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

Quantitative prediction of variant effects on alternative splicing in MAPT using endogenous pre-messenger RNA structure probing

Kumar, J., Lackey, L., Waldern, J. M., Dey, A., Mustoe, A. M., Weeks, K. M., Mathews, D. H., & Laederach, A. (2022) · eLife · doi:10.7554/elife.73888 · Cited by 24

Impacts of Alternative Splicing Events on the Differentiation of Adipocytes

Lin, J.-C. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160922169 · Cited by 23

New CD20 alternative splice variants: molecular identification and differential expression within hematological B cell malignancies

Gamonet, C., Bôle‐Richard, E., Delherme, A., Aubin, F., Toussirot, É., Garnache‐Ottou, F., Godet, Y., Ysebaert, L., Tournilhac, O., Dartigeas, C., et al. (2015) · Experimental Hematology and Oncology · doi:10.1186/s40164-016-0036-3 · Cited by 23

A new cis-acting motif is required for the axonal SMN-dependent Anxa2 mRNA localization

Rihan, K., Antoine, E., Maurin, T., Bardoni, B., Bordonné, R., Soret, J., & Rage, F. (2017) · RNA · doi:10.1261/rna.056788.116 · Cited by 23

A genetic screen implicates a CWC16/Yju2/CCDC130 protein and SMU1 in alternative splicing in Arabidopsis thaliana

Kanno, T., Lin, W., Fu, J. L., Matzke, A. J. M., & Matzke, M. A. (2017) · RNA · doi:10.1261/rna.060517.116 · Cited by 23

Variant snRNPs: New players within the spliceosome system

Vazquez‐Arango, P., & O’Reilly, D. (2017) · RNA Biology · doi:10.1080/15476286.2017.1373238 · Cited by 23

The Sm-core mediates the retention of partially-assembled spliceosomal snRNPs in Cajal bodies until their full maturation

Roithová, A., Klimešová, K., Pánek, J., Will, C. L., Lührmann, R., Staněk, D., & Girard, C. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky070 · Cited by 23

Transcriptome-wide analysis of alternative mRNA splicing signature in the diagnosis and prognosis of stomach adenocarcinoma

Shi, Y., Chen, Z., Gao, J., Wu, S., Gao, H., & Feng, G. (2018) · Oncology Reports · doi:10.3892/or.2018.6623 · Cited by 23

Disease modeling of core pre-mRNA splicing factor haploinsufficiency

Wood, K., Rowlands, C. F., Qureshi, W. M. S., Thomas, H. B., Buczek, W. A., Briggs, T. A., Hubbard, S. J., Hentges, K. E., Newman, W. G., & O’Keefe, R. T. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz169 · Cited by 23

UsnRNP trafficking is regulated by stress granules and compromised by mutant ALS proteins

Rossi, S., Rompietti, V., Antonucci, Y., Giovannini, D., Scopa, C., Scaricamazza, S., Scardigli, R., Cestra, G., Serafino, A., Carrı̀, M. T., et al. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104792 · Cited by 23

Regulation of RNA decay and cellular function by 3′-5′ exoribonuclease DIS3L2

Luan, S., Luo, J., Liu, H., & Li, Z. (2019) · RNA Biology · doi:10.1080/15476286.2018.1564466 · Cited by 22

Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome

Engal, E., Oja, K. T., Maroofian, R., Geminder, O., Le, T.-L., Marzin, P., Guimier, A., Mor, E., Zvi, N., Elefant, N., et al. (2023) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.10.013 · Cited by 22

IntS6 and the Integrator phosphatase module tune the efficiency of select premature transcription termination events

Fujiwara, R., Zhai, S.-N., Liang, D., Shah, A. P., Tracey, M. P., Ma, X.-K., Fields, C. J., Mendoza-Figueroa, M. S., Meline, M. C., Tatomer, D. C., et al. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.10.035 · Cited by 22

Role of PRMT1 and PRMT5 in Breast Cancer

Martinez, S., Sentis, S., Poulard, C., Trédan, O., & Romancer, M. L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168854 · Cited by 25

Structural and mechanistic basis for preferential deadenylation of U6 snRNA by Usb1

Nomura, Y., Roston, D., Montemayor, E., Cui, Q., & Butcher, S. E. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky812 · Cited by 23

Small ribonucleoprotein particle protein SmD3 governs the homeostasis of germline stem cells and the crosstalk between the spliceosome and ribosome signals in Drosophila

Yu, J. J., Luan, X., Yan, Y., Qiao, C., Liu, Y., Zhao, D., Xie, B., Zheng, Q., Wang, M., Chen, W., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201802536rr · Cited by 22

An in-silico human cell model reveals the influence of spatial organization on RNA splicing

Ghaemi, Z., Peterson, J. R., Gruebele, M., & Luthey-Schulten, Z. A. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007717 · Cited by 24

Cellular Sticking Can Strongly Reduce Complex Binding by Speeding Dissociation

Davis, C. M., & Gruebele, M. (2021) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.1c00950 · Cited by 22

AtMC1 Associates With LSM4 to Regulate Plant Immunity Through Modulating Pre-mRNA Splicing

Wang, S., Xue, M., He, C., Shen, D., Jiang, C., Zhao, H., & Niu, D. (2021) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-07-21-0197-r · Cited by 22

Therapeutic Targeting of Alternative RNA Splicing in Gastrointestinal Malignancies and Other Cancers

Şahin, İ., George, A., & Seyhan, A. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111790 · Cited by 22

Genomic dynamics associated with malignant transformation in IDH1 mutated gliomas

Park, C., Park, I. H., Lee, S., Sun, C.-H., Koh, Y., Park, S.-H., Eun, K. J., Yun, H., & Lee, S.-H. (2015) · Oncotarget · doi:10.18632/oncotarget.6189 · Cited by 22

Spliceosomal intronogenesis

Lee, S., & Stevens, S. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605113113 · Cited by 22

If the 5’ cap fits (wear it) – Non-canonical RNA capping

Potužník, J. F., & Cahová, H. (2024) · RNA Biology · doi:10.1080/15476286.2024.2372138 · Cited by 21

The Tumor Microenvironment Impairs Th1 IFNγ Secretion through Alternative Splicing Modifications of Irf1 Pre-mRNA

Bernard, A., Hibos, C., Richard, C., Viltard, E., Chevrier, S., Lemoine, S., Melin, J., Humblin, É., Mary, R., Accogli, T., et al. (2021) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-19-0679 · Cited by 21

Posttranslational splicing modifications as a key mechanism in cytarabine resistance in acute myeloid leukemia

Morales, M. L., García-Vicente, R., Rodríguez-García, A., Reyes‐Palomares, A., Vincelle-Nieto, Á., Alvarez, N. D. D., Ortiz-Ruiz, A., Garrido, V., Giménez, A., Carreño‐Tarragona, G., et al. (2023) · Leukemia · doi:10.1038/s41375-023-01963-4 · Cited by 21

Chemical Modulation of Pre-mRNA Splicing in Mammalian Systems

Boer, R. E., Torrey, Z. R., & Schneekloth, J. S. (2020) · ACS Chemical Biology · doi:10.1021/acschembio.0c00001 · Cited by 21

Functional and evolutionary analysis of the Arabidopsi s 4R-MYB protein SNAPc4 as part of the SNAP complex

Thiedig, K., Weißhaar, B., & Stracke, R. (2020) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaa067 · Cited by 21

Metabolic regulation of mRNA splicing

Cui, H., Shi, Q., Macarios, C. M., & SCHIMMEL, P. R. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.02.002 · Cited by 22

Identification of Methylation-Regulated Differentially Expressed Genes and Related Pathways in Hepatocellular Carcinoma: A Study Based on TCGA Database and Bioinformatics Analysis

Yu, L., Ma, B., Jiang, P., & Yang, H. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.636093 · Cited by 20

The spliceosome component Usp39 controls B cell development by regulating immunoglobulin gene rearrangement

Ruan, G., Li, Y., Chen, W., Huang, H., Zhang, R., Chen, C., Lam, K., Xu, S., & Ou, X. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110338 · Cited by 20

GEMINs: potential therapeutic targets for spinal muscular atrophy?

Borg, R. M., & Cauchi, R. J. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00325 · Cited by 20

Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation

Lanfranco, M., Cacciottolo, R., Borg, R. M., Vassallo, N., Juge, F., Bordonné, R., & Cauchi, R. J. (2017) · FEBS Letters · doi:10.1002/1873-3468.12853 · Cited by 20

Somatic SF3B1 mutations in myelodysplastic syndrome with ring sideroblasts and chronic lymphocytic leukaemia

Foy, A., & McMullin, M. F. (2019) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2019-205895 · Cited by 21

Diabetic polyneuropathy: Bridging the translational gap

Kobayashi, M., & Zochodne, D. W. (2020) · Journal of the Peripheral Nervous System · doi:10.1111/jns.12392 · Cited by 21

RNA Binding Motif 5 (RBM5) in the CNS—Moving Beyond Cancer to Harness RNA Splicing to Mitigate the Consequences of Brain Injury

Jackson, T. C., & Kochanek, P. M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00126 · Cited by 21

SF3B1 mutant myelodysplastic syndrome: Recent advances

Pellagatti, A., & Boultwood, J. (2020) · Advances in Biological Regulation · doi:10.1016/j.jbior.2020.100776 · Cited by 20

Nuclear Magnetic Resonance Structure of a Novel Globular Domain in RBM10 Containing OCRE, the Octamer Repeat Sequence Motif

Martin, B. T., Serrano, P., Geralt, M., & Wüthrich, K. (2015) · Structure · doi:10.1016/j.str.2015.10.029 · Cited by 20

Gemin4 is an essential gene in mice, and its overexpression in human cells causes relocalization of the SMN complex to the nucleoplasm

Meier, I. D., Walker, M. P., & Matera, A. G. (2018) · Biology Open · doi:10.1242/bio.032409 · Cited by 20

The Regulatory Roles of RNA-Binding Proteins in Plant Salt Stress Response

Wang, T. Q., Meng, K., Zhu, Z., Pan, L., Okita, T. W., Zhang, L., & Tian, L. (2025) · Plants · doi:10.3390/plants14091402 · Cited by 19

Lighting up the central dogma for predictive developmental biology

García, H. G., Berrocal, A., Kim, Y. J., Martini, G. D., & Zhao, J. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.10.010 · Cited by 19

PICLN modulates alternative splicing and light/temperature responses in plants

Mateos, J. L., Sánchez, S. E., Legris, M., Esteve-Bruna, D., Torchio, J. C., Petrillo, E., Goretti, D., Blanco‐Touriñán, N., Seymour, D. K., Schmid, M., et al. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac527 · Cited by 19

GPATCH4 regulates rRNA and snRNA 2′-O-methylation in both DHX15-dependent and DHX15-independent manners

Kanwal, N., Krogh, N., Memet, I., Lemus-Diaz, N., Thomé, C. C., Welp, L. M., Mizi, A., Hackert, P., Papantonis, A., Urlaub, H., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad1202 · Cited by 20

A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methods

Oh, R. Y., AlMail, A., Cheerie, D., Guirguis, G. F., Hou, H., Yuki, K. E., Haque, B., Thiruvahindrapuram, B., Marshall, C. R., Mendoza‐Londono, R., et al. (2024) · Human Genetics and Genomics Advances · doi:10.1016/j.xhgg.2024.100299 · Cited by 19

Mutations in the U11/U12-65K protein associated with isolated growth hormone deficiency lead to structural destabilization and impaired binding of U12 snRNA

Norppa, A. J., Kauppala, T., Heikkinen, H. A., Verma, B., Iwaï, H., & Frilander, M. J. (2017) · RNA · doi:10.1261/rna.062844.117 · Cited by 19

SWATH‐based proteomics reveals processes associated with immune evasion and metastasis in poor prognosis colorectal tumours

Lopez-Sanchez, L. M., Jiménez‐Izquierdo, R., Peñarando, J., Mena‐Osuna, R., Guil‐Luna, S., Toledano‐Fonseca, M., Conde, F., Villar, C., Díaz, C., Ortea, I., et al. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14693 · Cited by 19

Complex interactomes and post-translational modifications of the regulatory proteins HABP4 and SERBP1 suggest pleiotropic cellular functions

Colleti, C., Melo‐Hanchuk, T. D., da Silva, F. R. M., Saito, Â., & Kobarg, J. (2019) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v10.i3.44 · Cited by 19

Combinatorial control of Spo11 alternative splicing by modulation of RNA polymerase II dynamics and splicing factor recruitment during meiosis

Cesari, E., Loiarro, M., Naro, C., Pieraccioli, M., Farini, D., Pellegrini, L., Pagliarini, V., Bielli, P., & Sette, C. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2443-y · Cited by 19

Nusinersen ameliorates motor function and prevents motoneuron Cajal body disassembly and abnormal poly(A) RNA distribution in a SMA mouse model

Berciano, M. T., Puente-Bedia, A., Medina-Samamé, A., Rodríguez-Rey, J. C., Calderó, J., Lafarga, M., & Tapia, O. (2020) · Scientific Reports · doi:10.1038/s41598-020-67569-3 · Cited by 19

The potential roles of circular RNAs as modulators in traumatic spinal cord injury

Bie, F., Wang, K., Xu, T., Yuan, J., Ding, H., Lv, B., Liu, Y., & Lan, M. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111826 · Cited by 19

Dysregulation of splicing variants and spliceosome components in breast cancer

Gahete, M. D., Hermán‐Sánchez, N., Fuentes-Fayos, A. C., Lopez-Canovas, J. L., & Luque, R. M. (2022) · Endocrine Related Cancer · doi:10.1530/erc-22-0019 · Cited by 19

SRSF1 acts as an IFN-I-regulated cellular dependency factor decisively affecting HIV-1 post-integration steps

Sertznig, H., Roesmann, F., Wilhelm, A., Heininger, D., Bleekmann, B., Elsner, C., Santiago, M. L., Schuhenn, J., Karakoese, Z., Benatzy, Y., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.935800 · Cited by 22

RBM4a-regulated splicing cascade modulates the differentiation and metabolic activities of brown adipocytes

Lin, J.-C., Lu, Y.-H., Liu, Y., & Lin, Y. (2016) · Scientific Reports · doi:10.1038/srep20665 · Cited by 19

SF1 Phosphorylation Enhances Specific Binding to U2AF 65 and Reduces Binding to 3′-Splice-Site RNA

Chatrikhi, R., Wang, W., Gupta, A., Loerch, S., Maucuer, A., & Kielkopf, C. L. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.11.007 · Cited by 19

A Genetic Screen Identifies PRP18a, a Putative Second Step Splicing Factor Important for Alternative Splicing and a Normal Phenotype inArabidopsis thaliana

Kanno, T., Lin, W., Chang, C., Matzke, M. A., & Matzke, A. J. M. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200022 · Cited by 19

Alternative splicing: A key regulator in T cell response and cancer immunotherapy

Yong, C., Liang, Y., Wang, M., Jin, W., Fan, X., Wang, Z., Cao, K., Wu, T., Li, Q., & Chang, C. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107713 · Cited by 19

Decoding alternative splicing: A key player in plant biotic stress resistance

Zhu, J., Guo, W., Chen, J., & Sun, Z. (2025) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13951 · Cited by 18

Lipin 1 modulates mRNA splicing during fasting adaptation in liver

Wang, H., Chan, T. W., Vashisht, A. A., Drew, B. G., Calkin, A. C., Harris, T. E., Wohlschlegel, J. A., Xiao, X. G., & Reue, K. (2021) · JCI Insight · doi:10.1172/jci.insight.150114 · Cited by 18

The intrinsically disordered TSSC4 protein acts as a helicase inhibitor, placeholder and multi-interaction coordinator during snRNP assembly and recycling

Bergfort, A., Hilal, T., Kuropka, B., Ilik, İ., Weber, G., Aktaş, T., Freund, C., & Wahl, M. C. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac087 · Cited by 18

RNA binding proteins in MLL-rearranged leukemia

Tran, T. M., & Rao, D. S. (2022) · Experimental Hematology and Oncology · doi:10.1186/s40164-022-00343-5 · Cited by 18

Analyzing alternative splicing in Alzheimer’s disease postmortem brain: a cell-level perspective

Farhadieh, M., & Ghaedi, K. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1237874 · Cited by 18

DDX20: A Multifunctional Complex Protein

He, L., Yang, J., Yu, H., Yang, X., Shi, X., Zhang, D., Zhao, D., Yan, W., Bie, X., Chen, L., et al. (2023) · Molecules · doi:10.3390/molecules28207198 · Cited by 18

What is going on inside of phytochrome B photobodies?

Willige, B. C., Yoo, C. Y., & Guzmán, J. P. S. (2024) · The Plant Cell · doi:10.1093/plcell/koae084 · Cited by 18

Liquid-liquid phase separation in subcellular assemblages and signaling pathways: Chromatin modifications induced gene regulation for cellular physiology and functions including carcinogenesis

Chakraborty, S., Mishra, J., Roy, A., Niharika, N., Manna, S., Baral, T., Nandi, P., Patra, S., & Patra, S. K. (2024) · Biochimie · doi:10.1016/j.biochi.2024.05.007 · Cited by 18

The Application of Non-Coding RNAs as Biomarkers, Therapies, and Novel Vaccines in Diseases

Yang, L.-X., Li, H., Cheng, Z.-H., Sun, H.-Y., Huang, J., Li, Z., Li, X., Hu, Z., & Wang, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073055 · Cited by 18

Identification of Methylosome Components as Negative Regulators of Plant Immunity Using Chemical Genetics

Huang, S., Balgi, A. D., Pan, Y., Li, M., Zhang, X., Du, L., Zhou, M., Roberge, M., & Li, X. (2016) · Molecular Plant · doi:10.1016/j.molp.2016.10.006 · Cited by 18

The splicing factor transformer2 (tra2) functions in the Drosophila fat body to regulate lipid storage

Mikoluk, C., Nagengast, A., & DiAngelo, J. R. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.12.002 · Cited by 18

Accumulation of poly(A) RNA in nuclear granules enriched in Sam68 in motor neurons from the SMNΔ7 mouse model of SMA

Narcís, J. O., Tapia, O., Tarabal, O., Piedrafita, L., Calderó, J., Berciano, M. T., & Lafarga, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-27821-3 · Cited by 18

Negative cooperativity between Gemin2 and RNA provides insights into RNA selection and the SMN complex's release in snRNP assembly

Yi, H., Li, M., Shen, C., Kong, X., Wang, Y., Hou, Y., & Zhang, R. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1135 · Cited by 18

Allosteric regulation of U1 snRNP by splicing regulatory proteins controls spliceosomal assembly

Shenasa, H., Movassat, M., Forouzmand, E., & Hertel, K. J. (2020) · RNA · doi:10.1261/rna.075135.120 · Cited by 19

Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation

von Elsner, L., Chai, G., Schneeberger, P. E., Harms, F. L., Casar, C., Qi, M., Alawi, M., Abdel‐Salam, G. M. H., Zaki, M. S., Arndt, F., et al. (2021) · Brain · doi:10.1093/brain/awab403 · Cited by 18

Integrative Proteome and Phosphoproteome Profiling of Early Cold Response in Maize Seedlings

Xing, J., Tan, J., Feng, H., Zhou, Z., Deng, M., Luo, H., & Deng, Z. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126493 · Cited by 18

Modulation the alternative splicing of GLA (IVS4+919G>A) in Fabry disease

Chang, W.-H., Niu, D., Lu, C.-Y., Lin, S.-Y., Liu, T., & Chang, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175929 · Cited by 18

Ubiquitin carboxyl-terminal hydrolase isozyme L5 inhibits human glioma cell migration and invasion via downregulating SNRPF

Ge, J., Hu, W., Zhou, H., Yu, J., Sun, C., & Chen, W. (2017) · Oncotarget · doi:10.18632/oncotarget.23071 · Cited by 18

Functional and in-silico interrogation of rare genomic variants impacting RNA splicing for the diagnosis of genomic disordersPreprint

Ellingford, J. M., Thomas, H. B., Rowlands, C. F., Arno, G., Beaman, G. M., Gomes-Silva, B., Campbell, C., Gossan, N., Hardcastle, C. L., Webb, A. K., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/781088 · Cited by 18

SRSF6 modulates histone-chaperone HIRA splicing to orchestrate AR and E2F activity in prostate cancer

Montero‐Hidalgo, A. J., Jiménez‐Vacas, J. M., Gómez‐Gómez, E., Porcel-Pastrana, F., Sáez-Martínez, P., Pérez‐Gómez, J. M., Fuentes-Fayos, A. C., Blázquez‐Encinas, R., Sánchez‐Sánchez, R., González-Serrano, T., et al. (2024) · Science Advances · doi:10.1126/sciadv.ado8231 · Cited by 17

Identification, evolution and alternative splicing profile analysis of the splicing factor 30 (SPF30) in plant species

Zhang, D., Yang, J.-F., Gao, B., Liu, T.-Y., Hao, G., Yang, G., Fu, L.-J., Chen, M., & Zhang, J. (2019) · Planta · doi:10.1007/s00425-019-03146-x · Cited by 17

A UHM–ULM interface with unusual structural features contributes to U2AF2 and SF3B1 association for pre-mRNA splicing

Galardi, J. W., Bela, V. N., Jeffery, N. N., He, X., Glasser, E., Loerch, S., Jenkins, J. L., Pulvino, M. J., Boutz, P. L., & Kielkopf, C. L. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102224 · Cited by 17

Aberrant Retinal Pigment Epithelial Cells Derived from Induced Pluripotent Stem Cells of a Retinitis Pigmentosa Patient with the PRPF6 Mutation

Liang, Y., Tan, F., Sun, X., Cui, Z., Gu, J., Mao, S., Chan, H. F., Tang, S., & Chen, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169049 · Cited by 17

Alternative splicing in bladder cancer: potential strategies for cancer diagnosis, prognosis, and treatment

Montero‐Hidalgo, A. J., Pérez‐Gómez, J. M., Martínez‐Fuentes, A. J., Gómez‐Gómez, E., Gahete, M. D., Jiménez‐Vacas, J. M., & Luque, R. M. (2022) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1760 · Cited by 17

RNA levers and switches controlling viral gene expression

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