PolyASite 2.0: a consolidated atlas of polyadenylation sites from 3′ end sequencing

The Sequence Read Archive

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Proliferating Cells Express mRNAs with Shortened 3' Untranslated Regions and Fewer MicroRNA Target Sites

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A large-scale analysis of mRNA polyadenylation of human and mouse genes

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Ensembl 2019

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The UCSC Genome Browser database: 2019 update

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Patterns of Variant Polyadenylation Signal Usage in Human GenesPreprint

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A quantitative atlas of polyadenylation in five mammalsPreprint

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Progressive lengthening of 3′ untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development

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Polyadenylic Acid Sequences in the Heterogeneous Nuclear RNA and Rapidly-Labeled Polyribosomal RNA of HeLa Cells: Possible Evidence for a Precursor Relationship

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Alternative cleavage and polyadenylation in health and disease

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Beyond the RNA-dependent function of LncRNA genes

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Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation

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TDP-43 condensation properties specify its RNA-binding and regulatory repertoire

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High-throughput total RNA sequencing in single cells using VASA-seq

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A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brain

Joglekar, A., Prjibelski, A., Mahfouz, A., Collier, P., Lin, S., Schlusche, A. K., Marrocco, J., Williams, S. R., Haase, B., Hayes, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20343-5 · Cited by 229

Exon architecture controls mRNA m 6 A suppression and gene expression

He, P. C., Wei, J., Dou, X., Harada, B. T., Zhang, Z. S., Ge, R., Liu, C., Zhang, L., Yu, X., Wang, S., et al. (2023) · Science · doi:10.1126/science.abj9090 · Cited by 229

SQANTI3: curation of long-read transcriptomes for accurate identification of known and novel isoforms

Pardo-Palacios, F. J., Arzalluz-Luque, Á., Kondratova, L., Salguero, P., Mestre‐Tomás, J., Amorín, R., Estevan-Morió, E., Liu, T., Nanni, A. V., McIntyre, L. M., et al. (2024) · Nature Methods · doi:10.1038/s41592-024-02229-2 · Cited by 219

Alternative polyadenylation: methods, mechanism, function, and role in cancer

Zhang, Y., Liu, L., Qiu, Q., Zhou, Q. H., Ding, J., Lü, Y., & Liu, P. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-01852-7 · Cited by 158

Multivalent Proteins Rapidly and Reversibly Phase-Separate upon Osmotic Cell Volume Change

Jalihal, A. P., Pitchiaya, S., Xiao, L., Bawa, P., Jiang, X., Bedi, K., Parolia, A., Cieslik, M. P., Ljungman, M. E., Chinnaiyan, A. M., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.08.004 · Cited by 140

Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms

Patowary, A., Zhang, P., Jops, C. T., Vuong, C. K., Ge, X., Hou, K., Kim, M., Gong, N. N., Margolis, M. P., Vo, D., et al. (2024) · Science · doi:10.1126/science.adh7688 · Cited by 90

3’UTR Diversity: Expanding Repertoire of RNA Alterations in Human mRNAs

Hong, D., & Jeong-Yu, S. (2023) · Molecules and Cells · doi:10.14348/molcells.2023.0003 · Cited by 96

Long 3′UTRs predispose neurons to inflammation by promoting immunostimulatory double-stranded RNA formation

Dorrity, T. J., Shin, H., Wiegand, K. A., Aruda, J., Closser, M., Jung, E., Gertie, J. A., Leone, A., Polfer, R., Culbertson, B., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.adg2979 · Cited by 76

The landscape of alternative polyadenylation in single cells of the developing mouse embryo

Agarwal, V., Lopez-Darwin, S. L., Kelley, D. R., & Shendure, J. (2021) · Nature Communications · doi:10.1038/s41467-021-25388-8 · Cited by 66

The ENCODE4 long-read RNA-seq collection reveals distinct classes of transcript structure diversityPreprint

Reese, F., Williams, B. A., Balderrama-Gutierrez, G., Wyman, D., Çelik, M. H., Rebboah, E., Rezaie, N., Trout, D. E., Razavi-Mohseni, M., Jiang, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.15.540865 · Cited by 70

On the function and relevance of alternative 3′‐ UTRs in gene expression regulation

Pereira‐Castro, I., & Moreira, A. (2021) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1653 · Cited by 60

3′UTR heterogeneity and cancer progression

Chan, J. J., Tabatabaeian, H., & Tay, Y. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.10.001 · Cited by 58

TERA-Seq: true end-to-end sequencing of native RNA molecules for transcriptome characterization

Ibrahim, F., Oppelt, J., Maragkakis, M., & Mourelatos, Z. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab713 · Cited by 58

Pervasive transcriptome interactions of protein-targeted drugs

Fang, L., Velema, W. A., Lee, Y., Xiao, L., Mohsen, M. G., Kietrys, A. M., & Kool, E. T. (2023) · Nature Chemistry · doi:10.1038/s41557-023-01309-8 · Cited by 57

Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in ovarian cancer

Dondi, A., Lischetti, U., Jacob, F., Singer, F., Borgsmüller, N., Coelho, R., Aebersold, R. H., Ak, M., Alquaddoomi, F., Albert, S. I., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43387-9 · Cited by 55

scAPAtrap: identification and quantification of alternative polyadenylation sites from single-cell RNA-seq data

Wu, X., Liu, T., Ye, C., Ye, W., & Ji, G. (2020) · Briefings in Bioinformatics · doi:10.1093/bib/bbaa273 · Cited by 53

Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci

Yamaguchi, K., Ishigaki, K., Suzuki, A., Tsuchida, Y., Tsuchiya, H., Sumitomo, S., Nagafuchi, Y., Miya, F., Tsunoda, T., Shoda, H., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32358-1 · Cited by 51

The landscape of alternative polyadenylation during EMT and its regulation by the RNA-binding protein Quaking

Neumann, D., Pillman, K. A., Dredge, B. K., Bert, A. G., Phillips, C. A., Lumb, R., Ramani, Y., Bracken, C. P., Hollier, B. G., Selth, L. A., et al. (2023) · RNA Biology · doi:10.1080/15476286.2023.2294222 · Cited by 45

Deep learning of human polyadenylation sites at nucleotide resolution reveals molecular determinants of site usage and relevance in disease

Stroup, E. K., & Ji, Z. (2023) · Nature Communications · doi:10.1038/s41467-023-43266-3 · Cited by 40

Single-cell long-read sequencing in human cerebral organoids uncovers cell-type-specific and autism-associated exons

Yang, Y., Yang, R., Kang, B., Qian, S., He, X., & Zhang, X. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113335 · Cited by 41

SCAPTURE: a deep learning-embedded pipeline that captures polyadenylation information from 3′ tag-based RNA-seq of single cells

Li, G., Fang, N., Yuan, G.-H., Liu, C., Liu, X., Chen, L., Tian, B., & Yang, L. C. (2021) · Genome biology · doi:10.1186/s13059-021-02437-5 · Cited by 40

Sequencing of individual barcoded cDNAs using Pacific Biosciences and Oxford Nanopore Technologies reveals platform-specific error patternsPreprint

Mikheenko, A., Prjibelski, A. D., Joglekar, A., & Tilgner, H. (2022) · Genome Research · doi:10.1101/gr.276405.121 · Cited by 40

Quantifying 3′UTR length from scRNA-seq data reveals changes independent of gene expression

Fansler, M. M., Mitschka, S., & Mayr, C. (2024) · Nature Communications · doi:10.1038/s41467-024-48254-9 · Cited by 52

Benchmarking sequencing methods and tools that facilitate the study of alternative polyadenylation

Shah, A., Mittleman, B. E., Gilad, Y., & Li, Y. (2021) · Genome biology · doi:10.1186/s13059-021-02502-z · Cited by 37

Cancer-associated dynamics and potential regulators of intronic polyadenylation revealed by IPAFinder using standard RNA-seq dataPreprint

Zhao, Z., Xu, Q., Wei, R., Wang, W., Ding, D., Yang, Y., Yao, J., Zhang, L., Hu, Y., Wei, G., et al. (2021) · Genome Research · doi:10.1101/gr.271627.120 · Cited by 40

CFIm-mediated alternative polyadenylation remodels cellular signaling and miRNA biogenesis

Ghosh, S., Ataman, M., Bąk, M., Börsch, A., Schmidt, A., Buczak, K., Martin, G., Dimitriades, B., Herrmann, C., Kanitz, A., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac114 · Cited by 37

Evolution and function of developmentally dynamic pseudogenes in mammals

Qian, S. H., Chen, L., Xiong, Y.-L., & Chen, Z. (2022) · Genome biology · doi:10.1186/s13059-022-02802-y · Cited by 39

TREND-DB—a transcriptome-wide atlas of the dynamic landscape of alternative polyadenylation

Marini, F., Scherzinger, D., & Danckwardt, S. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa722 · Cited by 35

Integrator loss leads to dsRNA formation that triggers the integrated stress response

Baluapuri, A., Zhao, N. C., Marina, R. J., Huang, K.-L., Kuzkina, A., Amodeo, M. E., Stein, C. B., Ahn, L., Farr, J. S., Schaffer, A. E., et al. (2025) · Cell · doi:10.1016/j.cell.2025.03.025 · Cited by 39

Chromosomal‐level genome and metabolome analyses of highly heterozygous allohexaploid Dendrocalamus brandisii elucidate shoot quality and developmental characteristics

Jiang, J., Zhang, Z., Bai, Y., Wang, X., Dou, Y., Geng, R., Wu, C., Zhang, H., Lu, C., Gu, L., et al. (2023) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13592 · Cited by 31

MAAPER: model-based analysis of alternative polyadenylation using 3′ end-linked reads

Li, W. V., Zheng, D., Wang, R., & Tian, B. (2021) · Genome biology · doi:10.1186/s13059-021-02429-5 · Cited by 31

QuantifyPoly(A): reshaping alternative polyadenylation landscapes of eukaryotes with weighted density peak clustering

Ye, C., Zhao, D., Ye, W., Wu, X., Ji, G., Li, Q. Q., & Lin, J. (2021) · Briefings in Bioinformatics · doi:10.1093/bib/bbab268 · Cited by 31

An RNA foundation model enables discovery of disease mechanisms and candidate therapeuticsPreprint

Celaj, A., Gao, A. J., Lau, T., Holgersen, E. M., Lo, A., Lodaya, V., Cole, C. B., Denroche, R. E., Spickett, C., Wagih, O., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.20.558508 · Cited by 36

Dysregulated RNA polyadenylation contributes to metabolic impairment in non-alcoholic fatty liver disease

Jobbins, A. M., Haberman, N., Artigas, N., Amourda, C., Paterson, H. A. B., Yu, S., Blackford, S. J. I., Montoya, A., Dore, M. H., Wang, Y.-F., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac165 · Cited by 32

Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing

Mulroney, L., Wulf, M. G., Schildkraut, I., Tzertzinis, G., Buswell, J., Jain, M., Olsen, H. E., Diekhans, M., Junior, I. R. C., Akeson, M. A., et al. (2021) · RNA · doi:10.1261/rna.078703.121 · Cited by 27

Animal-APAdb: a comprehensive animal alternative polyadenylation database

Jin, W., Zhu, Q., Yang, Y., Yang, W., Wang, D., Yang, J., Niu, X., Yu, D., & Gong, J. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa778 · Cited by 26

scAPAdb: a comprehensive database of alternative polyadenylation at single-cell resolution

Zhu, S. Z., Lian, Q., Ye, W., Qin, W., Wu, Z., Ji, G., & Wu, X. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab795 · Cited by 26

Alternative polyadenylation determines the functional landscape of inverted Alu repeats

Ku, J., Lee, K., Ku, D., Kim, S., Lee, J., Bang, H., Kim, N., Do, H., Lee, H., Lim, C., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.01.008 · Cited by 23

mRNA initiation and termination are spatially coordinated

Calvo-Roitberg, E., Carroll, C. L., Kim, G., Sanabria, V. C., Venev, S. V., Mick, S. T., Paquette, J. D., Urióstegui-Arcos, M., Dekker, J., Fiszbein, A., et al. (2025) · Science · doi:10.1126/science.ado8279 · Cited by 23

Comprehensive characterization of somatic variants associated with intronic polyadenylation in human cancers

Zhao, Z., Xu, Q., Wei, R., Huang, L., Wang, W., Wei, G., & Ni, T. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab772 · Cited by 27

TDP-43 nuclear loss in FTD/ALS causes widespread alternative polyadenylation changesPreprint

Zeng, Y., Lovchykova, A., Akiyama, T., Liu, C., Guo, C., Jawahar, V. M., Sianto, O., Calliari, A., Prudencio, M., Dickson, D. W., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.22.575730 · Cited by 25

An isoform-resolution transcriptomic atlas of colorectal cancer from long-read single-cell sequencing

Li, Z., Zhang, B., Chan, J. J., Tabatabaeian, H., Tong, Q. Y., Chew, X. H., Fan, X., Driguez, P., Chan, C., Cheong, F., et al. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100641 · Cited by 27

Aptardi predicts polyadenylation sites in sample-specific transcriptomes using high-throughput RNA sequencing and DNA sequence

Lusk, R., Stene, E., Banaei‐Kashani, F., Tabakoff, B., Kechris, K. J., & Saba, L. M. (2021) · Nature Communications · doi:10.1038/s41467-021-21894-x · Cited by 23

Regulating the regulator: a survey of mechanisms from transcription to translation controlling expression of mammalian cell cycle kinase Aurora A

Cacioppo, R., & Lindon, C. (2022) · Open Biology · doi:10.1098/rsob.220134 · Cited by 21

Cochlear transcript diversity and its role in auditory functions implied by an otoferlin short isoform

Liu, H., Liu, H., Wang, L., Song, L., Jiang, G., Lü, Q., Yang, T., Hu, P., Cai, R., Zhao, X., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38621-3 · Cited by 25

TDP-43 loss induces extensive cryptic polyadenylation in ALS/FTDPreprint

Bryce-Smith, S., Brown, A., Mehta, P. R., Mattedi, F., Mikheenko, A., Barattucci, S., Zanovello, M., Dattilo, D., Yome, M., Kargbo-Hill, S. E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.22.576625 · Cited by 24

Challenges in identifying mRNA transcript starts and ends from long-read sequencing dataPreprint

Calvo-Roitberg, E., Daniels, R. F., & Pai, A. A. (2024) · Genome Research · doi:10.1101/gr.279559.124 · Cited by 24

Rapid UPF1 depletion illuminates the temporal dynamics of the NMD-regulated human transcriptome

Boehm, V., Wallmeroth, D., Wulf, P. O., Popp, O., Teixeira Alves, L. G., Reinecke, L., Riedel, M., Wyler, E., Franitza, M., Becker, K., et al. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.08.015 · Cited by 23

Macrophage differentiation is marked by increased abundance of the mRNA 3’ end processing machinery, altered poly(A) site usage, and sensitivity to the level of CstF64

Mukherjee, S., Graber, J. H., & Moore, C. L. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1091403 · Cited by 21

Merging short and stranded long reads improves transcript assembly

Kainth, A. S., Haddad, G. A., Hall, J. M., & Ruthenburg, A. J. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011576 · Cited by 21

M6A-methylated circPOLR2B forms an R-loop and regulates the biological behavior of glioma stem cells through positive feedback loops

Lin, H., Cui, Z., Tiange, E., Xu, H., Wang, D., Wang, P., Ruan, X., Liu, L., & Xue, Y. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06946-6 · Cited by 19

Functional and dynamic profiling of transcript isoforms reveals essential roles of alternative splicing in interferon response

Ueda, M. T., Inamo, J., Miya, F., Shimada, M., Yamaguchi, K., & Kochi, Y. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100654 · Cited by 20

Extensible benchmarking of methods that identify and quantify polyadenylation sites from RNA-seq data

Bryce-Smith, S., Bürri, D., Gazzara, M. R., Herrmann, C., Danecka, W., Fitzsimmons, C. M., Wan, Y. K., Zhuang, F., Fansler, M. M., Fernández, J. M., et al. (2023) · RNA · doi:10.1261/rna.079849.123 · Cited by 18

The RNA-Binding Protein HuD Regulates Alternative Splicing and Alternative Polyadenylation in the Mouse Neocortex

Sena, R. M., Twiss, J. L., Gardiner, A. S., Dell’Orco, M., Linsenbardt, D. N., & Perrone‐Bizzozero, N. I. (2021) · Molecules · doi:10.3390/molecules26102836 · Cited by 18

Implications of Poly(A) Tail Processing in Repeat Expansion Diseases

Joachimiak, P., Ciesiołka, A., Figura, G., & Fiszer, A. (2022) · Cells · doi:10.3390/cells11040677 · Cited by 17

Widespread occurrence of hybrid internal-terminal exons in human transcriptomes

Fiszbein, A., McGurk, M. P., Calvo-Roitberg, E., Kim, G., Burge, C. B., & Pai, A. A. (2022) · Science Advances · doi:10.1126/sciadv.abk1752 · Cited by 16

Sequential verification of transcription by Integrator and Restrictor

Estell, C., Łazowski, K., Eaton, J. D., & West, S. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.09.025 · Cited by 16

m6Am sequesters PCF11 to suppress premature termination and drive neuroblastoma differentiation

An, H., Hong, Y., Goh, Y. T., Koh, C. W. Q., Kanwal, S., Zhang, Y., Lu, Z., Yap, P. M. L., Neo, S. P., Wong, C., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.10.004 · Cited by 18

scAPAatlas: an atlas of alternative polyadenylation across cell types in human and mouse

Yang, X., Tong, Y., Liu, G., Yuan, J., & Yang, Y. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab917 · Cited by 17

MicroRNA‐mediated metabolic reprogramming of chimeric antigen receptor T cells

Rad, S. M. A. H., Halpin, J. C., Tawinwung, S., Suppipat, K., Hirankarn, N., & McLellan, A. D. (2022) · Immunology and Cell Biology · doi:10.1111/imcb.12551 · Cited by 18

PolyASite v3.0: a multi-species atlas of polyadenylation sites inferred from single-cell RNA-sequencing data

Moon, Y., Herrmann, C., Mironov, A., & Zavolan, M. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1043 · Cited by 16

Interplay between splicing and transcriptional pausing exerts genome-wide control over alternative polyadenylation

Gallardo, C. M., de Diego, A. S., Martínez‐A, C., & van Wely, K. H. M. (2021) · Transcription · doi:10.1080/21541264.2021.1959244 · Cited by 15

Kinetics of mRNA nuclear export regulate innate immune response gene expression

Lefaudeux, D., Sen, S., Jiang, K., Hoffmann, A., the UCLA Ribonomics Group, Arriola, J. G. S., Miller, N., Zhang, C., Chen, E. Y. H., Roy, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34635-5 · Cited by 16

Systematic screening identifies ABCG2 as critical factor underlying synergy of kinase inhibitors with transcriptional CDK inhibitors

van der Noord, V. E., van der Stel, W., Louwerens, G., Verhoeven, D., Kuiken, H. J., Lieftink, C., Grandits, M., Ecker, G. F., Beijersbergen, R. L., Bouwman, P., et al. (2023) · Breast Cancer Research · doi:10.1186/s13058-023-01648-x · Cited by 15

CFIm-mediated alternative polyadenylation safeguards the development of mammalian pre-implantation embryos

Li, N., Cai, Y., Zou, M., Zhou, J. P., Zhang, L., Zhou, L., Xiang, W., Cui, Y., & Li, H. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.11.016 · Cited by 14

REPAC: analysis of alternative polyadenylation from RNA-sequencing data

Imada, E. L., Wilks, C., Langmead, B., & Marchionni, L. (2023) · Genome biology · doi:10.1186/s13059-023-02865-5 · Cited by 14

Transcriptome sequencing suggests that pre-mRNA splicing counteracts widespread intronic cleavage and polyadenylation

Vlasenok, M., Margasyuk, S., & Pervouchine, D. D. (2022) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqad051 · Cited by 14

The peptide woods are lovely, dark and deep: Hunting for novel cancer antigens

Oreper, D., Klaeger, S., Jhunjhunwala, S., & Delamarre, L. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101758 · Cited by 13

Navigating the Multiverse of Antisense RNAs: The Transcription- and RNA-Dependent Dimension

Pagani, G., Pandini, C., & Gandellini, P. (2022) · Non-Coding RNA · doi:10.3390/ncrna8060074 · Cited by 12

Uncovering the dynamics and consequences of RNA isoform changes during neuronal differentiation

Ulićević, J., Shao, Z., Jasnovidova, O., Bressin, A., Gajos, M., Ng, A. H. M., Annaldasula, S., Meierhofer, D., Church, G. M., Busskamp, V., et al. (2024) · Molecular Systems Biology · doi:10.1038/s44320-024-00039-4 · Cited by 12

Differential Effects on the Translation of Immune-Related Alternatively Polyadenylated mRNAs in Melanoma and T Cells by eIF4A Inhibition

Biswas, B., Guemiri, R., Cadix, M., Labbé, C. M., Chakraborty, A., Dutertre, M., Robert, C., & Vagner, S. (2022) · Cancers · doi:10.3390/cancers14051177 · Cited by 12

Accurate transcriptome-wide identification and quantification of alternative polyadenylation from RNA-seq data with APAIQPreprint

Long, Y., Zhang, B., Tian, S., Chan, J. J., Zhou, J., Li, Z., Li, Y., An, Z., Liao, X., Wang, Y., et al. (2023) · Genome Research · doi:10.1101/gr.277177.122 · Cited by 12

Infernape uncovers cell type–specific and spatially resolved alternative polyadenylation in the brainPreprint

Kang, B., Yang, Y., Hu, K., Ruan, X., Liu, Y.-L., Lee, P., Lee, J., Wang, J., & Zhang, X. (2023) · Genome Research · doi:10.1101/gr.277864.123 · Cited by 11

U1 snRNP regulates alternative promoter activity by inhibiting premature polyadenylation

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Functional Polymorphism in Pak1–3′ Untranslated Region Alters Skin Tumor Susceptibility by Alternative Polyadenylation

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