Gene Reports · doi:10.1016/j.genrep.2018.03.017 · Cited by 6

The Simultaneous Coupling of Transcription and Splicing in Plants

Zhang, Y., & Ding, Y. (2020) · Molecular Plant · doi:10.1016/j.molp.2020.01.011 · Cited by 6

Elongation rate of RNA polymerase II affects pausing patterns across 3′ UTRs

Khitun, A., Brion, C., Moqtaderi, Z., Geisberg, J. V., Churchman, L. S., & Struhl, K. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105289 · Cited by 7

Examining the intersection between splicing, nuclear export and small RNA pathways

Nabih, A., Sobotka, J. A., Wu, M. Z., Wedeles, C. J., & Claycomb, J. M. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.05.027 · Cited by 6

Conserved sequences in the Drosophila mod(mdg4) intron promote poly(A)-independent transcription termination and trans-splicing

Tikhonov, M. V., Utkina, M. V., Maksimenko, O. G., & Georgiev, P. G. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky716 · Cited by 9

The florigen interactor BdES43 represses flowering in the model temperate grass Brachypodium distachyon

Cao, S., Luo, X., Xie, L., Gao, C., Wang, D., Holt, B. F., Lin, H., Chu, C., & Xia, X. (2019) · The Plant Journal · doi:10.1111/tpj.14622 · Cited by 6

Characterizing RNA Pseudouridylation by Convolutional Neural Networks

He, X., Zhang, S., Zhang, Y., Lei, Z., Jiang, T., & Zeng, J. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2019.11.015 · Cited by 7

Unraveling docking and initiation of mRNA export through the nuclear pore complex

Tingey, M., & Yang, W. (2022) · BioEssays · doi:10.1002/bies.202200027 · Cited by 6

Exploring the Impact of Cleavage and Polyadenylation Factors on Pre-mRNA Splicing Across Eukaryotes

Lepennetier, G., & Catania, F. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.041483 · Cited by 7

Mechanistic Insights Into Catalytic RNA–Protein Complexes Involved in Translation of the Genetic Code

Routh, S. B., & Sankaranarayanan, R. (2017) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2017.04.002 · Cited by 6

Methods for the analysis of transcriptome dynamics

Rodrigues, D. F., Costa, V. M., Silvestre, R., Bastos, M. D. L., & Carvalho, F. D. (2019) · Toxicology Research · doi:10.1039/c9tx00088g · Cited by 6

ASAPA: a bioinformatic pipeline based on Iso-Seq that identifies the links among alternative splicing, alternative transcription initiation and alternative polyadenylation

Wang, F., Jin, Z., Wang, S., Yang, L., Fan, Z., & Yao, Y. (2024) · Functional & Integrative Genomics · doi:10.1007/s10142-024-01332-z · Cited by 5

Disentangling genetic effects on transcriptional and post-transcriptional gene regulation through integrating exon and intron expression QTLs

Brümmer, A., & Bergmann, S. (2024) · Nature Communications · doi:10.1038/s41467-024-48244-x · Cited by 5

mRNA-Associated Processes and Their Influence on Exon-Intron Structure in Drosophila melanogaster

Lepennetier, G., & Catania, F. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.029231 · Cited by 5

Global Approaches to Alternative Splicing and Its Regulation—Recent Advances and Open Questions

Hsiao, Y.-H. E., Cass, A. A., Bahn, J. H., Lin, X., & Xiao, X. G. (2015) · Translational bioinformatics · doi:10.1007/978-94-017-7450-5_2 · Cited by 5

StAR, a bridge from ApoE, LDL, and HDL cholesterol trafficking to mitochondrial metabolism

Jefcoate, C. R. E., & Larsen, M. C. (2019) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2019.07.011 · Cited by 5

Conditional depletion of transcriptional kinases Ctk1 and Bur1 and effects on co-transcriptional spliceosome assembly and pre-mRNA splicing

Maudlin, I. E., & Beggs, J. D. (2021) · RNA Biology · doi:10.1080/15476286.2021.1991673 · Cited by 5

HiFENS: high-throughput FISH detection of endogenous pre-mRNA splicing isoforms

Shilo, A., Pegoraro, G., & Misteli, T. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac869 · Cited by 6

Programmed Delayed Splicing: A Mechanism for Timed Inflammatory Gene Expression 2267628

Dearborn, J. S., Frankiw, L., Limoge, D. W., Burns, C. S., Vlach, L., Turpin, P., Kirch, T., Miller, Z. D., Dowell, W., Languon, S., et al. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag141.1179 · Cited by 5

Genome evolution is driven by gene expression‐generated biophysical constraints through RNA‐directed genetic variation: A hypothesis

Auboeuf, D. (2017) · BioEssays · doi:10.1002/bies.201700069 · Cited by 5

Exploring the RNA Gap for Improving Diagnostic Yield in Primary Immunodeficiencies

Lye, J. J., Williams, A. P., & Baralle, D. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.01204 · Cited by 6

Phase separation of RNA-binding protein promotes polymerase engagement and transcriptionPreprint

Shao, W., Bi, X., Gao, B., Wu, J. F., Pan, Y., Yin, Y., Liu, Z., Zhang, W., Jiang, X., Ren, W., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.26.436939 · Cited by 5

Next-Generation Mapping of the ACINUS-Mediated Alternative Splicing Machinery and Its Regulation by O-glycosylation in ArabidopsisPreprint

Shrestha, R., Reyes, A. V., Carey, S., Karunadasa, S. S., Zhai, W., Byun, D., Lin, W., Li, J., Alerte, K., Cui, H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.04.631329 · Cited by 5

Epididymal extracellular vesicles harbor and convey mRNA to sperm for transfer to zygotes

Trigg, N. A., Lee, G. S., Leach, A. G., & Conine, C. C. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag330 · Cited by 5

Full-Length Transcriptome of the Great Himalayan Leaf-Nosed Bats (Hipposideros armiger) Optimized Genome Annotation and Revealed the Expression of Novel Genes

Bao, M., Wang, X., Sun, R., Wang, Z., Li, J., Jiang, T., Lin, A., Wang, H., & Feng, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054937 · Cited by 4

Neuronal RNA processing: cross-talk between transcriptional regulation and RNA-binding proteins

Ozbulut, H. C., & Hilgers, V. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1426410 · Cited by 4

Evaluating the breadth of nucleic acid-based payloads delivered in lipid nanoparticles to establish fundamental differences in development

Li, J., & Foged, C. (2024) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2024.2409142 · Cited by 5

Decoding the regulatory roles of circular RNAs in cardiac fibrosis

You, Q., Yu, J., Pan, R., Feng, J., Guo, H.-D., & Liu, B. (2024) · Non-coding RNA Research · doi:10.1016/j.ncrna.2024.11.007 · Cited by 5

True length of diverse capped RNA sequencing (TLDR-seq): 5′–3′-end sequencing of capped RNAs regardless of 3′-end status

Auxillos, J., Stigliani, A., Vaagensø, C., Garland, W., Niazi, A. M., Valen, E., Jensen, T. H., & Sandelin, A. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf240 · Cited by 4

The KH-domain genes FLK and HOS5 integrate flowering and stress responses in Arabidopsis thaliana

Rodríguez‐Cazorla, E., Ripoll, J. J., Candela, H., Aranda-Martínez, A., Zavala-Gonzalez, E. A., García‐Mina, J. M., Zamarreño, A. M., Martínez‐Laborda, A., & Vera, A. (2025) · Journal of Experimental Botany · doi:10.1093/jxb/eraf286 · Cited by 4

Advances in understanding and targeting eIF4E activity

D’Agostino, S., Davies, C., Powers, M. V., & Clarke, P. A. (2025) · Biochemical Society Transactions · doi:10.1042/bst20241045 · Cited by 7

Distinctive functioning of STARD1 in the fetal Leydig cells compared to adult Leydig and adrenal cells. Impact of Hedgehog signaling via the primary cilium

Kothandapani, A., Larsen, M. C., Lee, J., Jorgensen, J. S., & Jefcoate, C. R. E. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111265 · Cited by 4

Nanodynamo quantifies subcellular RNA dynamics revealing extensive coupling between steps of the RNA life cycle

Tarrero, L. C., Famà, V., D’Andrea, G., Maestri, S., de Polo, A., Biffo, S., Furlan, M., & Pelizzola, M. (2024) · Nature Communications · doi:10.1038/s41467-024-51917-2 · Cited by 4

Subversion of phosphorylated SR proteins by enterovirus A71 in IRES-dependent translation revealed by RNA-interactome analysis

Lee, K.-M., Wu, C., Fan, Y.-T., Chiang, H.-J., Lien, P.-Y., Wang, J.-P., Huang, Y., & Shih, S. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013242 · Cited by 4

Syntheses of C‐6 Aryl‐ and Alkynyl‐Substituted Thymidines from Thymidine trans‐5,6‐Bromohydrins

Wrigstedt, P. J., Iashin, V., Lagerblom, K., Keskiväli, J., Chernichenko, K. Y., & Repo, T. (2016) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201601219 · Cited by 4

Alternative Splicing (AS) Dynamics in Dwarf Soybean Derived from Cross of Glycine max and Glycine soja

Roy, N. S., Basnet, P., Ramekar, R. V., Um, T., Yu, J., Park, K.-C., & Choi, I. (2022) · Agronomy · doi:10.3390/agronomy12071685 · Cited by 4

Multi-scale gene regulation mechanism: Spatiotemporal transmission of genetic information

Xue, Y., Wang, J., He, Y., Patra, P., & Gao, Y. Q. (2022) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2022.102487 · Cited by 5

Inhibition of mitochondrial complex III or dihydroorotate dehydrogenase (DHODH) triggers formation of poly(A) + RNA foci adjacent to nuclear speckles following activation of ATM (ataxia telangiectasia mutated)

Miyake, S., & Masuda, S. (2022) · RNA Biology · doi:10.1080/15476286.2022.2146919 · Cited by 4

New Chromatin Run-On Reaction Enables Global Mapping of Active RNA Polymerase Locations in an Enrichment-free Manner

Gao, M., Li, Y., Shu, X., Dai, P., Cao, J., An, Y., Li, T., Huang, Y., Wang, F., Lu, Z., et al. (2022) · ACS Chemical Biology · doi:10.1021/acschembio.1c00951 · Cited by 4

Filamentous Fungi as Hosts for Heterologous Production of Proteins and Secondary Metabolites in the Post-Genomic Era

Rendsvig, J. K. H., Futyma, M. E., Jarczynska, Z. D., & Mortensen, U. H. (2020) · Springer eBooks · doi:10.1007/978-3-030-49924-2_10 · Cited by 4

Comprehensive Transcriptomic and Epigenomic Insights into Environmental Toxicant Exposures: The TaRGET II ResourcePreprint

Zhang, B., Miao, B., Fu, S., Coarfa, C., Kumar, R., Kuntala, P. K., Park, B., Grimm, S. L., Jangid, R. K., Colacino, J. A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.28.667191 · Cited by 4

The association of the RSC remodeler complex with chromatin is influenced by the prefoldin-like Bud27 and determines nucleosome positioning and polyadenylation sites usage in Saccharomyces cerevisiae

Cuevas-Bermúdez, A., Martinez-Fernandez, V., Garrido-Godino, A. I., Jordán‐Pla, A., Peñate, X., Martín‐Expósito, M., Gutiérrez, G., Govind, C. K., Chávez, S., Pelechano, V., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2023.194995 · Cited by 3

Genome-wide kinetic profiling of pre-mRNA 3′ end cleavage

Torres-Ulloa, L., Calvo-Roitberg, E., & Pai, A. A. (2023) · RNA · doi:10.1261/rna.079783.123 · Cited by 3

The ATP-dependent DEAD-box RNA helicase Dbp2 regulates the glucose/nitrogen stress response in baker’s yeast by modulating reversible nuclear retention and decay of SKS1 mRNA

Paul, S., Das, S., Banerjea, M., Chaudhuri, S., & Das, B. (2024) · Genetics · doi:10.1093/genetics/iyae221 · Cited by 3

Melanophilin inhibit the growth and lymph node metastasis of triple negative breast cancer via the NONO-SPHK1-S1P axis

Yao, X., Yuen, T., Qingchuan, C., Jianjun, Z., Liu, Y., & Sun, S. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06240-9 · Cited by 3

Coupling mechanisms coordinating mRNA translation with stages of the mRNA lifecycle

Famà, V., Tarrero, L. C., Albanese, R., Calviello, L., Biffo, S., Pelizzola, M., & Furlan, M. (2025) · RNA Biology · doi:10.1080/15476286.2025.2483001 · Cited by 3

The Reactivity of Thymine and Thymidine 5,6-Epoxides with Organometallic Reagents – A Route to Thymidine (6-4) Photoproduct Analogues

Wrigstedt, P. J., Kavakka, J. S., Heikkinen, S., Nieger, M., Räisänen, M. T., & Repo, T. (2016) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.6b00495 · Cited by 3

NineTeen Complex-subunit Salsa is required for efficient splicing of a subset of introns and dorsal–ventral patterning

Rathore, O. S., Silva, R. D., Ascensão-Ferreira, M., Matos, R., Carvalho, C., Marques, B., Tiago, M. N., Prudêncio, P., Andrade, R. P., Roignant, J., et al. (2020) · RNA · doi:10.1261/rna.077446.120 · Cited by 3

MicroRNA 452 regulates GTF2E1 expression in colorectal cancer cells

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3′‐end mRNA processing within apicomplexan parasites, a patchwork of classic, and unexpected players

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