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Regulation of androgen receptor splice variant AR3 by PCGEM1.

Zhang Z, Zhou N, Huang J, Ho TT, Zhu Z, Qiu Z, Zhou X, Bai C, Wu F, Xu M, Mo YY.

Oncotarget. 2016 Mar 29;7(13):15481-91. doi: 10.18632/oncotarget.7139.


Mechanism of alternative splicing and its regulation.

Wang Y, Liu J, Huang BO, Xu YM, Li J, Huang LF, Lin J, Zhang J, Min QH, Yang WM, Wang XZ.

Biomed Rep. 2015 Mar;3(2):152-158. Epub 2014 Dec 17.


Mechanisms and Regulation of Alternative Pre-mRNA Splicing.

Lee Y, Rio DC.

Annu Rev Biochem. 2015;84:291-323. doi: 10.1146/annurev-biochem-060614-034316. Epub 2015 Mar 12. Review.


Accurate inference of isoforms from multiple sample RNA-Seq data.

Tasnim M, Ma S, Yang EW, Jiang T, Li W.

BMC Genomics. 2015;16 Suppl 2:S15. doi: 10.1186/1471-2164-16-S2-S15. Epub 2015 Jan 21.


The association of ADORA2A and ADORA2B polymorphisms with the risk and severity of chronic heart failure: a case-control study of a northern Chinese population.

Zhai YJ, Liu P, He HR, Zheng XW, Wang Y, Yang QT, Dong YL, Lu J.

Int J Mol Sci. 2015 Jan 26;16(2):2732-46. doi: 10.3390/ijms16022732.


Regulation of mRNA abundance by polypyrimidine tract-binding protein-controlled alternate 5' splice site choice.

Hamid FM, Makeyev EV.

PLoS Genet. 2014 Nov 6;10(11):e1004771. doi: 10.1371/journal.pgen.1004771. eCollection 2014 Nov.


Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses.

Schrimpf R, Dierks C, Martinsson G, Sieme H, Distl O.

PLoS One. 2014 Oct 29;9(10):e109675. doi: 10.1371/journal.pone.0109675. eCollection 2014.


The adenosine deaminase gene polymorphism is associated with chronic heart failure risk in Chinese.

He HR, Li YJ, He GH, Wang YJ, Zhai YJ, Xie J, Zhang WP, Dong YL, Lu J.

Int J Mol Sci. 2014 Aug 28;15(9):15259-71. doi: 10.3390/ijms150915259.


A comprehensive survey of non-canonical splice sites in the human transcriptome.

Parada GE, Munita R, Cerda CA, Gysling K.

Nucleic Acids Res. 2014;42(16):10564-78. doi: 10.1093/nar/gku744. Epub 2014 Aug 14.


The splicing activator DAZAP1 integrates splicing control into MEK/Erk-regulated cell proliferation and migration.

Choudhury R, Roy SG, Tsai YS, Tripathy A, Graves LM, Wang Z.

Nat Commun. 2014;5:3078. doi: 10.1038/ncomms4078.


Systematical identification of splicing regulatory cis-elements and cognate trans-factors.

Wang Y, Wang Z.

Methods. 2014 Feb;65(3):350-8. doi: 10.1016/j.ymeth.2013.08.019. Epub 2013 Aug 22.


Pick one, but be quick: 5' splice sites and the problems of too many choices.

Roca X, Krainer AR, Eperon IC.

Genes Dev. 2013 Jan 15;27(2):129-44. doi: 10.1101/gad.209759.112. Review.


A complex network of factors with overlapping affinities represses splicing through intronic elements.

Wang Y, Xiao X, Zhang J, Choudhury R, Robertson A, Li K, Ma M, Burge CB, Wang Z.

Nat Struct Mol Biol. 2013 Jan;20(1):36-45. doi: 10.1038/nsmb.2459. Epub 2012 Dec 16.


Intronic splicing enhancers, cognate splicing factors and context-dependent regulation rules.

Wang Y, Ma M, Xiao X, Wang Z.

Nat Struct Mol Biol. 2012 Oct;19(10):1044-52. doi: 10.1038/nsmb.2377. Epub 2012 Sep 16.


Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins.

Wang ET, Cody NA, Jog S, Biancolella M, Wang TT, Treacy DJ, Luo S, Schroth GP, Housman DE, Reddy S, Lécuyer E, Burge CB.

Cell. 2012 Aug 17;150(4):710-24. doi: 10.1016/j.cell.2012.06.041.


Identification of conserved splicing motifs in mutually exclusive exons of 15 insect species.

Buendia P, Tyree J, Loredo R, Hsu SN.

BMC Genomics. 2012 Apr 12;13 Suppl 2:S1. doi: 10.1186/1471-2164-13-S2-S1.


Alternative splicing of RNA triplets is often regulated and accelerates proteome evolution.

Bradley RK, Merkin J, Lambert NJ, Burge CB.

PLoS Biol. 2012 Jan;10(1):e1001229. doi: 10.1371/journal.pbio.1001229. Epub 2012 Jan 3.


Son maintains accurate splicing for a subset of human pre-mRNAs.

Sharma A, Markey M, Torres-Muñoz K, Varia S, Kadakia M, Bubulya A, Bubulya PA.

J Cell Sci. 2011 Dec 15;124(Pt 24):4286-98. doi: 10.1242/jcs.092239. Epub 2011 Dec 22.


Loss of exon identity is a common mechanism of human inherited disease.

Sterne-Weiler T, Howard J, Mort M, Cooper DN, Sanford JR.

Genome Res. 2011 Oct;21(10):1563-71. doi: 10.1101/gr.118638.110. Epub 2011 Jul 12.

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