A day in the life of the spliceosome

Expansion of the eukaryotic proteome by alternative splicing

Nilsen, T. W., & Graveley, B. R. (2010) · Nature · doi:10.1038/nature08909 · Cited by 2,270

CRM1 Is an Export Receptor for Leucine-Rich Nuclear Export Signals

Fornerod, M. W. J., Ohno, M., Yoshida, M., & Mattaj, I. W. (1997) · Cell · doi:10.1016/s0092-8674(00)80371-2 · Cited by 2,086

Frequent pathway mutations of splicing machinery in myelodysplasia

Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., et al. (2011) · Nature · doi:10.1038/nature10496 · Cited by 2,029

Spliceosome Structure and Function

Will, C. L., & Luhrmann, R. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003707 · Cited by 1,829

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

Lorson, C. L., Hahnen, E., Androphy, E. J., & Wirth, B. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6307 · Cited by 1,536

Spliced segments at the 5′ terminus of adenovirus 2 late mRNA

Berget, S. M., Moore, C. L., & Sharp, P. A. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.8.3171 · Cited by 1,483

Understanding alternative splicing: towards a cellular code

Matlin, A. J., Clark, F., & Smith, C. W. J. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1645 · Cited by 1,299

An amazing sequence arrangement at the 5′ ends of adenovirus 2 messenger RNA

Chow, L. T., Gelinas, R. E., Broker, T. R., & Roberts, R. J. (1977) · Cell · doi:10.1016/0092-8674(77)90180-5 · Cited by 1,234

Are snRNPs involved in splicing?

Lerner, M. R., Boyle, J. A., Mount, S. M., Wolin, S. L., & STEITZ, J. A. (1980) · Nature · doi:10.1038/283220a0 · Cited by 1,192

Splicing regulation: From a parts list of regulatory elements to an integrated splicing code

Wang, Z., & Burge, C. B. (2008) · RNA · doi:10.1261/rna.876308 · Cited by 1,127

Differences in splicing factors may predict type 2 diabetes remission in the CORDIOPREV study

Ojeda‐Rodríguez, A., Torres-Peña, J. D., Larriva, A. P. A.-D., Rangel-Zúñiga, O. A., Podadera-Herreros, A., Boughanem, H., G-García, M. E., López-Moreno, A., Katsiki, N., Luque, R. M., et al. (2024) · iScience · doi:10.1016/j.isci.2024.111527 · Cited by 2

Selecting differential splicing methods: Practical considerations

Draper, B. J., Dunning, M., & James, D. C. (2025) · F1000Research · doi:10.12688/f1000research.155223.1 · Cited by 2

Minor Splicing Factor RNPC3 Is Essential for the Germinal Center B Cell Response

Wang, J., Ruan, G., Li, Y., Xiao, X., Zhu, Z., Chen, W., Huang, H., Zhang, R., Wang, R., Chen, M., et al. (2025) · European Journal of Immunology · doi:10.1002/eji.202451508 · Cited by 2

Interconversion and mechanisms between Lsm-type and Sm-type heteroheptameric rings: implications for spliceosome evolution and RNA metabolism

Li, M., Hou, Y., Hu, Y. W., Wang, Y., Shen, C., Luo, Y., Su, D., & Zhang, R. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf451 · Cited by 2

Splicing Shift of RAC1 Accelerates Tumorigenesis and Defines a Potent Therapeutic Target in Lung Cancer

Yan, Y., Wang, N., Xing, B., Yang, M., Shang, J., Bao, Y., Xiao, L., Zhang, N., Ren, Y., Liu, C., et al. (2025) · Advanced Science · doi:10.1002/advs.202503322 · Cited by 2

Different mRNAs encoding identical proteins: how and why?

Duan, Y., & Cao, Q. (2025) · Journal of Applied Genetics · doi:10.1007/s13353-025-00995-z · Cited by 2

Causes, Consequences and Challenges of Intron Retention in lncRNAs

Kumar, M., & Grammatikakis, I. (2025) · Molecular and Cellular Biology · doi:10.1080/10985549.2025.2539755 · Cited by 2

Alternative Splicing-Mediated Resistance to Antibody-Based Therapies: Mechanisms and Emerging Therapeutic Strategies

Choi, S., Kang, J., & Kim, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262411918 · Cited by 2

Identification and validation of palmitoylation metabolism related biomarkers in osteoarthritis using transcriptomic and single cell RNA sequencing analyses

Zhang, D., Liu, X., Zhang, W., Xiao, D., Zhao, W., Qiong, T., Wang, Y., & Sun, T. (2025) · Scientific Reports · doi:10.1038/s41598-025-31218-4 · Cited by 2

Spliceosomal Sm core assembly: AlphaFold 3 predicted structure and phosphorylation-dependent regulation of the human 6S complex

Grimmler, M., Reinhart, M., Alers, S., & Peter, C. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.12.013 · Cited by 2

Genome-wide screens identify core regulators of cell surface prion protein expression

Beauchemin, K. S., & Supattapone, S. (2026) · Scientific Reports · doi:10.1038/s41598-026-37137-2 · Cited by 2

Discovery and classification of new reptile cathelicidins by genome mining: study of their structure and genomic organization in Testudines and Squamata

Otazo‐Pérez, A., López, M. F., González-Acosta, S., Morales-delaNuez, A. J., & de la Lastra, J. M. P. (2026) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2026.105560 · Cited by 2

2′-O-methylation-dependent installation of N2-methylguanosine in the U6 internal stem loop facilitates efficient spliceosome assembly

Kleiber, N., Petrosyan, J., Greve, M., Thomé, C. C., Dybkov, O., Tay, L. L. E., Welp, L. M., Hackert, P., Touboul, D., Stark, H., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72355-2 · Cited by 2

Characterization of the virus-host RNA-RNA interactome across important human pathogenic RNA viruses

Damas, N. D., Seemann, S. E., Costa, R., Krambrich, J., Fossat, N., Rivera-Rangel, L. R., Fahnøe, U., Nielsen, L., Gorodkin, J., Bukh, J., et al. (2026) · PLoS Pathogens · doi:10.1371/journal.ppat.1014217 · Cited by 2

Zenit Ra Evaluation, A Solid-Phase Chemiluminescence Immunoassay for Detection of Anti-Cellular Antibodies

Madrid, E. M., Rodríguez, C. G., Ávila-García, M. D. G., Arrobas-Velilla, T., & Riejos, P. F. (2017) · Bioanalysis · doi:10.4155/bio-2016-0252 · Cited by 2

Clinical and Biological Significance of Sodium Channel Modifier 1 as a Component of the Minor Spliceosome in Hepatocellular Carcinoma

Ofuchi, T., Otsu, H., Hosoda, K., Ikehara, T., Higuchi, S., Tatsumi, T., Omachi, K., Tsujimoto, A., Hirose, K., Tsuda, Y., et al. (2025) · Annals of Surgical Oncology · doi:10.1245/s10434-025-17108-z · Cited by 2

The cancer-associated SF3B1K700E spliceosome mutation confers enhanced sensitivity to BV-6-induced cytotoxicity

Roets, L. E., Blayney, J. K., McMillan, H. P., Preston, P. J., Mutch, A., Mills, K., Savage, K. I., & Lappin, K. M. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07790-y · Cited by 2

Functional Evaluation of Splice Variants Using a Minigene Strategy

Nizou, A., Mahfoud, L., Janin, A., & Lia, A. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4726-4_11 · Cited by 2

cFLIP expression is altered in severe corticosteroid-resistant asthma

Lazarev, D., Miller, R. L., DiMango, E., Fu, X.-D., Li, H., Logan, C. J., & Manley, J. L. (2014) · Genomics Data · doi:10.1016/j.gdata.2014.05.003 · Cited by 2

Allele-specific alternative splicing of Drosophila Ribosomal protein S21 suppresses a lethal mutation in the Phosphorylated adaptor for RNA export (Phax) gene

Garcia, E. L. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkac195 · Cited by 2

Hemizygous splicing variant in CNKSR2 results in X‐linked intellectual developmental disorder

Lou, Y., Shi, X., Su, G., Guo, Y., Gao, L., Wang, Y., Miao, P., & Feng, J. (2024) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.2389 · Cited by 2

SFRS8 Regulates Memory by Modulating RNA Splicing of Synaptic Genes

Zeng, D., Liu, Q., & Zhang, J. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05036-8 · Cited by 2

Gene Regulation through mRNA Expression

Inose, H., Mukai, K., Ito, M., & Masuda, S. (2015) · Advances in Biological Chemistry · doi:10.4236/abc.2015.52005 · Cited by 2

A model of k-mer surprisal to quantify local sequence information content surrounding splice regions

Humphrey, S., Kerr, A. R. W., Rattray, M., Dive, C., & Miller, C. J. (2020) · PeerJ · doi:10.7717/peerj.10063 · Cited by 2

Comprehensive Analysis of Prognostic Alternative Splicing Signature Reveals Recurrence Predictor for Papillary Thyroid Cancer

Liu, M., Khushbu, R.-A., Chen, P., Hu, H., Tang, N., Ouyang, D., Wei, B., Zhao, Y., Huang, P. F., & Chang, S. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.705929 · Cited by 2

LncRNA BCLET variant confers bladder cancer susceptibility through alternative splicing of MSANTD2 exon 1

Liu, H., Wang, X., Guo, Z., Sun, G., Lv, Q., Qin, C., Yuan, L., Wang, Y., Du, M., Wang, M., et al. (2023) · Cancer Medicine · doi:10.1002/cam4.6072 · Cited by 2

Correlation betweenTICAM1gene polymorphisms and community‐acquired pneumonia in children

Yang, Y., Yang, S., Chen, Z., & Liu, L. (2020) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22503 · Cited by 2

Identification and initial characterization of POLIII-driven transcripts by msRNA-sequencing

Zorn, P., Misiak, D., Gekle, M., & Köhn, M. (2021) · RNA Biology · doi:10.1080/15476286.2020.1871216 · Cited by 2

The landscape of the alternatively spliced transcriptome remains stable during aging across different species and tissuesPreprint

Sieber, P., Barth, E., & Marz, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/541417 · Cited by 2

Type I PRMTs and PRMT5 Independently Regulate Both snRNP Arginine Methylation and Post-Transcriptional SplicingPreprint

Maron, M. I., Burgos, E. S., Gupta, V., Casill, A. D., Kosmyna, B., Chen, H., Gamble, M. J., Query, C. C., & Shechter, D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.18.389288 · Cited by 2

Transcription | Messenger RNA Processing in Eukaryotes

Wise, J. A., & Lou, H. J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00332-7 · Cited by 2

Characterization of the regulation of CD46 alternative splicing

Tang, S. J. (2016) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/65984 · Cited by 2

Extensive Dysregulation of SLK Splicing in Cancers Impacts MetastasisPreprint

Yang, Y., Hu, Y., Zhang, S.-R., Li, J., Guan, J.-W., Zhang, W., Sun, Y., Feng, X., Sun, J., Yang, Y., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.28.514146 · Cited by 2

Multifaced regulator: RNA binding proteins and their roles in hematopoiesis

Ren, Y., Huo, Y., Li, W., Wang, F., & Yu, J. (2019) · Blood Science · doi:10.1097/bs9.0000000000000008 · Cited by 1

Significance of RNA Processing Factors in Prognosis and Treatment of Hepatocellular Carcinoma: Implications for Precision Medicine

Zhan, R., Wang, S., Zheng, N., & Zhou, F. (2024) · Journal of Biomedical Nanotechnology · doi:10.1166/jbn.2024.3741 · Cited by 1

Addressing the tissue specificity of U5 snRNP spliceosomopathies

Kemal, R. A., & O’Keefe, R. T. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1572188 · Cited by 1

Targeted modification of cis-elements in the CUL3 gene to restore exon 9 inclusion for treating Gordon syndrome

Shi, X., Lu, S., Tang, Q., & Zhao, X. (2025) · Human Genomics · doi:10.1186/s40246-025-00820-y · Cited by 1

Nager Syndrome Revisited: Integrating In Vivo and In Vitro Models to Decipher SF3B4 ‐Dependent Tissue Coordination

Qin, J., Ulhaq, Z. S., & Tse, W. K. F. (2026) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.70007 · Cited by 1

Unlocking the potential of TNF: From biologic agents to small-molecule inhibitors

Huang, Y., Mu, L., Qu, Y., & Liu, Y. (2026) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2026.118780 · Cited by 1

U2AF2-regulated alternative splicing of UPP1 promotes NSCLC progression by enhancing glycolysis

Pan, H., Liang, X., Qin, Y., Xu, Y., Xue, K., Sun, L., Chai, W., Liu, X., Cao, Y., Li, J., et al. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02942-9 · Cited by 1

BCL11b interacts with RNA and proteins involved in RNA processing and developmental diseases

Sobhy, H., Rovere, M. D., Aït-Ammar, A., Kashif, M., Wallet, C., Daouad, F., Loustau, T., Lint, C. M. V., Schwartz, C., & Rohr, O. (2024) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2024.195065 · Cited by 1

Transcriptome‐based analysis of the molecular mechanism of recombinant protein expression in Periplaneta americana cells

Ma, C., Zhang, X., Li, X., Ding, W., Chen, H., & Feng, Y. (2024) · FEBS Journal · doi:10.1111/febs.17331 · Cited by 1

Multiple losses of aKRAB from PRDM9 coincide with a teleost-specific intron size distribution

Zinner, A.-C., & Jakt, L. M. (2024) · BMC Biology · doi:10.1186/s12915-024-02059-w · Cited by 1

Quantitative synthetic MRI reveals grey matter abnormalities in patients with spinal muscular atrophy types 2 and 3

Yan, C. P., Lan, S., Wang, H., Nie, H., Xiang, P., Xu, B., Su, S., Yang, Z., Tang, W., Li, Y., et al. (2025) · Quantitative Imaging in Medicine and Surgery · doi:10.21037/qims-24-1095 · Cited by 1

Reporting a Homozygous Case of Neurodevelopmental Disorder Associated With a Novel PRPF8 Variant

Mirinezhad, M. R., Mirzaei, F., Salmaninejad, A., Esfehani, R. J., Seyedtaghia, M. R., Farahmand, S., Toosi, M. B., Hashemian, S., & Lewis, M. E. S. (2025) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.70084 · Cited by 1

Pre-mRNA Splicing Functions in Plant Sexual Reproduction Development

Shao, D., Gao, X., & Wei, Y. (2025) · Plants · doi:10.3390/plants14101472 · Cited by 1

The splicing genes SmEa and SmEb regulate plant development during vegetative growth in poplar

Goretti, D., Collani, S., Marcon, A., Nilsson, O. R., & Schmid, M. (2025) · BMC Plant Biology · doi:10.1186/s12870-025-07676-3 · Cited by 1

Initial spliceosomal U4/U6 di-snRNA formation occurs in the cytoplasm of Saccharomyces cerevisiae and requires a guard protein mediated quality control

Wang, X., Guo, J., Li, J., & Krebber, H. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf1500 · Cited by 1

Splicing regulation and intron evolution in the short-intron ciliate model of endosymbiosis Paramecium bursaria

Nguyen, T. N. G., Kamal, M. M., Lin, C., & Leu, J. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag063 · Cited by 1

SMN deficiency-induced alternative splicing dysregulation in cardiac defects

Jiang, L., Wang, X., Cui, Y., Zhou, D., Yang, Z., Cheng, H., & Shanshan, M. A. O. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124361 · Cited by 1

Beyond housekeeping: snRNA diversity, regulation, and human disease

Liudkovska, V., de Jonge, A., & Cieśla, M. (2026) · Trends in Genetics · doi:10.1016/j.tig.2026.06.001 · Cited by 1

Alternative splicing is coordinated through interconnected response pathways to direct major features of fungal cell physiology

Neves‐da‐Rocha, J., Lopes, M. E. R., Azevedo, M. I. G., Petrucelli, M. F., Santos-Saboya, M. J., Rossi, A., & Martinez-Rossi, N. M. (2026) · Fungal Biology Reviews · doi:10.1016/j.fbr.2026.100506 · Cited by 1

Methylosome and survival motor neuron complexes are dispensable for plant viability in Arabidopsis thaliana

Goretti, D., Collani, S., Nardeli, S. M., Ratnakaram, H., Robert, S., & Schmid, M. (2026) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiag667 · Cited by 1

Dissecting the hybridization of oligonucleotides to structured complementary sequences

Peracchi, A. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.02.006 · Cited by 1

Interaction of spliceosomal U2 snRNP protein p14 with its branch site RNA target

Perea, W. (2016) · Cited by 1

Predicting DNA sequence splice site based on graph convolutional network and DNA graph construction

Rentao, L., Yelin, L., Guan, L., & Li, M. (2024) · Journal of King Saud University - Computer and Information Sciences · doi:10.1016/j.jksuci.2024.102089 · Cited by 1

ACTR10 Overexpression Facilitates the Progression and Tyrosine Kinase Inhibitor Resistance in Hepatocellular Carcinoma

Luo, J., Qin, K., He, R., Li, J. D., Huang, Z., Yin, B., Wu, T., Chen, Y., Qin, D. Y., Luo, J., et al. (2024) · World Journal of Oncology · doi:10.14740/wjon1944 · Cited by 1

Ion channel messenger RNA processing defects and arrhythmia

Dudley, S. C., & Zhou, A. (2014) · Current Biomarker Findings · doi:10.2147/cbf.s37417 · Cited by 1

General Aspects Related to Nonsense Mutations

Benhabiles, H., Jia, J., & Lejeune, F. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804468-1.00001-4 · Cited by 2

Structural Characterization of RNA Recognition Motif‐2 Domain of SART3

Bang, K., Cho, N. Y., Kim, W.-J., Kim, A., Song, H. K., Kim, E. E., & Kim, N. (2017) · Bulletin of the Korean Chemical Society · doi:10.1002/bkcs.11106 · Cited by 1

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells

Wei, H.-H., Liu, Y., Wang, Y., Lu, Q., Yang, X., Li, J., & Wang, Z. (2017) · Journal of Visualized Experiments · doi:10.3791/54967 · Cited by 1

Alternative Splicing and Aging

Yustis-Rubio, J. C., & Gómez-Verján, J. C. (2020) · Springer eBooks · doi:10.1007/978-3-030-40955-5_7 · Cited by 1

A putative frameshift variant in the CHM gene is associated with an unexpected splicing alteration in a choroideremia patient

Fioretti, T., Ungari, S., Savarese, M. C., Cattaneo, F., Pirozzi, E., & Esposito, G. (2020) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.1490 · Cited by 1

Induced pluripotent stem cells for modeling of spinal muscular atrophy

Welby, E., & Ebert, A. D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85764-2.00010-7 · Cited by 1

The Spliceosome and Pre-mRNA Splicing

Carrocci, T. J., & Hoskins, A. A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.10052-5 · Cited by 1

Messenger RNA Splicing Signals

Cygan, K. J., Taggart, A. J., Fairbrother, W. G., & Mount, S. M. (2017) · Wiley eBooks · doi:10.1002/9780470015902.a0000888.pub2 · Cited by 1

Riboglow: a multicolor riboswitch-based platform for live cell imaging of mRNA and small non-coding RNA in mammalian cellsPreprint

Braselmann, E., Wierzba, A. J., Polaski, J. T., Chromiński, M., Holmes, Z. E., Hung, S.-T., Batan, D., Wheeler, J. R., Parker, R., Jimenez, R., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/199240 · Cited by 1

A transcriptomic census reveals that Rbfox contributes to a broad but selective recapitulation of peripheral tissue splicing patterns in the thymusPreprint

Jansen, K., Shikama‐Dorn, N., Attar, M., Maio, S., Lopopolo, M., Buck, D., Holländer, G. A., & Sansom, S. N. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.06.980870 · Cited by 1

m RNA Splicing: Role of sn RNA s

Padgett, R. A. (2015) · Wiley eBooks · doi:10.1002/9780470015902.a0000879.pub3 · Cited by 1

Functional and Genetic Analysis of Choroid Plexus Development in Zebrafish

Henson, H. E. (2014) · doi:10.21007/etd.cghs.2014.0134 · Cited by 1

Lariat debranching by RNA DEBRANCHING ENZYME 1 depends on SICKLE in Arabidopsis thalianaPreprint

Kovak, E., Marshall, C. M., Molinari, M. D. C., Nepomuceno, A. L., & Harmon, F. G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.25.550414 · Cited by 1

Pan-tissue Transcriptome Analysis Reveals Sex-dimorphic Human AgingPreprint

Wang, S., Dong, D., Li, X., & Wang, Z. (2024) · eLife · doi:10.7554/elife.102449.1 · Cited by 1

Bioinformatic Analysis of Alternative Splicing

Acharya, K. K., Medini, R., Thakur, T., Agrawal, K., Das, A., Balagannavar, G. C., & Chitturi, N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95502-7.00204-9 · Cited by 1

Pan-tissue Transcriptome Analysis Reveals Sex-dimorphic Human AgingPreprint

Wang, S., Dong, D., Li, X., & Wang, Z. (2025) · eLife · doi:10.7554/elife.102449.2 · Cited by 1

Intron Retention Controls Localization of lncRNAs PURPL and MALAT1 to Promote Cell Proliferation and MigrationPreprint

Grammatikakis, I., Norkaew, C., song, Y. J., Behera, A. K., Pehrsson, E. C., Hartford, C. C. R., Kordale, S., Prasanth, R., Zhao, Y., Shrethsa, B., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.19.706780 · Cited by 1

Dramatically reduced spliceosome, intronome, and splicing efficiency in Cyanidiococcus yangmingshanensis and Cyanidium caldariumPreprint

Slat, V., Stark, M. R., & Rader, S. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.17.725761 · Cited by 1

Macromolecular Communication between Nucleus and Cytoplasm

Tartakoff, A. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30020-7

Small Nuclear RNA

Buratti, E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-374984-0.01437-6

ATPase dependent and independent roles of Brahma in transcription and pre-mRNA processing

Yu, S. (2015) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Assessing the relationship between chromatin and splicing factors in alternative splicing

Kremsky, I. (2015) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Gene expression regulation by well-known non-coding RNAs

Tan, J. (2014) · doi:10.32657/10356/64260

MED12 in hematopoietic stem cells—cell specific function despite ubiquitous expression

Keightley, M.-C., Nilsson, S. K., & Lieschke, G. J. (2017) · Stem Cell Investigation · doi:10.21037/sci.2016.12.04

Ambient temperature‐directed flowering time regulation : the role of alternative splicing

Verhage, D. S. L. (2017) · doi:10.18174/393113

Targeting Pre-mRNA Processing in Cancer

Webb, T. R., & Stamm, S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.12398-4

An Investigation Into The Molecular Basis Underlying Enhancement Of Transcription By The Intron In Budding Yeast

Agarwal, N. (2016) · Human Biology

Characterization of regulatory mechanisms for BIM exon 3 alternative splicing

Bhadra, M. (2017) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/69548

Computational modeling of splicing regulation

Lin, H. (2017) · IUScholarWorks (Indiana University) · doi:10.7912/c2/900

Das Spliceosom als Angriffspunkt für Pharmaka

León, B., Kashyap, M. K., Chan, W. C., Krug, K. A., Castro, J. E., Clair, J. J. L., & Burkart, M. D. (2017) · Angewandte Chemie · doi:10.1002/ange.201701065

Optimizing gene expression by adapting splicingPreprint

Frumkin, I., Yofe, I., Bar‐Ziv, R., Voichek, Y., & Pilpel, Y. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/220228

Characterization of RNA-modifying enzymes and their roles in diseases

Warda, A. S. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6612

Characterizing the role of ice1 in maintaining zebrafish neural stem cells

D’Amata, C. (2017) · TSpace (University of Toronto)

Targeting the ubiquitin proteasome system to develop novel therapeutic approaches for spinal muscular atrophy

Powis, R. A. (2016) · Edinburgh Research Archive (University of Edinburgh)

Negative Cooperativity between Gemin2 and RNA provides Insights into RNA Selection and the SMN Complex’s Release in snRNP AssemblyPreprint

Yi, H., Mu, L., Shen, C., Kong, X., Wang, Y., Hou, Y., & Zhang, R. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/312124

Large-scale study of rna processing alterations in multiple cancers

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