Zhao J, Yang D, Qieqieke Y, Han N, Jieensi H
Curr Med Sci. 2024; 44(6):1325-1336.
PMID: 39565507
DOI: 10.1007/s11596-024-2943-6.
Kramarek M, Soucek P, Reblova K, Grodecka L, Freiberger T
Nucleic Acids Res. 2024; 52(10):5959-5974.
PMID: 38426935
PMC: 11162779.
DOI: 10.1093/nar/gkae147.
Lopez-Oreja I, Gohr A, Playa-Albinyana H, Giro A, Arenas F, Higashi M
Life Sci Alliance. 2023; 6(11).
PMID: 37562845
PMC: 10415613.
DOI: 10.26508/lsa.202301955.
Dybkov O, Preussner M, El Ayoubi L, Feng V, Harnisch C, Merz K
Sci Adv. 2023; 9(9):eadf1785.
PMID: 36867703
PMC: 9984181.
DOI: 10.1126/sciadv.adf1785.
Ebrahimie E, Rahimirad S, Tahsili M, Mohammadi-Dehcheshmeh M
World J Stem Cells. 2021; 13(10):1394-1416.
PMID: 34786151
PMC: 8567453.
DOI: 10.4252/wjsc.v13.i10.1394.
Nucleotides in both donor and acceptor splice sites are responsible for choice in NAGNAG tandem splice sites.
Hujova P, Soucek P, Radova L, Kramarek M, Kovacova T, Freiberger T
Cell Mol Life Sci. 2021; 78(21-22):6979-6993.
PMID: 34596691
PMC: 11072513.
DOI: 10.1007/s00018-021-03943-2.
Extensive Changes in Transcription Dynamics Reflected on Alternative Splicing Events in Systemic Lupus Erythematosus Patients.
Papanikolaou S, Bertsias G, Nikolaou C
Genes (Basel). 2021; 12(8).
PMID: 34440434
PMC: 8392844.
DOI: 10.3390/genes12081260.
An extended catalogue of tandem alternative splice sites in human tissue transcriptomes.
Mironov A, Denisov S, Gress A, Kalinina O, Pervouchine D
PLoS Comput Biol. 2021; 17(4):e1008329.
PMID: 33826604
PMC: 8055015.
DOI: 10.1371/journal.pcbi.1008329.
Impact of acceptor splice site NAGTAG motif on exon recognition.
Hujova P, Grodecka L, Soucek P, Freiberger T
Mol Biol Rep. 2019; 46(3):2877-2884.
PMID: 30840204
DOI: 10.1007/s11033-019-04734-6.
Targeted RNA-Seq profiling of splicing pattern in the DMD gene: exons are mostly constitutively spliced in human skeletal muscle.
Bouge A, Murauer E, Beyne E, Miro J, Varilh J, Taulan M
Sci Rep. 2017; 7:39094.
PMID: 28045018
PMC: 5206723.
DOI: 10.1038/srep39094.
Merging Absolute and Relative Quantitative PCR Data to Quantify STAT3 Splice Variant Transcripts.
Turton K, Esnault S, DeLain L, Mosher D
J Vis Exp. 2016; (116).
PMID: 27768061
PMC: 5092172.
DOI: 10.3791/54473.
Coding exon-structure aware realigner (CESAR) utilizes genome alignments for accurate comparative gene annotation.
Sharma V, Elghafari A, Hiller M
Nucleic Acids Res. 2016; 44(11):e103.
PMID: 27016733
PMC: 4914097.
DOI: 10.1093/nar/gkw210.
It's a bit over, is that ok? The subtle surplus from tandem alternative splicing.
Szafranski K, Kramer M
RNA Biol. 2015; 12(2):115-22.
PMID: 25826565
PMC: 4615896.
DOI: 10.1080/15476286.2015.1017210.
Alternative splicing at GYNNGY 5' splice sites: more noise, less regulation.
Wang M, Zhang P, Shu Y, Yuan F, Zhang Y, Zhou Y
Nucleic Acids Res. 2014; 42(22):13969-80.
PMID: 25428370
PMC: 4267661.
DOI: 10.1093/nar/gku1253.
Physiological state co-regulates thousands of mammalian mRNA splicing events at tandem splice sites and alternative exons.
Szafranski K, Fritsch C, Schumann F, Siebel L, Sinha R, Hampe J
Nucleic Acids Res. 2014; 42(14):8895-904.
PMID: 25030907
PMC: 4132704.
DOI: 10.1093/nar/gku532.
A subtle alternative splicing event gives rise to a widely expressed human RNase k isoform.
Karousis E, Sideris D
PLoS One. 2014; 9(5):e96557.
PMID: 24797913
PMC: 4010519.
DOI: 10.1371/journal.pone.0096557.
A naturally occurring insertion of a single amino acid rewires transcriptional regulation by glucocorticoid receptor isoforms.
Thomas-Chollier M, Watson L, Cooper S, Pufall M, Liu J, Borzym K
Proc Natl Acad Sci U S A. 2013; 110(44):17826-31.
PMID: 24127590
PMC: 3816441.
DOI: 10.1073/pnas.1316235110.
Alternative mRNA splicing generates two distinct ADAM12 prodomain variants.
Duhachek-Muggy S, Li H, Qi Y, Zolkiewska A
PLoS One. 2013; 8(10):e75730.
PMID: 24116070
PMC: 3792144.
DOI: 10.1371/journal.pone.0075730.
Discovery and mass spectrometric analysis of novel splice-junction peptides using RNA-Seq.
Sheynkman G, Shortreed M, Frey B, Smith L
Mol Cell Proteomics. 2013; 12(8):2341-53.
PMID: 23629695
PMC: 3734590.
DOI: 10.1074/mcp.O113.028142.
New insights from existing sequence data: generating breakthroughs without a pipette.
Plocik A, Graveley B
Mol Cell. 2013; 49(4):605-17.
PMID: 23438857
PMC: 3590807.
DOI: 10.1016/j.molcel.2013.01.031.