Function of alternative splicing
Abstract
Almost all polymerase II transcripts undergo alternative pre-mRNA splicing. Here, we review the functions of alternative splicing events that have been experimentally determined. The overall function of alternative splicing is to increase the diversity of mRNAs expressed from the genome. Alternative splicing changes proteins encoded by mRNAs, which has profound functional effects. Experimental analysis of these protein isoforms showed that alternative splicing regulates binding between proteins, between proteins and nucleic acids as well as between proteins and membranes. Alternative splicing regulates the localization of proteins, their enzymatic properties and their interaction with ligands. In most cases, changes caused by individual splicing isoforms are small. However, cells typically coordinate numerous changes in 'splicing programs', which can have strong effects on cell proliferation, cell survival and properties of the nervous system. Due to its widespread usage and molecular versatility, alternative splicing emerges as a central element in gene regulation that interferes with almost every biological function analyzed.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Different splice variants can have distinct interaction partners and biological functions.
“RNA-seq can also distinguish between the expression of different splice variants [46, 47], which can have distinct interaction partners [48] and biological functions [49].”
From Gene co-expression analysis for functional classification and gene–disease predictions (2017) · cites this paper as [49]
Cites
AUGUSTUS: ab initio prediction of alternative transcripts
Stanke, M., Keller, O., Gunduz, I., Hayes, A., Waack, S., & Morgenstern, B. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl200 · Cited by 2,829 · see citing works
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
Christofk, H. R., Vander Heiden, M. G., Harris, M. H., Ramanathan, A., Gerszten, R. E., Wei, R., Fleming, M. D., Schreiber, S. L., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06734 · Cited by 2,820 · see citing works
The Spliceosome: Design Principles of a Dynamic RNP Machine
Wahl, M. C., Will, C. L., & Lührmann, R. (2009) · Cell · doi:10.1016/j.cell.2009.02.009 · Cited by 2,665 · see citing works
Tripathi, V., Ellis, J. D., Shen, Z., Song, D. Y., Pan, Q., Watt, A. T., Freier, S. M., Bennett, C. F., Sharma, A., Bubulya, P. A., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.08.011 · Cited by 2,223 · see citing works
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 1,424 · see citing works
Makeyev, E. V., Zhang, J., Carrasco, M. A., & Maniatis, T. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.015 · Cited by 1,395 · see citing works
Function of alternative splicing
Stamm, S., Ben‐Ari, S., Rafalska, I., Tang, Y., Zhang, Z., Toiber, D., Thanaraj, T. A., & Soreq, H. (2004) · Gene · doi:10.1016/j.gene.2004.10.022 · Cited by 1,373 · see citing works
Self-citationHITS-CLIP yields genome-wide insights into brain alternative RNA processing
Licatalosi, D. D., Mele, A., Fak, J. J., Ule, J., Kayikci, M., Chi, S. W., Clark, T. A., Schweitzer, A. C., Blume, J. E., Wang, X., et al. (2008) · Nature · doi:10.1038/nature07488 · Cited by 1,352 · see citing works
Stanke, M., Schöffmann, O., Morgenstern, B., & Waack, S. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-62 · Cited by 1,304 · see citing works
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 · see citing works
Sultan, M., Schulz, M. H., Richard, H., Magen, A., Klingenhoff, A., Scherf, M., Seifert, M., Borodina, T., Soldatov, A., Parkhomchuk, D., et al. (2008) · Science · doi:10.1126/science.1160342 · Cited by 1,293 · see citing works
Mechanisms of alternative splicing regulation: insights from molecular and genomics approaches
Chen, M., & Manley, J. L. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2777 · Cited by 1,284 · see citing works
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 · see citing works
HnRNP proteins controlled by c-Myc deregulate pyruvate kinase mRNA splicing in cancer
David, C. J., Chen, M., Assanah, M., Canoll, P., & Manley, J. L. (2010) · Nature · doi:10.1038/nature08697 · Cited by 1,179 · see citing works
Cooper, T. A., Wan, L., & Dreyfuss, G. (2009) · Cell · doi:10.1016/j.cell.2009.02.011 · Cited by 1,160 · see citing works
iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution
König, J., Zarnack, K., Rot, G., Curk, T., Kayikci, M., Zupan, B., Turner, D. J., Luscombe, N. M., & Ule, J. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1838 · Cited by 1,126 · see citing works
CLIP Identifies Nova-Regulated RNA Networks in the Brain
Ule, J., Jensen, K. B., Ruggiu, M., Mele, A., Ule, A., & Darnell, R. B. (2003) · Science · doi:10.1126/science.1090095 · Cited by 1,120 · see citing works
Regulation of Alternative Splicing by Histone Modifications
Luco, R. F., Pan, Q., Tominaga, K., Blencowe, B. J., Pereira‐Smith, O. M., & Misteli, T. (2010) · Science · doi:10.1126/science.1184208 · Cited by 1,099 · see citing works
Exon Recognition in Vertebrate Splicing
Berget, S. M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.6.2411 · Cited by 1,090 · see citing works
Alternative splicing and evolution: diversification, exon definition and function
Keren, H., Lev-Maor, G., & Ast, G. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2776 · Cited by 1,082 · see citing works
Splicing in disease: disruption of the splicing code and the decoding machinery
Wang, G., & Cooper, T. A. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2164 · Cited by 1,040 · see citing works
Belfiore, A., Frasca, F., Pandini, G., Sciacca, L., & Vigneri, R. (2009) · Endocrine Reviews · doi:10.1210/er.2008-0047 · Cited by 1,035 · see citing works
Dehm, S. M., Schmidt, L. J., Heemers, H. V., Vessella, R. L., & Tindall, D. J. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-0594 · Cited by 834 · see citing works
Alternative pre-mRNA splicing regulation in cancer: pathways and programs unhingedPreprint
David, C. J., & Manley, J. L. (2010) · Genes & Development · doi:10.1101/gad.1973010 · Cited by 815 · see citing works
Acid-Mediated Tumor Invasion: a Multidisciplinary Study
Gatenby, R. A., Gawlinski, E. T., Gmitro, A. F., Kaylor, B., & Gillies, R. J. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-4193 · Cited by 771 · see citing works
Structure and evolution of transcriptional regulatory networks
Babu, M. M., Luscombe, N. M., Aravind, L., Gerstein, M., & Teichmann, S. A. (2004) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2004.05.004 · Cited by 764 · see citing works
The Honey Bee Epigenomes: Differential Methylation of Brain DNA in Queens and Workers
Lyko, F., Foret, S., Kucharski, R., Wolf, S., Falckenhayn, C., & Maleszka, R. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000506 · Cited by 727 · see citing works
Feng, J., Bi, C., Clark, B. S., Mady, R., Shah, P., & Kohtz, J. D. (2006) · Genes & Development · doi:10.1101/gad.1416106 · Cited by 712 · see citing works
mSin1 Is Necessary for Akt/PKB Phosphorylation, and Its Isoforms Define Three Distinct mTORC2s
Frías, M. A., Thoreen, C. C., Jaffe, J. D., Schroder, W. A., Sculley, T. B., Carr, S. A., & Sabatini, D. M. (2006) · Current Biology · doi:10.1016/j.cub.2006.08.001 · Cited by 690 · see citing works
Differential chromatin marking of introns and expressed exons by H3K36me3
Kolasinska-Zwierz, P., Down, T. A., Latorre, I. J., Liu, T., Liu, X. S., & Ahringer, J. (2009) · Nature Genetics · doi:10.1038/ng.322 · Cited by 671 · see citing works
Escaping the Nuclear Confines: Signal-Dependent Pre-mRNA Splicing in Anucleate Platelets
Denis, M. M., Tolley, N. D., Bunting, M., Schwertz, H., Jiang, H., Lindemann, S., Yost, C. C., Rubner, F. J., Albertine, K. H., Swoboda, K. J., et al. (2005) · Cell · doi:10.1016/j.cell.2005.06.015 · Cited by 652 · see citing works
AceView: a comprehensive cDNA-supported gene and transcripts annotation
Thierry-Mieg, D., & Thierry-Mieg, J. (2006) · Genome Biology · doi:10.1186/gb-2006-7-s1-s12 · Cited by 629 · see citing works
Johnson, M. B., Kawasawa, Y. I., Mason, C. E., Krsnik, Ž., Coppola, G., Bogdanović, D., Geschwind, D. H., Mane, S. M., State, M. W., & Šestan, N. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.027 · Cited by 603 · see citing works
Yeo, G. W., Coufal, N. G., Liang, T. Y., Peng, G. E., Fu, X.-D., & Gage, F. H. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1545 · Cited by 572 · see citing works
Different levels of alternative splicing among eukaryotes
Kim, E., Magen, A., & Ast, G. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl924 · Cited by 545 · see citing works
Alternative splicing and disease
Tazi, J., Bakkour, N., & Stamm, S. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.09.017 · Cited by 541 · see citing works
Self-citationRomero, P. R., Zaidi, S., Fang, Y. Y., Uversky, V. N., Radivojac, P., Oldfield, C. J., Cortese, M. S., Sickmeier, M., LeGall, T., Obradovic, Z., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507916103 · Cited by 480 · see citing works
RNA-MEDIATED NEUROMUSCULAR DISORDERS
Ranum, L. P. W., & Cooper, T. A. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113014 · Cited by 472 · see citing works
Xue, Y., Zhou, Y., Wu, T., Zhu, T., Ji, X., Kwon, Y.-S., Zhang, C., Yeo, G., Black, D. L., Sun, H., et al. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.12.003 · Cited by 469 · see citing works
Nucleosome positioning as a determinant of exon recognition
Tilgner, H., Nikolaou, C., Althammer, S., Sammeth, M., Beato, M., Valcárcel, J., & Guigó, R. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1658 · Cited by 446 · see citing works
The Birth of an Alternatively Spliced Exon: 3' Splice-Site Selection in Alu Exons
Lev-Maor, G., Sorek, R., Shomron, N., & Ast, G. (2003) · Science · doi:10.1126/science.1082588 · Cited by 435 · see citing works
Control of alternative RNA splicing and gene expression by eukaryotic riboswitches
Cheah, M. T., Wachter, A., Sudarsan, N., & Breaker, R. R. (2007) · Nature · doi:10.1038/nature05769 · Cited by 430 · see citing works
Influence of RNA Secondary Structure on the Pre-mRNA Splicing Process
Buratti, E., & Baralle, F. E. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.24.10505-10514.2004 · Cited by 425 · see citing works
Clower, C. V., Chatterjee, D., Wang, Z., Cantley, L. C., Vander Heiden, M. G., & Krainer, A. R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914845107 · Cited by 424 · see citing works
Intron—exon structures of eukaryotic model organisms
Long, M., & Deutsch, M. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.15.3219 · Cited by 417 · see citing works
Ward, A. J., & Cooper, T. A. (2009) · The Journal of Pathology · doi:10.1002/path.2649 · Cited by 415 · see citing works
Cell Motility Is Controlled by SF2/ASF through Alternative Splicing of the Ron Protooncogene
Ghigna, C., Giordano, S., Shen, H., Benvenuto, F., Castiglioni, F., Comoglio, P. M., Green, M. R., Riva, S., & Biamonti, G. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.10.026 · Cited by 389 · see citing works
An ESRP‐regulated splicing programme is abrogated during the epithelial–mesenchymal transition
Warzecha, C. C., Jiang, P., Amirikian, K., Dittmar, K. A., Lu, H., Shen, S., Guo, W., Xing, Y., & Carstens, R. P. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.195 · Cited by 383 · see citing works
ASTALAVISTA: dynamic and flexible analysis of alternative splicing events in custom gene datasets
Foissac, S., & Sammeth, M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm311 · Cited by 377 · see citing works
Neuronal regulation of alternative pre-mRNA splicing
Li, Q., Lee, J.-A., & Black, D. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2237 · Cited by 376 · see citing works
Polypyrimidine Tract Binding Protein Antagonizes Exon Definition
Wagner, E. J., & García-Blanco, M. A. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.10.3281-3288.2001 · Cited by 376 · see citing works
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
Ko, J., Fuccillo, M. V., Malenka, R. C., & Südhof, T. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.12.012 · Cited by 369 · see citing works
Splign: algorithms for computing spliced alignments with identification of paralogs
Kapustin, Y., Souvorov, A. E., Tatusova, T. A., & Lipman, D. J. (2008) · Biology Direct · doi:10.1186/1745-6150-3-20 · Cited by 365 · see citing works
Regulation of Fas Alternative Splicing by Antagonistic Effects of TIA-1 and PTB on Exon Definition
Izquierdo, J. M., Oró, N. M., Bonnal, S., Martínez, C., Castelo, R., Guigó, R., Bilbao, D., & Valcárcel, J. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.06.015 · Cited by 364 · see citing works
SR Proteins Function in Coupling RNAP II Transcription to Pre-mRNA Splicing
Das, R., Yu, J., Zhang, Z., Gygi, M. P., Krainer, A. R., Gygi, S. P., & Reed, R. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.05.036 · Cited by 346 · see citing works
Self-citationCancer-associated regulation of alternative splicing
Venables, J. P., Klinck, R., Koh, C., Gervais-Bird, J., Bramard, A., Inkel, L., Durand, M., Couture, S., Froehlich, U., Lapointe, E., et al. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1608 · Cited by 340 · see citing works
Nucleosomes are well positioned in exons and carry characteristic histone modifications
Andersson, R., Enroth, S., Rada-Iglesias, A., Wadelius, C., & Komorowski, J. (2009) · Genome Research · doi:10.1101/gr.092353.109 · Cited by 325 · see citing works
Stanke, M., Tzvetkova, A., & Morgenstern, B. (2006) · Genome biology · doi:10.1186/gb-2006-7-s1-s11 · Cited by 320 · see citing works
An Alternative Splicing Network Links Cell-Cycle Control to Apoptosis
Moore, M. J., Wang, Q., Kennedy, C. J., & Silver, P. A. (2010) · Cell · doi:10.1016/j.cell.2010.07.019 · Cited by 316 · see citing works
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcriptsPreprint
Sanford, J. R., Wang, X., Mort, M. E., VanDuyn, N., Cooper, D. N., Mooney, S. D., Edenberg, H. J., & Liu, Y. (2008) · Genome Research · doi:10.1101/gr.082503.108 · Cited by 309 · see citing works
Grillo, G., Turi, A., Licciulli, F., Mignone, F., Liuni, S., Banfi, S., Gennarino, V. A., Horner, D. S., Pavesi, G., Picardi, E., et al. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp902 · Cited by 308 · see citing works
Splicing regulates NAD metabolite binding to histone macroH2A
Kustatscher, G., Hothorn, M., Pugieux, C., Scheffzek, K., & Ladurner, A. G. (2005) · Nature Structural & Molecular Biology · doi:10.1038/nsmb956 · Cited by 300 · see citing works
Graveley, B. R. (2005) · Cell · doi:10.1016/j.cell.2005.07.028 · Cited by 295 · see citing works
The soluble Interleukin 6 receptor: Generation and role in inflammation and cancer
Chalaris, A., Garbers, C., Rabe, B., Rose‐John, S., & Scheller, J. (2010) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2010.10.007 · Cited by 291 · see citing works
Yan, M., Kanbe, E., Peterson, L. F., Boyapati, A., Miao, Y., Wang, Y., Chen, I.-M., Chen, Z., Rowley, J. D., Willman, C. L., et al. (2006) · Nature Medicine · doi:10.1038/nm1443 · Cited by 279 · see citing works
The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing
Kishore, S., Khanna, A., Zhang, Z., Hui, J., Balwierz, P. J., Stefan, M., Beach, C. M., Nicholls, R. D., Zavolan, M., & Stamm, S. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddp585 · Cited by 279 · see citing works
Self-citationFemale-specific insect lethality engineered using alternative splicing
Fu, G., Condon, K. C., Epton, M. J., Gong, P., Jin, L., Condon, G. C., Morrison, N. I., Dafa’alla, T., & Alphey, L. (2007) · Nature Biotechnology · doi:10.1038/nbt1283 · Cited by 272 · see citing works
Olson, P. A., Tkatch, T., Hernández‐López, S., Ulrich, S., Ilijić, E., Mugnaini, E., Zhang, H., Борисович, Б. И., & Surmeier, D. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3327-04.2005 · Cited by 270 · see citing works
Llorian, M., Schwartz, S., Clark, T. A., Hollander, D., Tan, L.-Y., Spellman, R., Gordon, A., Schweitzer, A. C., de la Grange, P., Ast, G., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1881 · Cited by 263 · see citing works
No evidence for a shift in pyruvate kinase PKM1 to PKM2 expression during tumorigenesis
Bluemlein, K., Grüning, N., Feichtinger, R. G., Lehrach, H. R., Kofler, B., & Ralser, M. (2011) · Oncotarget · doi:10.18632/oncotarget.278 · Cited by 254 · see citing works
Chen, Z., Gore, B. B., Long, H., Ma, L., & Tessier‐Lavigne, M. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.016 · Cited by 251 · see citing works
Regulation of Alternative Splicing by Reversible Protein Phosphorylation
Stamm, S. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.r700034200 · Cited by 250 · see citing works
Self-citationVarani, L., Hasegawa, M., Spillantini, M. G., Smith, M. J., Murrell, J. R., Ghetti, B. F., Klug, A., Goedert, M., & Varani, G. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.8229 · Cited by 248 · see citing works
iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions
Wang, Z., Kayikci, M., Briese, M., Zarnack, K., Luscombe, N. M., Rot, G., Zupan, B., Curk, T., & Ule, J. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000530 · Cited by 242 · see citing works
RegRNA: an integrated web server for identifying regulatory RNA motifs and elements
Huang, H.-L., Chien, C.-H., Jen, K.-H., & Huang, H. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl333 · Cited by 239 · see citing works
Conservation of an RNA regulatory map between Drosophila and mammalsPreprint
Brooks, A. N., Yang, L. C., Duff, M. O., Hansen, K. D., Park, J. W., Dudoit, S., Brenner, S. E., & Graveley, B. R. (2010) · Genome Research · doi:10.1101/gr.108662.110 · Cited by 236 · see citing works
Disease-related Modifications in Tau Affect the Interaction between Fyn and Tau
Bhaskar, K., Yen, S.-H. C., & Lee, G. S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505895200 · Cited by 223 · see citing works
Behzadnia, N., Golas, M. M., Hartmuth, K., Sander, B. O., Kastner, B., Deckert, J., Dube, P., Will, C. L., Urlaub, H., Stark, H., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601631 · Cited by 218 · see citing works
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients
Sadakata, T., Washida, M., Iwayama, Y., Shoji, S., Sato, Y., Ohkura, T., Katoh-Semba, R., Nakajima, M., Sekine, Y., Tanaka, M., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29031 · Cited by 218 · see citing works
Péterfy, M., Phan, J. P., & Reue, K. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503885200 · Cited by 215 · see citing works
Günzel, D., Stuiver, M., Kausalya, P. J., Haisch, L., Krug, S. M., Rosenthal, R., Meij, I. C., Hunziker, W., Fromm, M., & Müller, D. (2009) · Journal of Cell Science · doi:10.1242/jcs.040113 · Cited by 214 · see citing works
Regulation of TMEM16A Chloride Channel Properties by Alternative Splicing
Ferrera, L., Caputo, A., Ubby, I., Bussani, E., Zegarra‐Moran, O., Ravazzolo, R., Pagani, F., & Galietta, L. J. V. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.046607 · Cited by 212 · see citing works
Survivin splice variants regulate the balance between proliferation and cell death
Caldas, H., Jiang, Y., Holloway, M. P., Fangusaro, J., Mahotka, C., Conway, E. M., & Altura, R. A. (2005) · Oncogene · doi:10.1038/sj.onc.1208350 · Cited by 200 · see citing works
Pre-mRNA Secondary Structures Influence Exon Recognition
Hiller, M., Zhang, Z., Backofen, R., & Stamm, S. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030204 · Cited by 199 · see citing works
Self-citationSlaaby, R., Schäffer, L., Lautrup-Larsen, I., Andersen, A. S., Shaw, A. C., Mathiasen, I. S., & Brandt, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605189200 · Cited by 198 · see citing works
SF2/ASF autoregulation involves multiple layers of post-transcriptional and translational control
Sun, S., Zhang, Z., Sinha, R., Karni, R., & Krainer, A. R. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1750 · Cited by 197 · see citing works
Self-citationLossin, C. (2008) · Brain and Development · doi:10.1016/j.braindev.2008.07.011 · Cited by 195 · see citing works
Unusual Intron Conservation near Tissue-Regulated Exons Found by Splicing Microarrays
Sugnet, C. W., Srinivasan, K., Clark, T. A., O’Brien, G. S., Cline, M., Wang, H., Williams, A., Kulp, D., Blume, J. E., Haussler, D. H., et al. (2006) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0020004 · Cited by 194 · see citing works
Adato, A., Lefevre, G. M., Delprat, B., Michel, V., Michalski, N., Chardenoux, S., Weil, D., El-Amraoui, A., & Petit, C. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi416 · Cited by 185 · see citing works
Cauffman, G., Liebaers, I., Steirteghem, A. V., & de Velde, H. V. (2006) · Stem Cells · doi:10.1634/stemcells.2005-0611 · Cited by 183 · see citing works
Xu, Q. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg786 · Cited by 183 · see citing works
Keats, J. J., Maxwell, C. A., Taylor, B. J., Hendzel, M. J., Chesi, M., Bergsagel, P. L., Larratt, L. M., Mant, M. J., Reiman, T., Belch, A. R., et al. (2005) · Blood · doi:10.1182/blood-2004-09-3704 · Cited by 183 · see citing works
fruitless regulates aggression and dominance in Drosophila
Vrontou, E., Nilsen, S. P., Demir, E., Kravitz, E. A., & Dickson, B. J. (2006) · Nature Neuroscience · doi:10.1038/nn1809 · Cited by 179 · see citing works
Stoilov, P. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh051 · Cited by 179 · see citing works
Collesi, C., Santoro, M. M., Gaudino, G., & Comoglio, P. M. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.10.5518 · Cited by 177 · see citing works
Chromatin, transcript elongation and alternative splicing
Kornblihtt, A. R. (2006) · Nature Structural & Molecular Biology · doi:10.1038/nsmb0106-5 · Cited by 173 · see citing works
Angiomotin Regulates Endothelial Cell-Cell Junctions and Cell Motility
Bratt, A., Birot, O., Sinha, I., Veitonmäki, N., Aase, K., Ernkvist, M., & Holmgren, L. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503915200 · Cited by 173 · see citing works
Genome-wide analysis of alternative splicing in Caenorhabditis elegansPreprint
Ramani, A. K., Calarco, J. A., Pan, Q., Mavandadi, S., Wang, Y., Nelson, A. C., Lee, L. J., Morris, Q., Blencowe, B. J., Zhen, M., et al. (2010) · Genome Research · doi:10.1101/gr.114645.110 · Cited by 170 · see citing works
The Roles of Versican V1 and V2 Isoforms in Cell Proliferation and Apoptosis
Wang, S., Wang, G., Wang, Y., Liang, J., Wen, J., Zheng, P.-S., Wu, Y., Lee, V., Slingerland, J. M., Dumont, D. J., et al. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-04-0295 · Cited by 169 · see citing works
Coupling Transcription and Alternative Splicing
Kornblihtt, A. R. (2007) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-77374-2_11 · Cited by 168 · see citing works
Structures of APRIL-Receptor Complexes
Hymowitz, S. G., Patel, D. R., Wallweber, H. J. A., Runyon, S., Yan, M., Yin, J., Shriver, S. K., Gordon, N. C., Pan, B., Skelton, N. J., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411714200 · Cited by 167 · see citing works
Functional genetic analysis of mutations implicated in a human speech and language disorder
Vernes, S. C., Nicod, J., Elahi, F. M., Coventry, J. A., Kenny, N., Coupe, A.-M., Bird, L. E., Davies, K. E., & Fisher, S. E. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl392 · Cited by 167 · see citing works
Narla, G., DiFeo, A. V., Yao, S., Banno, A., Hod, E. A., Reeves, H. L., Qiao, R., Camacho‐Vanegas, O., Levine, A. C., Kirschenbaum, A. M., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-0217 · Cited by 166 · see citing works
Sharma, S., Falick, A. M., & Black, D. L. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.07.014 · Cited by 165 · see citing works
Lipins: Multifunctional Lipid Metabolism Proteins
Csaki, L. S., & Reue, K. (2010) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.012809.104729 · Cited by 164 · see citing works
Insights into the connection between cancer and alternative splicing
Kim, E., Goren, A., & Ast, G. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.10.001 · Cited by 162 · see citing works
Datta, D. B., Flaxenburg, J. A., Laxmanan, S., Geehan, C. S., Grimm, M. R., Waaga-Gasser, A. M., Briscoe, D. M., & Pal, S. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-4345 · Cited by 162 · see citing works
Characterization of the Human LPIN1-encoded Phosphatidate Phosphatase Isoforms
Han, G., & Carman, G. M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.117747 · Cited by 161 · see citing works
Misquitta-Ali, C. M., Cheng, E., O’Hanlon, D., Liu, G., McGlade, C. J., Tsao, M., & Blencowe, B. J. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00709-10 · Cited by 160 · see citing works
Differential Role of N-Type Calcium Channel Splice Isoforms in Pain
Altier, C., Dale, C. S., Kisilevsky, A. E., Chapman, K., Castiglioni, A. J., Matthews, E. A., Evans, R. M., Dickenson, A. H., Lipscombe, D., Vergnolle, N., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0307-07.2007 · Cited by 159 · see citing works
Discovery and Analysis of Evolutionarily Conserved Intronic Splicing Regulatory Elements
Yeo, G. W.-M., Nostrand, E. L. V., & Liang, T. Y. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030085 · Cited by 158 · see citing works
Lee, J.-A., Tang, Z., & Black, D. L. (2009) · Genes & Development · doi:10.1101/gad.1837009 · Cited by 158 · see citing works
Identification of Common Genetic Variation That Modulates Alternative Splicing
Hull, J., Campino, S. G., Rowlands, K., Chan, M., Copley, R. R., Taylor, M. S., Rockett, K. A., Elvidge, G. P., Keating, B. J., Knight, J. C., et al. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030099 · Cited by 157 · see citing works
Pihlajamäki, J., Lerín, C., Itkonen, P., Boes, T., Floß, T., Schroeder, J., Dearie, F., Crunkhorn, S., Burak, M. F., Jiménez‐Chillarón, J. C., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.06.007 · Cited by 156 · see citing works
Self-citationDistribution of SR protein exonic splicing enhancer motifs in human protein-coding genes
Wang, J. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki810 · Cited by 156 · see citing works
Global regulation of alternative splicing during myogenic differentiation
Bland, C. S., Wang, E. T., Vu, A. Q., David, M. P., Castle, J. C., Johnson, J. M., Burge, C. B., & Cooper, T. A. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq614 · Cited by 153 · see citing works
Feng, Y., Li, X., Wang, L., Zhou, L., & Gorodeski, G. I. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602999200 · Cited by 152 · see citing works
Sharp, D. A., Lawrence, D. A., & Ashkenazi, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413962200 · Cited by 152 · see citing works
Alternatively spliced tissue factor induces angiogenesis through integrin ligation
van den Berg, Y. W., van den Hengel, L. G., Myers, H. R., Ayachi, O., Jordanova, E. S., Ruf, W., Spek, C. A., Reitsma, P. H., Bogdanov, V. Y., & Versteeg, H. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905325106 · Cited by 150 · see citing works
A Novel Splice Variant of GLI1 That Promotes Glioblastoma Cell Migration and Invasion
Lo, H., Zhu, H., Cao, X., Aldrich, A. J., & Ali‐Osman, F. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0886 · Cited by 150 · see citing works
Alternative splicing of conserved exons is frequently species-specific in human and mouse
Pan, Q., Bakowski, M. A., Morris, Q., Zhang, W., Frey, B. J., Hughes, T. R., & Blencowe, B. J. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.12.004 · Cited by 149 · see citing works
Gooding, C., Clark, F., Wollerton, M., Grellscheid, S., Groom, H. C. T., & Smith, C. W. J. (2006) · Genome biology · doi:10.1186/gb-2006-7-1-r1 · Cited by 149 · see citing works
Alternative mRNA Splicing Produces a Novel Biologically Active Short Isoform of PGC-1α
Zhang, Y., Huypens, P., Adamson, A. W., Chang, J. S., Henagan, T. M., Boudreau, A., Lenard, N. R., Burk, D. H., Klein, J. C., Perwitz, N., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.037556 · Cited by 148 · see citing works
Multiple Alternative Splicing Markers for Ovarian Cancer
Klinck, R., Bramard, A., Inkel, L., Dufresne‐Martin, G., Gervais-Bird, J., Madden, R., Paquet, É. R., Koh, C., Venables, J. P., Prinos, P., et al. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-2580 · Cited by 147 · see citing works
Nesprin-2 Giant (NUANCE) maintains nuclear envelope architecture and composition in skin
Lüke, Y., Zaim, H., Karakesisoglou, I., Jaeger, V. M., Sellin, L. K., Lu, W., Schneider, M., Neumann, S., Beijer, Å., Munck, M., et al. (2008) · Journal of Cell Science · doi:10.1242/jcs.019075 · Cited by 146 · see citing works
Novikov, L., Park, J. W., Chen, H., Klerman, H., Jalloh, A. S., & Gamble, M. J. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05244-11 · Cited by 146 · see citing works
Alternative splicing: global insights
Hallegger, M., Llorian, M., & Smith, C. W. J. (2010) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07521.x · Cited by 143 · see citing works
Useful ‘junk’: Alu RNAs in the human transcriptome
Häsler, J., Samuelsson, T., & Strub, K. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7084-0 · Cited by 142 · see citing works
Liu, Y., Surka, M. C., Schroeter, T., Lukiyanchuk, V., & Schmid, S. L. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-08-0890 · Cited by 141 · see citing works
Weise, A., Bruser, K., Elfert, S., Wallmen, B., Wittel, Y., Wöhrle, S., & Hecht, A. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp1197 · Cited by 139 · see citing works
An intronic element contributes to splicing repression in spinal muscular atrophy
Kashima, T., Rao, N., & Manley, J. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700343104 · Cited by 133 · see citing works
Motoyama, M., Yamazaki, S., Eto-Kimura, A., Takeshige, K., & Muta, T. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m412738200 · Cited by 131 · see citing works
Alternative splicing: role of pseudoexons in human disease and potential therapeutic strategies
Dhir, A., & Buratti, E. (2010) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07520.x · Cited by 129 · see citing works
Dynamic Regulation of Alternative Splicing by Silencers that Modulate 5′ Splice Site Competition
Yu, Y., Maroney, P. A., Denker, J. A., Zhang, X. H.-F., Dybkov, O., Lührmann, R., Jankowsky, E., Chasin, L. A., & Nilsen, T. W. (2008) · Cell · doi:10.1016/j.cell.2008.10.046 · Cited by 129 · see citing works
MicroRNAs coordinate an alternative splicing network during mouse postnatal heart development
Kalsotra, A., Wang, K., Li, P.-F., & Cooper, T. A. (2010) · Genes & Development · doi:10.1101/gad.1894310 · Cited by 129 · see citing works
Reciprocal intronic and exonic histone modification regions in humans
Huff, J. T., Plocik, A. M., Guthrie, C., & Yamamoto, K. R. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1924 · Cited by 128 · see citing works
Meseguer, S., Mudduluru, G., Escamilla, J. M., Allgayer, H., & Barettino, D. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.167817 · Cited by 127 · see citing works
Alternative Splicing of Vitamin D-24-Hydroxylase
Ren, S., Nguyen, L., Wu, S., Encinas, C., Adams, J. S., & Hewison, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414522200 · Cited by 126 · see citing works
FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus
Fletcher, R. B., Baker, J. C., & Harland, R. M. (2006) · Development · doi:10.1242/dev.02342 · Cited by 126 · see citing works
Liao, P. H., Yu, D., Li, G., Yong, T. F., Soon, J.-L., Chua, Y. L., & Soong, T. W. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705478200 · Cited by 125 · see citing works
Functional coupling of RNAP II transcription to spliceosome assemblyPreprint
Das, R., Dufu, K., Romney, B., Feldt, M. C., Elenko, M. P., & Reed, R. (2006) · Genes & Development · doi:10.1101/gad.1397406 · Cited by 125 · see citing works
Global analysis of positive and negative pre-mRNA splicing regulators in DrosophilaPreprint
Blanchette, M., Green, R. E., Brenner, S. E., & Rio, D. C. (2005) · Genes & Development · doi:10.1101/gad.1314205 · Cited by 124 · see citing works
Pineda‐Lucena, A., Ho, C. S. W., Mao, D. Y. L., Sheng, Y., Laister, R. C., Muhandiram, R., Lü, Y., Seet, B. T., Katz, S., Szyperski, T., et al. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.05.046 · Cited by 124 · see citing works
Sam68 Regulates a Set of Alternatively Spliced Exons during Neurogenesis
Chawla, G., Lin, C.-H., Han, A., Shiue, L., Ares, M., & Black, D. L. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01349-08 · Cited by 124 · see citing works
The discovery of split genes and RNA splicing
Sharp, P. A. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.04.002 · Cited by 122 · see citing works
Mango, R., Biocca, S., Vecchio, F. D., Clementi, F., Sangiuolo, F. C., Amati, F., Filareto, A., Grelli, S., Spitalieri, P., Filesi, I., et al. (2005) · Circulation Research · doi:10.1161/01.res.0000174563.62625.8e · Cited by 120 · see citing works
Kar, A. N., Fushimi, K., Zhou, X., Ray, P., Chen, S., Chen, X., Liu, Z., Chen, S., & Wu, J. Y. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01149-10 · Cited by 120 · see citing works
Autoregulation of Fox protein expression to produce dominant negative splicing factors
Damianov, A., & Black, D. L. (2010) · RNA · doi:10.1261/rna.1838210 · Cited by 120 · see citing works
Genomic features defining exonic variants that modulate splicing
Woolfe, A., Mullikin, J. C., & Elnitski, L. L. (2010) · Genome biology · doi:10.1186/gb-2010-11-2-r20 · Cited by 119 · see citing works
The ASAP II database: analysis and comparative genomics of alternative splicing in 15 animal species
Kim, N., Alekseyenko, A. V., Roy, M., & Lee, C. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl884 · Cited by 117 · see citing works
UMD (Universal Mutation Database): 2005 update
Béroud, C., Hamroun, D., Collod‐Béroud, G., Boileau, C., Soussi, T., & Claustres, M. (2005) · Human Mutation · doi:10.1002/humu.20210 · Cited by 116 · see citing works
Gavin, A. L., Duong, B. H., Skog, P. D., Aït‐Azzouzene, D., Greaves, D. R., Scott, M. L., & Nemazee, D. A. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.1.319 · Cited by 115 · see citing works
Bao, J., Lu, Z., Joseph, J. J., Carabenciov, D., Dimond, C. C., Pang, L., Samsel, L., McCoy, J. P., Leclerc, J., Nguyen, P., et al. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22531 · Cited by 115 · see citing works
Gonçalves, V., Matos, P., & Jordan, P. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp317 · Cited by 113 · see citing works
Ruggiu, M., Herbst, R., Kim, N., Jevsek, M., Fak, J. J., Mann, M. A., Fischbach, G., Burden, S. J., & Darnell, R. B. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813112106 · Cited by 113 · see citing works
Distinct functions of homeodomain-containing and homeodomain-less isoforms encoded by homothoraxPreprint
Noro, B., Culí, J., McKay, D. J., Zhang, W., & Mann, R. S. (2006) · Genes & Development · doi:10.1101/gad.1412606 · Cited by 112 · see citing works
Pan, Y., Xu, J., Xu, M., Rossi, G. C., Matulonis, J. E., & Pasternak, G. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811586106 · Cited by 112 · see citing works
Alternative trans ‐splicing: a novel mode of pre‐mRNA processing
Horiuchi, T., & Aigaki, T. (2006) · Biology of the Cell · doi:10.1042/bc20050002 · Cited by 111 · see citing works
Enzyme-inhibitor-like tuning of Ca2+ channel connectivity with calmodulin
Liu, X., Yang, P. S., Yang, W., & Yue, D. T. (2010) · Nature · doi:10.1038/nature08766 · Cited by 111 · see citing works
Mice exclusively expressing the short isoform of Smad2 develop normally and are viable and fertilePreprint
Dunn, N. R., Koonce, C. H., Anderson, D. C., Islam, A., Bikoff, E. K., & Robertson, E. J. (2005) · Genes & Development · doi:10.1101/gad.1243205 · Cited by 108 · see citing works
Byun, H.-J., Hong, I., Kim, E., Jin, Y., Jeoung, D., Hahn, J.-H., Kim, Y.-M., Park, S. H., & Lee, H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605483200 · Cited by 105 · see citing works
Ohkura, N., Takahashi, M., Yaguchi, H., Nagamura, Y., & Tsukada, T. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502173200 · Cited by 105 · see citing works
New isoforms of rat Aquaporin-4
Moe, S. E., Sorbo, J. G., Sogaard, R., Zeuthen, T., Ottersen, O. P., & Holen, T. (2008) · Genomics · doi:10.1016/j.ygeno.2007.12.003 · Cited by 103 · see citing works
Meijer, O. C., Kalkhoven, E., van der Laan, S., Steenbergen, P. J., Houtman, S., Dijkmans, T. F., Pearce, D., & de Kloet, E. R. (2004) · Endocrinology · doi:10.1210/en.2004-0411 · Cited by 103 · see citing works
Laguri, C., Sadir, R., Rueda, P., Baleux, F., Gans, P., Arenzana‐Seisdedos, F., & Lortat‐Jacob, H. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001110 · Cited by 103 · see citing works
Rao, N. L., Nguyen, S. M., Ngo, K., & Fung‐Leung, W. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.15.6521-6532.2005 · Cited by 103 · see citing works
López, V., & Kelleher, S. L. (2009) · Biochemical Journal · doi:10.1042/bj20081189 · Cited by 102 · see citing works
Thomas, C. P., Andrews, J. I., & Liu, K. Z. (2007) · The FASEB Journal · doi:10.1096/fj.07-8809com · Cited by 102 · see citing works
SFmap: a web server for motif analysis and prediction of splicing factor binding sites
Paz, I., Akerman, M., Dror, I., Kosti, I., & Mandel-Gutfreund, Y. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq444 · Cited by 102 · see citing works
Regulation of B cell homeostasis and activation by the tumor suppressor gene CYLD
Hövelmeyer, N., Wunderlich, F. T., Massoumi, R., Jakobsen, C. G., Song, J., Wörns, M., Merkwirth, C., Kovalenko, A., Aumailley, M., Strand, D. J., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070318 · Cited by 102 · see citing works
Levy, S. F., LeBoeuf, A. C., Massie, M. R., Jordan, M. A., Wilson, L., & Feinstein, S. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413490200 · Cited by 102 · see citing works
Characterization of GPRA, a Novel G Protein–Coupled Receptor Related to Asthma
Vendelin, J., Pulkkinen, V., Rehn, M., Pirskanen, A., Räisänen-Sokolowski, A. K., Laitinen, A., Laitinen, L. A., Kere, J., & Laitinen, T. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2004-0405oc · Cited by 102 · see citing works
Kol, G., Lev-Maor, G., & Ast, G. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi164 · Cited by 99 · see citing works
Gopalakrishnan, S., Emburgh, B. O. V., Shan, J., Su, Z. Z., Fields, C. R., Vieweg, J., Hamazaki, T., Schwartz, P. H., Terada, N., & Robertson, K. D. (2009) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-09-0018 · Cited by 99 · see citing works
Developments in RNA Splicing and Disease
Poulos, M. G., Batra, R., Charizanis, K., & Swanson, M. S. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000778 · Cited by 98 · see citing works
Sundvall, M., Korhonen, A., Paatero, I., Gaudio, E., Melino, G., Croce, C. M., Aqeilan, R. I., & Elenius, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708333105 · Cited by 97 · see citing works
Zhong, X., Liu, J. R., Kyle, J. W., Hanck, D. A., & Agnew, W. S. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl068 · Cited by 97 · see citing works
Novel Splice Variants of ING4 and Their Possible Roles in the Regulation of Cell Growth and Motility
Unoki, M., Shen, J., Zheng, Z., & Harris, C. C. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606296200 · Cited by 97 · see citing works
Zhu, B., Ramachandran, B., & Gulick, T. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502491200 · Cited by 96 · see citing works
ERK1c regulates Golgi fragmentation during mitosis
Shaul, Y. D., & Seger, R. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200509063 · Cited by 95 · see citing works
Alternative splicing: regulation of HIV‐1 multiplication as a target for therapeutic action
Tazi, J., Bakkour, N., Marchand, V., Ayadi, L., Aboufirassi, A., & Branlant, C. (2010) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07522.x · Cited by 92 · see citing works
Chen, A., Perrin, M. H., DiGruccio, M. R., Vaughan, J. M., Brar, B. K., Arias, C. M., Lewis, K. A., Rivier, J., Sawchenko, P. E., & Vale, W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409583102 · Cited by 92 · see citing works
Fox-3 and PSF interact to activate neural cell-specific alternative splicing
Kim, K. K., Kim, Y. C., Adelstein, R. S., & Kawamoto, S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1221 · Cited by 91 · see citing works
Voolstra, O., Kiefer, C., Hoehne, M., Welsch, R., Vogt, K., & von Lintig, J. (2006) · Biochemistry · doi:10.1021/bi060701u · Cited by 91 · see citing works
Jackson, K. A., Helston, R. M., McKay, J. A., O'Neill, E. D., Mathers, J. C., & Ford, D. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610535200 · Cited by 91 · see citing works
Andolfo, I., Falco, L. D., Asci, R., Russo, R., Colucci, S., Gorrese, M., Zollo, M., & Iolascon, A. (2010) · Haematologica · doi:10.3324/haematol.2009.020685 · Cited by 90 · see citing works
Das, D., Clark, T. A., Schweitzer, A. C., Yamamoto, M. L., Marr, H., Arribere, J., Minovitsky, S., Poliakov, A., Dubchak, I. L., Blume, J. E., et al. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm485 · Cited by 89 · see citing works
Daoud, R., Mies, G., Smialowska, A., Oláh, L., Hossmann, K.-A., & Stamm, S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-14-05889.2002 · Cited by 89 · see citing works
Self-citationMcCartney, C. E., McClafferty, H., Huibant, J.-M., Rowan, E. G., Shipston, M. J., & Rowe, I. C. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505270102 · Cited by 87 · see citing works
Atherosclerosis-related molecular alteration of the human Ca V 1.2 calcium channel α 1C subunit
Tiwari, S., Zhang, Y., Heller, J. A., Abernethy, D. R., & Soldatov, N. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606539103 · Cited by 87 · see citing works
Farris, W., Leissring, M. A., Hemming, M. L., Chang, A. Y., & Selkoe, D. J. (2005) · Biochemistry · doi:10.1021/bi0476578 · Cited by 87 · see citing works
Fujikake, N., Nagai, Y., Popiel, H. A., Kano, H., Yamaguchi, M., & Toda, T. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.074 · Cited by 87 · see citing works
Irimia, M., Rukov, J. L., Penny, D., & Roy, S. W. (2007) · BMC Evolutionary Biology · doi:10.1186/1471-2148-7-188 · Cited by 87 · see citing works
Hirschfeld, M., zur Hausen, A., Bettendorf, H., Jäger, M., & Stickeler, E. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-1997 · Cited by 86 · see citing works
Kan, Z. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki834 · Cited by 86 · see citing works
Matsushita, K., Tomonaga, T., Shimada, H., Shioya, A., Higashi, M., Matsubara, H., Harigaya, K., Nomura, F., Libutti, D. E., Levens, D., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-04-4459 · Cited by 86 · see citing works
Lonka‐Nevalaita, L., Lume, M., Leppänen, S., Jokitalo, E., Peränen, J., & Saarma, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5888-09.2010 · Cited by 85 · see citing works
Adams, P. J., Garcı́a, E., David, L. S., Mulatz, K., Spacey, S. D., & Snutch, T. P. (2009) · Channels · doi:10.4161/chan.3.2.7932 · Cited by 84 · see citing works
ApoE receptor 2 controls neuronal survival in the adult brain
Beffert, U., Nematollah Farsian, F., Masiulis, I., Hammer, R. E., Yoon, S. O., Giehl, K. M., & Herz, J. (2006) · Current Biology · doi:10.1016/j.cub.2006.10.029 · Cited by 84 · see citing works
Izquierdo, J. M., & Valcárcel, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.c600198200 · Cited by 84 · see citing works
Flagged first, then by citations
5 of the 559 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Mechanisms and Regulation of Alternative Pre-mRNA Splicing
Lee, Y., & Rio, D. C. (2015) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060614-034316 · Cited by 1,291 · see citing works
Gene co-expression analysis for functional classification and gene–disease predictions
van Dam, S., Võsa, U., van der Graaf, A., Franke, L., & de Magalhães, J. P. (2017) · Briefings in Bioinformatics · doi:10.1093/bib/bbw139 · Cited by 1,086 · see citing works
Molecular mechanisms of ROS production and oxidative stress in diabetes
Newsholme, P., Cruzat, V. F., Keane, K. N., Carlessi, R., & de Bittencourt, P. I. H. (2016) · Biochemical Journal · doi:10.1042/bcj20160503c · Cited by 878 · see citing works
Alternative Splicing Regulatory Networks: Functions, Mechanisms, and Evolution
Ule, J., & Blencowe, B. J. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.09.017 · Cited by 780 · see citing works
Introducing Protein Intrinsic Disorder
Habchi, J., Tompa, P., Longhi, S., & Uversky, V. N. (2014) · Chemical Reviews · doi:10.1021/cr400514h · Cited by 744 · see citing works
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing
Yang, X., Coulombe-Huntington, J., Kang, S., Sheynkman, G. M., Hao, T., Richardson, A., Sun, S., Yang, F., Shen, Y. A., Murray, R. R., et al. (2016) · Cell · doi:10.1016/j.cell.2016.01.029 · Cited by 583 · see citing works
Mechanism of alternative splicing and its regulation
Wang, Y., LIU, J., Huang, B., XU, Y.-M., LI, J., Huang, L., Jin, L., Zhang, J., Min, Q., Yang, W., et al. (2014) · Biomedical Reports · doi:10.3892/br.2014.407 · Cited by 478 · see citing works
Aberrant RNA splicing in cancer; expression changes and driver mutations of splicing factor genes
Sveen, A., Kilpinen, S. K., Ruusulehto, A., Lothe, R. A., & Skotheim, R. I. (2015) · Oncogene · doi:10.1038/onc.2015.318 · Cited by 463 · see citing works
Alternative splicing as a source of phenotypic diversity
Wright, C. J., Smith, C. W. J., & Jiggins, C. D. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00514-4 · Cited by 454 · see citing works
The Expanding Landscape of Alternative Splicing Variation in Human Populations
Park, E., Pan, Z., Zhang, Z., Lin, L., & Xing, Y. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.11.002 · Cited by 357 · see citing works
Self-citationAlternative Splicing May Not Be the Key to Proteome Complexity
Tress, M. L., Abascal, F., & Valencia, A. (2016) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.08.008 · Cited by 341 · see citing works
Misregulation of Pre-mRNA Alternative Splicing in Cancer
Zhang, J., & Manley, J. L. (2013) · Cancer Discovery · doi:10.1158/2159-8290.cd-13-0253 · Cited by 306 · see citing works
Proteomic and interactomic insights into the molecular basis of cell functional diversity
Bludau, I., & Aebersold, R. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0231-2 · Cited by 297 · see citing works
Zhang, R., Calixto, C. P. G., Márquez, Y., Venhuizen, P., Τzioutziou, N. A., Guo, W., Spensley, M., Entizne, J. C., Lewandowska, D., ten Have, S., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx267 · Cited by 290 · see citing works
Reyes, A., & Huber, W. (2018) · Nucleic Acids Research · doi:10.1093/nar/gkx1165 · Cited by 290 · see citing works
Regulation of pre-mRNA splicing: roles in physiology and disease, and therapeutic prospects
Rogalska, M. E., Vivori, C., & Valcárcel, J. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00556-8 · Cited by 269 · see citing works
The Spliceosome: The Ultimate RNA Chaperone and Sculptor
Papasaikas, P., & Valcárcel, J. (2015) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2015.11.003 · Cited by 248 · see citing works
Defective control of pre–messenger RNA splicing in human disease
Chabot, B., & Shkreta, L. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201510032 · Cited by 209 · see citing works
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 · see citing works
Martín, G., Márquez, Y., Mantica, F., Duque, P., & Irimia, M. (2021) · Genome biology · doi:10.1186/s13059-020-02258-y · Cited by 208 · see citing works
Dual function of C/D box small nucleolar RNAs in rRNA modification and alternative pre-mRNA splicing
Falaleeva, M., Pagès, A., Matuszek, Ż., Hidmi, S., Agranat-Tamir, L., Korotkov, K. V., Nevo, Y., Eyras, E., Sperling, R., & Stamm, S. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1519292113 · Cited by 209 · see citing works
Self-citationRNA-binding proteins control gene expression and cell fate in the immune system
Turner, M., & Díaz‐Muñoz, M. D. (2017) · Nature Immunology · doi:10.1038/s41590-017-0028-4 · Cited by 200 · see citing works
Alternative Splicing and Protein Diversity: Plants Versus Animals
Chaudhary, S., Khokhar, W., Jabre, I., Reddy, A. S. N., Byrne, L. J., Wilson, C. M., & Syed, N. H. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00708 · Cited by 204 · see citing works
SubCellBarCode: Proteome-wide Mapping of Protein Localization and Relocalization
Orre, L. M., Vesterlund, M., Pan, Y., Arslan, T., Zhu, Y., Fernandez-Woodbridge, A., Frings, O., Fredlund, E., & Lehtiö, J. (2019) · Molecular Cell · doi:10.1016/j.molcel.2018.11.035 · Cited by 201 · see citing works
Alternative splicing and the evolution of phenotypic novelty
Bush, S. J., Chen, L., Tovar-Corona, J. M., & Urrutia, A. O. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0474 · Cited by 193 · see citing works
The emerging role of alternative splicing in senescence and aging
Deschênes, M., & Chabot, B. (2017) · Aging Cell · doi:10.1111/acel.12646 · Cited by 167 · see citing works
Márquez, Y., Höpfler, M., Ayatollahi, Z., Barta, A., & Kalyna, M. (2015) · Genome Research · doi:10.1101/gr.186585.114 · Cited by 166 · see citing works
Targeting RNA splicing for disease therapy
Havens, M. A., Duelli, D. M., & Hastings, M. L. (2013) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1158 · Cited by 163 · see citing works
Bebee, T. W., Park, J. W., Sheridan, K. I., Warzecha, C. C., Cieply, B. W., Rohacek, A. M., Xing, Y., & Carstens, R. P. (2015) · eLife · doi:10.7554/elife.08954 · Cited by 161 · see citing works
Goldfish spexin: solution structure and novel function as a satiety factor in feeding control
Wong, M. K. H., Sze, K. H., Chen, T., Cho, C. K., Law, H. C.-H., Chu, I. K., & Wong, A. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00141.2013 · Cited by 157 · see citing works
Global changes of the RNA-bound proteome during the maternal-to-zygotic transition in Drosophila
Sysoev, V. O., Fischer, B., Frese, C. K., Gupta, I., Krijgsveld, J., Hentze, M. W., Castelló, A., & Ephrussi, A. (2016) · Nature Communications · doi:10.1038/ncomms12128 · Cited by 146 · see citing works
The RNA Splicing Response to DNA Damage
Shkreta, L., & Chabot, B. (2015) · Biomolecules · doi:10.3390/biom5042935 · Cited by 154 · see citing works
Tan, S. H., Karri, V., Tay, N. W. R., Chang, K. H., Ah, H. Y., Ng, P. Q., Ho, H. S., Keh, H. W., & Candasamy, M. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.12.101 · Cited by 148 · see citing works
Functional roles of alternative splicing factors in human disease
Cieply, B. W., & Carstens, R. P. (2015) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1276 · Cited by 142 · see citing works
Soneson, C., Matthes, K. L., Nowicka, M., Law, C. W., & Robinson, M. D. (2016) · Genome biology · doi:10.1186/s13059-015-0862-3 · Cited by 141 · see citing works
The importance of alternative splicing in adaptive evolution
Singh, P., & Ahi, E. P. (2022) · Molecular Ecology · doi:10.1111/mec.16377 · Cited by 140 · see citing works
Drift and conservation of differential exon usage across tissues in primate species
Reyes, A., Anders, S., Weatheritt, R. J., Gibson, T. J., Steinmetz, L. M., & Huber, W. K. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307202110 · Cited by 132 · see citing works
Alternative splicing: the pledge, the turn, and the prestige
Gallego-Paez, L. M., Bordone, M. C., Leote, A. C., Saraiva-Agostinho, N., Ascensão-Ferreira, M., & Barbosa‐Morais, N. L. (2017) · Human Genetics · doi:10.1007/s00439-017-1790-y · Cited by 133 · see citing works
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer
Farina, A. R., Cappabianca, L. A., Sebastiano, M., Zelli, V., Guadagni, S., & Mackay, A. R. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01616-9 · Cited by 131 · see citing works
FFPred 3: feature-based function prediction for all Gene Ontology domains
Cozzetto, D., Minneci, F., Currant, H., & Jones, D. T. (2016) · Scientific Reports · doi:10.1038/srep31865 · Cited by 127 · see citing works
DYRK1A inhibitors for disease therapy: Current status and perspectives
Liu, T., Wang, Y., Wang, J., Ren, C., Chen, H., & Zhang, J. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.114062 · Cited by 126 · see citing works
The state of play in higher eukaryote gene annotation
Mudge, J. M., & Harrow, J. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.119 · Cited by 122 · see citing works
Genetic Control of Gonadal Sex Determination and Development.
Stévant, I., & Nef, S. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.02.004 · Cited by 85 · see citing works
Park, J., Dempewolf, E., Zhang, W., & Wang, Z. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179410 · Cited by 116 · see citing works
Origin of exon skipping-rich transcriptomes in animals driven by evolution of gene architecture
Grau‐Bové, X., Ruiz‐Trillo, I., & Irimia, M. (2018) · Genome biology · doi:10.1186/s13059-018-1499-9 · Cited by 110 · see citing works
Genome-Wide Detection of Condition-Sensitive Alternative Splicing in Arabidopsis Roots
Li, W., Lin, W., Ray, P., Lan, P., & Schmidt, W. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.217778 · Cited by 115 · see citing works
RNA Quality Control as a Key to Suppressing RNA Silencing of Endogenous Genes in Plants
Liu, L., & Chen, X. (2016) · Molecular Plant · doi:10.1016/j.molp.2016.03.011 · Cited by 113 · see citing works
Genes with a large intronic burden show greater evolutionary conservation on the protein level
Gorlova, O. Y., Fedorov, A. N., Logothetis, C. J., Amos, C. I., & Gorlov, I. P. (2014) · BMC Evolutionary Biology · doi:10.1186/1471-2148-14-50 · Cited by 109 · see citing works
RNA splicing in human disease and in the clinic
Baralle, D., & Buratti, E. (2017) · Clinical Science · doi:10.1042/cs20160211 · Cited by 105 · see citing works
The fitness cost of mis-splicing is the main determinant of alternative splicing patterns
Saudemont, B., Popa, A., Parmley, J. L., Rocher, V., Blugeon, C., Necşulea, A., Meyer, É., & Duret, L. (2017) · Genome biology · doi:10.1186/s13059-017-1344-6 · Cited by 106 · see citing works
Chen, X., Liu, Y. M., Xu, C., Ba, L., Liu, Z., Li, X., Huang, J., Simpson, E. R., Gao, H., Cao, D., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20327-5 · Cited by 105 · see citing works
Tabrez, S. S., Sharma, R. D., Jain, V., Siddiqui, A. A., & Mukhopadhyay, A. (2017) · Nature Communications · doi:10.1038/s41467-017-00370-5 · Cited by 97 · see citing works
Song, X., Wan, X., Huang, T., Zeng, C., Sastry, N. G., Wu, B., James, C. D., Horbinski, C., Nakano, I., Zhang, W., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-19-1504 · Cited by 96 · see citing works
Neurodegenerative diseases: a hotbed for splicing defects and the potential therapies
Li, D., McIntosh, C. S., Mastaglia, F. L., Wilton, S. D., & Aung-Htut, M. T. (2021) · Translational Neurodegeneration · doi:10.1186/s40035-021-00240-7 · Cited by 96 · see citing works
An integrated transcriptional analysis of the developing human retina
Mellough, C., Bauer, R., Collin, J., Dorgau, B., Zerti, D., Dolan, D., Jones, C. M., Izuogu, O. G., Yu, M., Hallam, D., et al. (2019) · Development · doi:10.1242/dev.169474 · Cited by 93 · see citing works
Horikawa, I., Fujita, K., Jenkins, L. M. M., Hiyoshi, Y., Mondal, A. M., Vojtěšek, B., Lane, D. P., Appella, E., & Harris, C. C. (2014) · Nature Communications · doi:10.1038/ncomms5706 · Cited by 93 · see citing works
Alternative Splicing of G9a Regulates Neuronal Differentiation
Fiszbein, A., Giono, L. E., Quaglino, A., Berardino, B. G., Sigaut, L., von Bilderling, C., Schor, I. E., Steinberg, J. H. E., Rossi, M., Pietrasanta, L. I., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.02.063 · Cited by 88 · see citing works
Nonsense-mediated RNA decay and its bipolar function in cancer
Nogueira, G., Fernandes, R. O., García-Moreno, J. F., & Romão, L. (2021) · Molecular Cancer · doi:10.1186/s12943-021-01364-0 · Cited by 89 · see citing works
Systematic detection of functional proteoform groups from bottom-up proteomic datasets
Bludau, I., Frank, M., Dörig, C., Cai, Y., Heusel, M., Rosenberger, G., Picotti, P., Collins, B. C., Röst, H., & Aebersold, R. (2021) · Nature Communications · doi:10.1038/s41467-021-24030-x · Cited by 88 · see citing works
Liu, L., Xiao, Q., Gilbert, E. R., Cui, Z., Zhao, X., Wang, Y., Yin, H., Li, D., Zhang, H., & Zhu, Q. C. (2018) · Scientific Reports · doi:10.1038/s41598-018-25103-6 · Cited by 88 · see citing works
Enhanced protein isoform characterization through long-read proteogenomics
Miller, R., Jordan, B. T., Mehlferber, M., Jeffery, E. D., Chatzipantsiou, C., Kaur, S., Millikin, R. J., Dai, Y., Tiberi, S., Castaldi, P. J., et al. (2022) · Genome biology · doi:10.1186/s13059-022-02624-y · Cited by 89 · see citing works
An analysis of tissue-specific alternative splicing at the protein level
Rodrı́guez, J. M., Pozo, F., Domenico, T. D., Vázquez, J., & Tress, M. L. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008287 · Cited by 85 · see citing works
The Function of Pre-mRNA Alternative Splicing in Mammal Spermatogenesis
Song, H., Wang, L., Chen, D., & Li, F. (2019) · International Journal of Biological Sciences · doi:10.7150/ijbs.34422 · Cited by 85 · see citing works
Differential splicing across immune system lineages
Ergün, A., Doran, G., Costello, J. C., Paik, H. H.-I., Collins, J. J., Mathis, D. J., Benoist, C. O., Blair, D. A., Dustin, M. L., Shinton, S. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311839110 · Cited by 84 · see citing works
Zhao, Y., Hu, F., Zhang, X., Wei, Q., Dong, J., Bo, C., Cheng, B., & Ma, Q. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-1878-8 · Cited by 83 · see citing works
Lopez-Canovas, J. L., del Río-Moreno, M., García-Fernández, H., Jiménez‐Vacas, J. M., Moreno-Montilla, M. T., Sánchez‐Frías, M., Amado, V., L‐López, F., Fondevila, M. F., Ciria, R., et al. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.10.010 · Cited by 82 · see citing works
The Central Role of Noncoding RNA in the Brain
Guennewig, B., & Cooper, A. A. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801105-8.00007-2 · Cited by 79 · see citing works
NOVA2 regulates neural circRNA biogenesis
Knupp, D., Cooper, D. A., Saito, Y., Darnell, R. B., & Miura, P. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab523 · Cited by 76 · see citing works
Mallinjoud, P., Villemin, J.-P., Mortada, H., Espinoza, M. P., Desmet, F.-O., Samaan, S., Chautard, É., Tranchevent, L.-C., & Auboeuf, D. (2013) · Genome Research · doi:10.1101/gr.162933.113 · Cited by 77 · see citing works
Heat stress induced alternative splicing in catfish as determined by transcriptome analysis
Tan, S., Wang, W., Tian, C., Niu, D., Zhou, T., Jin, Y., Yang, Y., Gao, D., Dunham, R. A., & Liu, Z. (2018) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2018.11.008 · Cited by 76 · see citing works
CLASS2: accurate and efficient splice variant annotation from RNA-seq reads
Li, S., Sabunciyan, S., & Florea, L. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw158 · Cited by 76 · see citing works
Danan-Gotthold, M., Guyon, C., Giraud, M., Levanon, E. Y., & Abramson, J. (2016) · Genome biology · doi:10.1186/s13059-016-1079-9 · Cited by 76 · see citing works
Lin, Y. J., Chen, H., Li, Q., Li, W., Wang, J. P., Shi, R., Tunlaya‐Anukit, S., Shuai, P., Wang, Z., Ma, H., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714422114 · Cited by 76 · see citing works
Heberle, B. A., Brandon, J. A., Page, M. L., Nations, K. A., Dikobe, K. I., White, B. J., Gordon, L. A., Fox, G. A., Wadsworth, M. E., Doyle, P. H., et al. (2024) · Nature Biotechnology · doi:10.1038/s41587-024-02245-9 · Cited by 69 · see citing works
Bhattacharya, S., Levy, M. J., Zhang, N., Li, H., Florens, L. A., Washburn, M. P., & Workman, J. L. (2021) · Nature Communications · doi:10.1038/s41467-021-21663-w · Cited by 73 · see citing works
Shade, L. M. P., Katsumata, Y., Abner, E. L., Aung, K. Z., Claas, S. A., Qiao, Q., Heberle, B. A., Brandon, J. A., Page, M. L., Hohman, T. J., et al. (2024) · Nature Genetics · doi:10.1038/s41588-024-01939-9 · Cited by 72 · see citing works
RNA binding proteins in the regulation of heart development
Blech-Hermoni, Y. N., & Ladd, A. N. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.08.008 · Cited by 70 · see citing works
The cellular landscape of mid‐size noncoding RNA
Boivin, V., Faucher‐Giguère, L., Scott, M. S., & Elela, S. A. (2019) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1530 · Cited by 70 · see citing works
de la Fuente, L., Arzalluz-Luque, Á., Tardáguila, M., del Risco, H., Martí, C., Tarazona, S., Salguero, P., Scott, R., Lerma-Aguilera, A., Alastrue‐Agudo, A., et al. (2020) · Genome biology · doi:10.1186/s13059-020-02028-w · Cited by 66 · see citing works
Linker, S. M., Urban, L., Clark, S. J., Chhatriwala, M., Amatya, S., McCarthy, D. J., Ebersberger, I., Vallier, L., Reik, W., Stegle, O., et al. (2019) · Genome biology · doi:10.1186/s13059-019-1644-0 · Cited by 68 · see citing works
Involvement of PARP1 in the regulation of alternative splicing
Matveeva, E. A., Maiorano, J. N., Zhang, Q., Eteleeb, A. M., Convertini, P., Chen, J., Infantino, V., Stamm, S., Wang, J., Rouchka, E. C., et al. (2016) · Cell Discovery · doi:10.1038/celldisc.2015.46 · Cited by 67 · see citing works
Self-citationA survey of software for genome-wide discovery of differential splicing in RNA-Seq data
Hooper, J. E. (2014) · Human Genomics · doi:10.1186/1479-7364-8-3 · Cited by 67 · see citing works
Samaan, S., Tranchevent, L.-C., Dardenne, É., Espinoza, M. P., Zonta, E., Germann, S., Gratadou, L., Dutertre, M., & Auboeuf, D. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1216 · Cited by 67 · see citing works
Pan-cancer analysis of clinical relevance of alternative splicing events in 31 human cancers
Zhang, Y., Yan, L., Zeng, J., Zhou, H., Liu, H., Gan, Y., Yao, W., Chen, K., Ye, Z., & Xu, H. (2019) · Oncogene · doi:10.1038/s41388-019-0910-7 · Cited by 66 · see citing works
Identification of protein features encoded by alternative exons using Exon OntologyPreprint
Tranchevent, L.-C., Aubé, F., Dulaurier, L., Benoit‐Pilven, C., Rey, A., Poret, A., Chautard, É., Mortada, H., Desmet, F.-O., Chakrama, F. Z., et al. (2017) · Genome Research · doi:10.1101/gr.212696.116 · Cited by 64 · see citing works
Deficiency of the splicing factor RBM10 limits EGFR inhibitor response in EGFR-mutant lung cancer
Nanjo, S., Wu, W., Karachaliou, N., Blakely, C. M., Suzuki, J., Chou, Y., Ali, S. M., Kerr, D. L., Olivas, V. R., Shue, J., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci145099 · Cited by 69 · see citing works
Sieber, P. A., Voigt, K., Kämmer, P., Brunke, S., Schuster, S., & Linde, J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02313 · Cited by 65 · see citing works
Best, A. J., James, K., Dalgliesh, C., Hong, E., Chadegani, M. K., Curk, T., Xu, Y., Danilenko, M., Hussain, R., Keavney, B. D., et al. (2014) · Nature Communications · doi:10.1038/ncomms5760 · Cited by 64 · see citing works
Nishida, S., Kakei, Y., Shimada, Y., & Fujiwara, T. (2017) · The Plant Journal · doi:10.1111/tpj.13606 · Cited by 63 · see citing works
PHD finger protein 5A promoted lung adenocarcinoma progression via alternative splicing
Mao, S., Li, Y., Lu, Z., Che, Y., Huang, J., Lei, Y., Wang, Y., Liu, C., Wang, X., Zheng, S., et al. (2019) · Cancer Medicine · doi:10.1002/cam4.2115 · Cited by 62 · see citing works
Functional and clinical characteristics of focal adhesion kinases in cancer progression
Zhang, Z., Li, J., Jiao, S., Han, G., Zhu, J., & Liu, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1040311 · Cited by 62 · see citing works
Self-citationSplicing regulatory factors, ageing and age-related disease
Latorre, E., & Harries, L. W. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.04.004 · Cited by 63 · see citing works
Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration
Yin, J., Xin, X., Weng, Y., & Gui, Z. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186279 · Cited by 61 · see citing works
Widespread alternative exon usage in clinically distinct subtypes of Invasive Ductal Carcinoma
Bjørklund, S. S., Panda, A., Kumar, S., Seiler, M., Robinson, D., Gheeya, J., Yao, M., Alnæs, G. I. G., Toppmeyer, D., Riis, M. L. H., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05537-0 · Cited by 60 · see citing works
MECHANISMS IN ENDOCRINOLOGY: Alternative splicing: the new frontier in diabetes research
Juan‐Mateu, J., Villate, O., & Eizirik, D. L. (2016) · European Journal of Endocrinology · doi:10.1530/eje-15-0916 · Cited by 58 · see citing works
Systematic evaluation of isoform function in literature reports of alternative splicing
Bhuiyan, S. A., Ly, S. M., Phan, M., Huntington, B., Hogan, E., Liu, C. C., Liu, J., & Pavlidis, P. (2018) · BMC Genomics · doi:10.1186/s12864-018-5013-2 · Cited by 60 · see citing works
Discovery and Expression Analysis of Alternative Splicing Events Conserved among Plant SR Proteins
Rauch, H. B., Patrick, T. L., Klusman, K. M., Battistuzzi, F. U., Mei, W., Brendel, V., & Lal, S. K. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst238 · Cited by 59 · see citing works
Karri, V., Ramos, D., Bauzá‐Martinez, J., Odena, M. A., de Oliveira, E., Coort, S. L., Evelo, C. T., Mariman, E. C. M., Schuhmacher, M., & Kumar, V. (2018) · Journal of Proteomics · doi:10.1016/j.jprot.2018.06.020 · Cited by 63 · see citing works
Genome-wide identification of transcript start and end sites by transcript isoform sequencing
Pelechano, V., Wei, W., Jakob, P., & Steinmetz, L. M. (2014) · Nature Protocols · doi:10.1038/nprot.2014.121 · Cited by 58 · see citing works
MYCN controls an alternative RNA splicing program in high-risk metastatic neuroblastoma
Zhang, S., Wei, J. S., Li, S. Q., Badgett, T. C., Song, Y. K., Agarwal, S., Coarfa, C., Tolman, C., Hurd, L., Liao, H., et al. (2016) · Cancer Letters · doi:10.1016/j.canlet.2015.11.045 · Cited by 58 · see citing works
- Authors
- Kelemen, O., Convertini, P., Zhang, Z., Wen, Y., Shen, M., Falaleeva, M., & Stamm, S.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Stamm, Stefan
- Venue
- Gene
- Publisher
- Elsevier BV
- Published
- 2013-02
- Volume
- 514
- Issue
- 1
- Pages
- 1-30
- ISSN
- 0378-1119 (ISSN-L)
- OpenAlex
- W3042475334
- Cited by
- 743
- References
- 559
- Citations by year
- 2026: 29 · 2025: 49 · 2024: 57 · 2023: 55 · 2022: 73 · 2021: 82 · 2020: 77 · 2019: 64 · 2018: 52 · 2017: 56 · 2016: 46 · 2015: 38 · 2014: 40 · 2013: 25
- FWCI
- 3.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Gene (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM083187)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Keywords
- alternative splicing, protein isoforms, protein-protein interaction, protein-nucleic acid interactions, protein-membrane binding, protein localization, ligand binding, gene expression regulation, cell proliferation, cell survival, nervous system
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review