MicroRNAs regulate the expression of the alternative splicing factor nPTB during muscle development

Mfold web server for nucleic acid folding and hybridization prediction

Zuker, M. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg595 · Cited by 13,404

The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14

Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948

Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets

Lewis, B. P., Burge, C. B., & Bartel, D. P. (2005) · Cell · doi:10.1016/j.cell.2004.12.035 · Cited by 11,855

The Human Genome Browser at UCSC

Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., & Haussler, A. D. (2002) · Genome Research · doi:10.1101/gr.229102 · Cited by 10,400

Prediction of Mammalian MicroRNA Targets

Lewis, B. P., Shih, I.-H., Jones-Rhoades, M. W., Bartel, D. P., & Burge, C. B. (2003) · Cell · doi:10.1016/s0092-8674(03)01018-3 · Cited by 5,199

The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans

Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R., & Ruvkun, G. (2000) · Nature · doi:10.1038/35002607 · Cited by 4,989

Identification of Novel Genes Coding for Small Expressed RNAs

Lagos-Quintana, M., Rauhut, R., Lendeckel, W., & Tuschl, T. (2001) · Science · doi:10.1126/science.1064921 · Cited by 4,956

Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs

Lim, L. P., Lau, N. C., Garrett-Engele, P., Grimson, A., Schelter, J. M., Castle, J., Bartel, D. P., Linsley, P. S., & Johnson, J. M. (2005) · Nature · doi:10.1038/nature03315 · Cited by 4,755

Combinatorial microRNA target predictions

Krek, A., Grün, D., Poy, M. N., Wolf, R., Rosenberg, L., Epstein, E. J., MacMenamin, P., da Piedade, I., Gunsalus, K. C., Stoffel, M., et al. (2005) · Nature Genetics · doi:10.1038/ng1536 · Cited by 4,603

Human MicroRNA Targets

John, B., Enright, A. J., Aravin, A., Tuschl, T., Sander, C., & Marks, D. S. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020363 · Cited by 3,796

Rethinking the Meaning of Biological Information

Keller, E. F. (2009) · Biological Theory · doi:10.1162/biot.2009.4.2.159 · Cited by 21

Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties

Chwalenia, K., Oieni, J., Zemła, J., Lekka, M., Ahlskog, N., Coenen-Stass, A. M. L., McClorey, G., Wood, M. J. A., Lomonosova, Y. N., & Roberts, T. C. (2022) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2022.08.033 · Cited by 21

Genome-Wide Activities of RNA Binding Proteins That Regulate Cellular Changes in the Epithelial to Mesenchymal Transition (EMT)

Bebee, T. W., Cieply, B. W., & Carstens, R. P. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-1221-6_8 · Cited by 23

MicroRNA‐31 is required for astrocyte specification

Meares, G. P., Rajbhandari, R., Gerigk, M., Tien, C., Chang, C., Fehling, S. C., Rowse, A. L., Mulhern, K. C., Nair, S., Gray, G. K., et al. (2018) · Glia · doi:10.1002/glia.23296 · Cited by 23

miRNA-Based Regulation of Alternative RNA Splicing in Metazoans

Schorr, A. L., & Mangone, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111618 · Cited by 21

Novel role of microRNA146b in promoting mammary alveolar progenitor cell maintenance

Elsarraj, H. S., Hong, Y., Valdez, K. E., Carletti, M. Z., Salah, S. M., Raimo, M., Taverna, D., Prochasson, P., Bharadwaj, U., Tweardy, D. J., et al. (2013) · Journal of Cell Science · doi:10.1242/jcs.119214 · Cited by 22

Repressing the neuron within

Fairbrother, W. G., & Lipscombe, D. (2007) · BioEssays · doi:10.1002/bies.20696 · Cited by 20

Non-coding RNA in apicomplexan parasites

Matrajt, M. (2010) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2010.06.002 · Cited by 20

Genome-wide profiling of differentially spliced mRNAs in human fetal cortical tissue exposed to alcohol

Kawasawa, Y. I., Mohammad, S., Son, A. I., Morizono, H., Basha, A., Salzberg, A. C., Torii, M., & Hashimoto‐Torii, K. (2017) · Alcohol · doi:10.1016/j.alcohol.2017.05.001 · Cited by 20

Serum miRNAs as biomarkers for the rare types of muscular dystrophy

Koutsoulidou, A., Koutalianos, D., Georgiou, K., Kakouri, A. C., Oulas, A., Tomazou, M., Kyriakides, T. C., Roos, A., Papadimas, G. K., Papadopoulos, C., et al. (2022) · Neuromuscular Disorders · doi:10.1016/j.nmd.2022.03.003 · Cited by 20

Regulator of differentiation 1 (ROD1) binds to the amphipathic C‐terminal peptide of thrombospondin‐4 and is involved in its mitogenic activity

Sadvakassova, G., Dobocan, M. C., DiFalco, M. R., & Congote, L. F. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21817 · Cited by 19

Developmental regulation and evolution of muscle-specific microRNAs

Kusakabe, R., & Inoue, K. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.10.020 · Cited by 20

Reversine promotes browning of white adipocytes by suppressing miR‐133a

Kim, S., Park, J. W., Lee, M. G., Nam, K. H., Park, J. H., Oh, H., Lee, J., Han, J., Yi, S. A., & Han, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27148 · Cited by 18

miR-1/206 downregulates splicing factor Srsf9 to promote C2C12 differentiation

Bjorkman, K. K., Buvoli, M., Pugach, E. K., Polmear, M. M., & Leinwand, L. A. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0211-4 · Cited by 20

Micro-RNA mediated regulation of proliferation, self-renewal and differentiation of mammalian stem cells

Hime, G. R., & Somers, W. G. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.4.9913 · Cited by 18

Регуляторы скелетно-мышечного миогенеза

Kopantseva, E., Белявский, А. В., Kopantseva, E. E., & Belyavsky, A. V. (2016) · Molecular Biology · doi:10.7868/s0026898416010079 · Cited by 17

Functions of microRNAs in Drosophila development

Jones, C. I., & Newbury, S. F. (2010) · Biochemical Society Transactions · doi:10.1042/bst0381137 · Cited by 16

Alternative splicing of inner-ear-expressed genes

Wang, Y., Liu, Y., Nie, H., Ma, X., & Xu, Z. (2016) · Frontiers of Medicine · doi:10.1007/s11684-016-0454-y · Cited by 16

PTB and TIAR binding to insulin mRNA 3′- and 5′UTRs; implications for insulin biosynthesis and messenger stability

Fred, R. G., Mehrabi, S. F., Adams, C. M., & Welsh, N. (2016) · Heliyon · doi:10.1016/j.heliyon.2016.e00159 · Cited by 17

Expression and Regulation Profile of Mature MicroRNA in the Pig: Relevance to Xenotransplantation

Song, Z., Cooper, D. K. C., Cai, Z., & Mou, L. (2018) · BioMed Research International · doi:10.1155/2018/2983908 · Cited by 14

CELF and PTB proteins modulate the inclusion of the β-tropomyosin exon 6B during myogenic differentiation

Sureau, A., Saulière, J., Expert-Bezançon, A., & Marie, J. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.09.010 · Cited by 19

Fine-tuning of microRNAs in Type 2 Diabetes Mellitus

Rosado, J. A., Diez-Bello, R., Salido, G. M., & Jardín, I. (2017) · Current Medicinal Chemistry · doi:10.2174/0929867325666171205163944 · Cited by 16

IARA: a complete and curated atlas of the biogenesis of spliceosome machinery during RNA splicing

Rodrigues, K. S., Petroski, L. P., Utumi, P. H., Ferrasa, A., & Herai, R. H. (2023) · Life Science Alliance · doi:10.26508/lsa.202201593 · Cited by 13

Molecular regulation of endothelial cell activation: novel mechanisms and emerging targets

Charreau, B. L. (2011) · Current Opinion in Organ Transplantation · doi:10.1097/mot.0b013e3283446c52 · Cited by 15

Structural and functional analysis of myostatin-2 promoter alleles from the marine fish Sparus aurata: Evidence for strong muscle-specific promoter activity and post-transcriptional regulation

Nadjar-Boger, E., Hinits, Y., & Funkenstein, B. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2012.03.017 · Cited by 14

Downregulation of CCL2 induced by the upregulation of microRNA-206 is associated with the severity of HEV71 encephalitis

Zhang, G., Wang, J., Guo, Y., & Shi, B. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7142 · Cited by 14

Crafting a Blueprint for MicroRNA in Cardiovascular Diseases (CVDs)

Khan, S. U., Saeed, S., Sheikh, A. N., Arbi, F. M., Shahzad, A., Faryal, U., & Lu, K. (2023) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2023.102010 · Cited by 14

MicroRNA Dysregulation in Aging and Pathologies of the Skeletal Muscle

McCormick, R., & Goljanek‐Whysall, K. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.03.005 · Cited by 14

Expression patterns of regulatory lncRNAs and miRNAs in muscular atrophy models induced by starvation in vitro and in vivo

Lei, S., She, Y., Zeng, J., Chen, R., Zhou, S., & Shi, H. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10661 · Cited by 14

Temporal correlation between differentiation factor expression and microRNAs in Holstein bovine skeletal muscle

Miretti, S., Volpe, M. G., Martignani, E., Accornero, P., & Baratta, M. (2016) · animal · doi:10.1017/s1751731116001488 · Cited by 14

Differential evolution of signal-responsive RNA elements and upstream factors that control alternative splicing

Xie, J. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1688-y · Cited by 13

Physiological tissue-specific and age-related reduction of mouse TDP-43 levels is regulated by epigenetic modifications

Pacetti, M., Conti, L. D., Marasco, L. E., Romano, M., Rashid, M. M., Nubiè, M., Baralle, F. E., & Baralle, M. (2022) · Disease Models & Mechanisms · doi:10.1242/dmm.049032 · Cited by 15

Aberrant Exon 8/8a Splicing by Downregulated PTBP (Polypyrimidine Tract-Binding Protein) 1 Increases Ca V 1.2 Dihydropyridine Resistance to Attenuate Vasodilation

Lei, J., Liu, X., Song, M., Zhou, Y., Fan, J., Shen, X., Xu, X., Kapoor, I., Zhu, G., & Wang, J. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.315010 · Cited by 13

RNA-binding proteins switch gears to drive alternative splicing in neurons

Grabowski, P. J. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb0707-577 · Cited by 14

Splicing alterations in pancreatic ductal adenocarcinoma: a new molecular landscape with translational potential

Alors‐Pérez, E., Pedraza‐Arévalo, S., Blázquez‐Encinas, R., Moreno-Montilla, M. T., García‐Vioque, V., Berbel, I., Luque, R. M., Sáinz, B., Ibáñez‐Costa, A., & Castano, J. P. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02858-z · Cited by 12

Alternative splicing regulation of membrane trafficking genes during myogenesis

Hinkle, E. R., Wiedner, H. J., Torres, E. V., Jackson, M., Black, A. J., Blue, R. E., Harris, S. E., Guzmán, B. B., Gentile, G. M., Lee, E. Y., et al. (2022) · RNA · doi:10.1261/rna.078993.121 · Cited by 12

Human microRNA in norm and pathology

Rogaev, E. I., Borinskaya, S. A., Islamgulov, D. V., & Grigorenko, A. P. (2008) · Molecular Biology · doi:10.1134/s002689330805004x · Cited by 10

Key regulators of skeletal myogenesis

Kopantseva, E., & Belyavsky, A. V. (2016) · Molecular Biology · doi:10.1134/s0026893316010076 · Cited by 12

Functional characterization of the ribonucleoprotein, PTB-binding 1/Raver1 promoter region

Romanelli, M. G., Lorenzi, P., Avesani, F., & Morandi, C. (2007) · Gene · doi:10.1016/j.gene.2007.09.004 · Cited by 11

In silico Analysis of Polymorphisms in microRNAs Deregulated in Alzheimer Disease

Moraghebi, M., Maleki, R., Ahmadi, M., Negahi, A. A., Abbasi, H., & Mousavi, P. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.631852 · Cited by 10

Physiological and Pathological Functions of Mammalian MicroRNAs

Liu, M., Jiang, S., Lu, Z., Li, Y., & Young, K. H. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-046884-6.00223-2 · Cited by 10

Micromanaging Alternative Splicing during Muscle Differentiation

Bland, C. S., & Cooper, T. A. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.01.014 · Cited by 10

Evaluation of RNA purification methods by using different blood stabilization tubes: identification of key features for epidemiological studies

Carrillo-Ávila, J. A., de la Puente, R., Catalina, P., Rejón, J. D., Espín-Vallejo, L., Valdivieso, V., & Aguilar‐Quesada, R. (2020) · BMC Research Notes · doi:10.1186/s13104-020-04943-4 · Cited by 10

Functional studies of microRNA based on knockdown using Locked Nucleic Acid probes

Rasmussen, S. V., & Roberts, P. (2007) · Nature Methods · doi:10.1038/nmeth1034 · Cited by 9

Differences in micro-RNA expression profile between vastus lateralis samples and myotubes in COPD cachexia

Barreiro, E., Sancho‐Muñoz, A., Puig‐Vilanova, E., Salazar‐Degracia, A., Pascual-Guàrdia, S., Casadevall, C., & Gea, J. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00611.2018 · Cited by 9

PTBP2 exon 10 inclusion is associated with the progression of CML and it is BCR-ABL1 dependent

Nandagopalan, S. R., Subramaniam, A., Vadlamudi, Y., Biswas, S., Biswas, G., Pattnayak, N. C., & Chakraborty, S. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.01.018 · Cited by 8

Regulation of miR-206 in denervated and dystrophic muscles, and its effect on acetylcholine receptor clustering

Barden, J., Kosloski, O., Jadidian, A., & Akaaboune, M. (2024) · Journal of Cell Science · doi:10.1242/jcs.262303 · Cited by 7

PTBP 1 acts as a dominant repressor of the aberrant tissue‐specific splicing of ISCU in hereditary myopathy with lactic acidosis

Rawcliffe, D. F. R., Österman, L., Nordin, A., & Holmberg, M. (2018) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.413 · Cited by 5

Mechanism and Functions of Identified miRNAs in Poultry Skeletal Muscle Development – A Review

Collins, A. A., Zou, K., Li, Z., & Su, Y. (2019) · Annals of Animal Science · doi:10.2478/aoas-2019-0049 · Cited by 6

Functional, Structural, and Sequence Studies of MicroRNA

Mitra, C. K., & Korla, K. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-748-8_11 · Cited by 6

Micro RNAs in Development and Disease

Staton, A. A., & Giráldez, A. J. (2008) · Wiley eBooks · doi:10.1002/9780470015902.a0020863 · Cited by 6

Idiopathic inflammatory myopathy and non-coding RNA

Yang, Y., Hu, G., Wan, G., Li, M., Chang, B., & Yi, X. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1227945 · Cited by 6

Co- and post-transcriptional regulation of Rbm5 and Rbm10 in mouse cells as evidenced by tissue-specific, developmental and disease-associated variation of splice variant and protein expression levels

Ozuemba, B., Masilamani, T. J., Loiselle, J. J., Koenderink, B. W., Vanderbeck, K. A., Knee, J. M., Larivière, C., & Sutherland, L. C. (2016) · Gene · doi:10.1016/j.gene.2015.12.070 · Cited by 5

Great Potential of MicroRNA in Cancer Stem Cell

Xia, M. (2015) · Cited by 5

ESRP2–microRNA-122 axis promotes the postnatal onset of liver polyploidization and maturation

Bangru, S., Chen, J., Baker, N., Das, D., Chembazhi, U. V., Derham, J. M., Chorghade, S., Arif, W., Alencastro, F., Duncan, A. W., et al. (2025) · Genes & Development · doi:10.1101/gad.352129.124 · Cited by 4

Regulatory Factors that Reveal Three Distinct Adipocytes : The Brown, the White and the Brite

Waldén, T. B. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 4

Roles of miR-1, miR-133a, and miR-206 in calcium, oxidative stress, and NO signaling involved in muscle diseases

(2015) · RNA & DISEASE · doi:10.14800/rd.558 · Cited by 3

MicroRNAs in Skeletal Muscle Differentiation

Sun, H., Cao, Y., Zhao, Y. F., Lu, L., Zhou, L., Wang, L., Chen, X., & Wang, H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405544-5.00017-4 · Cited by 3

Biological activities and molecular interactions of the C-terminal residue of thrombospondin-4, an epitome of acidic amphipathic peptides

Congote, L. F., Sadvakassova, G., Dobocan, M. C., DiFalco, M. R., & Kriazhev, L. (2009) · Peptides · doi:10.1016/j.peptides.2009.12.011 · Cited by 3

The impact of microRNAs on the evolution of metazoan complexity

Dai, Z., & Chen, L. (2010) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2010.00105 · Cited by 3

Argonaute identity defines the length of mature mammalian micrornas

Juvvuna, P. K. (2013) · doi:10.32657/10356/51099 · Cited by 4

Guider et intégrer pour un épissage diversifié

Fisette, J., Michelle, L., Revil, T., & Chabot, B. (2009) · médecine/sciences · doi:10.1051/medsci/2009252175 · Cited by 3

[Expression profiles of miRNA-182 and Clock mRNA in the pineal gland of neonatal rats with hypoxic-ischemic brain damage].

Han, X., Ding, X., Xu, L., Liu, M., & Feng, X. (2016) · PubMed Central · doi:10.7499/j.issn.1008-8830.2016.03.016 · Cited by 2

Gene expression, cell determination, differentiation, and regeneration

Stockdale, F. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818422-6.00010-1 · Cited by 2

The role of microRNAs in muscle wasting and recovery during critical illness: a systematic review

Borja-Gonzalez, M., Coyne, S. M., Fagan, S., Casas-Martinez, J. C., Sannicandro, A. J., McNicholas, B., O'Connell, K., Laffey, J. G., Ó’Caoimh, R., McDonagh, B., et al. (2023) · JCSM Rapid Communications · doi:10.1002/rco2.80 · Cited by 2

On the road to the definition of the cardiac miRNome in human disease states

Latronico, M. V. G., & Condorelli, G. (2008) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2008.05.018 · Cited by 2

MicroRNA: from fundamental research to their application

Shirina, T. V., Bobrovskaya, M. T., & Kozlov, E. A. (2007) · Biopolymers and Cell · doi:10.7124/bc.000781 · Cited by 2

MicroRNAs in Skeletal Muscle Differentiation

Sun, H., Cao, Y., Zhao, Y. F., Lu, L., Zhou, L., Wang, L., Chen, X., & Wang, H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-820719-2.00013-2 · Cited by 1

From development to disease: the neuronal role of hnRNPs through the lens of Drosophila

Stefanelli, C., Colaianni, D., Pittà, C. D., & Mazzotta, G. M. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1819111 · Cited by 1

Splicing Silencing by the CUGBP2 Splicing Factor: Mechanism of Action and Combinatorial Code for Splicing Silencing with Implications for Autoregulation

Dembowski, J. A. (2009) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

MicroRNA expression in melanocytes and melanoma cells

Petkevich, A., Shubina, I. Z., Abramov, A., Mamedova, L. T., Самойленко, И. В., & Kiselevsky, M. V. (2018) · Russian Journal of Biotherapy · doi:10.17650/1726-9784-2018-17-3-6-11 · Cited by 1

Advances in the Treatment of Colorectal Cancer Using MicroRNA

Dang, K., Gao, Y., Qian, A., & Dong, J. (2019) · International Bhurban Conference on Applied Sciences and Technology (IBCAST) · doi:10.1109/ibcast.2019.8667146 · Cited by 1

MicroRNA in Muscle Development and Function

Deng, Z., & Wang, D. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8533-8_8 · Cited by 1

Developmental switch on the signaling for cardiomyocyte death: Insights into the regulation of apoptotic gene expression and into the control of DNA fragmentation

Zhang, J. (2009) · Repositori ObertUDL (University of Lleida) · Cited by 1

Correction: Transcriptome-Wide Prediction of miRNA Targets in Human and Mouse Using FASTH

Ragan, C., Cloonan, N., Grimmond, S. M., Zuker, M., & Ragan, M. A. (2009) · PLoS ONE · doi:10.1371/annotation/e0842765-3cae-4737-8b5b-96aeb12d7fb5 · Cited by 1

Gene Expression, Cell Determination, and Differentiation

Stockdale, F. E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-398358-9.00012-4 · Cited by 1

miR-1/206 down-regulates splicing factor Srsf9 to promote myogenesisPreprint

Bjorkman, K. K., Buvoli, M., Pugach, E. K., Polmear, M. M., & Leinwand, L. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/691162 · Cited by 1

ESRP2-microRNA-122 axis directs the postnatal onset of liver polyploidization and maturationPreprint

Bangru, S., Chen, J., Baker, N., Das, D., Chembazhi, U. V., Derham, J. M., Chorghade, S., Arif, W., Alencastro, F., Duncan, A. W., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.06.602336 · Cited by 1

Splicing Decisions Shape Neuronal Protein Function across the Transcriptome

Dembowski, J. A., & Grabowski, P. J. (2013) · Wiley eBooks · doi:10.1002/9783527665433.ch7

Gene Regulation by Transcription Factors and Splicing Factors Coupled With microRNAs in Animals*

Pang, J.-H., Ren, C.-H., Li, Z., Liu, H., & Zhang, C. (2009) · PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS · doi:10.3724/sp.j.1206.2008.00423

Studies on mammalian pre-mRNA splicing : connections to transcription and cancer

David, C. J. (2011) · doi:10.7916/d8931130

MICRO-RNA146B PROMOTES ALVEOLAR PROGENITOR CELL MAINTENANCE THROUGH PREFERENTIAL REGULATION OF STAT3B

Elsarraj, H. S. (2012) · KU ScholarWorks (The University of Kansas)

Guider et intégrer pour un épissage

Revil, T., & Chabot, B. (2009)

Identification of novel signaling pathways for cardiomyocyte differentiation and growth

Ye, J. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Regulation of Core Splicing Factors by Alternative Splicing and Nonsense-mediated mRNA Decay

Saltzman, A. L. (2012) · TSpace (University of Toronto)

Regulation of Alternative Splicing by microRNAs

Gaur, R. K. (2009) · CRC Press eBooks · doi:10.1201/9781420008708.ch14

A Comprehensive Profile of Mature MicroRNA in the PigPreprint

Wang, X., Cooper, D. K. C., Cai, Z., & Mou, L. (2017) · Preprints.org · doi:10.20944/preprints201709.0057.v1

A Genome-Scale Analysis of Alternative Splicing Regulation by Splicing Factors in C. elegans

Tan, J. H. (2018) · TSpace (University of Toronto)

Physiological and Pathological Functions of Mammalian MicroRNAs

Ma, X., Wang, L., Cao, Z., Hu, H., Lu, Z., Xu-Monette, Z. Y., Young, K. H., & Li, Y. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.95612-5

Étude des protéines de liaison à l'ARN des familles PTB et ARE-BP au cours du développement chez le xénope

Noiret, M. (2012) · OpenGrey (Institut de l'Information Scientifique et Technique)

Ptbp1-Activateded Co-Transcriptional Splicing Controls Epigenetic Status of Pluripotent Stem CellsPreprint

Iannone, C., Kainov, Y. A., Zhuravskaya, A., Hamid, F., Nojima, T., & Makeyev, E. V. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4058691

Faculty Opinions recommendation of MicroRNAs coordinate an alternative splicing network during mouse postnatal heart development.

Riley, P. R., & Petchey, L. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.3480956.3176054

WITHDRAWN:Genome-wide profiling of differentially spliced mRNAs in human fetal cortical tissue exposed to alcohol

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